field_job_occupational_field_parents_all

field_job_employment_type

job_organization_name

city

state

<h3>Job Description</h3>
Job Description
Principal Biostatistician
Statistics &amp; Data Corporation (SDC), a specialized contract research organization (CRO) headquartered in Arizona, delivering top-tier clinical trial services to pharmaceutical, biologic, and medical device/diagnostic companies since 2005. SDC providing a technology enabled service offering to provide clients with both clinical services expertise, as well as the technology they need to be successful in their clinical trials.
Job Location: AZ/MA/NC
Job Summary
Apply a high level of technical expertise to help guide and develop the more junior biostatistics staff members. Serve as a lead statistician on clinical studies and provide senior level peer review of work being accomplished by other biostatisticians in the department. Maintain the statistical and analytical integrity of clinical trials analyzed by SDC. Actively participate in writing statistical sections of protocols, preparing statistical analysis plans, preparing data deliverables for clinical study reports, interpreting analysis results, writing statistical sections of clinical study reports, and participating in meetings with drug regulatory agencies as required. Support business development and project management with strategic planning, proposals, pricing, and timeline planning.
Primary Responsibilities
• Serve as an internal consultant for biostatistics analysis tools and methods
• Serve as a subject matter expert during client and vendor meetings for biostatistics analysis support
• Actively support business development in capabilities presentations to prospective and current clients
• Effectively manage assigned clinical study budgets for biostatistics analysis support
• Develop, coach and mentor junior biostatistics department personnel
• Act as the lead statistician on clinical research projects and help with SAS programming
• Provide statistical expertise for study design of clinical trial protocols
• Write statistical methods section of the study protocol, as needed
• Write statistical analysis plans ensuring appropriate regulatory requirements and study objectives defined in the study protocol are followed
• Review CRFs to ensure consistency with protocol and statistical analysis plan (SAP)
• Program summary tables, data listings and graphical representations of clinical trials data
• Perform all analyses defined in the statistical analysis plan as well as any post-hoc analyses and relevant exploratory analyses of clinical trial data
• Prepare/review key sections of clinical study reports and various regulatory documents
• Perform statistical QC of all department outputs including analyses and clinical study reports
• Provide statistical support to answer questions from external clients (such as FDA, Investigators)
• Contribute to the development, maintenance, and training of standard operating procedures (SOPs)
• Represent the biostatistics department at regulatory meetings, sponsor meetings, and any other multifunctional meetings, as needed
• Manage biostatistics timelines, budgets, and client expectations
• Adhere to all aspects of the Statistics &amp; Data Corporation’s quality system
• Comply with Statistics &amp; Data Corporation’s data integrity &amp; business ethics requirements
• Perform other related duties incidental to the work described herein
• Adherence to all essential systems and processes that are required at SDC to maintain compliance to business and regulatory requirements
The above statements describe the general nature and level of work being performed by individuals assigned to this classification. This document is not intended to be an exhaustive list of all responsibilities and duties required of personnel so classified.
Requirements
Required Skills
• Effective leadership, budget forecast and implementation skills
• Excellent analytical skills, with the ability to process scientific and medical data
• Able to work independently and in teams
• Project management abilities including analytical evaluation, organization, delegation, flexible team management, negotiating and resource management skills
• Excellent knowledge of statistical programming
• Expertise in manipulating and analyzing SAS data
• Able to identify data issues, present problems, and implement solutions.
• Capable of communicating technical concepts clearly, concisely, and understandably to non-statistical colleagues and clients
• Excellent organizational and time management skills, with the ability to multi-task
• Familiarity with clinical trial design and analysis activities and basic knowledge of regulatory guidelines (FDA/CFR, ICH/GCP)
• Strong interpersonal communication and presentation skills
• Able to effectively collaborate across cross-functional teams
• Focus on quality at all times and in all situations
Education or Equivalent Experience
• A Master’s degree in biostatistics, statistics or other related, scientific field and at least eight years of relevant professional experience or a combination of education and experience.
Benefits
Why SDC
SDC is a team of diversified professionals who deliver exceptional Biometric Services, Consulting, and Technology Solutions to pharmaceutical, biologic, and medical device/diagnostic companies. Since 2005 our purpose has been to partner with sponsors to provide high quality and experienced team members to develop great medicines that save lives and cure diseases in the most efficient manner possible. Our global team operates as a value partner to our clients by fulfilling their needs as our own and delivering exceptional results. We are a specialty CRO in that we provide scalable service offerings, focused services area specialists, efficient project timelines, optimal technology solutions, and proven success and experience. Our commitment to our clients is the same commitment to our employees. By offering strong benefits including competitive pay, generous time off, attainable career advances, positive work/life balance and 401k matching (US), we are able to attract some of the most talented people in the industry. 
•We are committed to developing our employees. We recognize achievements, provide growth opportunities and career advancement, offer a flexible work schedule, engaging work culture and employee benefits. 
•We are passionate about our company culture. Our recognition program is directly tied to our core values of Energy, Integrity, Engagement, Innovation, Ownership, and Commitment. 
•We strive to provide a place of belonging to our employees with fun and engaging activities from SDC’s culture club.
•We are constantly growing and innovating to support our client and employee needs. Global in nature, we bring diverse perspectives enabling our growth in this ever-evolving industry. 
•With a proven track record, SDC has been successfully executing client clinical programs since 2005.
Take a look at how you can join our team!
#LI-Hybrid

Principal Biostatistician

<h3>Job Description</h3>
Job DescriptionSalary: 
JOB SUMMARY
The QC Microbiologist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols.
 
