Devens, MA, 01434, USA
7 days ago
Manager, Packaging Operations Supply Chain, Cell Therapy
**Working with Us** 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 rich in diversity. 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. Read more: careers.bms.com/working-with-us . **Position Summary:** The Packaging Operation Manager - Cell Therapy Supply Chain will oversee the Packaging Operation to support routine patient and/or healthy donor samples received, finished goods product labeling operations, and finished goods product shipment for Cell Therapy. **Knowledge, Skills, and Abilities:** + Knowledge of inventory systems preferred + This position will require supporting off-shift schedules, including holidays and weekends. + Must be comfortable being exposed to human blood components. **Duties and Responsibilities:** + Lead the day-to-day activities of the packaging operation for Devens Cell Therapy to ensure patient order delivery as required by the Patient Scheduling team. + Manage the creation, implementation, and compliance of all documentation and procedures for the packaging operation team. + Ensure the packaging operation associates are trained as per SOPs, Company Policies and that associates meet qualification requirements for the position to which they are assigned. + Maintain operating and storage areas ready and safe to operate as per SOPs + Identify tactical and operational issues to prevent deviations and maintain a compliance environment. + Lead and manage the development of corrective and preventative actions, deviation responses, and investigations. + Hire, mentor, and develop exceptional people: Conduct performance reviews and identify opportunities for career growth for manufacturing associates. + Manage implementation and maintenance of appropriate training curricula + Create an environment of teamwork, open communication, and a sense of urgency. Foster a safety culture and compliance with site policies and cGMP requirements. + Additional duties, tasks, and responsibilities as assigned by the Supply Chain department. **Education and Experience:** + Bachelor's degree in a relevant science or engineering discipline. + Advanced degree a plus + 5+ years of experience in cGMP manufacturing within a biopharmaceutical or cell therapy manufacturing environment + 3+ years of experience with direct reports required. + An equivalent combination of education, experience and training may substitute. + Experience in electronic batch records a plus. + Receiving and Shipping experience a plus **Working Conditions:** + Stand and Walk - Required to stand/walk while operating manufacturing/computer equipment for several hours at a time throughout the day. + Require working in a conference room environment for reasonable periods. + Require working in labs, productions, and warehouse environments + Will be required to wear personal protective equipment (PPE) and other clean room garments daily. This may include but is not limited to: safety shoes, safety glasses, aprons, face shields, lab coats, full full-body gowns, hairnets, gloves, and hearing protection. If you come across a role that intrigues you but doesn't 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. **Uniquely Interesting Work, Life-changing Careers** With a single vision as inspiring as Transforming patients' lives through scienceā„¢ , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. **On-site Protocol** BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role: Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/ (https://careers.bms.com/eeo-accessibility) eeo-accessibility to access our complete Equal Employment Opportunity statement. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/ Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. **Company:** Bristol-Myers Squibb **Req Number:** R1587007 **Updated:** 2024-11-15 05:39:36.803 UTC **Location:** Devens-MA 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.
Confirm your E-mail: Send Email