Contamination Control Specialist
Sanofi · Framingham, MA
- Level
- Specialist
- Team
- Controls
- Degree
- Required
- Experience asked
- 8+ years
- Industry
- Pharma & life sciences
- Posted
- 2 days ago
The role in 30 seconds
A specialist controls role at Sanofi (pharma & life sciences) in Framingham, MA.
- They ask for
- 8+ years · degree required
- Tools it names
- CAPA, FDA / GMP, Validation (IQ/OQ/PQ), Automation
Read from the posting. The full description is below.
From the plant jobs report · week of November 2, 2026
Controls Engineer roles in Massachusetts: typical posted base $120k–$178k.
Median of the low and high ends of 10 live postings that list pay, out of 27 controls 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 26 other live controls postings in Massachusetts.
- Base pay
- Not listed in this posting
- Experience asked
- More than usual (8+ vs 5+)
Typical $119k–$165k, from 9 postings that list pay.
Similar roles usually ask 5+ years.
Skills these teams ask for most
- PLC 81%
- ✓ Automation 78%
- Robotics 44%
- ✓ Validation (IQ/OQ/PQ) 30%
- Root cause 30%
- AutoCAD 26%
✓ = this posting asks for it too. % = share of similar postings that mention it.
Stands out: this posting asks for CAPA, which few similar roles mention. If you have it, lead with 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 Controls team at Sanofi
We found 7 people at this company and state: 5 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
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Write to John → (free) - 3
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Questions worth asking about this team:
- What does a normal week look like on your team?
- How did you land the job? What stood out in your interviews?
- 4
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- 5
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This plant: Sanofi in Framingham
1 other open role at this site · 7 people we found in controls roles at Sanofi.
- Area Maintenance Specialist · Reliability · Specialist
Full description from SanofiAs posted on their careers site.ShowHide
Responsibilities
- ◆Leading as SME specific subjects part of the Contamination Control SOP in her/his area of expertise
- ◆Conducting risk assessments related to contamination control
- ◆Overseeing sites activities and performance for contamination control systems in her/his scope of
responsibilities
- ◆Leading investigation following contamination control failures and proposing corrective and preventive actions (CAPA)
- ◆Collaborating with cross-functional teams to ensure product quality
- ◆Ensuring presence on the shop floor to oversee practices, identify gaps vs SOP for contamination control
- ◆Reviewing data from contamination control monitoring to propose improvements as necessary (from monitoring and trends)
- ◆Participating in audits and regulatory inspections and audits, providing expertise on contamination control
- ◆Supporting the preparation of validation protocol and supporting projects related to her/his area of expertise
- ◆Contributing as an SME to specific CoE/CoP with Global functions; implementing on site the best practices shared
requirements
and Good Manufacturing Practices (GMP) relevant to sterility assurance and microbiological control
- ✓Communication skills to communicate with a large number of functions (from shopfloor to management) and to present complex subjects
- ✓Ability to organize and lead routine investigations with a multi-disciplinary team
Qualifications
- ✓Bachelor's degree in Life Sciences, Sciences, Engineering or other related fields with 8+ years experience working in a regulated, cGXP environment OR
- ✓Master's degree in Life Sciences, Sciences, Engineering or other related fields with 6+ years of experience working in a regulated, cGXP environment.
Preferred Qualifications
- ✓Operations experience in one or more of the following areas: Quality Assurance, Quality Control, Manufacturing Technical Support, Facilities Engineering, or Automation is preferred.
- ✓Clear understanding of cGMP via experience in working in a regulated environment
- ✓Demonstrated knowledge of cGXP regulations and guidance.
- ✓Demonstrated experience with change control, CAPA and deviation quality systems.
- ✓Demonstrated experience with project management
Show full description ↓Show less ↑
Job Title: Contamination Control Specialist
Location: Framingham, MA
About The Job
The Sterility Assurance and Microbiology (Contamination Control) Department supports quality and manufacturing activities at Sanofi Framingham Biologics Campus by identifying possible trends from microbial contaminants that may interfere with the quality of the product during different stages of the manufacturing process. It aims to maintain a state of microbiological control in the Utility Systems and within the environment where the manufacturing process is executed. It assesses the aseptic behavior of the personnel involved in these processes; and contributes to the guarantee that the areas are operating in a state of environmental control.
Join a global network that powers how Sanofi delivers — seamlessly, purposefully, and at scale. In Manufacturing & Supply, you'll help reimagine how life-changing treatments reach people everywhere, faster.
About Sanofi
We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.
Main
Key Roles
- •Advise on contamination control protocols and procedures
- •Propose corrective and preventive actions to improve contamination controls
- •Advise cross-functional teams on best practices or expected improvements in her/his area of expertise
- •Presence on the shopfloor with formal traceability of the observations. Inform management and feedback operators
- •Contribute to quality documentation SOP and validation protocol
Additional Accountabilities
- •Experience in sterility assurance and microbiological or contamination control within a pharmaceutical or biotechnology environment
- •Ability to meticulously review and analyze documentation, processes, and products to ensure compliance with Sanofi GOP / Quality standards
- •In-depth knowledge of regulatory
About You
Basic
Skills
- •Experience with Trackwise or equivalent system
- •Experience with metrics and trending
- •Experience with analytical instrumentation
- •Experience with Environmental Monitoring and Critical Utilities
- •Ability to work independently with minimal supervision and direction
- •Ability to function well in a fast paced environment
- •High attention to detail and accuracy
- •Self-motivated and highly organized
- •Experience with project management
- •Hands on problem solving and strong analytical skills
- •Strong computer skills
Special Working Conditions
- •Ability to gown and gain entry to manufacturing and Quality Control areas.
Why Choose Us
- •Bring the miracles of science to life alongside a supportive, future-focused team.
- •Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
- •Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
- •Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.
- •Shape the future of medicine and vaccine delivery with cutting-edge technology, ensuring seamless launches and a resilient global supply.
- •Power industry-leading performance by leveraging digital, data, and AI-driven innovation – at speed and scale.
- •Transform lives worldwide by delivering life-changing treatments anywhere, anytime.