PRIMARY DUTIES AND RESPONSIBILITIES
<ul>
<li>Prepares and analyzes samples to determine microbiological quality through the following analyses: Microbial enumeration methods, absence of specified microorganisms, Sterility, endotoxin, and water quality analysis (bioburden, TOC, Conductivity).</li>
<li>Documents work in a clear and organized manner.</li>
<li>Revises procedures and ELNs under close supervision.</li>
<li>Follows all safety rules and regulations and conducts periodic safety audits.</li>
<li>Follows all cGMP rules and regulations.</li>
<li>Under close supervision confers with Microbiologists and other client personnel regarding research, procedures performed, related results and prepares reports.</li>
<li>Under close supervision will be trained to become proficient at assigned tasks in order to become subject matter experts.</li>
<li>Performs routine data generation and problem solving with a minimal rework.</li>
<li>Works under close supervision to ensure all work performed is executed in compliance with standard operating procedures, good manufacturing practices, and the regulations of the Food and Drug Administration.</li>
<li>Ensures all work performed strictly adheres to Company, client and Pharmacopeial methodologies.</li>
<li>Performs system maintenance and calibrations to ensure equipment is operating with specified requirements.</li>
<li>Proper handling of hazardous waste in compliance with the Company and DES hazardous waste rules.</li>
</ul>
REQUIREMENTS &amp; QUALIFICATIONS
Qualifications include a BA or BS degree in Microbiology or related science discipline with 0-2 years of related experience is required. Knowledge of cGMP and related compliance regulations and guidances is preferred.
 
SHIFT
Sunday-Wednesday, 1st shift.
 
MINIMUM SKILLS REQUIREMENTS
<ul>
<li>Must have the ability and skill to perform the detailed job requirements noted above competently, safely and proficiently.</li>
<li>A self-starter, motivated person who possesses good interpersonal skills capable of effectively interacting with all departments and client personnel.</li>
<li>Must have excellent organizational, verbal communication and technical documentation skills.</li>
<li>Solid computer skills.</li>
<li>Knowledge of safe laboratory practices, including the proper procedures in handling chemicals and samples.</li>
<li>Must be a team player with integrity and concern for the quality of Company products, services and staff members.</li>
</ul>

Microbiologist QC I

<h3>Job Description</h3>
Job Description
Location: Devens MA
Reports to: Director, Separations Sciences
FLSA Status: Exempt
Summary:
The Principal Application Scientist is responsible for conducting chromatography services, developing chromatographic methodology and providing technical insights to YMC America customers. This is a hands-on lab position that will utilize YMC chromatography products to conduct lab services mainly at internal YMC facilities and occasionally externally at customer sites. The developed insights will be used for promoting YMC products and for technical support / troubleshooting of clients who use YMC products.
The Principal Application Scientist will also be responsible for technical support of YMC chromatography media, technology and lab systems. They will be a “face of YMC technology” at customer sites and conferences. This will include support of instrument rentals, feasibility studies, methods development and other activities that enable customers to solve purification dilemmas by leveraging YMC technologies.
Responsibilities:
<ul>
<li>Conduct certain YMC America’s lab studies (Insight Services) under the direction of the Director, Separations Sciences. Lab facilities include those in Devens, MA and certain university collaborations. This role includes some instrument maintenance and support for the in-house lab/pilot facility.</li>
<li>Maintain a high-level working knowledge of YMC chromatography products (resins, columns, services and systems) and impart that understanding in the support of sales as a non-sales technical expert.</li>
<li>Assist in internal and external bench chromatography (CUBE) and pilot (TWIN) studies in the America’s. This includes the occasional on-site and remote set-up and training of lab instruments (Contichrom CUBE).</li>
<li>Influence potential customers to recognize the value and benefits of YMC resin and system technologies in a non-sales role.</li>
<li>Attend conferences and technical meetings as a representative of YMC America. </li>
<li>Deliver occasional presentations, papers and / or posters at industry events. Generate reports on competitive techniques and technologies.</li>
<li>Co-author white papers / applications notes that can be used to promote understanding of YMC products.</li>
<li>Assist in the review of results from external users of YMC products and provide feedback on how to better use the product in question.</li>
<li>Troubleshoot existing customer separation problems when their technical experiences / insights are applicable.</li>
<li>Play an active role in the development of new applications for existing analytical and prep products. </li>
</ul>
Required Experience &amp; Knowledge:
<ul>
<li>Bachelor’s degree in chemistry, chemical engineering, or a related field.</li>
<li>A minimum of three years’ experience as a lab scientist with an emphasis on Chromatography. </li>
<li>Must have a solid knowledge of chromatographic theory, techniques and associated instruments.</li>
<li>Hands-on experience with prep chromatography techniques and instrumentation. Particularly, as applied to peptide and/or oligonucleotide pharmaceutical compounds.</li>
<li>Ability to prioritize obligations, make self-directed decisions, multi-task, and function effectively with multiple deadlines. </li>
<li>Must be willing to travel up to 20% of the time.</li>
<li>Must possess strong documentation and technical writing skills and be able to apply relevant scientific principles and practices.</li>
<li>Must communicate clearly and concisely across levels, both orally and in writing, with a strong command of the English language.</li>
<li>Must be able to work under minimal supervision and able to work independently and in a team environment.</li>
</ul>
Preferred Skills and Experience:
<ul>
<li>A post-undergraduate degree in Chemistry, Chemical Engineering, or a related degree.</li>
<li>Experience of 3+ years performing lab services preferably related to the pharmaceutical industry, including some form of lab management responsibilities.</li>
<li>Working knowledge of automation systems for lab and production equipment in the life sciences related field.</li>
<li>Demonstrated experience in writing technical papers. Past publication experience is a plus.</li>
<li>Working knowledge of both large molecule biopharmaceutical processes and small molecule processes.</li>
<li>Language/communication skills with Spanish, German or Japanese is preferred.</li>
</ul>

