Offers “Sanofi”

Expires soon Sanofi

Process Engineer - VIE Contract (W/M)

  • Internship
  • Framingham, USA

Job description



iMove, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + Norway, Liechtenstein and Iceland) aged between 18 and 28.
PLEASE NOTE that since this program is primarily an international development program, candidates cannot apply to a VIE assignment in their own country of citizenship.
PLEASE NOTE that applications that are only submitted in French cannot be considered by our non-French speaking partners at Sanofi worldwide.
Therefore, only applications that are submitted in English will be considered.

We are looking for a candidate for a VIE mission of:

Process Engineer - VIE Contract (W/M)

Seeking a full-time Process Engineer (40hr/week) able to perform early stage fill/finish manufacturing process development in a pilot facility in a regulated cGMP environment. The candidate will participate in startup activities for a new fill/finish facility, including a new automated filling line under isolator. The candidate should also have experience writing SOPs, User Requirements, Change Controls, Deviations and Batch Records and coordinating activities with related groups (Quality, Validation, Metrology, Engineering and Facilities). The candidate should have the ability to operate complex systems and equipment in accordance with current GMPs and safety guidelines under limited supervision.

Responsibilities:

·  Perform early stage fill/finish manufacturing process development in a pilot facility in a regulated cGMP environment
·  Participate in start-up activities for a new fill/finish facility, including a new automated filling line under isolator
·  Write SOPs (Standard Operating Procedures), User Requirements, Change Controls, Deviations and Batch Records and coordinating activities with related groups (Quality, Validation, Metrology, Engineering and Facilities)
·  Operate complex systems and equipment in accordance with current GMPs (Good Manufacturing Practices) and safety guidelines under limited supervision

Basic Qualifications:

·  Education: Master's Degree in Process Engineering and 1+ years of related GMP manufacturing experience; knowledge and demonstrated understanding of GMP and how it applies to specific responsibilities and manufacturing operations; SOP writing
·  Experience: experience with automated manufacturing equipment (preferred)
·  Soft skills: strong verbal and written communications, effective time management and organizational skills are essential to succeed in this role; self-motivated, detailed oriented, flexible, team oriented, demonstrating good troubleshooting skills
·  IT tools: MS Office, Microsoft Project is appreciated
·  Languages: fluent English

Special Working Conditions:

·  Push/pull/lift up to 50 pounds to move loaded, wheeled carts with assistance from another worker
·  Frequent sitting, walking, standing, bending and squatting
·  May require standing and walking up to 70% of day
·  Frequent reaching between waist and shoulder level
·  Occasional reaching up and out
·  Repetitive grasping and movement of hands and fingers
·  May involve work with hazardous materials

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.

Make every future a success.
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