Scientist at Gilead Sciences

Foster City, California, United States

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Not SpecifiedCompensation

Mid-level (3 to 4 years), Senior (5 to 8 years)Experience Level

Full TimeJob Type

UnknownVisa

Biotechnology, PharmaceuticalsIndustries

Requirements

M.S. in Chemical Engineering, Bio-engineering, Biochemical Engineering, Biochemistry, or related field with >4 years (or B.S. with >6 years) of industrial experience in biologics purification development and/or scaleup operations
Hands-on experience with pilot scale purification, operation planning, and execution
Experience in tech transfer and process scale-up
Working knowledge of single-use manufacturing technology
Proficient with Unicorn and working experience with Akta system (e.g., Pure, Avant, Pilot, and Ready)
Experience in data analysis (e.g., JMP, Spotfire), creating and maintaining batch records, authoring operation procedures and reports
Working knowledge of lab automation, data management, data science, knowledge management, and data protection is a plus
Excellent communication, technical writing, and presentation skills, and aptitude for creative problem solving
Demonstrated ability to collaborate cross-functionally
Commitment to inclusion and diversity

Responsibilities

Maintain a state-of-the-art purification lab that enables rapid assessment of new biologics entities, purification process development, and scaleup
Participate in material generation planning and execute pilot scale purification operations
Support process scaleup and implementation in the Pilot Lab
Collect and analyze data from Pilot Lab runs in compliance with data integrity policy
Author and review batch records, protocols, and reports
Assist in transferring processes to the Pilot Lab in a timely manner and provide technical support for Pilot run atypical event investigations
Author and maintain Pilot Lab work instructions, standard operating procedures, and training plans
Support training for Pilot Lab operators
Contribute to biologics manufacturing platform development and new technology/innovation evaluation and implementation to enable fast first-in-human clinical trial timelines
Participate in cross-functional initiatives as needed
Adhere to department budget and all training, compliance, and safety requirements

Skills

Key technologies and capabilities for this role

biologics purificationpilot scale operationspurification process developmentlab operationsstaff trainingtechnology evaluationprocess scaleuptoxicology studies supportcross-functional collaboration

Questions & Answers

Common questions about this position

What degree is required for the Scientist position?

An M.S. in Chemical Engineering, Bio-engineering, Biochemical Engineering, Biochemistry, or related field is required.

What are the main responsibilities of this role?

The role involves executing pilot scale purification operations, maintaining Pilot Lab readiness, supporting training, participating in technology evaluation, and contributing to biologics development and cross-functional initiatives.

Is this a full-time position?

Yes, this is a full-time employment position.

What is the salary range for this Scientist role?

This information is not specified in the job description.

What does Gilead value in its employees and culture?

Gilead values collaboration, determination, a relentless drive to make a difference, and passionate, ambitious people who contribute to scientific innovations; it emphasizes great leadership, inclusion, development, and empowerment.

Gilead Sciences

Develops and commercializes biopharmaceuticals

About Gilead Sciences

Gilead Sciences focuses on discovering, developing, and commercializing medicines for various medical conditions, including HIV/AIDS, liver diseases, cancer, inflammatory and respiratory diseases, and cardiovascular issues. The company conducts extensive research and development to create new therapies, which are then marketed to healthcare providers, hospitals, and pharmacies after receiving regulatory approval. Gilead differentiates itself from competitors through its strong commitment to R&D and strategic partnerships, such as with SAP Ariba, to enhance its operations and product offerings. The company's goal is to improve health equity and access to care globally, working with communities to ensure that its medicines reach those in need.

Foster City, CaliforniaHeadquarters

1987Year Founded

$15,873.6MTotal Funding

IPOCompany Stage

Biotechnology, HealthcareIndustries

10,001+Employees

Benefits

Paid family time off and paid parental time off

Generous 401(k) contribution matching

Comprehensive medical plans that cover both physical and mental healthcare

Global Wellbeing Reimbursement

Time Off

Global Volunteer Day

Giving Together Program

Employee Support Programs

Flexible Work Options

Risks

Increased competition in HIV treatment from ViiV Healthcare's expanding drug portfolio.

Regulatory scrutiny over drug pricing could impact Gilead's U.S. market operations.

Patent expirations, like Truvada's, lead to increased generic competition and revenue loss.

Differentiation

Gilead's lenacapavir is recognized as the 2024 Breakthrough of the Year for HIV care.

Partnerships with LEO Pharma and Tubulis enhance Gilead's focus on inflammatory and cancer therapies.

Gilead's commitment to health equity initiatives like COMPASS and HepConnect sets it apart.

Upsides

Gilead's strategic partnerships expand its reach in inflammatory and oncology drug markets.

Investment in digital health technologies enhances Gilead's R&D and patient engagement.

Focus on sustainability improves Gilead's operational efficiency and corporate reputation.

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