PRINCIPAL APPLICATION SCIENTIST

<h3>Job Description</h3>
Job Description
Lantheus is headquartered in Bedford, Massachusetts with offices in New Jersey, Canada, and Sweden. For more than 60 years, Lantheus has been instrumental in pioneering the field of medical imaging and has helped physicians enhance patient care with its broad product portfolio. 
Lantheus is an entrepreneurial, agile, growing organization that provides innovative diagnostics, targeted therapeutics, and artificial intelligence (AI) solutions that empower clinicians to find, fight and follow disease. At Lantheus our purpose and values guide our behaviors in all interactions and play a vital role in creating a dynamic environment that contributes to our success. Every employee is crucial to our success; we respect one another and act as one knowing that someone’s health is in our hands. We believe in helping people be their best and are seeking to bring together a diverse group of individuals with different viewpoints and skill sets to be a part of a productive and inclusive team. 
Position Summary
Operates with a high degree of independence and is adept at conceptually outlining development, qualification, and life-cycle management studies with a focus on process analytical concepts to monitor and control critical steps in the manufacturing process of radiopharmaceuticals, ensuring consistent quality and safety meet current regulatory requirements on radiopharmaceutical drug products. Drives development and validation of new and improved radiochemical process controls in commercial processes; implements analytical methods and/or physicochemical characterizations in support of process development; radiolabeling processes and detection; and/or technology transfer to Contract Organizations. These efforts support the economical, efficient, and safe manufacture of radiolabeled precursors, bulk drug substances, and/or drug products. Lead PET CMO analytical operations and execution from late-stage development through site qualification. Engages in the development of complex strategies and testing requiring implementation of sophisticated, specialized scientific knowledge and advanced lab techniques, with latitude for independent judgment, decisions, and action. Radiopharmaceutical experience is preferred.
Essential Functions
<ul>
<li>Plans and drives multiple projects, requiring initiative and innovation, within Lantheus’ Quality system and governing regulations. Works on complex problems of diverse scope while serving as a technical analytical SME. Identifies, analyzes, and interprets project results. Evaluates results and examines implications to program.</li>
<li>Participate in technical troubleshooting sessions for processes and products manufactured in-house and at CMOs as needed and in investigating atypical/OOS results.</li>
<li>Performs routine laboratory, including working with radioactive materials, or oversees these actions at PET CMOs. Demonstrates ability to follow SOPs and Lantheus’ procedures as written. Tracks laboratory supplies and replenishes when needed. Maintains laboratory notebook, record keeping, and laboratory safety in accordance to common industry GLPs and Lantheus’, or CMO site, procedures.</li>
<li>Exhibits an increased understanding of radiochemistry, its regulations, stays aware of new scientific developments, and is able to incorporate these into their development/qualification activities.</li>
<li>Communicates scientific ideas and information in an appropriate and timely manner. Employs active listening skills to maintain clear communication to others. </li>
<li>Provides technical support to further program and Qualification activities at CMO/CROs; Authors technical transfer protocols and ensure acquired results are collected and documented according to cGMPs; Assists in completion of close-out reports and appropriate Change Controls. </li>
<li>Shows the ability and willingness to continually enhance functional and technical expertise. Assesses own strengths/ needs and learns from experience and feedback in order to continually enhance the level of functional and technical expertise. Takes action on developmental opportunities.</li>
<li>Accurately documents results in established formats. Able to write basic reports clearly and succinctly. Prepares written reports on all phases of laboratory and/or field experimental work. Presents results to colleagues at scientific meetings and to multidisciplinary audiences in program meetings. Writes comprehensive reports based on literature, lab and field data.</li>
<li>Maintains current knowledge of, and ensure all work activities are conducted in compliance with the full range of related internal and external systems, technology, regulatory requirements and related policies and procedures. Follows procedures to support intellectual property protection. May be responsible for preparing and defending patent disclosures and applications.</li>
<li>Actively promotes safety rules and awareness. Demonstrates good safety practices at all times including the appropriate use of protective equipment. Reports and takes initiative to correct safety &amp; environmental hazards.</li>
<li>Actively demonstrates the Lantheus values of Helping people be their best; Respect one another and act as one; Learn, adapt, and win; Know someone’s health is in our hands; and Own the solution and make it happen.</li>
</ul>
Typical Minimum Skills and Experience and Education 
<ul>
<li>Degree in Chemistry, Engineering, or related discipline or equivalent relevant industry experience.</li>
<li>Requires a minimum of a Ph.D. degree and 5+ years relevant industry work experience or a M.S. degree and 8+ years relevant work experience or a B.S. degree and 10+ years relevant industry work experience.</li>
<li>Scientific knowledge and experience in the technical aspects of radioanalytical chemistry and radiopharmaceutical process development and expertise in GMP documentation requirements with a working understanding of 21CFR 212 regulatory guidelines.</li>
<li>Previous experience working with radiopharmaceuticals and CMOs strongly preferred.</li>
</ul>
Other Requirements
<ul>
<li>Exceptional knowledge of scientific field of specialization. Familiar with Code of Federal Regulations parts 210 and 211 and supporting regulatory inspections.</li>
<li>Demonstrated skills in leading projects on an assigned team.</li>
<li>Able to properly handle and minimize exposure to potentially hazardous chemical, or radiological materials. Required to follow all safety procedures, and use personal and protective equipment provided.</li>
<li>Demonstrated competence in the design and documentation of complex experiments focused on a specific topic. Expanded scope to include multiple related questions for a given program.</li>
<li>Routine and or frequent lifting, with reasonable accommodations.</li>
<li>Demonstrated ability to effectively communicate ideas and information, both in oral and written form.</li>
<li>Travel (including international) is highly anticipated.</li>
</ul>
Lantheus is an equal opportunity employer that provides a workplace free from discrimination. All qualified applicants and employees are considered without regard to race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any other characteristic protected by law.
Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the Lantheus Talent Acquisition team at <a href="mailto:talentacquisition@lantheus.com" target="_blank">talentacquisition@lantheus.com</a>.

