Scientist, OSD Clinical Manufacturing - New Brunswick, NJ
Scientist, OSD Clinical Manufacturing - New Brunswick, NJ
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$ 96940 - 117500
1 Vacancy
Job Description
ATTENTION MILITARY AFFILIATED JOB SEEKERS- Our organization works with partner companies to source qualified talent for their open roles. The following position is available toVeterans Transitioning Military National Guard and Reserve Members Military Spouses Wounded Warriors and their Caregivers. If you have the required skill set education requirements and experience please click the submit button and follow the next steps. Unless specifically stated otherwise this role is On-Site at the location detailed in the job post.
Challenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here uniquely interesting work happens every day in every department. From optimizing a production line to the latest breakthroughs in cell therapy this is work that transforms the lives of patients and the careers of those who do it. Youll get the chance to grow and thrive through opportunities uncommon in scale and scope alongside high-achieving teams. Take your career farther than you thought possible.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits services and programs that provide our employees with the resources to pursue their goals both at work and in their personal lives.
Our Clinical Supply Operations is responsible for the supply of drug product administered to patients in clinical studies worldwide. In Global Product Development and Supply the team works closely with our partners to deliver quality products safely efficiently and on time while operationalizing the innovative technologies that will deliver the transformative medicines of tomorrow. As a member of our team you will get the chance to play a pivotal role to positively impact patients lives while developing professionally to achieve your own career goals.
Position Summary:
This position is needed to efficiently produce GMP compliant clinical materials in support of the BMS clinical portfolio.
Role & Responsibilities:
Effectively oversee batch execution and supervise technicians to ensure product is made in accordance with pertinent specifications and cGMP requirements.
Adherence to group master manufacturing schedule and escalation to management when timelines are at risk.
Generation and review of GMP documentation as necessary including batch records SOPs Work Instructions planned deviations operation alerts and CAPAs.
Coordinate activities with other departments to ensure timely release of products.
Interface with Pharmaceutics R&D to ensure proper technical transfer and scale-up of formulae and processes into Clinical Manufacturing and out to commercial manufacturing.
Complete batch feedback reports and provide recommendation for process procedure and batch record improvements to management.
Experience & Qualifications:
B.E./B.S. in Engineering or in a related science field
Experience in pharmaceutical manufacturing and/or formulation (3 years) required.
Experience with solid dosage dose manufacturing cGMPs and product or process development is preferred.
The ability to work in a GMP environment and the capability to plan and execute projects is required.
The starting compensation for this job is a range from $96940 - $117500 plus incentive cash and stock opportunities (based on eligibility).
The starting pay rate takes into account characteristics of the job such as required skills and where the job is performed. Final individual compensation will be decided based on demonstrated experience.
Employment Type
Full Time
