field_job_occupational_field_parents_all

field_job_employment_type

job_organization_name

city

state

<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 
We are seeking a highly motivated Senior Scientist I to join our Analytical Development team in the Product Development Science and Technology, Biologics Development Launch division. Our team is responsible for the development, qualification, and execution of analytical methods to provide product and process understanding for biological entities from discovery through commercial stages.
The successful candidate will be a part of the Biomolecular Interaction Group which is mainly focused on method development and implementation of various immunoassays to monitor process impurities and to assess potency of AbbVie’s Biologics to support product and process development for early-phase, late-phase, and commercial programs.&nbsp; Some of the techniques/methods utilized in the group include 1) ELISAs to monitor and detect process related impurities; 2) surface plasmon resonance using Biacore for assessment of antigen binding and binding of antibody Fc receptors; and 3) qPCR to measure levels of residual DNA and mycoplasma. The role will &nbsp;involves managing all analytical aspects of biologics products on the market, overseeing commercial methods throughout their lifecycle - from method transfer, performance monitoring, troubleshooting, to method enhancement. The individual will also play a key role in establishing commercial product specifications, stability programs, and regulatory filings. Collaboration with other analytical teams, process development, global QC, and manufacturing science and technology groups is a crucial part of this role to meet business objectives and program milestones.
Responsibilities:
<ul>
<li>Partner with Analytical Development groups to achieve commercial method readiness using traditional and advanced analytical techniques, including but not limited to ELISA, bioassays, spectrophotometric and compendial methods.</li>
<li>Participate in cross-functional, multi-site, global meetings / projects and oversee commercial analytical method transfer between sites, product/process investigations, method performance monitoring and troubleshooting.</li>
<li>Establish scientifically sound, analytical lifecycle strategies, including methods, stability, specification and change management that meet Health Authority best practices and expectations.</li>
<li>Participate in the preparation and review of technical documents to ensure global compliance - including validation protocols and reports, reference standard qualification reports and analytical test procedures.</li>
<li>Author regulatory submissions, support regulatory inspections and provide scientifically sound responses to agency deficiency letters.</li>
<li>Conduct periodic review of methods and work with program leads to design, execute remediation experiments, and implement changes to new or existing commercial methods when necessary.</li>
</ul>
Qualifications 
<ul>
<li>BS or equivalent education in Biology, Biochemistry, Engineering or related discipline and 8+ years of experience in the biopharmaceutical industry; MS and 6+ years experience; PhD and 3+ years experience.</li>
<li>Industry experience in method development, qualification, validation, and method transfer in support of development and/or commercialization of biological products. &nbsp;</li>
<li>Methods including but not limited to ELISA, western blot, qPCR, ddPCR, SPR and automation</li>
<li>Ability to lead and manage projects/teams of significant scope and complexity, while meeting all deliverables and timelines.</li>
<li>Ability to think critically and demonstrate troubleshooting and problem-solving skills.</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>
<li>
This job is eligible to participate in our long-term incentive&nbsp;programs​
</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>

Senior Scientist, II- Analytical Development ( On-site-Worcester, MA)