Senior Scientist II PET Analytical Development

<h3>Job Description</h3>
Job Description
Summary:
As a senior member of NCF’s Department of Ecological Research, Stewardship and Restoration, the Coastal Wetlands Research Ecologist is responsible for executing the Coastal and Wetland Ecology Research Program. They oversee research on the ecology of wetlands and coastal habitats related to restoration, habitat quality, ecosystem function, and resilience. Broad project topics include but are not limited to baseline coastal wetland habitat health, effectiveness of nature-based responses to climate change impacts, understanding impacts of climate change on coastal habitats, habitat restoration for function and improved resilience, and broad ecological research within the Program focus. 
Under the direction of the Vice President of Science and Stewardship, the Coastal Wetlands Research Ecologist is responsible for developing targeted inventory, monitoring and research projects related to their Program’s areas of interest (as described above) as well as overseeing and participating in the successful execution of these projects. They provide oversight, planning, and logistical support to NCF’s year-round Coastal Research Technician and related seasonal field staff. They also oversee and may participate in related research conducted by outside research partners working on NCF properties, work cooperatively on joint projects with other local and regional conservation organizations, and represent NCF on key committees, working groups and the like related to their program’s areas of expertise. 
The Coastal Wetlands Research Ecologist serves as a key senior member of the NCF Department of Ecological Research, Stewardship and Restoration, working closely and coordinating with senior level staff from the Wildlife Ecology, Plant Ecology and Botany, and Land Management and Stewardship Programs. Furthermore, they coordinate education, mentoring and outreach programming relevant to coastal wetland ecology in partnership with NCF’s Interpretive Education staff, contribute content to NCF’s social media, website, newsletters, annual reports, and other publications and provide team-oriented support for the successful implementation of NCF’s overall mission. 
Specific Responsibilities:
Staff Management
1. Supervise the Coastal Research Technician; assists in supervising seasonal field assistant(s) and volunteers working on coastal and wetland ecology related projects.
Coastal and Wetland Ecology Research
In coordination with the Vice President of Science and Stewardship, oversee all aspects of the Coastal and Wetlands Ecology Program of the NCF Department of Ecological Research, Stewardship and Restoration, including but not limited to the following: 
1. Provide leadership and strategic planning for current and future goals and projects related to the Program.
2. Develop and oversee the implementation of research, restoration and monitoring projects related to coastal and wetlands ecology and potential coastal resilience initiatives on NCF properties, including:
o Project design, field work, data collection and analysis, and interpretation and presentation of results in reports, scientific publications, and professional presentations.
o Staff oversight, delegation and support for all aspects of project implementation needed for success.
o Relevant grant opportunity identification and application for funding as opportunities arise.
3. Identify and target potential partnerships with academic and research institutions that complement the focus of the Coastal and Wetland Ecology Program, as well as the vision, mission and strategic goals of the overall department.
4. Represent NCF’s wetland ecology interests and coastal resilience initiatives at appropriate local and regional committees, working groups, professional networks and the like when appropriate.
5. Provide oversight and participate as appropriate in research conducted by outside investigators working on Foundation properties.
Stewardship, Land Management and Restoration
1. Play a leadership role in identifying, planning and implementing projects focused on wetland restoration and coastal resilience. 
2. Contribute expertise and collaborate on the development, planning and implementation of stewardship, land management and restoration projects on NCF properties.
3. Collaborate on joint projects with local and regional conservation organizations and governmental agencies involved in coastal resilience and coastal and wetland ecology projects, as needed.
4. Coordinate with NCF’s Department of Land Management regarding the need for land management staff and equipment support for Coastal and Wetland Ecology Program projects, as needed. 
Interpretive Education and Community Relations
1. Contribute content related to Coastal and Wetland Ecology Program projects to NCF’s website, social media outlets, newsletters, publications, press releases, video productions and the like, as well as outside requests for content.
2. Develop and participate in NCF’s interpretive education excursion programming aimed at providing experiences that educate participants in coastal resilience and wetland ecology, as well as other outside opportunities as they arise.
Development, Fundraising and Donor Relations
1. Work with the Vice President of Science and Stewardship to identify grant opportunities, write proposals and manage grant awards supporting NCF’s overall research, stewardship and restoration projects.
2. Participate as a senior department representative at fundraising, outreach and donor cultivation events to provide support for the Development Department’s efforts to connect donors with aspects of NCF’s mission that complement their interests.
Dates/Hours:
This is a full-time, year-round exempt position beginning in late-July 2025; exact dates are somewhat flexible. Hours are 40 hours per week, generally during normal business hours from Monday through Friday. Daily hours may be somewhat variable depending on particular projects: early-morning and late-night fieldwork may be required depending on weather, tides, etc. Weekend work will occasionally be required for certain field projects and non-profit events.
Field Work Environment:
A component of this position involves field work involving hiking, standing, bending, kneeling, and hauling field gear. Applicants should be accustomed to occasionally working in inclement weather or at sites with variable terrain, poison ivy, biting insects, etc. such as salt marshes and other wetlands. Nantucket is an area with a high incidence of tick-borne disease so precautions to minimize risk are encouraged. 
TO APPLY:
Applications accepted ONLY through our hiring website: <a href="https://apply.workable.com/nantucket-conservation-foundation/" target="_blank">https://apply.workable.com/nantucket-conservation-foundation/</a>
Application Packet: ONE PDF DOCUMENT including cover letter, resume, contact information for 3 professional references and an unofficial copy of your college transcripts. Incomplete application packets will not be considered. 
Application deadline is June 27, 2025, by 5pm. Applications will be reviewed on a rolling basis so apply early for consideration.
Click APPLY to job and fill out the form. Upload your Application Packet using the “Upload Resume” Link. 
Requirements
1. Master’s degree in Ecology, Botany, Wetland Ecology, Coastal Ecology, Natural Resource Management, Environmental Science, or a related biological/ecological field.
2. At least five years of relevant work experience post-graduate school.
3. Proven organizational skills and ability to independently prioritize, plan, lead and oversee multiple projects.
4. Experience in experimental design, field work (especially freshwater wetland and salt marsh field sampling in New England), data collection, quality control and data analysis (including statistics proficiency).
5. Working knowledge of community and ecosystem ecology; familiarity with plant and wildlife identification. 
6. Proven ability to effectively supervise, mentor, and develop team members, including providing feedback, setting performance goals, supporting professional growth, and fostering a positive, collaborative work environment.
7. Exceptional verbal and written communication skills, with the ability to convey complex information clearly and persuasively to diverse audiences, tailor messaging to different stakeholders, and produce high-quality reporting.
8. Collaboration experience and ability to work well in teams with others from a variety of experience levels to both efficiently execute projects and contribute to departmental strategic planning and oversight.
9. Proficiency with ArcGIS (ArcPro) and experience with interpreting and presenting geospatial research results, database management, map making, and the use of GPS units to collect data in the field.
10. Experience working with environmental monitoring loggers. 
11. Proficiency with Microsoft Office applications and data analysis software. 
12. Valid driver’s license required. 
Benefits
Salary commensurate with experience starting at $80,000, based on a 40-hour work week. Housing is provided in a shared, employee house at an adjusted rate -- salary is negotiable if housing is not needed. Work-related transportation is provided during working hours. Eligible to participate in the Foundation's full-time employee benefit plans and programs (subject to required waiting periods) including group health insurance, group life and accidental death insurance, disability insurance, dental insurance, 401K Plan, paid employee vacation and sick time, and paid holidays.

