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<h3>Job Description</h3>
Job Description
EnSafe is seeking a Senior Hydrogeologist to join our team of environmental professionals working on complex and rewarding projects across the country based out of any of EnSafe’ s offices listed.
EnSafe is an employee-owned global environmental consulting and engineering firm. We strive to provide cutting-edge, creative solutions for our clients. EnSafe specializes in custom solutions in Environmental Management and Planning, Civil Design Engineering, Environmental Restoration, Natural &amp; Water Resources, Health &amp; Safety, and Technology, with offices operating within the U.S. 
What We Are Looking For
As Senior Hydrogeologist, you will lead and contribute to multidisciplinary projects involving environmental site investigation, remediation, groundwater modeling, and regulatory compliance. We offer a workplace culture that promotes autonomy, continuous learning, and professional growth. 
What You Will Be Doing: 
<ul>
<li>Designing, directing, and executing complex site investigations, including the planning and implementation of drilling, geophysical logging, aquifer testing, sampling of various media, and installation of monitoring and recovery wells.</li>
<li>Leading project teams in developing conceptual site models and conducting contaminant fate and transport evaluations.</li>
<li>Managing and overseeing field activities, ensuring health and safety compliance, subcontractor coordination, and efficient scheduling.</li>
<li>Interpreting hydrogeologic data and synthesizing field and analytical results to support reporting, risk assessments, remedial design, and regulatory decision-making.</li>
<li>Practical use of advanced groundwater models to support site characterization and remediation/optimization strategies.</li>
<li>Writing and reviewing technical reports, work plans, sampling plans, and standard operating procedures (SOPs).</li>
<li>Serving as a technical advisor, mentoring junior staff, performing quality control reviews, and helping the next generation of hydrogeologists grow.</li>
<li>Interfacing with clients and regulatory agencies as a subject matter expert, providing strategic guidance, presenting findings, and supporting negotiations.</li>
<li>Performing optimization of passive and active remedial alternatives, including LTM.</li>
<li>Building, calibrating, and validating analytical and numerical soil, groundwater, surface water, sediment, and indoor air (attenuation) modeling.</li>
<li>Providing litigation support for discovery, affidavits, deposition, and trial.</li>
<li>Performing sequence stratigraphy evaluations and reporting.</li>
<li>Performing statistical evaluations, background studies, and associated reporting.</li>
<li>Travel up to approximately 30% may be required, including occasional overnight trips.</li>
</ul>
What You Will Need:
<ul>
<li>Bachelor's or Master’s degree in Hydrology, Hydrogeology, Geology, Engineering, or a closely related field.</li>
<li>15–20 years of professional experience, preferably in environmental consulting. </li>
<li>Professional Geologist or Engineer licensure (by exam).</li>
<li>Strong background in hydrogeologic site characterization, groundwater flow and transport modeling and analysis, and environmental remediation/remedy optimization.</li>
<li>Proficiency with regulatory programs including CERCLA, RCRA, and state-specific programs.</li>
<li>Demonstrated ability to lead projects and teams, manage multiple priorities, mentor/supervise employees, and communicate effectively with diverse audiences.</li>
<li>Advanced skills in data analysis, report writing, and preparation of maps, tables, charts, and figures.</li>
<li>Experience using hydrogeologic modeling tools, including but not limited to MODFLOW, MT3D codes, VISTAS, EVS, etc. </li>
<li>Familiarity with GIS applications.</li>
<li>Excellent verbal and written communication skills. </li>
<li>Current 40-hour HAZWOPER certification.</li>
</ul>
About EnSafe
EnSafe began as a two-person firm in 1980, navigating complex regulatory compliance issues on behalf of our clients. We nurture our people with growth and development opportunities. We build enduring, trustful relationships with each of our clients, with a focus on high ethical and safety standards. We build this reputation by attracting high-quality people and retaining them for the long term.
At EnSafe, we are dedicated to building a diverse, inclusive, and authentic workplace, so if you’re excited about this role but your past experience doesn’t align perfectly with every qualification in the job description, we encourage you to apply anyway. You may be just the right candidate for this or other roles at our company.
EnSafe is committed to being an EEO employer and all qualified candidates will receive consideration without regard to race, color, religion, national origin, citizenship, age (except for bona fide occupational qualifications), sex, disability, sexual orientation, gender identity, marital status, military or veteran status, any other status protected by federal, state, or local law, or association with a person on the basis of one or more of the foregoing.
Check us out on the web at <a href="http://www.ensafe.com" target="_blank">www.ensafe.com</a>
#LI-MR1

Senior Hydrogeologist

<h3>Job Description</h3>
Job DescriptionDescription:

Kula Bio is at the forefront of sustainable agriculture, providing pioneering nitrogen solutions that empower farmers to increase crop yields and support environmental stewardship. Our cost-effective biofertilizer leverages and enhances a natural process to deliver significant, sustained nitrogen to the soil.
 
