Process Dev Engineering Senior Scientist, Media Development

Reposted 8 Days Ago
Be an Early Applicant
Boston, MA, USA
In-Office
123K-185K Annually
Senior level
Biotech • Pharmaceutical
The Role
The role involves developing cost-effective cell culture media, optimizing processes, troubleshooting raw material challenges, and supporting tech transfer for GMP manufacturing while potentially managing juniors.
Summary Generated by Built In

Job Description

General Summary:

Cell, gene and biologic therapies are rapidly growing parts of Vertex Pharmaceuticals, where research, development, and clinical manufacturing are highly integrated together at our new R&D site in Boston Seaport.

Vertex is seeking a talented individual to join our Process Development team to support media development and optimization efforts. The focus of this position is to support advancement of the innovative stem cell culture medium development and optimization for cell and gene therapy applications. This position will collaborate with cross functional teams to advance media optimizations to enable process scaling, cost of goods reduction, and process robustness improvement through fundamental process understanding. The ideal candidate has deep expertise in media development and optimization, fundamental cell culture process understanding, thrive in a fast-paced environment and proven ability to perform under pressure. The position will be based in Boston, MA.

Key Duties and Responsibilities:

  • Develop robust and cost-effective cell culture media for commercial scale manufacturing.
  • Define and implement technical roadmaps for media development and optimization, ensuring alignment with business priorities and leadership strategy.
  • Troubleshoot complex raw material sourcing and control challenges, with a strong understanding of GMP, regulatory, and quality requirements.
  • Develop and optimize high-throughput, small-scale media screening toolboxes to enhance media development processes.
  • Stay up to date with emerging analytical tools, omics technologies and scientific advancements to drive hypothesis guided media optimization.
  • Generate and review technical reports, regulatory filings, source documents, patents and external publications.
  • Support media preparation protocol transfer to pilot team and support GMP manufacturing tech transfer.
  • Foster strong partnerships with internal and external stakeholders, proactively managing relationships to ensure alignment and efficient execution.
  • Potential of managing or mentoring a small group of junior level employees.
  • Lead by example, work closely with the team in the lab and conduct hands-on experiments. Foster a culture of innovation and continuous improvement.

Knowledge and Skills:

  • Strong fundamental knowledge in cell culture metabolism and biological pathways, and extensive experience of medium development (stem cell culture experience is preferred)
  • In-depth understanding and extensive experience of cell culture process development, perfusion process development, and bioreactors across scales. Experience with high throughput and automated cell culture platforms is highly preferred.
  • Extensive knowledge and experience on raw material control and sourcing considerations.
  • Solid knowledge and experience with statistical principles and design of experiments (DOE).
  • Must have a working knowledge of cGMP.
  • Excellent verbal and written communication skills.
  • Ability to handle multiple tasks while meeting timelines and adapting to changing priorities.
  • Strong people skills and ability to work with diverse team dynamics, and potential in the future to manage a team.
  • Excellent organizational skills and high attention to detail.
  • Strong people skills and ability to work with diverse teams

Education and Experience:

  • Degree in relevant engineering or scientific discipline (e.g., chemical or biochemical engineering, natural or life sciences).
  • PhD with 2-5 years of relevant industry work experience, or a MS with 6-9 years of relevant industry experience, or a BS with 8-11 years of industry experience.

Participation in weekend work rotation with the broader team required.

Pay Range:

$123,200 - $184,800

Disclosure Statement:

The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, experience, and other job-related factors permitted by law.

At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations.  From medical, dental and vision benefits to generous paid time off (including a week-long company shutdown in the Summer and the Winter), educational assistance programs including student loan repayment, a generous commuting subsidy, matching charitable donations, 401(k) and so much more.

Flex Designation:

On-Site Designated

Flex Eligibility Status:

In this On-Site designated role, you will work five days per week on-site with ad hoc flexibility.  

Note: The Flex status for this position is subject to Vertex’s Policy on Flex @ Vertex Program and may be changed at any time.

#LI-Onsite

Company Information

Vertex is a global biotechnology company that invests in scientific innovation.

Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at [email protected]

Skills Required

  • Degree in relevant engineering or scientific discipline (chemical/biochemical engineering, natural/life sciences)
  • PhD with 2-5 years or MS with 6-9 years or BS with 8-11 years of relevant industry experience
  • Strong knowledge in cell culture metabolism and biological pathways, extensive experience in medium development
  • Experience in cell culture process development, perfusion process development, bioreactors
  • Knowledge and experience with statistical principles and design of experiments (DOE)
  • Working knowledge of cGMP
  • Excellent verbal and written communication skills
  • Ability to handle multiple tasks and changing priorities
  • Strong people skills for teamwork dynamics
  • Participation in weekend work rotation

Vertex Pharmaceuticals Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Vertex Pharmaceuticals and has not been reviewed or approved by Vertex Pharmaceuticals.

  • Parental & Family Support Policies provide 12 weeks of 100% paid bonding leave for all U.S. parents with additional fully paid time for birth parents. Family-forming supports include adoption and surrogacy assistance, fertility options like IVF and egg cryopreservation, breast‑milk shipping, subsidized childcare, backup care, and a DCFSA match.
  • Leave & Time Off Breadth Time off includes roughly four weeks of vacation, 13 holidays, sick time, and two companywide shutdowns (summer and year‑end). Some roles also include flexible or unlimited time off and paid volunteer time.
  • Retirement Support Programs include a 401(k) plan with employer contributions and an employee stock purchase plan. Filings describe employer contributions occurring in company stock, supporting long‑term ownership.

Vertex Pharmaceuticals Insights

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The Company
HQ: Boston, MA
5,000 Employees
Year Founded: 1989

What We Do

Vertex is a global biotechnology company that invests in scientific innovation to create transformative medicines for people with serious and life-threatening diseases. We discovered and developed the first medicines to treat the underlying cause of cystic fibrosis (CF), a rare, life-threatening genetic disease. In addition to clinical development programs in CF, Vertex has more than a dozen ongoing research programs focused on the underlying mechanisms of other serious diseases. Founded in 1989 in Cambridge, Massachusetts, our corporate headquarters is now located in Boston’s Innovation District, and our international headquarters is in London, United Kingdom. We currently employ approximately 3,500 people in the United States, Europe, Canada, Australia and Latin America with nearly two-thirds of our staff dedicated to research and development. Vertex is consistently recognized as one of the industry’s top places to work by Science Magazine, The Boston Globe, Boston Business Journal and the San Diego Business Journal. Our research and medicines have also received esteemed recognitions, including the Robert J. Beall Therapeutics Development Award, the French Prix Galien and the British Pharmacological Society awards.

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