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Là où les miracles
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Job Title: Production Technician - Vaccines

Location: Swiftwater, PA

Hours: Monday - Friday 6:00 a.m. - 2:30 p.m.

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.

The Swiftwater site is in northeast Pennsylvania and is home to the production of over 120 million doses of injectables that help prevent diseases and enhance patients' quality of life. Our teams follow current Good Manufacturing Practices (cGMP) and procedures while working in a fast-paced team environment.

The production technician (All levels of technicians represent the “heartbeat”) is the “heartbeat” of the manufacturing facilities and is responsible for the high quality and efficient production of our injectables in accordance with current good manufacturing practices (cGMP) for all relevant regulatory agencies (e.g. FDA). Positions within production facilities may change based off of business needs and seasonality.

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:

• Follows all procedures put into effect to ensure your safety as well as the safety of others. 

• Participates in monthly safety meetings. 

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

• Actively participates in safety walk throughs coordinated by the department’s safety team. 

• Provides input for potential safety issues as well as contributing ideas for corrective and preventative actions.

• Follows effective procedures to ensure the production of a safe and efficacious product. 

• Works to understand cGMP’s. 

• Identifies areas of deficiency to the leadership team and offers potential suggestions for improvements. 

• Participates in both deviation investigations when appropriate and implementation plans to ensure a quality product.

• Works with the leadership team to complete deviation investigations and root cause analysis. 

• Works to complete quality documentation (PDR’s, logbooks, etc.) accurately in a timely manner. 

• CFR (code of federal regulations) / PAI inspection readiness. 

• FDA audit understanding and awareness.

• Participates in team meetings. 

• Actively communicates improvement ideas, issues, concerns, etc. to team members. 

• Participates in cross functional teams where necessary to complete projects in an effective and timely manner.

• Ensures proper process area operation by pre and post run set up and maintenance of equipment. 

• Recommends changes to PDR's, SOPS and SWIs when warranted. 

• Write and edit documents under supervision. 

• Seeks out cross training in other areas whenever possible. 

• Responsible for assisting in writing and assisting incident investigations, CAPA's, change controls, along with assisting the higher tech levels and Principle Investigators with projects.

• All other duties as assigned.

About You

• You are professional, detail-oriented, coachable, and a trainable person who thrives in a fast-paced team environment.

• Education: High school diploma or GED required, associate degree or bachelor's degree preferred.

• Experience:

  • Minimum of6 months of prior manufacturing or warehouse work experience,oracollege degree.

• Military Service:

  • Veteranswho served in theU.S. military(active duty) or areNational Guard membersare encouraged to apply.
  • Must have received anhonorable,general, ormedical discharge.

• Soft skills: Cooperates willingly with colleagues, establishes rapport in a friendly and courteous manner. Maintains positive working relationships and is willing to help others.

• Technical skills: Basic computer skills and previous production experience preferred.

• Languages: Reading, writing, comprehension, communication in English is preferred, but all multi-lingual languages welcomed.

• Special Requirements: Product specific vaccination is required. Able to receive influenza vaccine, required for building access. Pursue progress, discover extraordinary

Sanofi Benefits Include the Following:

· Onsite Gym

· Onsite Cafeteria

· Onsite Health and Wellness Center

· Immediate benefits package including medical, dental, vision, paid time off including company holidays

· 401k company match

· Development opportunities including mentorship and tuition reimbursement

· Involvement and engagement opportunities in Employee Resource Groups (ERG) that touch both local and global networks

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.

Toujours Progresser. Découvrir l’Extraordinaire.

Rejoignez Sanofi et entrez dans une nouvelle ère de la science – où votre parcours peut être aussi transformateur que le travail que nous accomplissons. Nous investissons en vous pour que vous alliez plus loin, accélériez votre réflexion et accomplissiez ce qui n’a jamais été fait auparavant. Vous contribuerez à repousser les limites, à bousculer les conventions et à concevoir des solutions plus intelligentes pour les communautés que nous servons. Prêt·e à poursuivre les miracles de la science et à améliorer la vie des gens ? Poursuivons le progrès et découvrons l’extraordinaire – ensemble.

Chez Sanofi, nous croyons dans l’égalité des chances, sans distinction de race, de couleur, d’ascendance, de religion, de sexe, d’origine, d’orientation sexuelle, d’âge, de citoyenneté, d’état civil, de handicap, d’identité de genre ou de tout autre critère protégé par la loi.