Research & Development Analytical Scientist Job at Argenta (Shawnee)

Scientist II/Sr. Scientist I, Analytical Research and Development

We are seeking a Scientist II/ Senior Scientist I with hands‑on experience in ph...

Location

United States , Cambridge

Salary:

130000.00 - 180000.00 USD / Year

Beam Therapeutics

Expiration Date

Until further notice

Requirements

Degree in a relevant discipline (biochemistry, biotechnology, biological sciences, bioengineering, or related fields)
Minimum PhD with 2+ years or BS/MS with 10-15 years industry experience
Must have hands-on experience on analytical method development, optimization, qualification, and testing at GMP or non-GMP environments, supporting clinical phase programs
Experience with analysis of RNAs, proteins, protein conjugates, lipids, and lipid nanoparticles (LNPs) is highly desirable
Extensive experience with at least one or several of the analytical techniques is required: HPLC (RP, IPRP, SEC, IEX), capillary gel electrophoresis, ELISA
Experience with qPCR, DNA and RNA extraction, western blotting, UV spectrophotometry, DLS, MALS, mass spectrometry, and compendial testing will be a plus
Experience with analytical CMC development, method transfer, and QC technical support is highly desirable
A good understanding of ICH Q2 and Q14, with working knowledge on analytical Quality by Design concept
Familiarity with data analysis software such as Openlab, Chromeleon, and statistical software such as JMP
Team player with excellent oral and written communication skills

Job Responsibility

Lead early through late phase method development, optimization, and transfer for lot release, stability, and characterization of drug substances, critical materials, and drug products
Establish technical leadership as subject matter expert in multiple analytical techniques during method development and transfer and provide technical troubleshooting support when needed
Work with cross-functional groups including Research & Development, Quality Control, and Process Development teams to participate in various aspects of method development, transfer, characterization, comparability, and investigation
Coordinate routine sample testing including requests from Research and Development groups and Process Development teams
Author and review SOPs, technical reports, and assist in the preparation of CMC regulatory submissions
Analyze, track, and trend data to monitor analytical assays and ensure consistency in assay performance
Maintaining detailed documentation of experiments in ELN system
Adapting to a fast-paced, dynamic research environment
Mentor and train junior scientists
Living Beam Therapeutics core values

Fulltime

Analytical Development Scientist

Analytical Development Scientist. Provide measurement science to generate and im...

Location

United Kingdom , Huddersfield

Salary:

17.91 - 18.91 GBP / Hour

SRG

Expiration Date

Until further notice

Requirements

Degree (BSc, MSc, or equivalent) in Chemistry or Analytical Chemistry with a proven track record in analytical method development
Knowledge of HSE systems, QA procedures, and compliance responsibilities
Comprehensive experience with chemical and physical analytical techniques such as LC, GC, MS, NMR, FTIR, SEM, EDS, and PSD
Strong background in analytical chemistry, critical data analysis (statistics/DoE), method development, calibration, modelling, validation, and technical transfer
Significant experience supporting manufacturing operations including process monitoring, data analysis, troubleshooting, and implementing process improvements
Problem Solving: Ability to analyse complex problems and generate creative, original solutions
Management: Strong time management, work planning (>4 weeks), team coordination, and meeting management skills
Laboratory/Analytical: Comprehensive practical and theoretical knowledge
Research Skills: Literature/database searching, and ability to interpret complex information
Communication: Clear verbal, written, and presentation skills

Job Responsibility

Provide measurement science to generate and improve manufacturing processes for new and existing products through improved understanding
Support manufacturing processes and projects to meet business targets
Utilise laboratory and plant information efficiently to identify improvements and implement change in line with good change‑management principles and procedures
Collaborate with internal and external partners to deliver analytical aspects of process development and manufacturing support
Remain up to date with scientific developments and proactively identify opportunities to apply them to project work
Plan, manage and conduct non‑routine chemical and physical analysis, analytical development, and process analytical technology projects to support new and existing manufacturing processes
Provide expertise and advice in Analytical Chemistry to both local and global teams under guidance of the Specialist Team Leader
Support development of other scientists in analytical techniques and best practices
Use knowledge and experience to improve safe ways of working in partnership with Departmental Safety Leadership teams
Manage, record and communicate activities in compliance with site, company, and regulatory requirements

Analytical Chemistry Development Scientist 1

Looking for local candidates, contract position, potential long term depending o...