Coastal Wetlands Research Ecologist

<h3>Job Description</h3>
Job Description
John Turner Consulting (JTC), an environmental and engineering consulting firm serving New England, is seeking an experienced Senior Geologist to join our Portsmouth, NH office.
This is a strategic hire for a senior-level environmental professional ready to lead, mentor, and grow a team, with flexibility to work in a hybrid schedule.
Your Role
In this leadership role, you will oversee site investigation and remediation projects, supervise junior technical staff, and contribute to business development. You will bring a strong command of regulatory compliance at local, state, and federal levels, and have the potential to generate up to $1 million in annual revenue through project leadership and client management.
Responsibilities
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Lead environmental site assessments, investigation, and remediation projects throughout New England
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Prepare and review technical documents, including sampling plans, remedial action plans, and regulatory reports
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Manage and mentor junior staff, promoting professional development and safety
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Interface with regulatory agencies such as NHDES, MassDEP, MEDEP, and EPA
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Support and drive business development, including proposal writing and client outreach
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Maintain responsibility for project scope, budget, and schedule
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Contribute to strategic planning and help grow JTC’s environmental practice
Qualifications
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 15+ years in environmental consulting with increasing technical and leadership responsibilities
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; New Hampshire Professional Geologist (PG) required; multi-state licensure is a plus
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Demonstrated ability to maintain and grow a portfolio of work worth $1M+ annually
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Strong knowledge of environmental programs (RCRA, CERCLA, TSCA)
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Hands-on experience with New England environmental regulations and permitting
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Successful collaboration with local, state, and federal regulatory agencies
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Experience managing and mentoring junior staff
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Strong organizational and communication skills
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Bachelor’s degree in Geology, Environmental Engineering, or a related field required; Master’s degree preferred
Why Join JTC?
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Competitive 401(k) plan with company match
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Comprehensive medical, dental, vision, and prescription coverage
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Generous vacation, sick leave, holidays, and family medical leave
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Hybrid work environment with a balance of office, home, and field time
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Opportunities for advancement, mentorship, and professional development
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Collaborative, supportive culture committed to quality and safety

Senior Geologist

<h3>Job Description</h3>
Job Description
Boston Metal is commercializing cutting­­-edge­ extractive metallurgy technology that will revolutionize primary metals production by improving metal quality while decreasing cost and lowering environmental impact. This fast-paced startup company is looking for a Senior Scientist to join the team. 
The Senior Scientist will collaborate with the R&amp;D team on the laboratory-scale research programs as well as with the process, operations, and engineering teams for the development activities of full-scale industrial experiments.
Responsibilities include but are not limited to:
<ul>
<li>Lead the development of electrometallurgical processes for new products using new feedstocks for our Critical Metals program.</li>
</ul>
<ul>
<li>Carry out thermodynamic and electrochemical calculations to support process development.</li>
</ul>
<ul>
<li>Track metrics such as conductivity, voltage, current efficiency, and specific energy consumption. </li>
</ul>
<ul>
<li>Collaborate with process development, engineering, operations, and supply chain to keep a focus on scalability while optimizing process parameters. </li>
</ul>
<ul>
<li>Conduct experiments and analyze data on existing high temperature electrochemical testing setup.</li>
</ul>
<ul>
<li>Regular presentation and communication of results within the technical team, to senior management, and company-wide.</li>
</ul>
Requirements
Strong theoretical background in electrochemistry with proven ability to perform data analysis and first-principles modeling, track record in novel electrochemical research, demonstrated ability to independently plan and implement research programs.
7+ years of experience with electrochemical research or metallurgy in a technical environment. MS/PhD from accredited university or college in one or more of the following areas: Materials Science, Chemical Engineering, Chemistry, process metallurgy or a closely related field. 
<ul>
<li>Demonstrated technical leadership experience</li>
<li>Experience with experimental electrochemical cell setup and characterization</li>
<li>Familiarity with chemical engineering principles (e.g., mass and energy balances, thermodynamics, transport phenomena)</li>
<li>Experience developing a MATLAB or Python based data analysis pipeline, and using graphical plotting software for data analysis and visualization</li>
<li>Experience in research and working with large datasets </li>
<li>Materials or metallurgical research</li>
<li>Experience with high-temperature setup/system</li>
<li>Experience with thermodynamic modeling and calculations (FactSage preferred)</li>
<li>Analysis Scripting in Matlab or Python</li>
<li>Experience using Labview</li>
<li>Materials characterization</li>
<li>Portuguese language experience preferred</li>
<li>Intermittent travel to our Brazil facility </li>
</ul>
Benefits
Additional Information:
We are people first with a comprehensive benefits package that can be customized to fit your needs. Our full benefits package offers health, dental, vision, life and disability insurance, paid vacation, sick &amp; holidays, health savings account with a company contribution, dependent care account plan, paid parental and bonding leave and a 401k with company matching provision.
We are flexible with salary expectations for the Senior Scientist Critical Metals position, with a targeted range of $130 - $190K annually based on your experience and qualifications.
You will be working in a small team environment where teamwork and good relationships with other team members is critical. We operate pilot plants and labs and many of our staff members are required to wear Personal Protection Equipment (PPE) and you should be prepared to do so as well when necessary.
Boston Metal is an equal opportunity employer who considers all qualified applicants equally for employment. We do not discriminate on the basis of race, color, religion, national origin, age, sex, gender identity, sexual orientation, pregnancy or pregnancy-related condition, disability, ancestry, genetic information, veteran or military status, or any other characteristics protected by applicable federal, state or local law.

