Sanofi Group Senior Manufacturing Associate in Framingham, Massachusetts
*12-hour rotating day shift position including rotating holidays and weekends and overtime as per business needs*
*Great promotion opportunity to build leadership skills*
Position in a cGMP biologics facility which includes small scale and large scale upstream operations. Initial job responsibilities will include performing a diverse range of manufacturing related activities. The Manufacturing Associate will be responsible for performing a variety of complex tasks under general guidance and in accordance with the manufacturing instruction set and current GMPs
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 and participates as needed in investigations.
Maintains cleanliness and orderliness of process area.
Ensures production area is stocked with supplies.
Prepares and operates large scale manufacturing equipment and systems.
Performs Batch record review, procedures revisions, and work order generations.
Fulfills role of lead trainer on numerous operations and is an area SME.
Utilizes manufacturing knowledge to improve process operations and affect positive change.
Demonstrates ability to troubleshoot basic mechanical operations.
Effectively utilizes Microsoft office applications.
Mentors less experienced operators and performs support function for supervisor.
Leads team to the execution of the daily work plan.
May attend meetings in absence of supervisor.
May lead shift handover or act as shift lead in the absence of a supervisor.
* Key Responsibilities may differ among employees with the same job title and may change over time, in accordance with business needs.
An ongoing commitment to conducting our global business according to the highest legal and ethical standards, and 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 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 product.
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.
- High School Diploma/GED with 5-7 years in CGMP manufacturing environment, or Bachelor’s degree with 3-5 years of experience.
Bachelor’s degree with 4-6 years of experience in bulk biologics cGMP manufacturing.
Familiarity with Manufacturing Control Systems (i.e. DeltaV).
Extended experience in large-scale purification operations.
Experience in a GXP environment.
Experience facilitating and delivering training.
Experience reviewing and creating controlled documents.
Experience in leading teams.
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).
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.
At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.