<h3>Job Description</h3>
Job Description
Job Title: Chemist II – Stability Testing (Quality Control) Job Location: Fall River, MA (On-site) Schedule: 8:00 AM – 5:00 PM (May vary based on business needs) Classification: Full-Time, Exempt Relocation Assistance: Up to $6,000 available Work Authorization: US Citizen, Green Card, H1B Transfer, TN Visa, OPT-EAD
About the Role:
We are seeking a QC Chemist II – Stability Testing to join our Quality Control Department. The selected candidate will be responsible for performing and overseeing stability testing for pharmaceutical formulations under various environmental conditions, ensuring data integrity, and compliance with cGMP guidelines.
Key Responsibilities:
<ul>
<li>
Conduct routine and advanced stability testing in a laboratory setting.
</li>
<li>
Operate and maintain instruments such as HPLC, GC, ICP, Karl Fischer, and Particle Size Analyzers.
</li>
<li>
Perform raw material testing and release.
</li>
<li>
Lead investigations into out-of-specification (OOS) or deviations and document findings.
</li>
<li>
Ensure adherence to cGMP, Good Documentation Practices (GDP), and data integrity principles.
</li>
<li>
Prepare and review documentation, including lab notebooks and reports.
</li>
<li>
Participate in audits and ensure inspection readiness.
</li>
<li>
Collaborate with cross-functional teams, including QA and manufacturing.
</li>
<li>
Support training and mentoring of junior team members.
</li>
<li>
Execute additional duties as assigned by departmental leadership.
</li>
</ul>
Required Qualifications:
<ul>
<li>
Bachelor’s degree (BS/BA) in Chemistry or a related physical science.
</li>
<li>
Minimum 3 years of experience in formulation stability testing in a pharmaceutical setting.
</li>
<li>
Working knowledge of analytical instruments including HPLC, GC, ICP, Karl Fischer, and particle size analyzers.
</li>
<li>
Familiarity with MDI (Metered Dose Inhaler) testing is a strong plus.
</li>
<li>
Experience with various dosage forms (liquid, solid, tablets, capsules) is desirable.
</li>
<li>
Strong command of English – spoken and written.
</li>
<li>
Proficiency with Microsoft Office and scientific software.
</li>
<li>
Excellent analytical, documentation, and communication skills.
</li>
<li>
Must be authorized to work in the United States and be available to work on-site full-time.
</li>
</ul>
Preferred Qualifications:
<ul>
<li>
Experience working with inhalation products (MDIs).
</li>
<li>
Previous work in a fast-paced, regulated pharmaceutical QC lab environment.
</li>
<li>
Experience leading or contributing to laboratory investigations.
</li>
</ul>
Work Environment Physical Requirements:
<ul>
<li>
Work in a cGMP laboratory or manufacturing environment requiring the use of personal protective equipment (PPE).
</li>
<li>
Regular exposure to solvents, powders, and chemical substances.
</li>
<li>
Must be able to stand or walk for 75% or more of an 8-hour shift.
</li>
<li>
Must be able to lift up to 10 kg unassisted.
</li>
<li>
Must be able to sit and work at a computer for extended periods.
</li>
</ul>
Compensation Benefits:
<ul>
<li>
Competitive salary based on experience ($75K–$105K)
</li>
<li>
Bi-weekly pay
</li>
<li>
Paid Time Off (PTO)
</li>
<li>
Health Insurance (Medical, Dental, Vision) – starts on Day 1
</li>
<li>
Disability Insurance
</li>
<li>
Overtime and shift differential as applicable
</li>
<li>
401(k) with company match
</li>
<li>
Career advancement opportunities and ongoing training
</li>
<li>
Company-sponsored events
</li>
</ul>
Important Notes:
<ul>
<li>
Candidates must have prior pharmaceutical (not biopharma) experience.
</li>
<li>
Chemistry background is highly preferred.
</li>
<li>
Candidates should clearly indicate experience with formulations including MDI, liquid, solid, tablets, and capsules in their resume.
</li>
<li>
No Green Card sponsorship available; H1B transfers are acceptable.
</li>
</ul>

QC Chemist II

<h3>Job Description</h3>
Job DescriptionWe are looking for a skilled, resourceful, and collaborative Senior Geotechnical Project Manager to join our client's team in Burlington, Vermont. The Senior Geotechnical Project Manager will work closely with a team of staff engineers and scientists on challenging and exciting projects largely in urban environments. This is a fast-paced and dynamic position, with opportunities to be challenged, contribute to project outcomes, interact routinely with project Principals and clients, and is designed to support your professional growth. Essential Functions – What You Will DoTo perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed are representative of the knowledge, skill and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Develop new business opportunities. Manage and grow client relationships. Prepare proposals and project budgets. Manage project budgets and prepare invoices. Manage and supervise staff engineers. Set technical strategy and oversee production of technical work products. Plan and coordinate field investigation programs. Interpret and analyze field and laboratory data. Coordinate and oversee construction administration for development projects. Manage preparation of reports, design plans, data tables, specifications, and other deliverables. Formulate conclusions, recommendations, and geotechnical strategies for development projects.Qualifications Minimum of ten years relevant experience and a BS in Civil Engineering (Geotechnical Focus) or seven years relevant experience and a MS in Civil Engineering (Geotechnical Focus). Possess Professional Engineering Licensure. Strong attention to detail and understanding of geotechnical engineering. Experience with geotechnical field work and construction earthwork. Strong organizational and time management skills combined with the flexibility to work with shifting priorities. Desire and affinity for networking and business development. Awareness and general understanding of environmental considerations (i.e., contaminated soil and groundwater management during construction). Client-service orientation with the ability to anticipate needs and deliver to meet expectations. Excellent verbal and written communication skills. Work well as a team member, with a collaborative communication style.If you meet these requirements and qualifications, please apply or reach out to <a href="mailto:mforde@aectac.com" target="_blank">mforde@aectac.com</a>.

Geotechnical Project Manager

<h3>Job Description</h3>
Job DescriptionJob Title: Biologist Location: Boston, MA 02210 Duration: 12 Months+ Shift: Standard shift Pay range: $38 - $41/ hr. on W2 Job Description:
<ul>
<li>Perform cell-based and molecular biology assays, including cell viability, ELISA, immunofluorescence, flow cytometry, and functional assays. </li>
<li>Make observations, evaluate data, interpret results, and maintain good written records of laboratory procedures, results, and conclusions.</li>
<li>Comply with standard laboratory practices and company policies.</li>
</ul>
 Qualification/ Requirements:
<ul>
<li>B.S in biology, molecular biology, biotechnology, or related field</li>
<li>Basic laboratory skills and aseptic technique.</li>
<li>Prior experience with tissue culture and cell-based and molecular biology assays. Experience with ELISAs, immunofluorescence, and cry sectioning is a plus. </li>
<li>Outstanding interpersonal skills and established collaborative working habits.</li>
<li>Excellent oral and written communication skills.</li>
</ul>
 #sczr2