Location

United States , Salt Lake City

Salary:

25.00 - 28.00 USD / Hour

MillenniumSoft Inc

Expiration Date

Until further notice

Requirements

Experience / understanding of working in a lab
Lab work experience a strong plus
Ability to write detailed technical protocols and reports
Strong communication skills
Strong ability to learn
Bachelor’s degree or higher in a STEM major (Examples: Chemistry, chemical engineering, biomedical engineering, materials science)
Need US Citizens Or GC Holders Only

Job Responsibility

Provide technical skill, analytical testing, and engineering support for design and development activities for various medical device products
Support current products in roles of quality, research & development, pilot-scale manufacturing, supply continuity, and cost improvement
Focus will be on analytical chemistry and chemical work in the lab
Execute technical and cross-functional project work

Fulltime

Analytical Chemistry Development Scientist

This is a full-time contract position, with potential for long-term engagement, ...

Location

United States , Salt Lake City

Salary:

Not provided

MillenniumSoft Inc

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Chemistry, Chemical Engineering, Biomedical Engineering, Materials Science, or related field
Experience or understanding of lab work is required, with hands-on lab experience strongly preferred
The ability to write detailed technical protocols and reports is advantageous
Strong communication skills
Strong learning ability
Proficiency in analytical chemistry and/or in vitro biological testing
Understanding of lab protocols and procedures
Strong written and verbal communication skills
Ability to learn quickly and adapt to new tasks

Job Responsibility

Provide technical support for technology development in medical device products, including research & development and pilot-scale manufacturing projects
Conduct analytical chemistry and/or in vitro biology work using lab instruments
Execute technical and cross-functional project tasks
Follow standard operating procedures (SOP) and test methods
Coordinate lab maintenance activities
Perform other duties as directed by the Supervisor to support business operations

Fulltime

Research Scientist - MCED Assay Development

The Research Scientist works both independently and collaboratively on multiple ...

Location

United States , San Diego

Salary:

100000.00 - 150000.00 USD / Year

Exact Sciences

Expiration Date

Until further notice

Requirements

PhD in life sciences, medical technology, clinical laboratory science, chemical/physical/biological science, or related field
or Master’s degree in life sciences, medical technology, clinical laboratory science, chemical/physical/biological science, or related field and 4 years of related experience in lieu of a PhD
or Bachelor’s degree in life sciences, medical technology, clinical laboratory science, chemical/physical/biological science, or related field and 6 years of related experience in lieu of PhD
1+ years of experience in medical device/IVD, biotech, life science, or pharmaceutical industry
Demonstrated ability to apply molecular biology and/or biochemical techniques
Demonstrated understanding of GMP, ISO, and Quality Systems
Good knowledge of molecular biology and/or biochemistry and/or next-generation sequencing (NGS) and genomics
Basic knowledge of statistical and mathematical methods in biology/genetics/genomics
including experience with statistical software, such as JMP
Proficient computer skills to include Internet navigation, Email usage, and word processing

Job Responsibility

Work on complex scientific problems that require strong analytical thinking and creative problem solving
Independently design, execute, and analyze bench-level experiments, operating and maintaining relevant scientific instrumentation and escalating issues as needed
Apply and optimize existing methods and technologies while proposing and evaluating new experimental approaches
Exercise sound judgment within established practices and policies to select methods, interpret data, and drive to clear, actionable conclusions
Maintain accurate, complete, and compliant laboratory documentation in accordance with legal, ISO, and QSR requirements
Contribute scientific insight to project planning and experimental design, generating and communicating development plans for key project components
Prepare clear reports and presentations of results, conclusions, and next steps for technical teams and project stakeholders
Collaborate effectively with cross-functional project teams to achieve departmental and project objectives

What we offer

Paid time off (including days for vacation, holidays, volunteering, and personal time)
Paid leave for parents and caregivers
A retirement savings plan
Wellness support
Health benefits including medical, prescription drug, dental, and vision coverage
Bonus eligibility

Fulltime

Scientist Organic Chemistry | R&D Analytical Development

As a Scientist Organic Chemistry, you will join the Advanced Molecular Analysis ...

