RMF Production Technician- Vaccines

Sanofi; Swiftwater (Monroe County); On-site; USD 10,000 - 60,000; Full time

Job summary

Sanofi is seeking a motivated RMF Production Technician to join their Biologics Team in Swiftwater, PA. This full-time position involves ensuring compliance with FDA regulations and performing manufacturing activities in a cGMP environment. Candidates will work on the startup of a new manufacturing facility and develop technical skills in the biopharmaceutical industry.

Benefits

Health and wellbeing benefits

14 weeks’ gender-neutral parental leave

Qualifications

• 2+ years in cGMP or pharmaceutical or warehouse experience.
• Military experience considered.
• Ability to lift up to 50 lbs.

Responsibilities

• Ensure compliance with FDA regulations.
• Perform equipment set up and operations tasks.
• Identify and prevent deviations.

Skills

Communication

Technical knowledge

Leadership

Education

HS diploma or GED

Associates degree

Bachelors degree

Job description

RMF Production Technician- Vaccines page is loaded

RMF Production Technician- Vaccines

Apply locations Swiftwater, PA time type Full time posted on Posted 2 Days Ago time left to apply End Date: July 31, 2025 (30+ days left to apply) job requisition id R2802270

Job Title: RMF Production Technician- Vaccines

Location: Swiftwater, PA

About the Job

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. Your job, as a Production Technician - Vaccine within our Biologics Team, will have the potential to transform the practice of medicine, turning the impossible into possible for millions of people.

This is a 2nd shift position. Must be able to work weekends and holidays as needed.

About the Job

This position is to become part of the Production team to support the engineering, construction, qualification, validation, and licensure of the B55 Recombinant Manufacturing Facility. This position contributes as a member of a cross-functional team to support the startup of the cGMP manufacturing facility for Flublok /Panblok drug substance in Swiftwater PA and will later continue to support the cGMP commercial. manufacturing of drug substances requiring a high degree of relationship building, communication, technical knowledge, and leadership.

Sanofi is seeking a motivated professional candidate to operate within Biologics production and perform manufacturing activities. This is an exciting opportunity for a candidate to develop technical skills and learn about the biopharmaceutical industry. The production technician will operate in a cGMP manufacturing area performing equipment set up and operations tasks to meet all standards for safety, quality, and efficiency. The candidate will perform production in accordance with volume fluctuation, business need, and effective procedures.

This position may be required to be moved or temporarily flexed to another department or building within the Biologics operations due to business needs. Additionally, candidates should expect to work in multiple buildings. Some overtime/off shift work hours may be required based on business needs.

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.

Main Responsibilities:

• Ensuring that processes are always compliant with FDA regulations.

• Works to become trained in all assigned training modules.

• Identifying and preventing deviations and assisting in investigation and root cause analysis.

• Helping with deviation investigations, Corrective and Preventive Actions (CAPA), Change Control Requests (CCR), and other assigned projects.

• Ensuring that quality documents like Electronic Batch Records (eBRs) and electronic logbooks are completed accurately and on time.

• Ensuring documentation is completed accurately and in real-time is crucial for compliance and quality control.

• Preparing areas for the next shift helping to maintain smooth operations and efficiency.

• Responsibly use material in an efficient matter to reduce waste.

• Sharing improvement ideas, issues, concerns to team members along with providing solutions.

• Proactive in identifying and solving production issues to ensure smooth operations.

• Follow all procedures put into effect to ensure your safety as well as the safety of others. Participate in monthly safety meetings.

• Report all safety issues, concerns, incidents, and near misses to the team leadership promptly.

• Actively participate in safety walkthroughs coordinated by the department’s safety team.

• Provide input on potential safety issues and contribute ideas for the corrective and preventative actions.

About You

Required Qualifications

• HS diploma or GED and 2+ years in cGMP or pharmaceutical or warehouse experience, military experience considered

• Associates with 1+ years in cGMP or pharmaceutical or warehouse experience, military experience considered

• Bachelors with 0+ years in cGMP or pharmaceutical or warehouse experience

Special Working Conditions

• Ability to lift up to 50 lbs.

• Ability to stand on average 8 hours per shift.

• Ability to gown and gain entry to manufacturing areas.

• Ability to be flexible with work schedule. Potentially modified shifts for training and business needs including holidays and weekend

• May require personnel to flex into another platform within MTech and/or another M&S department, as well as the possibility to work weekends, holidays or off shift hours based on business need.

• May also include working in an aseptic processing area.

• Fit testing requirements of N95 may be required depending on the area you are assigned

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.

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.

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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:

$19.63 - $26.18

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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Sanofi is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.

With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us visiting www.sanofi.com or via our movie We are Sanofi

Why Sanofi

As an organization, we change the practice of medicine; reinvent the way we work; and enable people to be their best versions in career and life. We are constantly moving and growing, making sure our people grow with us. Our working environment helps us build a dynamic and inclusive workplace operating on trust and respect and allows employees to live the life they want to live.