 As a Research Associate you will work with the Discovery and Product Development team to plan and execute plant trials to validate product efficacy and test product prototypes. This role will focus on development, implementation, and data collection from plant assays that will lead to understanding the performance of the product. On a regular day, you will support validation of product efficacy through experimental design and set-up. You will implement crop growth protocols, handle microbial cultures, collect assay data, and present results. You will cultivate plants in controlled environmental conditions, monitor plant health and collect key data on plant growth, use and maintain laboratory equipment, and work closely with the broader team in a collaborative effort to meet project goals and timelines.
Requirements:

Qualifications:
<ul>
<li>BS in Plant Biology, Plant Science, Agronomy, Crop Science, Horticulture, or related sciences with at least 1 year of relevant hands-on research experience.</li>
<li>Experience working in greenhouses, controlled environmental chambers, and research fields.</li>
<li>Experience with plant care and maintenance including seed germination, propagation, seedling care, transplantation, nutrient and fertilizer delivery, plant phenotyping, and stress monitoring.</li>
<li>Ability to perform hands-on work in greenhouse, outdoor, and laboratory environments, including standing for extended periods and lifting moderate weights up to 50 lbs. (e.g., trays, soil, supplies).</li>
<li>Skilled at implementing standard experimental protocols and workflows including appropriate application of nutrients and/or amendments according to experimental design. Experience working in wet lab settings and practicing safe handling of chemicals and biologicals.</li>
<li>Experience with good aseptic technique including handling microorganisms or microbial products under sterile conditions.</li>
<li>Proficiency in data collection, management, and presentation including experience in use of Excel and PowerPoint – experience with Prism or other statistical analysis software is ideal.</li>
<li>Proficiency in lab record keeping including good note taking practices – experience with electronic lab notebooks like SciNote is ideal.</li>
<li>Strong critical thinking skills, demonstrating an ability to identify failure points, troubleshoot experiments, and propose practical solutions.</li>
<li>Strong communication skills and the ability to clearly communicate progress, challenges, and results.</li>
<li>Willing to work in a collaborative, timeline-driven environment.</li>
</ul>
 
Salary range $60,000 - $65,000 per year

Research Associate - Plant Trials

<h3>Job Description</h3>
Job Description
POSITION SUMMARY:&nbsp;
<ul>
<li>We are seeking a scientist to join our Systems Immunology Lab in Client Inflammation &amp; Immunology Research Unit. The successful candidate will be responsible for generating massive single-cell perturbational data using functional genomics and single cell transcriptomics technologies in collaboration with a small team.</li>
</ul>
&nbsp;
POSITION RESPONSIBILITIES:&nbsp;
<ul>
<li>Generate custom lentiviral libraries and maintain extensive&nbsp;cell cultures. Generate edited pools of cells via lentiviral transduction and arrayed electroporation. Develop, modify, and customize such procedures as needed to succeed in specific cell lines and types, and at large scale.</li>
<li>Generate single-cell data via several commercial workflows, including from 10x Genomics.</li>
</ul>
&nbsp;
ORGANIZATIONAL RELATIONSHIPS:&nbsp;
<ul>
<li>Reports to a lead scientist in Systems Immunology Lab.</li>
<li>Collaborates with and supports several multi-disciplinary experimental teams on a per-project basis.</li>
</ul>
&nbsp;
EDUCATION AND EXPERIENCE:&nbsp;
<ul>
<li>Bachelors or Masters + 3 years of experience in Biology, Immunology, or a related field</li>
</ul>
&nbsp;
TECHNICAL SKILLS REQUIREMENTS:&nbsp;
<ul>
<li>3+ years of hands-on experience with standard cell culture techniques including primary&nbsp;immune cells&nbsp;handling and isolation, maintenance of cell lines and in vitro stimulation of primary immune cells, experience with standard molecular biology techniques including lentivirus infection, qPCR, western blot, and flow cytometry.</li>
<li>Bonus: direct experience in pooled cell screening of immune cells using CRISPRi, CRISPRa, and other methods of in vitro gene editing.</li>
</ul>
&nbsp;
PHYSICAL POSITION REQUIREMENTS:&nbsp;
<ul>
<li>Typical bench work, including sitting, pipetting, lifting ?10lb items Interview Process: 1st Teams screen (Camera-On) 2nd Onsite (2hr with Stakeholders) Duration: 6-</li>
</ul>
Company DescriptionLanceSoft is a certified Minority Business Enterprise (MBE) and an equal opportunity employer. 
<h3>Company Description</h3>
LanceSoft is a certified Minority Business Enterprise (MBE) and an equal opportunity employer.