Location

Belgium , Beerse

Salary:

Not provided

Randstad

Expiration Date

August 05, 2026

Requirements

PhD in Organic Chemistry (or a related field) is highly preferred
candidates with a Master’s degree and a minimum of 6 years of relevant experience will also be considered
proven expertise in nitrosamines chemistry and hands-on experience with Mass Spectrometry (Triple Quadrupole and High-Resolution MS) is a significant advantage
strong background in developing chromatographic methods and familiarity with regulatory frameworks (ICH, EMA, FDA) and GMP guidelines
fast learner with scientific curiosity, a self-steering pro-active attitude, and ability to work effectively in a global team
fluent in English (written and spoken)
knowledge of Dutch is a plus
ready to work onsite 5 days a week in Beerse, Belgium

Job Responsibility

Support the feasibility and development of innovative analytical methods, ranging from complex sample preparation to advanced chromatographic separations for trace impurity quantification
lead comprehensive investigations into nitrosamine formation and chemical reactivity from early-stage research through late-stage development
work closely with cross-functional teams and initiate partnerships with universities and research institutions to expand our external innovation network
utilize your experience to review documents and report scientific findings accurately
maintain a safe laboratory environment in strict accordance with GMP, environmental, and health regulations

Fulltime

Senior Research Scientist - Toxicology

We are looking for a dynamic and detail-oriented Senior Research Scientist to jo...

Location

Canada , Vancouver

Salary:

112000.00 - 150000.00 CAD / Year

AbCellera Biologics

Expiration Date

Until further notice

Requirements

PhD in Toxicology or a related field, and a minimum of 5-8 years of related industry experience supporting biologics development
candidates with a MSc and 10+ years of relevant experience will also be considered
extensive hands-on experience with in vitro and/or in vivo toxicology studies
demonstrated proficiency with nonclinical safety assessment of large molecules/ biologics
strong organizational, critical problem-solving, and analytical skills to assess complex datasets and propose strategic solutions
excellent scientific writing, communication, and collaboration skills to effectively lead scientific discussions and influence decision-making
DABT accreditation (highly desirable, but not required)

Job Responsibility

Leading the design, planning, and oversight of in vitro safety and/or in vivo toxicology studies, ensuring alignment with global regulatory guidelines and strategic company objectives
Serving as a subject matter expert (SME) for Nonclinical Safety within cross-functional project teams, actively representing the function in internal and external stakeholder meetings
Providing critical assessment of complex toxicology data, translating and communicating clear, actionable risk-benefit evaluations and strategic recommendations to project teams and executive leadership
Maintaining comprehensive and meticulous recording of nonclinical safety study data as required by Good Laboratory Practice (GLP)
Authoring and critically reviewing the in vitro safety, toxicology, and safety pharmacology sections of Regulatory documentation (such as INDs, CTAs, IBs, and BLAs)
Collaborating seamlessly with scientists across various matrixed teams at AbCellera to ensure high data quality and accelerate program advancement
Contributing to the development of our toxicology programs and performing as a nonclinical safety/toxicology representative as needed
Maintaining an active scan and synthesis of published toxicology literature and evolving regulatory guidance relevant to AbCellera’s product portfolio, translating insights into internal best practices

What we offer

Equity
annual bonus dependent on team and company performance
6% (non-match) RRSP contribution
CAD $1,500 annual Active Lifestyle Allowance
annual vacation
professional development opportunities
comprehensive health benefits
Scientific and technical mentorship
strong sense of community and connections through work, clubs, and socials

Fulltime

Research Scientist II - Toxicology

We are looking for a dynamic and detail-oriented Research Scientist II to join o...

Location

Canada , Vancouver

Salary:

100000.00 - 125000.00 CAD / Year

AbCellera Biologics

Expiration Date

Until further notice

Requirements

PhD in Toxicology or related biological science field and a minimum of 2-5 years of related experience in an academic or industry environment
candidates with a MSc and 7+ years of relevant experience will also be considered
hands-on experience with in vitro and/or in vivo toxicology studies
strong desire to learn and develop proficiency with nonclinical safety assessment of large molecules/biologics
strong analytical and problem-solving skills
excellent communication and collaboration skills

Job Responsibility

Designing, planning, and supporting the execution of in vitro and/or in vivo toxicology studies as needed, adhering to the appropriate regulatory guidelines and communicating toxicology study results internally
Updating and maintaining proper recording of nonclinical safety study data, as required by Good Laboratory Practice (GLP)
Assisting with the authoring of toxicology sections of Regulatory documentation
Collaborating with scientists across various teams at AbCellera to ensure high data quality and that studies meet the company’s objectives
Contributing to the development of our toxicology programs and participating as a nonclinical safety/toxicology representative as needed
Maintaining an active scan of published toxicology data relevant to AbCellera’s product portfolio, and continuously expanding your knowledge base

What we offer

Equity
annual bonus dependent on team and company performance
6% (non-match) RRSP contribution
CAD $1,500 annual Active Lifestyle Allowance
annual vacation
professional development opportunities
comprehensive health benefits
scientific and technical mentorship

Fulltime

Select Country

Research & Development Analytical Scientist

Job Description

Job Responsibility

Requirements

Looking for more opportunities?