Manufacturing and Supply
Where the
miracles of
science are made
a reality for patients

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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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.