Exception - Professional Scientist

<h3>Job Description</h3>
Summary:
Entry-level Lab Scientist role within an Immunology team, ideal for recent graduates with a background in biology, immunology, or biotechnology. The position supports hands-on experimental work involving immune cell isolation, sterile cell culture, differentiation, flow cytometry, and functional immune assays.
 
Key responsibilities include isolating primary immune cells, maintaining and differentiating cell cultures, preparing and analyzing flow cytometry samples, and conducting immune cell–based functional and cytotoxicity assays. The role requires strong attention to detail, adherence to SOPs and biosafety practices, and effective collaboration within a research team.
 
Preferred candidates have exposure to immune assays, flow cytometry data analysis, and are eager to learn advanced immunology techniques in a collaborative research environment.

Biologist

<h3>Job Description</h3>
Job DescriptionRole Summary
<ul>
<li>Responsibilities: You will be responsible for devising and performing statistical analysis plans and then communicating the methodologies and results of these to our clients in the healthcare sector</li>
<li>Salary: $73,000 to $76,000 depending on qualifications and previous experience</li>
<li>Benefits: Discretionary profit share bonuses paid twice per year, hybrid and flexible working options, generous vacation allowance, private medical and dental insurance, 401K plan with up to a 5% employer contribution, life insurance, full funding and study leave for external training and more</li>
<li>Role Type: Full-time, permanent </li>
<li>Start Date: We are currently recruiting for start dates in early 2026 and you will be asked to state your availability on your application form</li>
<li>Application Deadlines: Whilst there are no set application deadlines, we strongly recommend applying as early as possible. The role, or particular start dates, may close when suitable candidates are found</li>
<li>Location: This role is available in our Boston office </li>
</ul>
About the Role
Our Statistics team provide statistical and analytical expertise across Costello Medical, devising statistical analysis plans and performing data analysis within R, Excel, Stan, SQL and BUGS software. They are also responsible for communicating the methodologies and results in both written and oral formats to drug and device manufacturers, and doctors. The statistical analyses vary across patient-level clinical trial data, observational study (real-world) data, and published aggregate data. Our work involves a range of techniques such as basic statistical analysis of individual patient data, regression analysis, survival analysis and complex Bayesian network meta-analysis using both standard and emerging methods.
You will work in project teams alongside colleagues from all specialities to ensure that statistics projects are completed to an exceptionally high standard, on time and in line with client expectations. You will receive training in the technical aspects of the role, project management skills and effective client communication. Delivering project work requires close collaboration with clients and, following a successful induction period, you will increasingly participate in client calls and face-to-face meetings with external stakeholders. 
Our team typically work on several projects at one time and the results of each analysis can feed into publications, value materials, health economic models or health technology assessment submissions. You will therefore be exposed to a wide variety of our services and a broad range of therapeutic areas. To read more about our recent articles and publications, please visit our website: <a href="https://www.costellomedical.com/research/articles-publications/" target="_blank">https://www.costellomedical.com/research/articles-publications/</a>
Hybrid Working Policy: We believe that having face-to-face time in the office holds many benefits and is central to ensuring that the community we have created, where people have a workplace they belong to and feel part of, is never lost. At the same time, we recognize that homeworking can improve work life balance, reduce commuting times and costs, and provide the opportunity to juggle personal commitments. Therefore, we offer flexible working arrangements that allow our colleagues to work from home for up to half of the time, measured across a 2-week rolling period. Please note that as part of our wider flexible working policy, employees may work outside of Massachusetts for up to 4 weeks annually
A Day in the Life of a Statistician
To learn more about a typical day for a Statistician at Costello Medical, please click here: <a href="https://www.costellomedical.com/day-in-the-life/statistician.html" target="_blank">https://www.costellomedical.com/day-in-the-life/statistician.html</a>
Career Profile
We offer many opportunities for personal and professional development at Costello Medical. Please click below to read firsthand accounts from our colleagues about their time with the company: <a href="https://www.costellomedical.com/careers/working-at-costello-medical/" target="_blank">https://www.costellomedical.com/careers/working-at-costello-medical/</a>
About Costello Medical
Costello Medical is a rapidly growing global healthcare agency specializing in medical communications, market access and health economic and outcomes research. We work with a wide range of clients, including the industry’s most successful pharmaceutical and medical technology companies, patient and public health bodies and charitable organizations. We have been listed in the Top 100 Best Companies to Work For list since 2017, the Boston Globe’s Top Places to Work list in 2025, and were proud to receive B Corporation accreditation in 2022. Please click here to learn more about us, our work and our mission: <a href="https://www.costellomedical.com/" target="_blank">https://www.costellomedical.com/</a>