Biologist

<h3>Job Description</h3>
Job Description
Description:
<ul>
<li>
Identifies and validates molecular targets that play a key role in a particular disease process.
</li>
<li>
Studies origin, relationship, development, anatomy, functions, and chemical processes of living organisms.
</li>
<li>
Analyzes materials to determine their toxic or nontoxic properties, binding and efficacy. Isolates or purifies analyses, and identifies hormones,minerals, proteins, and/or cultures of microorganisms to determine their biological properties.
</li>
<li>
Examines and conducts research on chemical aspects chemistry of cells andcell division.
</li>
<li>
May identify and produce small quantities of new drugs, pharmaceutical compounds and/or nutrients.
</li>
<li>
May develop an assay which employs in-vitro and/or in-vivo biological and immunological systems.
</li>
<li>
May experiment with animals and tissue to determine the effect of new drug compound entities utilizing in-vivo, in-vitro and ex-vivomodels on cells, tissues and whole animal systems.
</li>
<li>
Performs experiments and procedures demonstrating proficiency with a broad range of scientific or technology techniques; executes high-quality experiments and delivers and interprets data with colleagues and/or project teams.
</li>
<li>
Executes experiments and procedures requiring specific scientific or technical knowledge and laboratory techniques; delivers high-quality data to impact drug discovery, technology, and/or early development projects.
</li>
<li>
Generates hypotheses to test, troubleshoots issues and designs and executes the next set of experiments with some input from senior lab members/manager.
</li>
<li>
Approaches work with urgency, manages basic research activities in parallel.
</li>
<li>
Provides basic data analysis to interpret own experiments - assesses whether experimental hypothesis was appropriately tested and answered.
</li>
<li>
Works collaboratively across teams and trains other members of team in areas of technical expertise as needed.
</li>
<li>
Participates constructively in working teams and at lab meetings.
</li>
<li>
Steps in to support general lab responsibilities.
</li>
<li>
Generates hypotheses, independently executes experiments, and uses results to assist in the design of the next experiment.
</li>
<li>
Recognizes problems and provides input on solutions; suggests new approaches to established procedures to progress key drug discovery, technology, and/or early development projects.
</li>
<li>
Works collaboratively across lab with all members.
</li>
<li>
Expected to be an excellent lab citizen.
</li>
<li>
Uses understanding of experimental hypothesis and works with manager and colleagues to troubleshoot issues and help design and execute next experiment.
</li>
<li>
Experimental results support progression of drug discovery, technology, and/or early development projects.
</li>
<li>
Distribution of marketing samples (where applicable)
</li>
</ul>
Work Experience:
<ul>
<li>
PhD is required
</li>
<li>
Requires an understanding of one or more of the following: molecular biology, biochemistry, microbiology, cell biology, biophysics, virology and/or immunology.
</li>
<li>
The successful candidate will be proficient:
<ul>
<li>
expressing and purifying recombinant proteins from bacteria, insect and mammalian cells,
</li>
<li>
the ability to characterize small molecule and protein-protein interactions using biophysical techniques including SPR, DSF, SEC-MALLS, analytical ultracentrifugation and ITC and
</li>
<li>
previous experience solving protein structures using x-ray crystallography and cryoEM microscopy.
</li>
</ul>
</li>
<li>
Functional Breadth.
</li>
<li>
Collaborating across boundaries.
</li>
<li>
Skills:
</li>
<li>
Algorithms.
</li>
<li>
Analytical Skill.
</li>
<li>
Analytical Thinking.
</li>
<li>
Chemical Biology.
</li>
<li>
Clinical Research.
</li>
<li>
Clinical Trials.
</li>
<li>
Collaboration.
</li>
<li>
Communication Skills.
</li>
<li>
Curiosity.
</li>
<li>
Data.
</li>
<li>
Data Analysis.
</li>
<li>
Design Of Experiments.
</li>
<li>
Detail Oriented.
</li>
<li>
Diversity &amp; Inclusion.
</li>
<li>
Drug Discovery.
</li>
<li>
Ethics.
</li>
<li>
Hypothesis Testing.
</li>
<li>
Immunology.
</li>
<li>
Laboratory.
</li>
<li>
Lifesciences.
</li>
<li>
Mammalian Cell Culture.
</li>
<li>
Medical Research.
</li>
<li>
Molecular Biology.
</li>
<li>
Organization.
</li>
<li>
Problem Solving Skills.
</li>
<li>
Project Teams.
</li>
<li>
Reports Writing.
</li>
<li>
Research.
</li>
<li>
Science.
</li>
<li>
SOP (Standard Operating Procedure).
</li>
<li>
Time Management Skills.
</li>
</ul>
Benefits:
Healthcare Insurance: Synectics offers eligible employees and their dependents healthcare coverage through BlueCross BlueShield of Illinois. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. Premiums are subsidized by Synectics. 
Dental Insurance: Synectics offers eligible employees and their dependents a dental plan through MetLife. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. 
Vision Insurance: Synectics offers eligible employees vision insurance through VSP. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics.401(k) Plan: The Synectics Inc. Investment Savings Retirement Plan. Synectics offers all employees who are 21 years of age or older the opportunity to invest in the 401(k) Plan on the first enrollment date that is at least 30 days after employment begins. Enrollment dates are each January 1st, April 1st, July 1st, and October 1st.
Technical Certification Bonus: Synectics is pleased to award its employees a bonus of up to $500 for an approved professional certification. In determining the bonus amount, Synectics will consider the cost of the test(s) for any certification relating to your current position, achieved during your employment with us. Only one Certification Bonus per calendar year may be awarded per employee. Only current, active employees will be eligible to receive this bonus. It will be awarded 90 days after the Synectics office has received documentation confirming the successful completion of the certification.
Synectics is an equal opportunity employer.

