Manufacturing Associate

Sanofi EU; Framingham (MA); On-site; USD 60,000 - 75,000; Full time

Job summary

Sanofi in Framingham, MA is seeking a Manufacturing Associate to perform diverse, regulated manufacturing tasks on rotating night shifts (7pm-7am).

The role emphasizes adherence to cGXP and GMP standards, operating large-scale equipment, maintaining clean production areas, and accurately completing batch records and documentation. Training others and potential lead responsibilities may arise as you contribute to safe, reliable manufacturing operations.

Qualifications

• High school diploma or GED with 3–5 years in a cGXP environment, or Bachelor's with 1–3 years in a cGXP setting.
• Experience operating production equipment and completing production documentation.

Responsibilities

• Follow GMPs and safety procedures in all tasks.
• Operate and maintain large scale manufacturing equipment.
• Complete production documentation accurately.
• Identify deviations and participate in investigations.
• Train less experienced operators when needed.
• Assist in leading manufacturing operations.

Skills

GMP knowledge

Documentation skills

Training others

Equipment operation

Education

Bachelor's degree in a related field

High school diploma or GED

Tools

DeltaV

Job description

Job title: Manufacturing Associate

Location: Framingham, MA

Shift: Rotating night shift 7pm-7am

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.

Position Overview / Key Responsibilities:

This position is responsible for performing a variety of complex tasks under general guidance and in accordance with current GMP's.

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:

• Practices and promotes safe work habits and adheres to Sanofi’s safety procedures and guidelines.
• Effectively demonstrates understanding of GMPs and how they apply to specific responsibilities.
• Follows verbal and written procedures in operating production equipment and performing processing steps; accurately completes appropriate production documentation.
• Identifies, escalates, and documents events that deviate from normal operation; participate as needed in investigations.
• Maintains cleanliness and orderliness of process area.
• Maintains production area with supplies.
• Prepares and operates large scale manufacturing equipment and systems
• Performs clean in place operations to prepare equipment for manufacturing operations.
• Performs batch record review, procedure revisions, and work order generation.
• May be responsible for training less experienced or new operators.
• May be designated as a lead operator on manufacturing operations.
• Utilizes manufacturing knowledge to improve process operations and affect positive change.
• Demonstrates ability to troubleshoot basic mechanical operations.
• Effectively utilizes Microsoft office applications.

About You

Leadership Qualifications:

An ongoing commitment to conducting our global business according to the highest legal and ethical standards, and to continually pursue excellence in the development and delivery of all our products and services.

This includes:

• Adhering to all applicable laws and regulations of the places in which we conduct business, as well as our own company policies and procedures.
• Being honest and treating people with respect and courtesy.
• Constantly striving to make Sanofi a great place to work, and a company respected for the quality of its people and products.
• Acting as role models for our fellow employees by acting responsibly, fairly, and honestly in our dealings and exercising sound judgment in performing our jobs.

Basic Qualifications:

• High school diploma/GED with 3-5 years of experience in a cGXP manufacturing environment, or Bachelor’s Degree with 1-3 years of experience in a cGXP manufacturing environment.

Preferred Qualifications:

• Familiarity with Manufacturing Control Systems (i.e. DeltaV).
• Experience in large-scale manufacturing operations.
• Experience in a GXP environment.
• Experience facilitating and delivering training.
• Experience creating controlled documents.

Special Working Conditions:

• Ability to lift up to 50 lbs
• Ability to stand on average 10 hours per shift.
• Ability to gown and gain entry to manufacturing areas
• Ability to work twelve hour rotating shift and every other weekend, including scheduled holidays.
• Ability to work day and night shift, as applicable.
• Ability to work in a cold room environment (2-10 degrees C)

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 US Services and its U.S. affiliates are Equal Opportunity employers committed to a culturally inclusive 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.

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.