Senior Specialist, QC Compliance, Cell Therapy - Devens, MA
Senior Specialist, QC Compliance, Cell Therapy - Devens, MA
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$ 89530 - 108500
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.
At Bristol Myers Squibb we are reimagining the future of cell therapy. With our bold ambition backed by a best-in-the-industry team and long-term commitment we are leading the way to unlock the full promise of cell therapy as we strive to put more patients on the path to a cure. If you are ready to challenge yourself accelerate your career and give new hope to patients theres no better place than here at BMS with our Cell Therapy team.
The Senior Specialist QC Compliance Cell Therapy is responsible for leading QC deviation laboratory investigations CAPAs and change control. May provide support during health agency
inspection.
Shifts Available:
Monday Friday Standard Working Hours Hybrid
Responsibilities:
Lead and author QC deviations laboratory investigations CAPAs and other quality records
Work with QC SMEs to conduct root cause analysis.
Ensure timely and compliant closure of investigations deviations CAPAs and other quality records.
Perform document revision project CAPA and deviation/investigation change mgmt. actions related tasks and/ or continuous improvement efforts.
Train and mentor others on deviation investigation and CAPA process/ procedures.
May support health agency inspection as equipment area subject matter expert.
Communicate effectively with management and cross functional teams (e.g. present investigation findings at governance forums)
Additional Qualifications/Responsibilities
Basic Requirements:
Ability to accurately and completely understand follow interpret and apply Global Regulatory and cGMP requirements.
High problem-solving ability/mentality critical thinking technically adept and logical.
Ability to communicate effectively with peers department management and cross-functional peers about task status roadblocks and needs.
Ability to work in a fast-paced team environment action oriented highly organized to meet deadlines and prioritize work.
The starting compensation for this job is a range from $89530 - $108500 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.
Required Experience:
Senior IC
Employment Type
Full Time