Senior Scientist Critical Metals

<h3>Job Description</h3>
Job DescriptionDEKA Research &amp; Development has an immediate opening for a Biocompatibility &amp; Toxicology Senior Scientist to join our team focused on medical device and combination product development. The individual in this role will work directly with Research &amp; Development, Regulatory &amp; Clinical Affairs and Quality Engineering to formulate and execute biocompatibility and toxicological evaluation strategies that support development objectives and world-wide regulatory approvals.&nbsp; How you will make a difference as a&nbsp;Biocompatibility &amp; Toxicology Senior Scientist:
<ul>
<li>Work in close association with customers and development teams to define and execute biocompatibility/toxicology evaluations, including establishing requirements for biological safety of medical devices and combination products</li>
<li>Lead the preparation and conduct of biocompatibility/toxicology test programs</li>
<li>Lead interactions with external consultants and contract laboratories including in-person meetings, teleconferences, and other communications as needed to support program objectives</li>
<li>Develop and deploy mechanisms to continually maintain state of the art knowledge and understanding related to biocompatibility and toxicological safety of medical devices, including relevant standards and test methods.&nbsp; Insure processes and procedures maximize resource efficiency and minimize time to market</li>
<li>Insure the organization stays up to date on global regulatory changes to medical device biocompatibility standards and requirements through monitoring regulatory authority and industry resources</li>
<li>Coach and mentor internal and external partners on effective strategies and tactics</li>
<li>Interface with customers on biocompatibility and toxicology issues</li>
</ul>
Skills you will need to be successful:
<ul>
<li>MS in a technically related field (toxicology, materials science, chemical engineering, biomedical engineering or related).</li>
<li>Minimum of 7 years direct work experience in a medical device and/or combination product development role with demonstrated success in planning and conducting biocompatibility and toxicological evaluations</li>
<li>Expertise in U.S. and international medical device biocompatibility requirements including ISO 10993 standards, Good Laboratory Practices, and guidance from regulatory authorities</li>
<li>Demonstrated practical knowledge of the laboratory methods and analytical techniques associated with medical device and/or combination product biocompatibility and chemical characterization evaluations</li>
<li>Demonstrated ability to establish consensus and work collaboratively across functions and development teams</li>
<li>Excellent written and verbal communication skills including the ability to effectively communicate at all levels of the organization and with external partners</li>
</ul>
About DEKA:
One hour from the beach, Boston, and the mountains, the historic Amoskeag Millyard once housed the largest textile mills in the world. It is now home to DEKA Research and Development, where we are taking the same innovation and cutting-edge technology into the modern age.
Behind DEKA’s brick walls sits a team of professionals who strive to make a difference every day through thoughtful engineering, design, and manufacturing. Here at DEKA, some of the most innovative and life-changing products of our time are created, and new ideas are always welcome and explored.
 &nbsp;
Powered by JazzHR
5oUNcxSkY2