Research Associate

<h3>Job Description</h3>
Job DescriptionMaterials Scientist - Aerospace - Technical Ceramics- Relocation available! This Jobot Job is hosted by: Matt Swaneveld Are you a fit? Easy Apply now by clicking the "Apply Now" buttonand sending us your resume. Salary: $100,000 - $150,000 per year 
A bit about us:
 We are a leader in manufacturing advanced materials and are known for our custom designed technical solutions. Due to growth, we are looking for a Materials Scientist to assist in our well structured engineering department. As a Materials Scientist, you will be responsible for developing and testing new materials, analyzing and improving existing materials, and ensuring that all materials meet our high standards of quality and performance. This is a challenging and exciting role that requires a deep understanding of ceramics, materials, raw material testing, and scientific principles. If you have a background in technical ceramics and are looking to take the next step in your career, please read on! 
Why join us?
 
<ul>
<li> We are an industry leader with an assortment of versatile advanced material products</li>
<li> Stable company with well over 50+ years behind us</li>
<li> Great starting salary </li>
<li> Comprehensive benefits package including health/dental/wellness/and more</li>
<li> 401K+ employee match </li>
<li> Relocation assistance package if needed</li>
</ul>
 
Job Details
 Qualifications: 
<ul>
<li> Bachelor's degree in Materials Science, Ceramics, or a related field (Master's / PhD preferred) </li>
<li> Industry experience with Aerospace/Defense/ITAR/Medical</li>
<li> 9+ years of experience in ceramics, materials, or a related field</li>
<li> Potential to obtain a government security clearance</li>
<li> Strong knowledge of scientific principles and research methods</li>
<li> Experience with raw material testing and analysis</li>
<li> Excellent problem-solving skills and attention to detail</li>
<li> Strong communication and collaboration skills</li>
<li> Ability to work independently and as part of a team</li>
<li> Experience with advanced scientific equipment and techniques</li>
<li> Ability to write technical reports and present findings to management and other stakeholders</li>
</ul>
 Responsibilities: 
<ul>
<li> Conduct research and development activities to create new materials that meet our specific needs and requirements</li>
<li> Analyze and improve existing materials to enhance their performance, durability, and reliability</li>
<li> Perform raw material testing to ensure that all materials meet our quality standards</li>
<li> Collaborate with other scientists and engineers to develop new products and improve existing ones</li>
<li> Use advanced scientific equipment and techniques to analyze and test materials</li>
<li> Keep up-to-date with the latest developments in materials science and technology</li>
<li> Write technical reports and present findings to management and other stakeholders</li>
</ul>
 If you are a skilled and experienced Materials Scientist with a passion for innovation and a commitment to quality, we want to hear from you. This is an exciting and rewarding opportunity to work in a dynamic and fast-paced environment, where you will have the opportunity to make a real impact on the manufacturing industry. Interested in hearing more? Easy Apply now by clicking the "Apply Now" button. Jobot is an Equal Opportunity Employer. We provide an inclusive work environment that celebrates diversity and all qualified candidates receive consideration for employment without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. Sometimes Jobot is required to perform background checks with your authorization. Jobot will consider qualified candidates with criminal histories in a manner consistent with any applicable federal, state, or local law regarding criminal backgrounds, including but not limited to the Los Angeles Fair Chance Initiative for Hiring and the San Francisco Fair Chance Ordinance.Company DescriptionJobot is on a mission to connect good people with good jobs. By combining AI-powered technology with the expertise of Jobot Pros, our experienced recruiters, we help you find career opportunities that align with your goals and values. Founded in 2018 and employee-owned since 2024, Jobot is committed to fostering a culture of kindness, respect, innovation, and connection. As an industry leader, we’ve been recognized as a top workplace by Forbes, Fortune, USA Today, and Staffing Industry Analysts (SIA). Ready to find a good job? Create your profile today at Jobot.com.

