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Associate Scientist Cell Line Development Jobs (NOW HIRING)

Senior Scientist, Cell Science

Redmond, WA · On-site

$90K - $140K/yr

The Senior Scientist in the Cell Science Department is responsible for the development and ... Design and execute cell line development workflows, including vector design, transfection, clone ...

Associate Scientist/Scientist - Cell-Based Assay Core Facility Title: Associate Scientist/Scientist ... development, and core laboratory services for clinical trials. Cell-based Assay Core Lab The Cell ...

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Associate Scientist Cell Line Development information

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How much do associate scientist cell line development jobs pay per hour?

As of Jul 23, 2026, the average hourly pay for associate scientist cell line development in the United States is $35.92, according to ZipRecruiter salary data. Most workers in this role earn between $27.88 and $40.87 per hour, depending on experience, location, and employer.

What are some common challenges faced by Associate Scientists in Cell Line Development, and how can they be addressed?

Associate Scientists in Cell Line Development often encounter challenges such as optimizing cell growth conditions, maintaining cell line stability, and troubleshooting low productivity or contamination issues. Addressing these challenges requires strong attention to detail, effective documentation, and collaboration with cross-functional teams such as upstream process development and quality control. Regular communication with senior scientists and participation in team meetings can also help in problem-solving and ensuring project timelines are met. Staying updated on the latest techniques and technologies in cell line engineering further supports overcoming these obstacles.

What does an Associate Scientist in Cell Line Development do?

An Associate Scientist in Cell Line Development is responsible for creating and optimizing cell lines that are used in the production of biopharmaceutical products. Their work involves culturing cells, performing genetic modifications, and conducting experiments to select the best cell lines for manufacturing proteins or other biologics. They also document their findings, analyze data, and collaborate with other scientists to ensure the cell lines meet regulatory and quality standards. This role is vital in the early stages of drug development, as robust cell lines are essential for consistent and scalable production.

What is the difference between Associate Scientist Cell Line Development vs Associate Scientist Bioprocess Development?

AspectAssociate Scientist Cell Line DevelopmentAssociate Scientist Bioprocess Development
Required CredentialsBachelor's or Master's in Life Sciences, Molecular Biology, or related fieldsBachelor's or Master's in Biotechnology, Chemical Engineering, or related fields
Work EnvironmentLaboratory focused on cell line creation and characterizationLaboratory and pilot plant focused on process scale-up and manufacturing
Employer & Industry UsageBiotech and pharmaceutical companies developing cell lines for biologicsBiotech and pharma companies optimizing bioprocesses for production

Associate Scientist Cell Line Development primarily focuses on creating and characterizing cell lines for biologic production, while Associate Scientist Bioprocess Development concentrates on scaling up and optimizing manufacturing processes. Both roles require similar educational backgrounds and are essential in biologics development, but they differ in their specific focus within the biopharmaceutical pipeline.

What are the key skills and qualifications needed to thrive as an Associate Scientist in Cell Line Development, and why are they important?

To thrive as an Associate Scientist in Cell Line Development, you need a strong background in cell biology, molecular biology, and protein expression, typically supported by a relevant science degree. Familiarity with technical tools such as flow cytometry, cell culture systems, CRISPR gene editing platforms, and data analysis software is essential. Attention to detail, strong problem-solving abilities, and effective teamwork are standout soft skills in this role. These skills ensure high-quality cell line generation, reproducible results, and successful collaboration in fast-paced biopharmaceutical environments.
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Executive Director, Head of Cell Line & Cell Culture Dev

Jj

Spring House, PA

Full-time

Posted 22 days ago


Job description

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.Learn more at jnj.com.

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Enterprise Management

Job Sub Function:

Executive Management

Job Category:

People Leader

All Job Posting Locations:

Malvern, Pennsylvania, United States of America, Spring House, Pennsylvania, United States of America

Job Description:

Johnson & Johnson -- About Innovative Medicine

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

Learn more at https://www.jnj.com/innovative-medicine

Role Overview

The Executive Director, Cell Line and Cell Culture Development is a senior scientific and people leader within Proteins Development - API, accountable for the global strategy, execution, and organizational leadership of mammalian cell line development and upstream process development across the protein therapeutics portfolio.

