Manufacturing and Supply
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Job title: QC Lab Shift Team Leader - QC Chemistry Scheduler

Main Responsibilities:

• Daily scheduling of laboratory work, anticipating and resolving equipment issues, material and personnel scheduling conflicts

• Oversees the day to day running of the Laboratories, directing the workload of the Analysts to ensure Stability testing windows, and In Process and Release cycle times are met.

• Facilitating the scheduling of equipment to ensure support of routine assays, projected related work, and validation studies to minimize the impact to the production schedules

• Implementing the department master schedule; identifying and assisting in resolving gaps in master schedule

• Collaborating with operations planner/scheduler and attending site scheduling/planning meetings to align schedules to ensure deliverables are met

• Tracking and communicating the status of work-in-progress, material and equipment availability, pending material expiration dates, and schedule changes

• Monitoring and verifying inventory balances to ensure adherence to schedule

• Developing, tracking and reporting key performance indicators for the Chemistry laboratory

• Creating daily lab schedules and document process sequences, cycle times, and conflicts

• Manage laboratory projects and key initiatives that directly support the QC Chemistry team

• Provide Motivation, inspiration, and feedback to staff under general supervision.

• Act as the primary contact for cross functional teams with various departments, including Manufacturing

• Facilitates operational excellence through continuous improvement initiative such as SOP revisions and process changes.

In addition, the QC Lab Shift Team Leader is expected to:

• Work independently under minimal supervision and direction.

• Participate in determining objectives or significant projects or assignments.

• Perform work that requires decision making and the consistent exercise of independent judgment and discretion.

• Represent the department in cross-functional teams with limited direct supervision. 

About You

Basic Qualifications:

• Bachelor's Degree and 6 years Quality and/or Operations experience in a CGMP Laboratory Environment or

• Master’s degree in Life Science and 4 years Quality and/or Operations experience in a CGMP Laboratory Environment

• Experience with One-LIMS, SmartQC (Scheduling) or Veeva software

• Effective skills in time management, organization, teamwork, collaboration, and leadership

• Strong computer, verbal, and written communication skills

Preferred Qualifications:

• Experience working in a Quality Control Chemistry Laboratory

• Bachelor's Degree in a science or technical related field

• Strong Project Management Experience

• Experience with Scientific technical writing including authoring and revising SOPs

This is a Monday – Friday, on site position in Framingham, Massachusetts.

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.