Manufacturing Associate- rotating day shift Job at Production at SanofiLocation Framingham, Massachusetts Job Category Production Requisition Number POS_00473187-0003
Sanofi, a global healthcare leader, discovers, develops and distributes therapeutic solutions focused on patients’ needs. Sanofi has core strengths in diabetes solutions, human vaccines, innovative drugs, consumer healthcare, emerging markets, animal health and Genzyme.
At Sanofi US, we are committed to the growth of our people, connected in purpose by career, life and health.
Headquartered in Bridgewater, NJ, Sanofi US is part of a leading global healthcare company dedicated to discovering, developing and distributing therapeutic solutions focused on patients’ needs.
Sanofi has core strengths in diabetes solutions, human vaccines, innovative drugs, consumer healthcare, emerging markets, animal health and Genzyme.
Sanofi US employs approximately 17,000 people across the country all dedicated to protecting health, enhancing life and responding to the hopes and potential healthcare needs of seven billion people around the world.
Commitment is our Strength. Ready to grow together?
Sanofi US endeavors to make our career center accessible to any and all users. If you are experiencing difficulty and need assistance applying online, please call 1-800-207-8049 Option 7, then Option 3.
Sanofi US Services, 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.
This position is responsible for performing a variety of complex tasks under SOPs and in accordance with current cGMPs.
·Prepare large scale components and equipment for GMP production.
·Perform clean in place and sterilization operations to prepare equipment for manufacturing operations.
·Escalate issues to a supervisor or higher level co-worker.
·Review and create operation documents and batch records.
·Identify subtle variances from typical manufacturing operations; communicate to a supervisor and other support groups.
·Facilitate and execute daily work plan.
·May be responsible for training less experienced or new operators.
·May be responsible for batch record review, as a delegate.
·Effectively demonstrate understanding of cGMPs and how it applies to specific responsibilities.
·Maintain orderliness of
·Monitor operations to ensure compliance with
·Complete process documentation in accordance with good documentation practices (GDP).
·Practice and promote safe work habits and adheres to Genzyme’s safety
·Work under direct supervision to a supervisor or a shift lead.
·Perform support function for more senior operators.
·May be designated as a lead operator on manufacturing operations.
·Utilize manufacturing knowledge to im
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 of our products and services. This includes:
·Respecting the laws and operating within the applicable 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 Genzyme 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.
·High school diploma, Biotech Certification with 3-5 years in a cGMP manufacturing environment, or
·Associate’s Degree or equivalent and 1+ years of experience in a cGMP manufacturing environment, or Bachelor’s Degree in science related field with 1-2 years experience
Preferred Qualifications:Extended experience in using autoclaves.
Experience in a GMP environment.
Experience facilitating and delivering training.
Experience reviewing and creating controlled documents.
Experience in column packing and
Experience in Lean manufacturing and MDI (management for daily improvement) participation. 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 a twelve hour rotating shift and every other weekend, including scheduled holidays.
Ability to work day or night shift, as applicable.
Job : Production
Primary Location : United States-Massachusetts-Framingham
Job Posting : Nov 14, 2016, 4:16:33 PM
Job Type : Regular
Employee Status : Regular