Senior Materials Scientist

<h3>Job Description</h3>
Job DescriptionMaterials Scientist - Aerospace - Technical Ceramics- Relocation available! This Jobot Job is hosted by: Matt Swaneveld Are you a fit? Easy Apply now by clicking the "Apply Now" buttonand sending us your resume. Salary: $100,000 - $150,000 per year 
A bit about us:
 We are a leader in manufacturing advanced materials and are known for our custom designed technical solutions. Due to growth, we are looking for a Materials Scientist to assist in our well structured engineering department. As a Materials Scientist, you will be responsible for developing and testing new materials, analyzing and improving existing materials, and ensuring that all materials meet our high standards of quality and performance. This is a challenging and exciting role that requires a deep understanding of ceramics, materials, raw material testing, and scientific principles. If you have a background in technical ceramics and are looking to take the next step in your career, please read on! 
Why join us?
 
<ul>
<li> We are an industry leader with an assortment of versatile advanced material products</li>
<li> Stable company with well over 50+ years behind us</li>
<li> Great starting salary </li>
<li> Comprehensive benefits package including health/dental/wellness/and more</li>
<li> 401K+ employee match </li>
<li> Relocation assistance package if needed</li>
</ul>
 
Job Details
 Qualifications: 
<ul>
<li> Bachelor's degree in Materials Science, Ceramics, or a related field (Master's / PhD preferred) </li>
<li> Industry experience with Aerospace/Defense/ITAR/Medical</li>
<li> 9+ years of experience in ceramics, materials, or a related field</li>
<li> Potential to obtain a government security clearance</li>
<li> Strong knowledge of scientific principles and research methods</li>
<li> Experience with raw material testing and analysis</li>
<li> Excellent problem-solving skills and attention to detail</li>
<li> Strong communication and collaboration skills</li>
<li> Ability to work independently and as part of a team</li>
<li> Experience with advanced scientific equipment and techniques</li>
<li> Ability to write technical reports and present findings to management and other stakeholders</li>
</ul>
 Responsibilities: 
<ul>
<li> Conduct research and development activities to create new materials that meet our specific needs and requirements</li>
<li> Analyze and improve existing materials to enhance their performance, durability, and reliability</li>
<li> Perform raw material testing to ensure that all materials meet our quality standards</li>
<li> Collaborate with other scientists and engineers to develop new products and improve existing ones</li>
<li> Use advanced scientific equipment and techniques to analyze and test materials</li>
<li> Keep up-to-date with the latest developments in materials science and technology</li>
<li> Write technical reports and present findings to management and other stakeholders</li>
</ul>
 If you are a skilled and experienced Materials Scientist with a passion for innovation and a commitment to quality, we want to hear from you. This is an exciting and rewarding opportunity to work in a dynamic and fast-paced environment, where you will have the opportunity to make a real impact on the manufacturing industry. Interested in hearing more? Easy Apply now by clicking the "Apply Now" button. Jobot is an Equal Opportunity Employer. We provide an inclusive work environment that celebrates diversity and all qualified candidates receive consideration for employment without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. Sometimes Jobot is required to perform background checks with your authorization. Jobot will consider qualified candidates with criminal histories in a manner consistent with any applicable federal, state, or local law regarding criminal backgrounds, including but not limited to the Los Angeles Fair Chance Initiative for Hiring and the San Francisco Fair Chance Ordinance.Company DescriptionJobot is on a mission to connect good people with good jobs. By combining AI-powered technology with the expertise of Jobot Pros, our experienced recruiters, we help you find career opportunities that align with your goals and values. Founded in 2018 and employee-owned since 2024, Jobot is committed to fostering a culture of kindness, respect, innovation, and connection. As an industry leader, we’ve been recognized as a top workplace by Forbes, Fortune, USA Today, and Staffing Industry Analysts (SIA). Ready to find a good job? Create your profile today at Jobot.com. 
<h3>Company Description</h3>
Jobot is on a mission to connect good people with good jobs. By combining AI-powered technology with the expertise of Jobot Pros, our experienced recruiters, we help you find career opportunities that align with your goals and values.\r\n\r\nFounded in 2018 and employee-owned since 2024, Jobot is committed to fostering a culture of kindness, respect, innovation, and connection. As an industry leader, we’ve been recognized as a top workplace by Forbes, Fortune, USA Today, and Staffing Industry Analysts (SIA).\r\n\r\nReady to find a good job? Create your profile today at Jobot.com.

