
Associate Director, Quality Control - Technical Services
Vertex Pharmaceuticals · Boston, MA
- Level
- Director+
- Team
- Quality
- Base pay
- $159k–$238k
- Travel
- 20%
- Degree
- Required
- Experience asked
- 8+ years
- Industry
- Pharma & life sciences
- Posted
- Recently
The role in 30 seconds
A director-level quality role at Vertex Pharmaceuticals (pharma & life sciences) in Boston, MA.
- They ask for
- 8+ years · degree required
- Tools it names
- FDA / GMP, Validation (IQ/OQ/PQ), Automation
- Base pay
- $159k–$238k
- Day to day
- about 20% travel
Read from the posting. The full description is below.
From the plant jobs report · week of October 19, 2026
Quality Engineer roles in Massachusetts: typical posted base $107k–$149k. This one lists $159k–$238k.
Median of the low and high ends of 50 live postings that list pay, out of 70 quality engineer openings in Massachusetts, read from manufacturers' own careers sites.
Massachusetts plant jobs report →Pay by team and state →What moves pay →
How this role compares
Against 69 other live quality postings in Massachusetts.
- Base pay
- About 67% above similar roles
- Experience asked
- More than usual (8+ vs 5+)
Typical $100k–$138k, from 39 postings that list pay.
Similar roles usually ask 5+ years.
Skills these teams ask for most
- Root cause 69%
- ✓ FDA / GMP 60%
- ✓ Validation (IQ/OQ/PQ) 51%
- CAPA 50%
- ISO 13485 46%
- FMEA 37%
✓ = this posting asks for it too. % = share of similar postings that mention it.
At a glance
Pulled from the posting text. If it's not listed here, the posting didn't say.
How to get in at this plant
Five moves over a week or two. The first one takes ten minutes.
- 1
Pick 2–3 people on the Quality team at Vertex Pharmaceuticals
We found 3 people at this company and state: 1 in this kind of role, 2 leaders. Engineers who joined in the last year or two reply the most. See them ↓
- 2
Send a short, curious note
One real question about their work. No favors yet. Each person gets a different note, written for this role.
Write to Alexander → (free) - 3
Turn a reply into a short call
Questions worth asking about this team:
- What does a normal week look like on your team?
- Which standards drive the work here: ISO 13485, IATF 16949, AS9100?
- How much of the job is customer complaints versus prevention?
- The posting says about 20% travel. Between which sites?
- How did you land the job? What stood out in your interviews?
- 4
Apply with someone vouching for you
If the call went well, ask whether they’d pass your résumé to the hiring manager. Send your résumé link, apply that day, and let them know.
- 5
Bring proof to the interview
One page of before-and-after numbers from projects you led: scrap, OEE, cycle time, cost. Plant managers hire on results.
This plant: Vertex Pharmaceuticals in Boston
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Full description from Vertex PharmaceuticalsAs posted on their careers site.ShowHide
Responsibilities
The
Education and Experience
- ✓Requires the following or the equivalent combination of education and experience: Master degree and 8+ years, or Bachelor's and 10+ years in pharmaceutical/biopharmaceutical industry with 6 years of increasing management responsibility, or the equivalent combination of education and experience
- ✓Expertise in QC principles, concepts, industry practices, and standards.
- ✓Experience in method development, validation, and transfer of non-compendial and compendial analytical methods for small molecule using various techniques such as LC/GC chromatography, dissolution, Karl Fischer, FTIR, and XRPD
- ✓Deep knowledge in regulatory
requirements
and guidelines (ICH, CFR, FDA) with respect to small molecule manufacturing and release/stability testing.
- ✓Audit/inspection interaction experience with health authorities
- ✓Demonstrated ability to work independently and effectively to timelines in a virtual environment (i.e., internal partners, external CROs, CMOs, CTLs, etc.) and manage QC deliverables effectively.
- ✓Excellent written and verbal communication skills.
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.
Show full description ↓Show less ↑
Job Description
General Summary
The Associate Director, QC Technical Services – Small Molecule will lead the technical services group responsible for GMP release and stability testing activities at external laboratories supporting commercial small molecule programs at Vertex. The role is responsible for the development and maintenance of relationships with the external testing sites to provide strategic and operational oversight for QC activities, drive compliance, monitor performance and support continuous improvement activities. The role also includes operational oversight of quality event management, stability execution, regulatory support, and cross-functional collaboration to ensure uninterrupted commercial supply to patients.
This position reports directly to the Senior Director of QC Operations and Stability
of this position may include, but are not limited to, the following
- •Provide strategic and operational oversight for GMP release and stability testing conducted at external laboratories in support of commercial supply.
- •Oversee contract testing laboratories performing QC testing of drug substance, drug product intermediate, and drug products, ensuring alignment with timelines, quality standards, and quality agreements.
- •Ensure the group maintains compliant execution of QC processes in accordance with SOPs, policies, and applicable industry guidance.
- •Accountable for oversight of external data review processes, including appropriate assessment, escalation, and follow-up for OOS, OOE, OOT, and adverse performance or product trends.
- •Provide leadership oversight for KPI monitoring and CTL performance management to support reliable, compliant, and efficient testing operations.
- •Oversee quality event management within the function, including change controls, deviations, adverse stability trends, and CAPAs, ensuring timely resolution and appropriate escalation.
- •Lead cross-functional alignment with MS&T, AS&T, Supply Management, Regulatory Affairs, Program Management, and Quality Assurance to support commercial small molecule programs.
- •Provide functional accountability for QC input to regulatory submissions
- •Ensure the group is prepared to support audits and inspections at CMOs and contract laboratories.
- •Build and maintain strong relationships with internal stakeholders and external laboratories to support quality, compliance, and continuity of supply.
- •Support development and strengthening of internal quality systems relevant to the technical services function.
- •Support career development of direct reports
Knowledge and Skills
- •Demonstrated experience in biotech or pharmaceutical industry, in a analytical leadership role working with or in cGMP testing laboratories.
- •Proven experience in building and growing a high-performance team
- •Strong quality and compliance background in a commercial GMP environment with expertise in developing QC strategies, monitoring performance metrics, and driving continuous improvement initiatives.
- •Problem solver with a hands-on approach and ability to anticipate adverse scenarios and provide contingency plans to address them
- •Demonstrated technical background in analytical chemistry with small molecules
- •Solid project management skills and experience managing complex projects.
- •Strong verbal and written communication skills: ability to express oneself clearly and concisely, by adjusting style, language and/or terminology as appropriate for the audience.
- •Strong leadership and proven ability to collaborate and build relationships is critical.
- •Ability to work calmly and make sound decisions in a fast-moving environment of uncertainty and change
- •Ability to travel, national and international, up to 20%
Pay Range
$158,800 - $238,200
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
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