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Fill Finish Engineer Jobs (NOW HIRING)

Main responsibilities Work as a Subject Matter Expert (SME) providing support to Manufacturing, Engineering, and Capital Projects with a focus on fill-finish-related projects: * Assist and develop ...

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Fill Finish Engineer information

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$25

$53

$76

How much do fill finish engineer jobs pay per hour?

As of May 30, 2026, the average hourly pay for fill finish engineer in the United States is $53.63, according to ZipRecruiter salary data. Most workers in this role earn between $43.27 and $62.26 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Fill Finish Engineer, and why are they important?

To thrive as a Fill Finish Engineer, you need a solid background in chemical or biomedical engineering, experience in aseptic processing, and a relevant engineering degree. Familiarity with automated filling equipment, GMP regulations, and validation protocols is typically required, along with certifications such as Six Sigma or Lean Manufacturing. Strong problem-solving abilities, attention to detail, and effective communication skills help fill finish engineers excel in cross-functional teams and ensure product quality. These skills are essential to maintain regulatory compliance, minimize contamination risks, and support efficient, high-quality pharmaceutical manufacturing.

What are some common challenges faced by Fill Finish Engineers in a pharmaceutical manufacturing setting?

Fill Finish Engineers often encounter challenges related to maintaining strict sterility and regulatory compliance during the filling and packaging processes. They need to troubleshoot equipment malfunctions quickly to minimize production downtime and ensure product quality. Additionally, adapting to frequent changes in production schedules, batch sizes, and new drug formulations requires flexibility and a strong understanding of process optimization. Effective collaboration with quality assurance, validation, and production teams is essential to meet both safety and output goals.

What are Fill Finish Engineers?

Fill Finish Engineers are specialized professionals in the pharmaceutical and biotechnology industries who oversee the final stages of drug manufacturing. They are responsible for managing the processes of filling vials, syringes, or other containers with pharmaceutical products and ensuring proper sealing and packaging. Their role is crucial to maintaining product sterility, quality, and regulatory compliance. Fill Finish Engineers work closely with quality assurance, manufacturing, and engineering teams to optimize operations and troubleshoot any issues. They also play a key role in validating equipment and processes to meet industry standards.

What is the difference between Fill Finish Engineer vs Manufacturing Technician?

AspectFill Finish EngineerManufacturing Technician
CredentialsBachelor's degree in engineering or related field, often with GMP trainingHigh school diploma or associate degree, on-the-job training
Work EnvironmentCleanroom settings in pharmaceutical or biotech manufacturingProduction floors, manufacturing lines in similar industries
Industry UsageCommonly used in pharmaceutical, biotech, and sterile manufacturingUsed across manufacturing sectors, including pharma and biotech
Job FocusDesign, oversee, and optimize fill finish processes for sterile productsOperate equipment, assist in production, and ensure process adherence

The Fill Finish Engineer typically has a higher level of education and focuses on process design and optimization in sterile manufacturing environments. Manufacturing Technicians support daily operations and equipment handling. Both roles are essential in pharmaceutical production, but the engineer's role is more specialized in process development and validation.

Process Engineer (Fill-Finish)

Process Engineer (Fill-Finish)

Sanofi

Swiftwater, PA • On-site

Full-time

Posted 23 days ago


Sanofi rating

8.2

Company rating: 8.2 out of 10

Based on 58 frontline employees who took The Breakroom Quiz

27th of 70 rated pharmaceutical


Job description

Job Title: Site Schedule

  • Location: Swiftwater, PA

About the Job

Sanofi is an innovative global healthcare company with one purpose: to pursue scientific miracles to improve lives. Our team strives to transform the practice of medicine, connecting our science to communities in meaningful ways. Within our Sanofi Manufacturing & Supply Ambition, we're redefining our strategy, culture, and processes to make a tangible impact worldwide.

In this role, you'll join the Engineering & Projects team at our Swiftwater site. You will be responsible for providing engineering services to assigned projects and assisting on production floor troubleshooting assignments. You will be the one to determine how user requirements and quality requirements will be satisfied within design solutions that utilize the laws of engineering, mathematics and physics coupled with process engineering aptitude.

You will be required to manage a significant number of engineering deliverables and tasks, each with their own deadline. In addition to technical competence, this position requires the ability to work well in a cross-functional team to accomplish the best technical solution that also considers compliance, safety, operability and maintainability and project constraints.

As a Process Engineer, you will be a technical leader who knows their assigned equipment and processes and is passionate about collaboration and problem-solving. You will seek to grow Sanofi's capability by delivering and supporting process equipment that is optimally suited for the end user.

About Sanofi:

We deliver 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.

Main responsibilities

Work as a Subject Matter Expert (SME) providing support to Manufacturing, Engineering, and Capital Projects with a focus on fill-finish-related projects:

  • Assist and develop technically sound process equipment concepts and scope

  • Specify and design process equipment

  • Manage equipment vendors as required to meet requirements, cost, and schedule

  • Develop and execute commissioning and qualification documentation as required

  • Involve site Maintenance, Operations, Engineering, Quality, and Continuous Improvement teams throughout the design process.

  • At the conclusion of each project, ensure knowledge transfer to allow for appropriate support of process equipment.

Undertaking routine tasks related to the process equipment area:

  • Training and development

  • Interface with Operations to ensure the manufacturing process equipment consistently meets production requirements

  • Provide input to quality and safety systems

  • Providing advanced technical support to diagnose and resolve complex system issues, minimizing downtime

  • Identifying improvement opportunities for critical process systems

  • Implementing process improvements to enhance efficiency, safety, and quality

Related KPIs & Metrics :

  • Compliance (deviations, Corrective Action Preventive Action (CAPA), change control, training)

  • Work order metrics

  • Comisionan & Qualification (CQ) completion rate

  • Deviations and discards due to equipment issues

About You

Basic Qualifications

  • Minimum Bachelor of Science, Engineering (Chemical or Mechanical preferred) or related fields.

  • Minimum 5-+ years of experience in aseptic processing, sterile manufacturing, or fill-finish engineering experience. Hands on experience with filling equipment and aseptic barriers.

Other Qualities:

  • Technical knowledge of drug product processes, and understanding of automated mechanical systems

  • Strong analytical skills (ability to apply engineering principles to design)

  • Hands-on engineering troubleshooting skills

  • Knowledge of GMP (Good Manufacturing Processes) regulatory requirements for manufacturing and CQ activities

  • Sound organizational, written, and oral communication skills

  • Experience with lyophilization, CIP/SIP systems, and filling technologies

  • Experience in sterile manufacturing

  • Ability to lead small projects as a project manager

  • Understanding of the impact of utilities on equipment design and operation

  • Understanding of cost, schedule, and scope management including progress measurement

  • Knowledgeable of the automation design and testing processes

  • English: Proficiency in both written and spoken English.

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 andwellness 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 Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse 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.

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.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!

US and Puerto Rico Residents Only

Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally inclusive and diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; natural or protective hairstyles; 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:

$100,500.00 - $145,166.66

All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs. Additional benefits information can be found through the LINK.


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About Sanofi

Sourced by ZipRecruiter

At Sanofi R&D North America, we deliver meaningful solutions for patients. We transform science into breakthrough, best-in-class and first-in-class medicines and vaccines. We believe in creating a diverse and inclusive workforce - and workplace - which brings together the collective brainpower of over 2,000 colleagues and provides you with an exciting place to grow and develop. We set the bar high, and we deliver.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

Bridgewater, NJ, US

Year founded

2004

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