<h3>Job Description</h3>
Job DescriptionPrincipal Scientist, Translational Sciences Job summary: PharmaEssentia Innovation Research Center (PIRC) is seeking a highly motivated principal scientist to join our Translational Sciences team and contribute to the development of first-in-class and best-in-class biotherapeutics, including cytokines, antibodies, and antibody-drug-conjugates. &nbsp;The successful candidate will contribute to the design, execution, and interpretation of translational biomarker and mechanism of action (MOA) studies to support the development and regulatory approval of novel therapeutics as they transition from late discovery into first in human clinical trials and beyond.&nbsp; You will also drive translational and early clinical activities aimed at maximizing the potential of BESREMI, PharmaEssentia’s marketed drug for the treatment of myeloproliferative neoplasms, including indication expansion and novel combinations. &nbsp;To this end, you will work cross-functionally with clinical development, clinical operations, regulatory affairs as well as with academic investigators and clinical CROs to explore new applications for BESREMi.&nbsp; Additionally, you will provide scientific leadership, mentorship, and cross-functional collaboration within the Translational Sciences team and across other departments. The Company: It’s not often that you get the chance to make a real impact on the lives of others, while expanding your own possibilities. You’ll find that rare opportunity at PharmaEssentia. Join us, and let’s transform lives, together. PharmaEssentia Corporation is a rapidly growing biopharmaceutical innovator. We are leveraging deep expertise and proven scientific principles to deliver effective new biologics for challenging diseases in the areas of hematology, oncology and immunology, with one approved product and a diversifying pipeline. We believe in the potential to improve both the health and quality of life for patients with limited options today through the combination of rigorous research and innovative thinking. Founded in 2003 by a team of Taiwanese American executives and renowned scientists from U.S. biotechnology and pharmaceutical companies, today we are listed on the Taipei Exchange (TPEx: 6446) and are expanding our global presence with operations in the U.S., Japan, China and Korea, along with a world-class biologics production facility in Taichung. Our new research center, PharmaEssentia Innovation Research Center (PIRC), will build upon our invention and discovery-based innovation efforts originally established in Taiwan that led to a transformative advancement for treating polycythemia vera (one of the myeloid proliferative neoplasms). At PIRC, we aim to expand our current expertise in related therapeutic areas and identify novel therapeutic approaches in early to mid-stage discovery and development. Data scientists will leverage artificial intelligence and machine learning to inform new target and indication selection. The company is also recruiting for talented scientists who have deep knowledge in immunology, translational science, bioinformatics and biologics platforms to develop novel drugs leveraging disease-driving biology, novel technology in protein engineering, antibody discovery and new modalities. Summary of Key Responsibilities: &nbsp;
<ul>
<li>Further Exploration of BESREMi: Collaborate with clinical development to further explore the potential of BESREMi in MPN and other areas of Oncology. Conduct translational studies internally or externally via CROs, and drive investigator-initiated trials (IITs) or company sponsored clinical trials to maximize the clinical potential of BESREMi. </li>
<li>Study Design and Execution: Lead the design, planning, and execution of translational studies in indication-relevant animal models and primary human cellular and tissue systems to identify and validate biomarkers and explore drug candidate mechanism of action. &nbsp;Collaborate with cross-functional teams to ensure alignment with discovery and development goals as well as regulatory requirements.</li>
<li>Data Analysis and Interpretation: Oversee the analysis, interpretation, and reporting of in vitro and in vivo pharmacology/translational biomarker data, including pharmacokinetic and pharmacodynamic parameters, exposure-response relationships, and safety/tolerability profiles. Provide scientific insights to inform decision-making and optimize study outcomes.</li>
<li>Drug Development Strategy: Contribute to the development and implementation of clinical pharmacology strategies to support the progression of investigational drugs through all phases of clinical development. Generate scientific rationale for dose selection, formulation optimization, and therapeutic target validation.</li>
<li>Scientific Leadership: Serve as a subject matter expert in translational biomarkers, target biology and candidate therapeutic mechanism of action, providing guidance and mentorship to junior scientists, clinicians, and project teams. Contribute to the scientific literature through publications, presentations, and participation in professional conferences and working groups.</li>
<li>Cross-Functional Collaboration: Collaborate closely with colleagues in data sciences, biologics, immunology/pharmacology, clinical development, clinical operations and regulatory affairs to integrate translational biomarker and mechanism of action insights into overall drug development strategies. Foster a culture of scientific excellence, innovation, and collaboration. </li>
<li>Regulatory Interaction: Work with regulatory affairs and CROs to support the preparation and review of regulatory submissions, including investigational new drug (IND) applications, biologics license applications (BLA), and marketing authorization applications (MAA). Address inquiries and provide scientific justifications for study designs, endpoints, and data analyses.</li>
</ul>
 Qualifications: &nbsp;
<ul>
<li>M.D or Ph.D. in oncology, immunology, immuno-oncology, pharmacology, pharmaceutical sciences, or a related discipline.</li>
<li>8+ years’ experience in the pharmaceutical or biotechnology industries, including a proven track record of leadership and scientific achievement in translational sciences.</li>
<li>Expertise in in vivo model design and biomarker discovery, both internally and via CROs and academic collaborations. </li>
<li>Experience with primary human cellular/tissue-based assays to guide/inform indication selection, biomarker discovery and mechanism-of-action.</li>
<li>Experience with immuno-oncology and autoimmune disease/chronic inflammation targets and associated in vitro and in vivo models.</li>
<li>Experience in clinical trial design and/or clinical operations in either company-sponsored, or IIT clinical trials. </li>
<li>Experience working closely with academic collaborators and managing all aspects of sponsored research agreements or IITs.</li>
<li>Strong analytical skills, with proficiency in pharmacokinetic/pharmacodynamic software (e.g., NONMEM, Phoenix WinNonlin, R) is preferred.</li>
<li>Excellent communication and presentation skills, with the ability to effectively convey complex scientific concepts to diverse audiences.</li>
<li>Demonstrated leadership capabilities, including the ability to mentor and develop talent, foster teamwork, and drive results in a dynamic environment.</li>
</ul>
 Conclusion: As a Principal Scientist in Translational Sciences, you will play a pivotal role in advancing the understanding of drug pharmacology and contributing to the development of innovative therapeutics to address unmet medical needs. Your scientific expertise, leadership skills, and collaborative approach will be critical for driving drug development programs forward, maximizing the potential of BESREMi and ultimately improving patient outcomes at PIRC. EEO Statement: At PharmaEssentia Innovation Research Center (PIRC), we are committed to providing an environment of mutual respect where equal employment opportunities are available to all applicants without regard to race, color, religion, sex, pregnancy (including childbirth and related medical conditions), national origin, age, physical and mental disability, marital status, sexual orientation, gender identity, gender expression, genetic information (including characteristics and testing), military and veteran status, and any other characteristic protected by applicable law. PIRC believes that diversity and inclusion among our team are critical to our success as a global company, and we seek to recruit, develop and retain the most talented people from a diverse candidate pool.&nbsp; PIRC does not accept unsolicited agency resumes. Staffing agencies should not send resumes to our HR team or to any PIRC employees. PIRC is not responsible for any fees related to unsolicited resumes from staffing agencies.
At PharmaEssentia, our goal is to treat as many people with cancer as possible. That means challenging the status quo with better science that leads to better lives. By joining our team, you will not only expand your own possibilities, but you will contribute to expanding options for people with cancer.
<a href="https://us.pharmaessentia.com/careers/" target="_blank">https://us.pharmaessentia.com/careers/</a>
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Principal Scientist, Translational Sciences

