Activités Industrielles
Là où les miracles
de la science
deviennent une réalité pour les patients

Job Title: Production Operator- Vaccines

Location: Swiftwater, PA

About the Job

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.

Performs production in accordance with volume fluctuation, business need, and effective procedures.  Responsible for Manufacturing actives in assigned area.  Performs production in accordance with volume fluctuation, business need, and effective procedures. 

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 people’s lives.

Main Responsibilities:

Safety:

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

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

• Actively participates in safety walkthroughs 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.

• Utilizes +QDCI boards for Safety issues

• Attends Safety Meetings.

Quality:

• FDA audit understanding and awareness.  Ensures process in areas is following proper procedures at all times

• Identifies possible deviation occurrences and prevents or aids in investigations and root cause analysis. 

• Ensures completion of quality documentation (BFR’s, logbooks, etc) accurately in a timely manner.

• Understands the function of the quality group and works with them to maintain a positive rapport.

• Maintains acceptable execution with no emerging negative trends in procedural deviations

Delivery:

• Performs production in accordance with volume fluctuation, business need, and effective procedures. Must be flexible to ensure staffing for changing business volume and needs

•  Completes tasks and corresponding documentation as required by cGMP to ensure document completion.

• Works to prepare assigned areas for the oncoming shifts to ensure continuous operation.

• Must ensure maintenance of gowning and Physical dexterity to complete proper set up of machines so not to impact the safety, quality, and integrity of the product.

• All other duties as assigned. Adheres to all other company time keeping and attendance policies.

•  Ensures all Final Container materials required for production are available prior to need. These materials must be ready for aseptic filling operations to ensure the safety, quality, purity, and integrity of the product is maintained.

•  Ensures the completion of Real Time SAP transactions in an accurate and timely manner to ensure accurate inventory.

Cost:

• Executes procedure as documented to avoid deviations.

• Responsibly uses material in an efficient manner to reduce waste.

• Utilizes Filling Standards to capture and Record HRxHR and Change Over Activities.

• Actively communicates improvement ideas, issues, concerns, etc. to team members along with providing solutions.

Involvement:

• Trains and orients new team members (at any level) as assigned. 

• Follows proper documentation as required by cGMP.

• Has a thorough working knowledge of cGMP’s and works to help others understand. 

• In on time and attends and participates in Shift Change.

• Maintains acceptable training as described in key requirements.

• All other duties as assigned.

Context of the job/major challenges

• Performs production in accordance with volume fluctuation, business need, and effective procedures. Must be flexible to ensure staffing for changing business volume and needs.

• Works with Senior Technicians, leads, and managers to ensure operational area is running as intended to meet all operational goals. 

• Must attend shift change daily to ensure preparedness for work day.

• Completes Real Time SAP transactions on all aspects of Inventory Management.

• Obtains and Maintains access to necessary systems as needed (SAP, RT Reports , eDoc, HMI, SCADA access, Virtual Standards, etc.).

• Reports production issues and observations and relays to leadership team.

• Understands science behind process steps and technology including aseptic processing.  

• Works to prepare area for oncoming shifts.

• Is trained to complete Environmental Monitoring sampling and corresponding documentation.

• Works with lead technicians and managers to ensure continuous operation.

• Maintains aseptic work environment.

• Must be able to train and work in multiple production areas in the Filling umbrella including material movement, prep, and the aseptic corridor.

• Must ensure training and gowning status is acceptable all time to ensure agility to work in aseptic production areas.

• Must be able to complete training in all areas as required this includes aseptic filling and machine operation.

Dimensions/Scope

This role is for a nonexempt employee working in the Filling  Department.  Their Bi-weekly pay is based on previous experience and education time. 

Their responsibilities are, but are not limited to:

About You

Requirements

Certifications and Education/experience

• Requires good mechanical skills, computer skills and is detail oriented. Must have basic mechanical aptitude, computer skills, good comprehension skills, retention skills, troubleshooting and manual dexterity.

• Prior or related cGMP or Pharmaceutical experience recommended

• HS diploma or equiv and 3+ years in cGMP or Pharmaceutical experience

• Associates with 2 + yrs in cGMP or Pharmaceutical experience

• Bachelors with 1 + yrs in cGMP or Pharmaceutical experience

• Proficiency in at least but not limited to three areas of operations or product line.

• Must be a qualified trainer in one or more areas. Must be proficient in at least one of the following areas: BFR review, Environmental monitoring, Utliliy Sampling, Documentation Coordinator, logbook review, technical writing (SWI revisions).  

• Must have knowledge and access to systems (SAP, Trackwise, Master , EMS, PMS, SCADA, RT Reports, Labware).

• Must have knowledge and access to systems in applicable buildings and processes which have these systems (SFD, PI)

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.