Sanofi Vaccines US Inc. Posted September 3, 2026

B87 Filling and Formulation Manager

Swiftwater, United States Full time
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Sanofi Vaccines US Inc. is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Job Title: Aseptic Filling and Formulation Manager

Location: Swiftwater, PA

About the Job

This Aseptic Filling and Formulation Manager​ will lead aseptic filling and formulation operations in a new, state-of-the-art facility during a critical startup and qualification phase. You will be responsible for the overall safety, quality, compliance, productivity, and performance of your assigned team as the facility progresses through Development Aseptic Process Simulations (media fills) in Q4 2026 and Process Performance Qualifications (PPQs) in 2027, with a target of full commercial readiness in 2028.

You are a hands-on, forward-thinking leader who brings deep GMP expertise, a digital-first mindset, and the courage to challenge conventional processes. You thrive in dynamic, fast-paced environments and are energized by the opportunity to build something from the ground up. You lead with curiosity, inspire your team to continuously learn and improve, and hold yourself and others accountable to the highest standards.

Schedule Note: This role requires a flexible schedule during the startup and qualification phases, with a transition to an assigned shift (2nd or 3rd) during commercial operations. C&Q activities will predominantly occur on first shift; media fills, PPQs, and commercial launch activities will require shift-aligned hours as applicable.

What We Offer

A rare opportunity to build operations from the ground up in a state-of-the-art aseptic facility

A leadership role at the center of a high-visibility startup and qualification program

Exposure to cutting-edge aseptic processing technology and next-generation manufacturing practices

Career development and growth within a dynamic, expanding organization

A collaborative, innovative work environment that values curiosity, digital thinking, and challenging the status quo

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 lives.

Main Responsibilities

Lead startup operations for aseptic filling and formulation in a new facility environment, serving as the operational anchor through all phases of commissioning, qualification, and commercial readiness

Drive preparation and execution of Development Aseptic Process Simulations (media fills / APS) by Q4 2026

Oversee PPQ execution and commercial readiness activities throughout 2027, ensuring inspection readiness by December 2027

Apply innovative, analytically driven solutions to complex startup and qualification challenges

Champion a digital-first approach to operations, leveraging technology, data analytics, and digital tools to optimize performance and decision-making

Challenge conventional processes and drive continuous improvement across the operation

Build and develop a high-performing, agile team aligned with company values and culture

Ensure strict GMP compliance and regulatory readiness at all times

Work effectively across cross-functional teams in a fast-paced, multi-priority startup environment

Serve as Subject Matter Expert (SME) for aseptic operations during all Commissioning & Qualification (C&Q) and Validation activities

Startup & Qualification Leadership

Lead the operations team through all facility startup, commissioning, and qualification phases

Drive execution of Environmental Monitoring Performance Qualifications (EMPQs)

Oversee smoke studies and cleanroom qualification activities

Lead Development Aseptic Process Simulations (media fills) beginning Q4 2026

Direct PPQ execution in 2027 in accordance with validation protocols and regulatory expectations

Drive inspection readiness actions to ensure the facility is prepared for regulatory inspection (FDA PAI in 2027)

Ensure all C&Q activities are executed in compliance with applicable regulatory standards (cGMPs, CBER, WHO, EP, and other governing bodies)

Operational Excellence

Own shift performance across aseptic filling and formulation operations in support of startup projects and/or routine manufacturing activities

Drive execution performance using SMS 2.0 standards, routines, and digital tools

Leverage digital systems, including eOOE, iObeya, SAP, Qualipso, and Ocularis, to optimize operations, enable real-time decision-making, and maintain operational visibility

Lead critical operational functions including 5W2Hs, Gembas, MSV/LSVs, real-time reviews, eBR approval, Sartocheck, Paltronic, and Ops Tracker audits

Lead real-time problem solving in a dynamic, evolving environment

Support on-time closure of quality items and deviations to meet site performance metrics and product release requirements

Provide analysis and recommendations to management on quality systems matters

Participate in cost reduction and efficiency initiatives

Leadership & Team Development

Build, lead, and develop a highly trained operations team from startup through commercial launch

Foster a culture of learning, innovation, accountability, and challenging the status quo

Empower team members and ensure accountability at all levels of the organization

Demonstrate strong interpersonal and coaching behaviors

Drive cross-functional collaboration and process optimization across the facility and broader M&S organization

Assist with team development, training, and competency building throughout all phases

Digital Mindset & Innovation

Champion digital transformation initiatives within operations

Utilize data analytics and digital tools to drive informed, real-time decision-making

Identify and implement technology-enabled process improvements

Lead adoption of Industry 4.0 principles within aseptic operations

Model a digital-first approach and encourage the team to leverage available technology to its fullest potential

About You

This is a 2nd Shift leadership role, with flexible scheduling during startup and qualification phases.