Biocompatibility & Toxicology Senior Scientist

<h3>Job Description</h3>
Job Description
Who We Are: 
At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented and diverse workforce in our industry. Our commitment to uncompromising focus on quality, compliance, safety, and excellence in delivery shapes everything we do. We are not just looking for skills; we are seeking innovative individuals who have a mindset open to learning and growth, and a desire to make a difference.
Veranova is a global leader in the development and manufacturing of complex active pharmaceutical ingredients (APIs) for pharma and biotech customers. With deep technical expertise and impressive flexibility, we develop solutions and processes that support and accelerate innovation. 
Join us on our mission to enable current and next-generation therapeutics to improve and save the lives of patients. 
Role Overview:
The Scientist I - Process Research &amp; Development (PRD) is responsible for conducting small to large scale chemical reactions to optimize synthetic routes of active pharmaceutical ingredients (APIs) under the direction of project technical leads to deliver projects on target with quantity, quality, time, and within budget.
Core Responsibilities: 
<ul>
<li>Delivers experimental output with a high scientific integrity, both on time and target, and of high quality with guidance. </li>
<li>Exhibits safety awareness, safely conducts lab and other operations and hold themselves accountable for safe behavior in the work environment. </li>
<li>Maintains technical equipment and services.</li>
<li>Acts on feedback and show continuous commitment to learning and development.</li>
<li>Lead technical and operational areas and support troubleshooting for complex scientific issues under minimal guidance.</li>
<li>Expertly shares knowledge, skills and experience, communicating internally and externally. May lead focused projects as key contact. </li>
<li>Keeps accurate, legible and complete records of all experiments, observations, and equipment. </li>
<li>Writes high quality reports and delivers presentations to customers and management with some guidance in alignment with project milestones.</li>
<li>Contributes to sustaining good customer relations and identifies new commercial opportunities.</li>
<li>Actively contributes to the technical development of the department and company.</li>
<li>Accomplishes additional duties within the employee’s skills and abilities per reasonable request.</li>
</ul>
Qualifications: 
Required
<ul>
<li>PhD degree (or equivalent experience) in a chemistry related discipline.</li>
<li>2+ years hand on experience with PhD; 5+ years hand-on experience if Master's degree.</li>
<li>Proficiency with relevant lab and analytical techniques.</li>
<li>Previous industry experience in relevant areas.</li>
<li>Proficiency with relevant analytical techniques within an industry environment.</li>
<li>Ability to write clear and concise technical reports.</li>
<li>Good understanding of Microsoft Office and other relevant technical software platforms</li>
<li>Skilled in written and spoken communication and proven ability to effectively interact with management. </li>
<li>Demonstrates good judgment, quick decision-making skills, and the ability to work independently and in a team environment.</li>
</ul>
Physical Demands &amp; Work Environment:
<ul>
<li>Stand, walk, and manually operate objects, tools, or controls; reach with hands or arms; climb, balance, stoop, kneel, or crouch when necessary for the job activity.</li>
<li>Lift and/or move up to 50 pounds.</li>
<li>Specific vision abilities include near, distance, peripheral, color perception, and the ability to adjust focus.</li>
<li>Regularly work with moving mechanical parts and may work with toxic or caustic chemicals. </li>
<li>The work may be performed in humid areas with low or high temperatures. </li>
<li>This work may need to work with a respirator or operate with full-body Tyvek suits and supplied air or PAPR.</li>
</ul>
Our Commitment:
<ul>
<li>Health &amp; Wellness: Comprehensive health &amp; Wellness benefits. Access to mental health resources and wellness programs. Generous PTO and holiday pay policies. </li>
<li>Financial Wellness: Comprehensive total compensation package that includes competitive base salary, Defined Contribution Pension program, eligibility for performance-based bonuses, and attractive 401(k) Plan with company match.</li>
<li>Professional Development: Opportunities for continuous learning through LinkedIn Learning, workshops, conferences, and mentorship. Tuition Assistance for Undergraduate and Graduate degree programs.</li>
<li>Inclusive Culture: At Veranova an inclusive culture is integral to our values. We are committed to ensuring that everyone can bring their full self to work and thrive in their career.</li>
</ul>
How to Apply: 
At Veranova, we are on a mission to meet people that believe in our values and can contribute to the team in a variety of ways. Please visit <a href="http://www.veranova.com" target="_blank">www.veranova.com</a> to view all open roles and join our Talent Community to stay connected and learn about opportunities as they arise. 
We value a range of experiences and perspectives. If you want to be part of improving and saving the lives of patients, we encourage you to apply regardless of whether you meet every qualification listed. 
If you are a veteran, first responder, or in the process of transitioning from service member to civilian life, we encourage you to apply. Your experience brings invaluable skills and insights that can contribute to our team.
For applicants who may require a reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email to <a href="mailto:talentacquisition@veranova.com" target="_blank">talentacquisition@veranova.com</a> in order to confirm your request for an accommodation. Please include the job number, title, and location of role. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Veranova employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Additional Information:
Applicants for this role must be authorized to work in the United States without further employer sponsorship.
Agency and Search Firm Representatives: Veranova does not accept unsolicited resumes from agencies and/or search firms for this job posting. 
Important Notice Regarding Recruitment Scams: Veranova is committed to providing a professional and secure recruitment experience for all applicants. Unfortunately, fraudulent job postings and recruitment scams are becoming more prevalent. We want to ensure that all candidates are aware of potential scams. Please see our notice here.
<ul>
<li>Legitimate communications from Veranova will only come from official email addresses using our domain: @veranova.com.</li>
<li>Legitimate LinkedIn communications will only come from active Veranova employees.</li>
<li>Veranova will never ask candidates for sensitive personal information during the application process (e.g., bank account details or social security number).</li>
<li>Veranova will never ask candidates for payment (e.g., for equipment, training, or background checks).</li>
</ul>
If you have any doubts or concerns about the authenticity of a job posting, please reach out to our HR department: <a href="mailto:pharm.hr@veranova.com" target="_blank">pharm.hr@veranova.com</a> (US) or <a href="mailto:UKHR@veranova.com" target="_blank">UKHR@veranova.com</a> (UK).
All your information will be kept confidential according to EEO guidelines.
Veranova is an Equal Opportunity Employer. It is the policy of Veranova to provide equal employment access and opportunity to all persons regardless of age, race, color, national origin, religion, sex, sexual orientation, gender identity and/or expression, physical or mental disability, genetic information, citizenship, marital status, veteran status, or any other characteristic protected by federal, state, or local law.
All applications are carefully considered, and your details will be stored on our secure Application Management System. This is used throughout Veranova for the selection of suitable candidates for our vacancies as they arise. Veranova respects your privacy and is committed to protecting your personal information. For more information about how your personal data is used please view our privacy notice.

