Analytical Development Principal Scientist, Microbiology & Viral Safety
Company websitevrtx.com (Vertex Pharmaceuticals, opens in new tab)
Base salary $140,800 to $211,200
Employer-published annual base salary, USD. Advertised base range in Boston, MA
You apply on the employer's own site. Six Figure Work does not handle applications.
- LocationBoston, MA
- WorkplaceWorkplace not stated
- Status at last checkSource accepting applications when checked
- Last checked (17 min ago) · observed since
About this job
Job Description
We are seeking a highly skilled Principal Scientist, Analytical Development – Microbiology & Viral Safety to provide strategic and technical leadership for microbiology and viral safety testing across multiple development programs. This role will serve as the subject matter expert for microbiological and virological assays, supporting control strategy development, process development, regulatory submissions, and commercial readiness.
The ideal candidate will bring deep expertise in microbiological and virological risk assessment, as well as assay evaluation, development, qualification, validation, and lifecycle management. This individual will also demonstrate strong cross-functional collaboration skills and a passion for scientific innovation.
Key Duties and Responsibilities:
- Serve as the primary subject matter expert for microbiology and viral safety assays across cell and gene therapy and biologics programs, providing strategic and technical leadership to support development, manufacturing, and regulatory objectives
- Lead the development, qualification, validation, transfer, implementation, and lifecycle management of microbiological assays, including mycoplasma, sterility, Gram stain, and endotoxin methods, as well as viral safety assays
- Provide technical guidance to cross-functional teams on microbiological and virological risk assessment, assay selection, and testing strategies to support product development, process changes, investigations, and regulatory milestones
- Author and review technical dossiers, validation plans, protocols, reports, and scientific justifications to support regulatory submissions, health authority interactions, and inspection readiness
- Drive innovation in rapid and alternative microbiological methods to improve testing efficiency, strengthen manufacturing support, and enable scalable solutions for clinical and commercial programs
- Lead the evaluation, development, validation, transfer, and implementation of rapid and alternative microbiological methods in collaboration with internal stakeholders and external testing laboratories
- Represent the organization in external scientific forums, industry consortia, and collaborative initiatives to strengthen internal capabilities and advance best practices in adventitious agent safety
- Lead wet lab development activities, including hands-on experimental work
Knowledge and Skills:
- Strong expertise in microbiology, virology, and adventitious agent safety
- Strong knowledge of regulatory expectations for microbiological and viral safety testing for clinical and commercial products
- Experience supporting regulatory submissions, inspections, and health authority interactions
- Demonstrated ability to work effectively across cross-functional teams and with external partners
- Strong written, verbal, and scientific communication skills
- Experience in cell and gene therapy, biologics, or advanced therapy medicinal products (ATMPs)
- Familiarity with rapid and alternative microbiological methods and implementation strategies
- Participation in industry working groups, scientific forums, or consortia.
- Strong understanding of GMP environments and manufacturing support requirements
Education and Experience:
- Advanced degree in Microbiology, Virology, Biological Sciences, Pharmaceutical Sciences, or a related field; PhD preferred, with MS candidates considered based on significant relevant experience
- PhD and 4+ years, or Master's and 7+ years, or Bachelor's and 10+ years
- Significant industry experience in assay development, qualification, validation, transfer, and lifecycle management
At Vertex, we embrace continuous learning and encourage employees to stay informed on advances in AI, technology, automation, and industry trends. We seek talent who bring an external perspective, demonstrate curiosity and sound judgment, and thoughtfully adopt new capabilities that improve decision-making, drive innovation, increase efficiency, and help deliver better outcomes for patients.
Pay Range:
$140,800 - $211,200Disclosure 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 DesignatedFlex 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]
Source: Vertex Pharmaceuticals on Workday · View original posting (opens in new tab)
Pay in context
This role's base floor ($140,800) is above 32% of the 310 Science & Research roles in Massachusetts listed on this site; 1 other lists the same floor. Their median floor is $159,500; the middle half runs from $129,730 to $190,600.
Only jobs on this site count, and each one publishes a base salary of $100,000 or more, so this compares six-figure jobs with each other, not with the whole market. Computed Nov 7, 2026.
This listingAnalytical Development Principal Scientist, Microbiology & Viral Safety$140,800 to $211,200
Senior HCP Marketing Manager, US Kidney - Pove$140K to $210K
Discovery Immunology Principal Research Scientist$140K to $210K
Sr. AV and Events Platforms Administrator$140K to $210K
Analytical Development Principal Scientist$140,800 to $211,200
S2P Process Design & Standards Senior Manager$139,100 to $208,700
Senior Manager, Manufacturing Operations (3rd Shift)$139,100 to $208,700
Chart as a table
| Role | Published base |
|---|---|
| Analytical Development Principal Scientist, Microbiology & Viral Safety (this listing) | $140,800 - $211,200 |
| Senior HCP Marketing Manager, US Kidney - Pove | $140K - $210K |
| Discovery Immunology Principal Research Scientist | $140K - $210K |
| Sr. AV and Events Platforms Administrator | $140K - $210K |
| Analytical Development Principal Scientist | $140,800 - $211,200 |
| S2P Process Design & Standards Senior Manager | $139,100 - $208,700 |
| Senior Manager, Manufacturing Operations (3rd Shift) | $139,100 - $208,700 |
Observed changes
- First observed on the employer's board
- Began meeting the published-salary criteria
- Observed since
- Employer-stated posting date
- 2026-09-14
Where this pay comes from
Location as the employer wrote it: Boston, MA
$140,800 - $211,200
- Method
- Employer text, read with fixed rules and re-verified
- Checked
- Rule set
- us-base-v2
The pay passage appears in the employer's own job text. Fixed, deterministic rules located it, and the passage below was checked against the stored copy of the posting.
What we verified
- The pay figures come from the employer's own listing, quoted exactly above.
- The pay is an annual base salary in US dollars with a minimum of at least $100,000.
- The role was publicly listed on the employer's job board when last checked.
We do not verify what the employer will actually offer, whether the employer is still recruiting for the role, or anything beyond what the employer published. Full methodology.
