Lead scientific development of small molecule formulation and manufacturing processes, ensuring regulatory compliance and quality standards.
Compensation
The salary range for this position is: $146,540.00 - $189,640.00. Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package.
Responsibilities
Organizes, files and retrieves project‑related records
Maintains laboratory functions
Operates laboratory instrumentation and training others
Designs and executes experiments for cross‑functional projects
Troubleshoots analytical methods and manufacturing processes
Support the formulation and characterization efforts for biotherapeutic drug product discovery and development across different therapeutic areas, performing protein analytical techniques and facilitating tech transfer activities.
Compensation
$103,000.00-131,000.00 Annual
Responsibilities
Perform protein analytical techniques to inform formulation and process optimization
Assess biotherapeutic stability as a function of formulation and process
Facilitate tech transfer activities
Document experiments using electronic lab notebook
We seeking an Associate Scientist to join the Cell Line Development team to conduct CHO-based cell line engineering and screening for human therapeutics, executing synthetic biology studies and new technology evaluations.
Responsibilities
Perform CHO cell line development processes including transfection, cloning, characterization, and cell banking using state-of-the-art equipment.
Complete comprehensive documentation of studies in an Electronic Lab Notebook (ELN).
Help identify emerging practices for biologics cell line development and manufacturing to shape scientific strategies and develop improved workflows.
Contribute to innovation focused on the development of novel cell line development workflows and applications.
Work on novel, high-impact CLD research projects that go beyond standard molecules and workflows, with results intended for publication and/or patent filings.
Engineer to support lipid nanoparticle (LNP) process development, scale‑up, and characterization for gene editing therapies.
Compensation
Pay Rate: $65.00 – $68.00/hr on W2 (Without Benefits)
Responsibilities
Support the design, manufacturing and characterization of lipid nanoparticles (LNPs) for screening critical process parameters (CPPs) and critical material attributes (CMAs) that impact critical quality attributes (CQAs).
Support the design and execution of a wide range of experiments including DoEs to advance LNP technology and process development.
Participate in defining equipment specification/selection, draft procedures and recommended operating parameters/ranges
Write protocols, perform experiments, organize and analyze data, interpret results, record experiments in an electronic lab notebook, and summarize work in presentations and technical reports
Assist in ordering supplies, making reagents, and maintaining a safe and high-performing laboratory
Requirements
Bachelor's/Master's degree in chemical engineering, bioengineering, chemistry, pharmaceutical sciences, or another related field
Nice to have: lipid nanoparticle formulations and analytical characterization methods
Senior Scientist in the Pharmacokinetics, Dynamics, Metabolism and Bioanalytics group, responsible for developing and validating LC/MS methods and leading automation-enabled discovery workflows.
Compensation
$117,000.00 - $184,200.00
Responsibilities
Design and execute LC-MS methods for therapeutic antibodies, peptides, and drug conjugates
Provide scientific leadership for automation-enabled discovery workflows
Utilize bioanalytical approaches to characterize large molecule drug properties
Collaborate with subject-matter experts in Boston, South San Francisco and West Point
Requirements
Ph.D. in biochemistry, chemistry, pharmacology, pharmaceutical sciences, biomedical engineering or related field
Master’s degree in biochemistry, chemistry, pharmacology, pharmaceutical sciences, biomedical engineering or related field
Bachelor’s degree in biochemistry, chemistry, pharmacology, pharmaceutical sciences, biomedical engineering or related field
The Quality Control Technician II will be responsible for sampling, testing, inspecting, and releasing inbound raw materials for the Solutions division.
Compensation
Competitive Pay – Starting at $24 an hour
Responsibilities
Maintain order and appropriate labeling of the Quarantine area
Place non-conforming materials on Hold with correct labeling and documentation
Assist Quality Management in investigating issues and applying corrective and preventive actions as instructed
Manage retesting of aging inventory
Work with procurement and inventory management to prioritize testing of expiring materials
Requirements
High school diploma or equivalent
Associate's or Bachelor’s degree in Food Science or a similar scientific discipline
Nice to have: HACCP Certification
Nice to have: Associate's or Bachelor’s degree in Food Science or a similar scientific discipline
Lead and manage a downstream process team to develop purification processes for next-generation AAV gene therapy and execute early-stage process development.
Compensation
The salary for this position is expected to range between $108,500 and $201,500 per year for Principal Scientist I, and between $119,700 and $222,300 per year for Principal Scientist II.
Responsibilities
Lead and manage a 3-5 person downstream process team and provide technical support, training, and SME knowledge to assist with the professional development of direct reports.
Coordinate activities with associates across upstream process and analytical teams.
Develop strategies in collaboration with Disease Areas and partner with various line functions to support early drug discovery from target selection and validation through lead compound selection and developability assessment.
Serve as a subject matter expert to transfer manufacturing process knowledge to Technical Research & Development team and advance pipeline programs into clinical phases.
Lead effort and work collaboratively with Technical Research & Development to develop innovative and cost-effective downstream processes for next-generation AAV.
Requirements
PhD in bioprocessing, biochemical engineering, gene therapy or a related field
Associate Scientist, Cell Line DevelopmentAsimov · Boston, US
Senior Scientist, PharmacokineticsMerck · West Point, US+2 more