Requirements
About You
The successful candidate will be someone who enjoys problem solving and thinking outside the box to develop innovative solutions. In line with the company’s values, you will be passionate about improving patient outcomes by applying your statistical knowledge and technical skills to the healthcare industry.
Essentialrequirements for the role are:
<ul>
<li>A degree level or higher qualification in a scientific or mathematical discipline (minimum GPA 3.3) with a focus on statistics and data analysis. </li>
<li>Proficiency in the R programming language, and the willingness and ability to rapidly develop your programming skills</li>
<li>The technical and mathematical ability, coupled with the written and oral communication skills, to explain complex techniques and results to non-experts</li>
<li>A willingness to trial, explore or recommend new software or techniques that may suit specific projects</li>
<li>A high degree of accuracy and attention to detail, along with the ability to maintain a high level of customer service and the quality of deliverables under multiple competing demands</li>
<li>A high level of organisation, with the flexibility to respond to changing deadlines</li>
<li>The ability to use your initiative and work independently, in addition to working collaboratively within project teams</li>
<li>Excellent written English, which will be assessed during the selection process</li>
</ul>
Desired requirements for the role are:
<ul>
<li>A Masters degree or PhD in a scientific or mathematical discipline </li>
<li>Experience with Python Stan, SQL</li>
<li>Experience in and/or knowledge of medical data, clinical processes or trials</li>
</ul>
Joining Costello Medical from Academia
At Costello Medical, we warmly welcome applicants from academia who are looking to transitioning into a role within a commercial, industry-based setting. We understand the unique perspectives and valuable skills that academic professionals bring to our team. To support your career change, we offer comprehensive training, mentorship programs, and a work culture that fosters collaboration, growth and innovation. We are committed to facilitating a smooth transition and helping you thrive in an industry-based setting.
Many of our team members have successfully made this transition, and they share how their expertise has been transformed into fulfilling, impactful careers with us. Learn more here: <a href="https://www.costellomedical.com/careers/working-at-costello-medical/joining-from-academia/" target="_blank">https://www.costellomedical.com/careers/working-at-costello-medical/joi…</a>
Benefits
What We Offer
Alongside our award-winning company culture, where every team member is celebrated, respected, and has their voice heard, our comprehensive benefits package includes:
<ul>
<li>A starting salary of $73,000 to $76,000 per annum, depending on your qualifications and previous experience, as well as a discretionary profit share bonus paid twice per year. Please note that we have established salary bands that ensures a fair and consistent approach for all applicants, eliminating the need for individual negotiations</li>
<li>23 days’ vacation leave increasing by 1 day each year to a maximum of 27 days. 6 public holidays plus 1 floating vacation day to use on a holiday of your choosing</li>
<li>Flexible, reasonable working hours and the chance to work from home for up to half of your working time</li>
<li>Private medical insurance with a company contribution, as well as dental and vision cover and life insurance</li>
<li>Retirement savings via a 401k plan with up to a 5% employer match</li>
<li>Paid funding for external education and study leave</li>
<li>Paid and unpaid sabbaticals based on length of service</li>
</ul>
Please click here to learn about our full reward package and the other benefits of working for Costello Medical: <a href="https://www.costellomedical.com/careers/benefits-package-in-the-us/" target="_blank">https://www.costellomedical.com/careers/benefits-package-in-the-us/</a>
The Application Process
You are required to submit your resume and a cover letter via our online application form. In your cover letter, you must explain why you think you would be suited to the role and why you would like to join Costello Medical, with examples to support both. Your resume should clearly state the dates of all qualifications and grades achieved where applicable.
Our recruitment process includes a telephone interview with a member of our Talent Acquisition team. Following this, you will also be sent a technical assessment, using R programming, and a proofreading exercise that we ask you to complete in your own time. If successful, you will be invited to an interview which will include a short presentation you can prepare for in advance. Our standard recruitment process lasts around 6 weeks, however, this can be adapted if necessary.
As an equal opportunity employer, we are committed to fostering a diverse and inclusive workforce and, throughout the recruitment process, there are a number of reasonable adjustments we can provide. Please click here to learn more.
Please note that, whilst we embrace AI to innovate and improve processes, your role may involve confidential data that cannot be uploaded to AI. Therefore, it is important for us to assess your own skills and abilities, so we recommend that you do not rely solely on this technology to generate any application materials.
Visa Sponsorship
We welcome applications from international candidates, but we are unfortunately unable to provide visa sponsorship for working visas. Therefore, you must have the right to work in the US independently from the company. However, we are able to consider those on a temporary visa, such as an OPT visa

