Supervisor Manufacturing

Job title: Supervisor Manufacturing

Location: Framingham, MA

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.

Position in a cGMP biologics facility which includes solution preparation, equipment preparation, upstream operations, and downstream operations.  Initial job responsibilities will include performing a diverse range of  manufacturing related activities during plant start-up from Operational Commissioning/Shakedown through process validation (PV) and Product Change Over.

The primary job function post PV runs will be Downstream Operations.  Responsibilities will also include supporting Upstream and Support Operations as necessary. The  Manufacturing Supervisor will be responsible for performing a variety of complex tasks under general guidance and in accordance with the manufacturing instruction set and current GMPs.  

We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?

Main Responsibilities:

• Select, develop, and motivate qualified staff to effectively carry out department functions and   provide for the continuity of supervisory and specialized skills.

• Provide leadership, guidance, and direction to staff consistent with cGMP and company corporate quality governance.

• Coach and mentor staff in all aspects of their job performance and career development including training, feedback, rewards, and disciplinary action.

• Develop work plans, assign tasks, and supervise a large team or multiple small teams

• Implement and administer policies and procedures that typically affect individual subordinate employees.

• Establish key performance indicators, maintain, and report applicable department or organizational metrics.

• Represent business unit in Project team meetings related to global initiatives.

• Interact with project teams and research groups as they impact the quality operation.

• Perform internal audits of the SOPs and documentation related to QS Enterprise Systems and other functions that receive CQO QA oversight.

• Lead and implement continuous improvement projects.

• Ensure projects are completed on schedule.

Additional Responsibilities:

• Ensure execution of manufacturing activities in strict accordance with production batch records, standard operation procedures, and cGMP.

• Maintains a safe working environment and reporting of incidents/accidents to Site Leadership.

• Implement and maintain production schedules.

• Ensure manufacturing personnel are trained to perform all assigned functions and tasks.

• Partner with Manufacturing Managers and Quality to ensure manufacturing areas are inspection ready at all times.

• Ensure manufacturing personnel are compliant with annual safety and cGMP training.

• Operate complex systems and equipment in accordance with production batch records, SOPs, and cGMP.

• Utilize documentation control systems to author, review, and improve documentation

• Utilize process knowledge and investigation skill set to identify and resolve departmental issues.

• Escalate production floor issues related to procedures, materials, process, equipment, automation, utilities, and/or information systems to Manufacturing Management and/or appropriate functional area(s).

• Adhere to site scheduling processes.

• Ensure personnel identify and document events that deviate from procedure.

About You

Basic Qualifications

• High School Diploma or GED with 5+ years of experience in a cGXP-regulated environment, or a Bachelor’s degree with 3+ years of relevant experience.

• Proven leadership experience

• Hands-on experience in cGMP manufacturing operations

• Demonstrated ability to coach, mentor, and train team members effectively.

• Physically capable of lifting up to 50 pounds as part of routine job duties.

Preferred Qualifications

• Experience in the biotech or pharmaceutical industry.

• Strong people and process management capabilities.

• Solid background in operations, ideally within a regulated manufacturing environment.

Position Details

• 7PM-7AM- rotating NIGHT SHIFT position including rotating holidays and weekends

• Will qualify for night shift differential

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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