This role is accountable for fitforstage development of all proteinderived molecules from early development through latestage development to commercialization, as well as providing deep technical and nextgeneration process development support to commercial products as needed-ensuring robust, scalable, compliant, and costeffective processes that enable rapid portfolio progression and reliable patient supply.

The Executive Director operates as a key member of the Proteins Development - API leadership team, partnering across Proteins Development - API and beyond including Biologics Discovery Process Research, Biologics Development China Core, Drug Product Development and Delivery, Analytical Development, CMC, Quality, Regulatory, Manufacturing, Procurement, and J&J Innovative Medicine Supply Chain to deliver integrated solutions aligned with enterprise priorities.

Key ResponsibilitiesScientific & Technical Strategy
  • Define and own the global strategy to build, deploy, and continuously advance worldclass cell line, media, and cell culture platforms that remain competitive and fitforpurpose across the portfolio.
  • Ensure development approaches and work packages are fitforstage, platformaligned, and positioned to enable rapid clinical progression, best product and process at launch, and robust lifecycle management.
  • Provide senior scientific leadership across cell line generation, clone selection, media and feed strategy, upstream process optimization, scaleup, and process characterization.
  • Serve as the enterprise subjectmatter authority for CLD and upstream development within CMC governance, portfolio, and technical review forums.
Program & Portfolio Delivery
  • Ensure on quality, on time, and on budget cell line development and cell culture development in support of integrated CMC plans.
  • Partner with Biologics Discovery Process Research and CMC program leadership to align scope, timelines, resources, and risk postures.
  • Accountable for proactive identification and management of technical and operational risks related to cell line and cell culture development.
  • Support technology transfer and GMP manufacturing readiness, including troubleshooting, deviation support, and continuous process improvement.
External Manufacturing & Partnerships
  • Provide executive oversight of CDMO performance, ensuring delivery against technical, quality, compliance, and timeline expectations.
  • Act as senior escalation point for complex issues involving external partners and manufacturing sites.
Regulatory & Quality Alignment
  • Own cell line and cell culture-related regulatory strategy, ensuring phaseappropriate content for IND, BLA, and global submissions.
  • Partner closely with Quality and Regulatory Affairs to ensure development activities meet global regulatory and compliance expectations.
  • Represent cell line and cell culture development in regulatory interactions as required.
People, Culture & Organizational Leadership
  • Build, lead, and develop a highperforming organization, including senior leaders and technical experts.
  • Establish clear expectations and accountability for scientific rigor, delivery excellence, safety, quality, and budgetary compliance, and talent development.
  • Drive a culture aligned with J&J CREDO, C.E.O Leadership Imperatives, emphasizing accountability, collaboration, inclusion, and continuous improvement.
  • Ensure succession planning and capability building to support longterm organizational sustainability.
QualificationsEducation

PhD in Cell Biology, Biochemistry, Chemical Engineering, Biotechnology, or related scientific discipline.

Experience
  • 10+ years of experience in biologics CMC with deep expertise in mammalian cell line development and cell culture process development.
  • Demonstrated leadership at Senior Director or Executive Director level within large pharma or advanced biotech organizations.
  • Proven track record delivering upstream processes through clinical development and GMP manufacturing.
  • Strong experience working within matrixed, global organizations and with external manufacturing partners.
  • Demonstrated ability to influence senior stakeholders and operate effectively within enterprise governance models.

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson and Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, please email the Employee Health Support Center (ra-employeehealthsup@its.jnj.com) or contact AskGS to be directed to your accommodation resource.

Required Skills:

Preferred Skills:

Budget Management, Business Continuity Planning (BCP), Competitive Landscape Analysis, Continuous Improvement, Corporate Management, Developing Others, Empowering People, Inclusive Leadership, Leadership, Managerial Courage, Operational Excellence, Performance Measurement, Stakeholder Engagement, Standard Operating Procedure (SOP), Strategic Analysis, Strategic Change, Vendor Management