Statistician

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
Purpose
Independently generate precise, reliable and reproducible data in a timely manner. Demonstrate experimental precision and strong data interpretation skills and should possess understanding of core discipline.
Responsibilities
<ul>
<li>Perform routine tasks competently and independently, and generate reliable and consistent results.</li>
<li>Analyze and critique results, noting significant deviations.</li>
<li>Troubleshoot experiments and instrumentation.</li>
<li>Learn and understand new experimental techniques.</li>
<li>Demonstrate skill in multiple techniques and appropriately modify protocols, as required, to suit the changing needs of research or development sciences.</li>
<li>Place data in proper scientific context by consulting and citing relevant literature.</li>
<li>Demonstrate technical proficiency in his/her field.</li>
<li>Impact projects predominantly through lab and/or pilot plant based activities.</li>
<li>Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, controlled drug and radioactive compounds, GxP compliance, and animal care where applicable.</li>
</ul>
Qualifications 
Qualifications
<ul>
<li>Bachelor’s Degree, or equivalent education, with typically 3 or more years’ experience or Master’s Degree or equivalent education (no additional experience.</li>
<li>Theoretical and practical knowledge to carry out job function.</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;of this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and&nbsp;we&nbsp;may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the&nbsp;future. ​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​
</li>
<li>
This job is eligible to participate in our short-term incentive&nbsp;programs.&nbsp;​
</li>
</ul>
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of any bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Scientist Development Rotational Program ( SDP)Associate, Scientist II

<h3>Job Description</h3>
Job DescriptionJob Title: Research Associate Formulation Scientist Location: Lexington, MA 02421 Duration: 6 months+ (Possible Extension) Pay Rate: $37.97/hr. on w2 TOP SKILLS PER MGR: 1. Experience in preparing injectable formulations for animal studies 2. Experience creating ELN entries and managing formulation requests / workflows 3. Highly communicative and able to quickly solve problems as they arise JOB DESCRIPTION: About the Department: Our Research &amp; Development organization brings together the best minds in life science innovation. The teams located in facilities in Lexington, Watertown, Cambridge and Seattle reflect the full R&amp;D continuum, from early research through late-stage clinical development. Here, we are building for the future, creating a distinct R&amp;D community based on collaboration, partnerships, and cutting-edge research across multiple modalities and therapeutic areas. We recognize that improving human health starts here and that patients rely on us. Our R&amp;D hub merges biotech speed and agility with large pharmaceutical company quality, resources, and stability, uniting the best of both worlds to develop new medicines for patients. The Position: Client is seeking a highly motivated formulation scientist to join its Pharmaceutical Research Sciences department in Lexington, Massachusetts. The candidate will be responsible for the formulation and characterization of peptides, proteins, small molecules, and bioconjugates. Relationships: This position reports to the Head of Pharmaceutical Formulation Sciences. Internal relationships include project teams and research colleagues in Lexington MA. Individual Contributor: does not manage other employees or contingent workers. Essential Functions:
<ul>
<li>Prepare peptide and protein injectable formulations for in vitro and in vivo studies including selection of buffers, excipients, surfactants and conducting the relevant biophysical characterization and stability studies</li>
<li>Collaborate with cross-functional teams to ensure the selected dosage form meets the desired biophysical and biochemical profile and contribute to early screening strategies and execution</li>
<li>Operate, maintain, and troubleshoot lab instruments such as biophysical and analytical characterization equipment</li>
<li>Conduct laboratory work in a safe, efficient manner that ensures a safe working environment for colleagues</li>
</ul>
 Qualifications:
<ul>
<li>Bachelor's Degree required. Degree within subject matter expertise (biological, biochemical, or pharmacological sciences) preferred</li>
<li>2+ years’ relevant technical experience required</li>
<li>Strong knowledge and expertise in biophysical characterization and injectable formulation development</li>
<li>Experience with spectroscopy, calorimetry, light scattering, and other biophysical methods for peptide and protein injectable formulations is a plus</li>
<li>Proficient in data analysis and interpretation for drawing conclusions and making recommendations</li>
<li>Experience in managing projects and working collaboratively with cross-functional teams</li>
<li>Excellent scientific communication skills and ability to engage with stakeholders effectively</li>
<li>Strong attention to detail and ability to document experimental work with electronic laboratory notebooks (ELN)</li>
<li>General knowledge of cGMP, GLP, and regulatory requirements for pharmaceutical industries a plus.</li>
</ul>
 #sczr2