Scientist - Process Research & Development

<h3>Job Description</h3>
Job DescriptionRepertoire Immune Medicines is a biotechnology company working to unlock and direct the remarkable power of the human immune system to treat cancer and autoimmune disease. The company&nbsp;was&nbsp;founded on the belief that&nbsp;understanding&nbsp;the repertoire of T cell receptor (TCR)-antigen&nbsp;immune synapses&nbsp;that maintain health and drive disease represents one of the greatest opportunities for innovation in medical science. Repertoire scientists created and developed the DECODETM&nbsp;platform, which allows in-depth characterization of TCR-antigen pairs, and the ability to&nbsp;deploy this information in the form of&nbsp;novel targeted immune medicines&nbsp;to fundamentally reprogram the immune system to kill tumors or induce immune homeostasis. From its sites in Cambridge, Massachusetts and Zurich, Switzerland, Repertoire’s team is advancing a pipeline of DECODE-enabled immune medicines. For cancer, we are developing a pipeline of TCR bispecifics molecules for treatment of multiple cancer types. Repertoire is progressing through IND-enabling studies with its lead development candidate and is planning to initiate a Phase 1/2 clinical trial in multiple cancer indications.&nbsp; In addition, we are developing a pipeline of mRNA tolerizing vaccines for treatment of autoimmune diseases. Repertoire was founded&nbsp;in 2019 by Flagship Pioneering and&nbsp;is supported by a strong investor base.&nbsp; The company entered into a collaboration and license agreement with Genentech in April of 2025 to discover and develop innovative T cell-targeted immune medicines for an autoimmune indication.&nbsp; In addition, Repertoire entered a strategic partnership in April of 2024 with Bristol Myers Squibb to develop tolerizing vaccines for up to three autoimmune diseases.&nbsp; Principal Scientist/Associate Director, Translational Sciences (Oncology) We are seeking a highly motivated and experienced Principal Scientist/Associate Director in Translational Sciences that will be responsible for developing, implementing, and executing cross-functional activities to bridge preclinical and clinical development programs, across multiple therapeutic areas and drug modalities. A successful candidate will have a deep knowledge and focus on protein therapeutics, immune-oncology drug development, and genomic capabilities.&nbsp; Reporting to the Vice President, Project Lead and Head of Translational Medicine, this accomplished professional will have deep expertise in biomarkers in oncology to lead the design, implementation, and oversight of biomarker strategies for Phase I clinical trials in solid tumors. The ideal candidate will have a strong background in circulating tumor DNA (ctDNA), genomic profiling, and immune/DNA-based assays, as well as hands-on experience managing biomarker vendors and ensuring high-quality execution of exploratory biomarker analyses. Key Responsibilities 
<ul>
<li>Design and execute translational biomarker strategies to support mechanism-of-action, PK/PD, dose predictions, and patient stratification in Phase I/II first-in-human oncology trials.</li>
<li>Integrate preclinical and clinical data to generate hypotheses and guide data-driven decision-making in early development.</li>
<li>Lead development and implementation of exploratory and translational biomarkers, including immune profiling, ctDNA, and genomic assays, with a strong understanding of solid tumor biology.</li>
<li>Evaluate and oversee protein biomarker assays relevant to therapeutic response and resistance.</li>
<li>Manage external vendors and CROs for biomarker assay development, sample testing, and data delivery; ensure high-quality execution and troubleshooting as needed.</li>
<li>Oversee sample logistics (tumor tissue, liquid biopsies) to ensure integrity and timely analysis.</li>
<li>Partner closely with Clinical Development and Discovery Research teams to ensure translational plans align with clinical objectives and regulatory strategies.</li>
<li>Work closely with leadership to develop, manage, and deliver translational research timelines, budgets, metrics, and milestones.</li>
<li>Demonstrate a strong work ethic and ability to work well in team environment.</li>
<li>Communicate key findings and recommendations to senior leadership.</li>
</ul>
 Qualifications 
<ul>
<li>PhD, MD, or equivalent in cancer biology, oncology, immunology, molecular biology, or related field.</li>
<li>8+ years of biotech/pharma experience in translational sciences or biomarker research, ideally in a biotech or pharmaceutical environment.</li>
<li>Deep understanding of solid tumor biology, immune biomarkers, and ctDNA/genomic analysis, along with hands-on experience managing biomarker execution in early-phase clinical trials.</li>
<li>Strong understanding of drug development for protein therapeutics and immune-oncology mechanisms.</li>
<li>Demonstrated experience supporting Phase I/II first-in-patient clinical studies.</li>
<li>Experience incorporating ctDNA endpoints into Phase I/II oncology clinical trials, including exploratory biomarker strategies and regulatory considerations.</li>
<li>Experience transferring and overseeing assays at CROs or central labs.</li>
<li>Working knowledge of pharmacokinetics (PK) and anti-drug antibody (ADA) assessments for protein therapeutics, and ability to integrate PK/ADA findings with biomarker and clinical data to guide early development decisions.</li>
<li>Hands-on or oversight experience with circulating tumor DNA (ctDNA), including use in solid tumor clinical trials for patient stratification and treatment response monitoring.</li>
<li>Entrepreneurial mindset, excellent communication skills, and passion for advancing new therapies for patients.</li>
</ul>
The base salary for this role ranges from $150,000 to $215,000&nbsp;and is determined based on a candidate’s skills, experience, and internal equity. In addition to a competitive base salary, Repertoire offers a broad range of benefits designed to attract, retain, and motivate top talent, including medical, dental, vision, and life insurance, flexible time off, a 401(k) retirement plan, and short- and long-term incentive opportunities. Compensation and benefits are based on Repertoire’s good faith estimate at the time of publication and may be updated in the future. &nbsp;Repertoire is committed towards social responsibility and developing an inclusive culture.&nbsp; Much as the power of the immune system lies in the diversity of T and B cells, our work requires the creativity and ingenuity of a diverse workforce.&nbsp; We believe in actively pursuing equity in all facets of the work experience at Repertoire.&nbsp; We will continue to educate ourselves about the inequities and barriers present in our society and take action as a company where we can make a difference. Repertoire is proud to be an Equal Opportunity Employer. Recruitment &amp; Staffing Agencies: Repertoire Immune Medicines (“Repertoire”) does not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to Repertoire or its employees is strictly prohibited unless contacted directly by Repertoire’s internal Human Resources team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of Repertoire, and Repertoire will not owe any referral or other fees with respect thereto.
Powered by JazzHR
Sc8SLX5mN7

758 Science Jobs