Process Dev Engineering Senior Scientist, Media Development

Vertex Pharmaceuticals Inc

Boston, MA

JOB DETAILS
SALARY
$123,200–$184,800 Per Year
SKILLS
Analysis Skills, Biochemistry, Biology, Biotech and Pharmaceutical, Cell Cultures, Chemical Engineering, Communication Skills, Continuous Improvement, Cost Control, Cross-Functional, Current Good Manufacturing Practice (cGMP), Detail Oriented, Drug Development, Experiment Design, GMP (Good Manufacturing Practices), Gene Therapy, High Throughput, Identify Issues, Interpersonal Skills, Leadership, Legal, Manufacturing, Manufacturing Technology, Mentoring, Multimedia, Multitasking, Organizational Skills, Patents, Presentation/Verbal Skills, Process Development, Process Engineering, Process Improvement, Publications, Regulations, Regulatory Reports, Regulatory Submissions, Relationship Management, Research & Development (R&D), Stem Cells, Team Lead/Manager, Team Player, Time Management, United States Department of Energy (DOE), Writing Skills
LOCATION
Boston, MA
POSTED
30+ days ago

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 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.

Minimum Requirements

  • 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.
  • 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.
  • Participate in weekend work rotation with the broader team.
  • Authorized to work in the US.

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 ApplicationAssistance@vrtx.com

About the Company

V

Vertex Pharmaceuticals Inc

Vertex is a global biotechnology company that aims to discover, develop and commercialize innovative medicines so people with serious diseases can lead better lives. In addition to our clinical development programs focused on cystic fibrosis, Vertex has more than a dozen ongoing research programs aimed at other serious and life-threatening diseases. Founded in 1989 in Cambridge, Mass., Vertex today has research and development sites and commercial offices in the United States, Europe, Canada and Australia. For six years in a row, Science magazine has named Vertex one of its Top Employers in the life sciences. For additional information and the latest updates from the company, please visit www.vrtx.com
COMPANY SIZE
5,000 to 9,999 employees
INDUSTRY
Biotechnology/Pharmaceuticals
FOUNDED
1989
WEBSITE
https://www.vrtx.com/