Research Associate Formulation Scientist

<h3>Job Description</h3>
Job Description
MOVING YOUR WORLD by focusing on your success:
FUCHS offers a challenging and rewarding working environment where employees are encouraged to develop and grow.&nbsp; We stand behind our core values: trust, creating value, respect, reliability, and integrity. Ours is a culture that fosters creativity and empowerment, values work/life balance, and gives you the freedom to excel. At FUCHS we aim to nurture your capabilities, ideas and career.
&nbsp;
Salary:
FUCHS offers a competitive salary commensurate with experience in a similar position. The salary range for this position is $22.00 - $27.00 per hour, but actual salary will vary depending upon a new hire’s experience and qualifications as well as internal equity.
&nbsp;
Your responsibilities:
The Compounder works in the production department and is responsible for manufacturing of specialty lubricants. The Compounder must follow product folders to ensure all specification levels are met.&nbsp; The Compounder must adhere to all regulations, policies, and procedures for health, safety, and environmental compliance.
<ul>
<li>Wear mandatory PPE at all times.</li>
</ul>
<ul>
<li>Set up and operate production equipment in accordance with current good manufacturing practices and standard operating procedures</li>
<li>Review folder, calculate requirements, and verify weight of material</li>
<li>Documents production by completing forms, reports, logs, and records of equipment and batches</li>
<li>Locate material and supplies, and verify lots and weights according to the manufacturing order</li>
<li>Prepare and load raw materials into equipment</li>
<li>Must complete daily assigned tasks to meet production volume and schedule</li>
<li>Ensure that end products conform to FUCHS quality standards in accordance with 6S standards</li>
<li>Prepare finished goods for shipment by packing, labeling and loading on dock</li>
<li>Ensure that work environment is maintained clean, safe and organized</li>
<li>Keep equipment operating by following operating instructions; troubleshooting breakdowns;</li>
<li>Updates job knowledge by participating in training opportunities</li>
<li>Utilization of lean manufacturing techniques throughout production</li>
</ul>
<ul>
<li>Maintains material-handling equipment by completing pre-use inspections</li>
<li>Maintains inventory by identifying, labeling, and placing materials and supplies in stock; recording location of inventory</li>
</ul>
<ul>
<li>Responsible for responding to assigned corrective actions per the CAR system</li>
<li>Some heavy lifting (up to 75-lbs.) may be required</li>
<li>Ability to stand for long periods of time</li>
</ul>
&nbsp;
Qualifications we are looking for:
<ul>
<li>High school diploma or equivalent</li>
<li>2+ years working in chemical manufacturing experience</li>
<li>Computer literate required</li>
</ul>
<ul>
<li>Experience in a manufacturing environment</li>
<li>Mechanical ability preferred</li>
<li>Knowledge of material handling equipment</li>
</ul>
&nbsp;
&nbsp;
These are your benefits:
FUCHS offers a challenging and rewarding working environment where employees are encouraged to develop and grow as professionals.&nbsp; In this role, you will have the opportunity to work on projects that will expand your experience and challenge your abilities in the global marketplace.&nbsp; The position also offers an excellent compensation package and a comprehensive suite of benefits.&nbsp;Detailed benefit information can be found at this link: <a href="https://fuchs.com/us/en/benefits" target="_blank">https://fuchs.com/us/en/benefits</a>.
&nbsp;
FUCHS Lubricants Co. is an equal employment opportunity (EEO)/AA employer and strongly supports diversity in the workplace (m/f/d/v).
&nbsp;
Do you have any questions?&nbsp;Rosalinda Almanza (<a href="mailto:rosalinda.almanza@fuchs.com" target="_blank">rosalinda.almanza@fuchs.com</a>) will be more than happy to answer them!

