Lead molecular virology research and develop viral vector and RNA delivery platforms, overseeing independent and team-based projects from in vitro to in vivo validation.
Compensation
$125,000—$175,000 USD
Responsibilities
Design, execute, and oversee molecular virology and mammalian cell culture experiments
Develop high-throughput screening assays and workflows
Analyze and interpret complex datasets
Collaborate with computational scientists and therapeutic experts
Maintain rigorous scientific documentation
Requirements
Ph.D. in Virology, Molecular Biology, Microbiology, Biochemistry or a closely related life science discipline
Responsible for supporting QC testing for in-process, final product, and stability samples, including data review/verification. Perform method troubleshooting, training, and transfer/validation. Execute document revisions, projects, deviations/investigations/CAPA, and continuous improvement efforts.
Compensation
Summit West - NJ - US: $40.97 - $49.64per hour
Responsibilities
Perform method transfer/validation and routine testing of in-process, final product, and stability samples.
Anticipate and perform routine troubleshooting and problem solving with minimal guidance.
Perform data verification, data review and review of GMP documentation for general and complex methods.
Perform document revision, project, CAPA and deviation/ investigation related tasks and/ or continuous improvement efforts.
Train and mentor others on QC test methods, processes and procedures.
Perform biochemical and immunological assays in a cGMP laboratory environment to support clinical and commercial therapeutics.
Compensation
The expected salary range for this position based on the primary location of California is $60,600 - $112,500 Annual. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance.
Responsibilities
Perform biochemical and immunological cell-based and non-cell-based assays
Support process development, product characterization, stability studies, in-process testing, and lot release testing
Review and release assay data across electronic and paper-based formats
Prepare laboratory reagents and monitor assay performance
Present quality results to cross-functional teams
Requirements
Bachelor’s degree in Biological Sciences or related field
Responsible for movement and control of QC samples and materials in a GMP regulated environment, including cold chain storage, inventory, and sample tracking.
Compensation
Devens - MA - US: $27.35 - $33.14 per hour
Responsibilities
Handle test samples throughout the sample lifecycle: receipt, storage, distribution, transfer, and disposal
Facilitate cold chain transfers of samples
Ensure samples and materials are appropriately labelled and maintain sample tracking, labelling and chain of custody records
Maintain inventory and distribution of QC samples and materials
Record performance metrics for the sample management group
Requirements
Associate's degree in Chemistry, Microbiology or related science
High school diploma/GED with 2+ years of relevant work experience
Nice to have: knowledge of regulatory standards as they apply to GMP laboratories
Nice to have: experience with cold chain sample storage and transfer in a GMP regulated environment
Lead scientist responsible for laboratory work, experimental design, material characterization, and data interpretation to support drug product development.
Responsibilities
Design and conduct research experimentation
Assist in characterization needs for formulation development
Perform material characterization of APIs and excipients
Operate analytical instrumentation such as Inverse Gas Chromatography (IGC)
Review and approve relevant documentation for compliance (ELN)
Requirements
Bachelor's degree in a related field
Master's degree in Chemical Engineering, Mechanical Engineering, Pharmaceutical Science, Materials Science, Chemistry, or a related discipline
A Research Associate role focused on sterility testing and endotoxin testing on pharmaceutical products within a laboratory setting.
Compensation
$100,000 USD + equity options
Responsibilities
Prepare, handle, and incubate media and test systems under aseptic conditions in a cleanroom or isolator environment
Perform sterility testing of drug products, raw materials, and components using membrane filtration or direct inoculation
Conduct bacterial endotoxin testing using CRL Endosafe according to USP
Handle microbial cultures, including test strains such as S. aureus, P. aeruginosa, C. albicans, and B. subtilis, for growth promotion and suitability testing
Support qualification and routine monitoring of cleanrooms, isolators, biosafety cabinets, and autoclaves
Leading strategies for the validation, verification, and transfer of analytical and compendial methods supporting clinical and commercial biologics, while shaping analytical strategies across the CMC lifecycle.
Responsibilities
Leading all aspects of analytical method validation, transfer, and compendial method verification across clinical development and method lifecycle stages
Developing and implementing strategies for analytical method validation, verification, transfer, and ongoing lifecycle management
Leading cross-functional teams in assay troubleshooting and OOS/OOT investigations during method validation and transfer activities
Designing investigation plans and supporting the execution of laboratory experiments to identify root causes and develop scientifically sound solutions
Reviewing analytical test procedures, method performance metrics, and testing results across the global testing network
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