New · posted Oct 16
Sanofi · Pharmaceuticals
Filter Validation Execution Lead
- Swiftwater, PA
- On-site
- Full-time
- Senior & Principal
Closes Oct 30, 2026 · 15 days left
The role
Sanofi delivers 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families.
Sanofi Global MSAT (Manufacturing Sciences, Analytics, and Technology) acts as a crucial link between our R&D and Manufacturing facilities, playing a vital role in securing the present portfolio and delivering future launches of high-quality and innovative drugs and vaccines. By driving its own transformation, Global MSAT fulfills an important function by providing day-to-day manufacturing support, focusing on technical and process aspects, effective life cycle management, process robustness enhancement, and yield improvements to optimize performance.
We are an innovative global healthcare company that helps the world stay ahead of infectious diseases by delivering more than 500 million vaccine doses a year. Across different countries, our talented teams are exploring new technologies to protect people and promote healthy communities. We chase the miracles of science every single day, pursuing progress to make a real impact on millions of patients around the world.
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
Location: Swiftwater, PA
Terms of employment
The hired candidate will execute role as an individual contributor.
The hired candidate will work during normal business hours (8am – 5pm Monday – Friday), but flexibility for occasional work outside of these hours is necessary.
Preferred Start Date: September 2026
What you need
Educations
Bachelor’s degree in basic sciences, mathematics, engineering, or pharmacy with 2+ years’ work experience in Filter Validation field.
Candidates should possess educational and professional experience, commensurate with the position.
Experience
Demonstrated experience managing execution deliverables to achieve strategic objectives.
Preferred: 2+ years of experience in protocol writing, data pack assembly and report writing for filter validation.
Contributing to collaboration and harmonization initiatives in support of a vision for future production processes and technologies.
Demonstrated ability to work with a high level of autonomy with limited guidance.
Experience in cleaning, shipping, and Extractables and Leachable (E&L) validation is a plus.
Soft skills
Behaves according to company values and competencies.
Encourages and ensures proactive and strong collaboration internally and across functions; forward thinking with an attitude of optimization, efficiency, continuous improvement, and smooth transitions between functions.
Use experience and knowledge to propose continuous improvements that deliver efficiency gains.
Proactively anticipates and effectively communicates successes, constraints, conflicts, solutions, and actions for resolution.
Proactively resolves conflicts, removes roadblocks to execution within sphere of influence; escalates to functional management when appropriate.
Technical skills
Knowledge of regulatory expectations around filter design, qualification, and testing (e.g., FDA, EMA, PDA Technical Reports).
2+ years of hands-on experience for qualification and testing of filters used in vaccine manufacturing.
Strong communication skills with the ability to discuss technical topics effectively through both oral and written communication.
What you'll do
The Filter Validation Execution Lead is responsible for designing and executing development and validation studies for sterilizing-grade filters, virus filtration filters, bioburden reduction filters, and vent filters.
Responsible for managing the execution of studies aligned with the project schedule and communicating with stakeholders (external labs, the project team, and MSAT Management).
Partner with MSAT product experts to assess new filtration needs, and support screening studies to define and optimize filter selection.
Responsible for drafting, reviewing, and approving documents such as filter validation protocols, reports, Validation Project Plans (VPP), technical assessments, and deviations.
Responsible for driving Corrective and Preventive Actions (CAPAs) and Change Controls related to filter development and validation.
Responsible for coaching and mentoring junior personnel and contractors on technical knowledge regarding filter validation principles and practices.
Support the Subject Matter Expert (SME) to optimize the filter validation program and ensure the program remains compliant with changes to guidelines related to filter validation.
Support all internal and external audits and regulatory inspections related to filter validation.
Participate in the filtration validation expertise network within Sanofi and externally.
Lead and/or participate in any filter validation investigations and troubleshooting activities.
Build and maintain strong relationships with partners, cross-functional experts, and customers to achieve technical objectives.
Pay and benefits
$85,500 – $123,500 a year
Employer providedNorth America Applicants Only
The salary range for this position is:
$85,500.00 - $123,500.00
All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.
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.
14weeks
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.
Where you'll work
Swiftwater, PAOn-siteOpen in Maps (opens in a new tab)
More jobs in Swiftwater, PA
From the posting
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 lives.
Pursue progress, discover extraordinary
Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.
Equal opportunity, accessibility and legal noticesSanofi's statements, word for word
Sanofi Inc. and its U.S. affiliates are Equal Opportunity employers committed to a culturally inclusive workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
Sanofi US endeavours to make our career center accessible to any and all users. If you are experiencing difficulty and need assistance applying online, please call 1-866-SANOFI2 (1-866-726-6342) or click here
Job intelligence
The context around this role
Live data · October 16, 2026
Salary intelligence
How the pay compares
This role's midpoint is 14% below the US median for Validation & CQV roles at this level.
This roleEmployer provided
Senior & Principal roles in the US47 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $85,500 | — | $123,500 |
| All US (middle half) | $108,000 | $121,000 | $132,500 |
This role: Sanofi's own published range. Comparisons: the base pay employers published on open Validation & CQV roles at the same level on Regulatory Jobs, October 16, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Validation & CQV
The general path across 117 open Validation & CQV roles on Regulatory Jobs, with the titles they carry most. Not Sanofi's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 34 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Validation and qualification13
- Collaboration and leadership11
- Lab testing and methods3
- Documentation and SOPs3
- Quality systems and risk3
- Investigations and CAPA2
- GMP and compliance1
Regulatory intelligence
The rules behind this role
Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.
Company hiring pulse
Sanofi on Regulatory Jobs
- 18
- Open roles
- 16
- Distinct roles
- 6
- Locations
By discipline
- Quality10 56%
- Regulatory6 33%
- Compliance & Safety2 11%
By level
- Senior & Principal7 39%
- Manager4 22%
- Associate & Specialist3 17%
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Filter Validation Execution Lead at Sanofi
Applications close October 30. $86K–$124K a year, employer provided.