Chemical Compounder

<h3>Job Description</h3>
Job Description
RQM+ is The MedTech CRO, accelerating innovation to patient impact. Our tailored solutions deliver regulatory and quality expertise, FDA-recognized laboratory services, clinical trials, and reimbursement strategies across device types and therapeutic areas to bring life-changing technologies to patients — faster, safer, better.
We don’t make MedTech. We make MedTech happen.
Our experienced teams are cohesive, collaborative, and proactive, constantly seeking to improve and evolve while remaining laser-focused on customer success. RQM+ elevates the MedTech experience through best-in-class service and clear, concise communication. We serve as an extension of our customers establishing and maintaining excellent client and site relationships and providing direct access to our technology platforms for real-time data and study transparency.
Job Summary:
The Senior Chemist I is designed for an experienced, independent chemist and will perform laboratory analyses and support scientific data interpretation. This role will be responsible for conducting a variety of analyses, interpreting data, and developing technical reports for customer projects. The Senior Chemist I will leverage strong scientific knowledge and experience to ensure accurate and efficient testing while maintaining a focus on meeting client and internal standards. This role requires the ability to work autonomously with minimal supervision, while still collaborating effectively with laboratory teams and other departments to meet project goals.
Primary Responsibilities:
<ul>
<li>
Perform laboratory experiments to develop, optimize, and validate analytical methods (HPLC, GC, LCMS, GCMS). 
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Prepare and analyze samples for routine testing, stability studies, and in-process controls, ensuring accuracy and reproducibility. 
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Operate, calibrate, and maintain analytical instruments (e.g., HPLC, GC, LCMS, GCMS) and troubleshoot issues to minimize downtime. 
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<li>
Support advanced analysis and writing of challenging, complex customer projects and related business needs. 
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Collaborate with Laboratory Chemists, Study Directors, and Research &amp; Development teams to ensure alignment with project goals and timelines. 
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<li>
Review and assess data for trends and discrepancies and suggest improvements where applicable. 
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<li>
Ensure compliance with regulatory guidelines, laboratory safety protocols, and best practices during all laboratory activities. 
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<li>
Maintain thorough documentation of experimental procedures, results, and data interpretations. 
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Contribute to the development of laboratory methods and procedures. 
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Provide technical support and mentorship to junior team members as needed. 
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Act as support on primary review report writing process and finalization. 
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Champion laboratory safety protocols, regulatory compliance, and adherence to industry best practices, continuously evaluating and improving safety measures in the lab. 
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Keep up to date with the latest scientific literature, emerging technologies, and industry innovations, ensuring that the laboratory maintains a competitive edge in scientific advancements. 
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Any other duties and tasks as directed by the supervisor. 
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</ul>
Requirements:
<ul>
<li>
Bachelor’s Degree in relevant field with 7+ years’ experience; Masters 3+ years’ experience; Ph.D. 0-2 years’ experience. 
</li>
</ul>
<ul>
<li>
Proficiency in performing and interpreting laboratory experiments using techniques such as HPLC, GC, LCMS, GCMS. 
</li>
</ul>
<ul>
<li>
Advanced knowledge and understanding of analytical method development. 
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Advanced knowledge and understanding of scientific report writing.
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Advanced knowledge and understanding of investigative and regulatory techniques.
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Advanced practitioner of all scientific methods and troubleshooting.
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<li>
Advanced practitioner of all software with a deep understanding of settings and features.
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Ability to be innovative and use the software to solve problems.
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Ability to perform well under pressure and work with minimum supervision.
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Demonstrate the ability to perform work accurately and efficiently
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Computer proficiency and experience with all MS products
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<li>
Computer skills proficiency and ability to learn new software.
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Detail-oriented self-starter with ability to manage multiple projects, work independently, and learn new disciplines.
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Excellent verbal and written communication skills.
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Demonstrates the drive and energy to be effective.
</li>
</ul>
Behaviors: Action-Oriented, Approachability, Building Effective Teams, Business Acumen, Career Ambition, Composure, Courage (Managerial), Customer Focus, Decision Quality, Informing, Integrity &amp; Trust, Interpersonal Savvy, Planning
Supervisory Responsibilities:
This position will have no supervisory responsibilities. 
Work Environment/Physical Demands: This job operates in a professional office environment. This role routinely uses standard office equipment such as computers, phones, photocopiers and filing cabinets. The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. The employee is occasionally required to sit; climb or balance; and stoop, kneel, crouch or crawl. The employee must frequently lift or move objects up to 10 pounds and occasionally lift or move objects up to 25 pounds.
Being an industry leader in Medtech is just the beginning for RQM+. We consider our employees our biggest asset and we invest heavily in ongoing learning and development. Providing a rewarding place to work is rooted deep in our core values. From an industry leading compensation package to a deeply engrained focus on work life balance, RQM+ has a unique offering for regulatory and quality professionals. At RQM+, you are not just another employee, you are a member of RQM+ family. Make your impact today!
We invite you to apply if you have an interest in learning more about our organization and beginning your journey with us.
Job Opportunity Verification
At RQM+, we prioritize the security of our job applicants. To ensure a safe application process:
All legitimate RQM+ job opportunities are listed on our official careers page: rqmplus.com/careers
Every candidate going through the interview process will participate in a voice and/or video interview.
Exercise caution with unsolicited job offers or requests for sensitive information.

