Field Quality, QA Operations Senior Specialist - Devens, MA

Job DescriptionATTENTION MILITARY AFFILIATED JOB SEEKERS - Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans, 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 aren't 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. You'll 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. Position: Field Quality, QA Operations Senior SpecialistLocation: Devens, MAShift : 7:00 am to 3:30 pm Monday to Friday Key Responsibilities•Quality floor support of complex manufacturing activities•Performs manufacturing batch production record review in support of product release in accordancewith specifications and SOPs.•Perform walkthroughs of GMP areas documenting observations and areas of concern.•Perform training on routine facility Quality tasks for new team members.•Supports return to service walkthroughs and Manufacturing inspection readiness walkthroughs perprocedures as needed.•Assures all electronic and paper documentation, which requires QA review is in compliance with corporateand site procedures, cGMP regulations, and other industry guidelines.•May support review of quality master data.•Authors and revises QA specific SOPs and may provide QA review and approval of manufacturing related SOPs.•May provide guidance to less experienced staff.•Support the Quality approval of Master Batch Records or Syncade Recipes.•Supports the Quality review and closure of no impact manufacturing deviations.•May support release of incoming or manufactured products.•Routine QA Floor Support Activities, including alarm review, logbook review, etc.•Other duties as assigned.Additional Qualifications/ResponsibilitiesQualifications & Experience•B.S. in science, engineering, biochemistry or related discipline, or its equivalent•A minimum of 4 years of relevant experience in a regulated environment with 2 years focused on quality.Work is largely performed in a modern manufacturing facility where one must be aware of the presence of workplace standards including pressurized liquids gases, steam and hazardous chemicals. Use of Personal Protective Equipment (PPE) will be required in some portions of the facility, including appropriate gowning for working in a clean room environment.If you come across a role that intrigues you but does not perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.The starting compensation for this job is a range from $89,780.00 USD to $116,900.00 USD 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.