<h3>Job Description</h3>
Job Description
This is a remote position. As a Senior Research Scientist within the R&amp;I team, you will deliver Crisis Text Line’s insights related to mental health crises, coping, and crisis support to improve practice, policy, and the broader field of mental health support globally. Reporting to the VP of Impact Evaluation &amp; Storytelling, you will analyze the more than 11 million crisis conversations since 2013 to conduct research, monitor emerging trends, and generate insights to help people thrive. In collaboration with other teams across the organization, you will work to meet organization-wide business needs for data and insights on Crisis Text Line’s impact for texters, volunteers, and society across languages, cultures, and contexts. As an individual contributor, you will work in close collaboration with all members of the R&amp;I team to ensure our work is grounded in technical and methodological rigor to satisfy scientific scrutiny, engaging with a range of cross-functional internal partners.&nbsp;
Responsibilities:&nbsp;
Crisis Text Line is a fast moving, growing organization with a big vision and a critical mission. To serve our mission and vision, the person in each role must be agile and flexible to meet the needs of the business, aligning their work with priorities as defined by their manager and team leaders.
&nbsp;
Data Analytics and Visualization
Contribute to the delivery of new research insights related to Crisis Text Line’s impact in in the U.S. and globally by:
<ul>
<li>Developing, implementing, optimizing, and documenting complex SQL queries to support research projects&nbsp;</li>
<li>Planning, developing, and executing compelling and accurate data visualizations, including stand-alone visualizations and data dashboards</li>
<li>Selecting, applying, and presenting complex statistical analyses, including inferential statistics (e.g. generalized estimating equations, poisson regression)</li>
</ul>
&nbsp;
Data Verification&nbsp;
Meet organization-wide business needs for data and insights verification and content by:
<ul>
<li>Validating and providing code reviews for complex SQL queries performed by other team members</li>
<li>Supporting team dashboard development for team efficiency</li>
<li>Manage the research impact requests process; respond efficiently and accurately to organization-wide inquiries regarding the dataset&nbsp;</li>
<li>Supporting the development, review, and data verification for external-facing content referencing Crisis Text Line data and insights, as appropriate&nbsp;</li>
</ul>
&nbsp;
Data Storytelling&nbsp;
Work with the R&amp;I team to evidence and amplify Crisis Text Line’s impact for texters, our volunteer community, and broader society by contributing to report production for internal and external audiences. 
<ul>
<li>Support the team in translating clinical and technical analytic findings into data storytelling, by drafting key messages to be incorporated into reports for broad, nontechnical audiences.&nbsp;</li>
<li>Contribute to delivery of impact measurement efforts, conducting desk research on metrics and measurement, tracking metrics, and supporting evaluation efforts.</li>
</ul>
&nbsp;
Functional/ Technical Skills
Qualifications:
<ul>
<li>4+ years of combined training and experience in computational social science, natural language processing, computer science, statistics, mixed-methods evaluation or research, or related disciplines</li>
<li>2+ years of experience with SQL in a professional setting</li>
<li>2+ years of experience in programming languages used for data manipulation and computational statistics (such as Python, R) in a professional setting</li>
<li>Knowledge and demonstrated experience using rigorous quantitative or mixed research methods, analyzing data using multiple approaches, and reporting results</li>
<li>Solid writing skills, with an ability to translate research results into non-technical insights for broad consumption</li>
<li>Experience working in cross-functional or matrix teams</li>
</ul>
Reliable High-Speed Internet Required:&nbsp;Must have a stable high-speed internet connection to support seamless remote collaboration, virtual meetings, online job tasks, etc.
Currently, this position is offered on a 6-month contract. The full salary range for this position, across all United States geographies, is $50-$60 per hour.&nbsp;The upper portion of the salary range is typically reserved for existing employees who demonstrate strong performance over time. Starting salary will vary by location, qualifications, and prior experience; during the interview process, candidates will learn the starting salary range applicable for their location. We pay competitively in the tech-forward nonprofit space and offer a robust benefits package.
Only candidates in the following states will be eligible for employment:&nbsp;CA, CO, CT, FL, GA, HI, IL, IN, IA, MD, MA, MI, MO, NJ, NM, NY, NC, OH, PA, TN, TX, UT, VA, WA.
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Senior Research Scientist (6-month contract)