Basic Qualifications

Bachelor's degree in Life Sciences, Engineering, or a related field with 1+ years of pharmaceutical/GMP manufacturing operations experience and 6+ months of people leadership experience (formal or demonstrated leadership capability, e.g., team captain, project lead, supervisory role) OR High School Diploma with 5+ years of pharmaceutical/GMP manufacturing operations experience and 1+ years of people leadership experience (formal or demonstrated leadership capability, e.g., team captain, project lead, supervisory role)

Demonstrated experience in aseptic processing operations (Drug Substance, Drug Product, Biologics)

Strong working knowledge of GMPs and regulatory compliance requirements

Proven leadership experience with the ability to build, develop, and manage teams

Excellent technical writing, communication, and interpersonal skills

Ability to work flexible hours, including extended shifts and weekends, to support qualification activities and production schedules

Proficiency with digital systems and data analytics tools

Preferred Qualifications

Experience in facility or production line startup, commissioning, or qualification activities

Background in media fill execution and aseptic process validation (APS/PPQ)

People management experience with a demonstrated track record of hiring and developing a new team

Knowledge of continuous improvement methodologies (Lean, Six Sigma, or equivalent)

Experience with Lean manufacturing operating systems

Familiarity with Industry 4.0 concepts and digital manufacturing tools

Change management experience in a regulated manufacturing environment

Ability to influence across functions and organizational levels without direct authority

Previous experience in biologics, vaccines, or sterile drug product manufacturing.

Soft Skills:

Leadership Presence: Ability to inspire, develop, and hold teams accountable in a startup environment

Digital-First Mindset: Comfort leveraging technology, data, and digital platforms to drive operational performance

Intellectual Curiosity: Genuine desire to continuously learn, improve, and explore new approaches

Courage to Challenge: Willingness to question the status quo and drive meaningful change

Critical Thinking: Strong analytical and problem-solving capabilities applied to complex qualification and operational challenges

Proactive Collaboration: Partners cross-functionally with a focus on optimization, efficiency, and shared outcomes

Communication Excellence: Communicates progress, issues, and resolution actions clearly and accurately across all organizational levels

Anticipation & Proactivity: Identifies and communicates constraints, conflicts, and risks before they escalate

Conflict Resolution: Resolves execution roadblocks within sphere of influence; escalates appropriately when needed

Agility & Adaptability: Thrives in a fast-paced, multi-priority startup environment with evolving demands

Accountability & Ownership: Takes full ownership of team performance, quality outcomes, and operational results

TIMELINE & EXPECTATIONS

2025–2026 - Startup & Qualification, Facility startup, C&Q activities, EMPQs, Smoke Studies, Media Fills

Q1 2027 - Development Aseptic Process Simulations (APS)

2027 - PPQ Execution, PPQ campaigns, inspection readiness, regulatory preparation

2028+ - Commercial Operations - Transition to routine commercial operations leadership.

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.

Sanofi US Services 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.

#GD-SP

#LI-SP

#VHD

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.

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

US and Puerto Rico Residents Only

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.

North America Applicants Only

The salary range for this position is:

$90.000,00 - $130.000,00

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.

Job details

Seniority
Manager
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Swiftwater, United States
Employment type
Full time

How this role compares

Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.

We currently track 493 comparable Manager Manufacturing & CMC roles across 73 biopharma companies.

493Comparable roles tracked
443Currently active
73Companies hiring similar roles
31Countries represented

Salary context

150 of 493 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Associate Director, Digital Scientific Workflows · Merck $0/hr – $0/hr (≈ $0–$0/yr)
Highest disclosed · Regional Manager - Megasys · Merck KGaA $220,000/yr – $250,000/yr
Peer group range $0 – $235,000 (median $151,700)

Where these roles are based

Top locations among the 493 comparable roles

United States299
India65
United Kingdom16
Ireland15
Netherlands13
Japan10

+ 25 more countries

Seniority mix

493 of 493 peers have a known seniority level

Manager264
Associate154
Associate Director75

Therapeutic area mix

4 of 493 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Rare Disease2
Vaccines & Infectious Disease2

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The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

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Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
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Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.