Bristol Myers Squibb Technical Lead Commercial Manufacturing Upstream in Providence, Rhode Island
At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.
Works on routine manufacturing assignments as well as assignments that are very complex in nature where independent action and a high degree of initiative are required in resolving problems and making recommendations. – striving for right first time through adherence of GMP activities.
Change control identifiers – works in conjunction with bioprocess associate/specialists to identify key improvements initiatives and direct changes to project leads for initiation
Investigation identifiers – initiate investigation following alignment with QA floor
Communicate and resolve operational variances.
Serve as the “acting” Shift Supervisor/Manager in absence of Shift Supervisor/Manager – Coordinate, direct and oversee work execution and manage personnel related issues.
Executes real time process monitoring – including equipment and key process parameters review and work with Shift Supervisor/Manager to drive required decisions
Drive implementation of process enhancement and new technology in partnership with Project lead and Manufacturing Technology team.
Participate in performance review discussion
Leads complex investigations on floor – drives technical issues in working with cross functional team members
Support real time process reports review and resolve open issues. Trend issues and strives to right first time.
Technical trainer for the shift – provides consistent training to the staff
Execute and drive continuous improvements
Support Tech transfer team through active participation in ensuring that new process can fit and executes in sustainable manner
Being resource to support routine investigations and CAPAs– author, review, approval, in case of excess investigation beyond planned capacity.
Assigned area owner – drive facility upkeeps
Adheres to Good Manufacturing Practices and standard operating procedures.
Weighs and checks raw materials. Assembles, cleans and sterilizes process equipment, monitors processes.
Completes electronic work instructions and maintains clean room environment to comply with regulatory requirements.
Operates and trains others all production equipment within the assigned functional area (i.e. Upstream: Media formulation equipment, glass washers, dispensary, bioreactors, harvest equipments or Downstream: Buffer equipment, glass washers, chromatography skids, membrane operations, column packing skids, etc.)
Effectively uses process automation systems (i.e. Delta V and Syncade Interactions, OSI/Pi Historian) and some supporting business systems (i.e. SAP. Trackwise, Maximo etc.).
Ensures less experienced manufacturing personnel comply with Standard Operating Procedures (SOPs) and electronic work instructions and that training is completed on time.
Assists with the coordination and implementation of special projects such as validation or complex investigations.
May provide scheduling and work assignment guidance to peers. Modifies group work plan, schedule or assignments to meet shift/unit priorities, maintains operational efficiency, making corrections as necessary, regularly provides training and operational guidance to other staff. Advises Shift Supervisor/Manager on improvements which may optimize work processes and informs of work issues requiring management action.
*Works on a 12 hour (5PM to 5AM) rotating shift 36/48 which involves working all holidays that fall on the schedule. Required to work every rotating weekends, some holidays, and during adverse weather conditions in support of manufacturing facility. Flexibility to work irregular hours and short notice overtime. This role is inclusive of a 20% shift differential and 8 hours built in over time.
Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
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 company is committed to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace adjustments and ongoing support in their roles. Applicants can request an approval of accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application, or any part of the recruitment process direct your inquiries to email@example.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.
Company: Bristol Myers Squibb
Req Number: R1539641
Updated: 2021-06-19 02:39:21.774 UTC
Location: Providence,Rhode Island
Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.
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