Senior Chemist I

<h3>Job Description</h3>
Job Description
About the Team:
The Sensors Division specializes in the development of advanced sensor systems, with a particular focus on airborne and surface-based radar, space-based sensing, electronic warfare, and underwater acoustics. This position is within the Space Missions and Sensing (SMS) Sector of the Sensors Division. In this sector, we develop and deliver technology to advance space-based sensing, space control, and counter-sensing missions.
The Role:
The SMS Sector is seeking a Senior RF signal processing scientist to support algorithm development in a Research &amp; Development environment. In this role, you will be an integral part of a team developing a cutting-edge space-based radar system. Your responsibilities will include utilizing and advancing existing signal processing algorithms and analytics tools. This position offers significant opportunities for career growth within a fast-paced and rapidly expanding company.
What you will do:
<ul>
<li>Design signal processing and data exploitation algorithms that support day to day satellite operations</li>
<li>Conduct performance analysis through simulations and real-world testing to validate system performance</li>
<li>Communicate effectively with internal teams and stakeholders to convey technical concepts and project updates</li>
</ul>
Who you are:
<ul>
<li>Active Security Clearance at the Secret (S) level</li>
<li>BS or MS in Physics, Applied Mathematics, Electrical Engineering</li>
<li>3-5+ years of experience depending on degree</li>
<li>Radar signal processing, statistical signal processing background (detection, estimation)</li>
<li>Proficiency in MATLAB and/or Python programming languages</li>
</ul>
Even Better:
<ul>
<li>Past experience in space-based remote sensing (e.g. SAR, signal exploitation)</li>
<li>Expertise in linear algebra, mathematical optimization a plus</li>
<li>PhD in Applied Mathematics, Electrical Engineering with research background related to radar, radar signal processing in lieu of experience</li>
</ul>
Pay Information Full-Time Salary Range: $134,000 - $184,000
The salary range listed is based on external market data. Offers are based on factors, such as but not limited to, the candidate's experience, education, training, key skills/critical skills, security clearances, and prevailing market and business conditions.
STR is a growing technology company with locations near Boston, MA, Arlington, VA, near Dayton, OH, Melbourne, FL, and Carlsbad, CA. We specialize in advanced research and development for defense, intelligence, and national security in: cyber; next generation sensors, radar, sonar, communications, and electronic warfare; and artificial intelligence algorithms and analytics to make sense of the complexity that is exploding around us.
STR is committed to creating a collaborative learning environment that supports deep technical understanding and recognizes the contributions and achievements of all team members. Our work is challenging, and we go home at night knowing that we pushed the envelope of technology and made the world safer.
STR is not just any company. Our people, culture, and attitude along with their unique set of skills, experiences, and perspectives put us on a trajectory to change the world. We can't do it alone, though - we need fellow trailblazers. If you are one, join our team and help to keep our society safe! Visit us at <a href="http://www.str.us" target="_blank">www.str.us</a> for more info.
 STR is an equal opportunity employer. We are fully dedicated to hiring the most qualified candidate regardless of race, color, religion, sex (including gender identity, sexual orientation and pregnancy), marital status, national origin, age, veteran status, disability, genetic information or any other characteristic protected by federal, state or local laws.
If you need a reasonable accommodation for any portion of the employment process, email us at <a href="mailto:appassist@str.us" target="_blank">appassist@str.us</a> and provide your contact info.
Pursuant to applicable federal law and regulations, positions at STR require employees to obtain national security clearances and satisfy the requirements for compliance with export control and other applicable laws.

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