<h3>Job Description</h3>
Job Description(Sr.) Research Associate, Protein Sciences Job Summary: PharmaEssentia is a global biopharmaceutical company committed to developing innovative therapies to address unmet medical needs in oncology, hematology, and immunology. With a strong foundation in disease biology, biologics and translational science, we are expanding our research capabilities to fuel the next generation of breakthroughs. PharmaEssentia Innovation Research Center (PIRC) is seeking a highly motivated and collaborative (Senior) Research Associate, Protein Sciences to join our Biologics Platform team. In this role, you will play a vital part in advancing our pipeline of innovative biotherapeutics—including cytokines, antibodies, and antibody-drug conjugates—by supporting the characterization and optimization of therapeutic candidates for clinical development. Your expertise in Protein Science will be key to cross-functional drug discovery efforts. As a valued contributor to a growing and dynamic team, you’ll help drive our mission to develop transformative therapies for patients. Summary of Key Responsibilities: 
<ul>
<li>Perform biophysical and biochemical characterization to assess protein binding, stability, and developability properties to support research activities and project goals.</li>
<li>Perform complementary cell-based binding and functional assays to enable a comprehensive evaluation of protein function and selection of lead molecules. </li>
<li>Design, optimize, and validate assay protocols to ensure reproducibility between projects and teams.</li>
<li>Demonstrate strong attention to detail and a commitment to quality in organization and documentation.</li>
<li>Analyze data, interpret the results, and effectively communicate the results to internal teams.</li>
</ul>
 Essential Qualifications: Bachelor’s or Master’s degree in biochemistry, biophysics, molecular biology, or a related field with 3+ years research experience in an academic or industry setting.
<ul>
<li>Expertise in protein biochemistry, including experience with biologics characterization and analytical techniques such as BLI/SPR, ELISA, MSD, HPLC, and cell-based assays. </li>
<li>Skill in common mammalian cell culture protocols using primary cells and tumor cell lines.</li>
<li>Proficiency in data analysis/visualization software like GraphPad Prism.</li>
<li>Excellent written and oral communication, organization, and problem-solving skills.</li>
<li>Brings an enthusiastic, flexible, and team-oriented mindset to science. </li>
</ul>
 Preferred Qualifications:
<ul>
<li>Knowledge in antibody structure and function, and experience with antibody drug discovery and multi-specific antibody formats. </li>
<li>Knowledge of expression vector design and cloning (e.g., Gibson assembly), as well as protein purification methods (e.g., affinity, IEX, and SEC). </li>
<li>Experience with flow cytometry for binding assays, cell-based functional assays, and immunophenotyping.</li>
</ul>
EEO Statement: At PharmaEssentia Innovation Research Center (PIRC), we are committed to providing an environment of mutual respect where equal employment opportunities are available to all applicants without regard to race, color, religion, sex, pregnancy (including childbirth and related medical conditions), national origin, age, physical and mental disability, marital status, sexual orientation, gender identity, gender expression, genetic information (including characteristics and testing), military and veteran status, and any other characteristic protected by applicable law. PIRC believes that diversity and inclusion among our team are critical to our success as a global company, and we seek to recruit, develop and retain the most talented people from a diverse candidate pool.&nbsp; PIRC does not accept unsolicited agency resumes. Staffing agencies should not send resumes to our HR team or to any PIRC employees. PIRC is not responsible for any fees related to unsolicited resumes from staffing agencies. &nbsp;
At PharmaEssentia, our goal is to treat as many people with cancer as possible. That means challenging the status quo with better science that leads to better lives. By joining our team, you will not only expand your own possibilities, but you will contribute to expanding options for people with cancer.
<a href="https://us.pharmaessentia.com/careers/" target="_blank">https://us.pharmaessentia.com/careers/</a>
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