Specialist, Label Control and Material Operations in Devens, MA

Bristol-Myers Squibb • Devens, MA

83d • $83,540 - $101,228 • Hybrid

About The Position

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. 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.

Requirements

• Bachelor's degree preferred. High school diploma/ Associates degree with equivalent combination of education and work experience may be considered.
• 2+ years of relevant cGMP experience.
• Experience in FDA/EMA regulations in biopharmaceuticals or cell therapy manufacturing is preferred.
• Experience with quality management systems preferred.
• Experience with electronic system and databases such as Manufacturing Execution systems (MES), Enterprise Resource Planning (ERP) preferred.
• Experience with labeling software and commercial label printers preferred.

Responsibilities

• Issue clinical and commercial final drug product labels
• Verify the legibility and accuracy of drug product labels in accordance with approved procedures and label specifications
• Ensure areas are maintained in state of compliance to always be ready for health authority inspection or audits
• Perform basic troubleshooting; communicate and resolve discrepancies independently and escalate as required
• Author and review department owned documents
• Maintain compliance with assigned learning plan
• Support integration of newer team members
• Support internal and external inspections as required
• Assess discrepancies for entry into quality system and initiate deviations as applicable
• Participate in cross-department and cross-functional meetings, communicate in professional manner and share data/ knowledge within team
• Build relationships with specialized functions

Benefits

• Medical, pharmacy, dental and vision care
• Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP)
• Financial well-being resources and a 401(K)
• Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection and survivor support
• Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility
• Parental, caregiver, bereavement, and military leave
• Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources
• Other perks like tuition reimbursement and a recognition program

What This Job Offers

• Job Type: Full-time
• Industry: Chemical Manufacturing
• Education Level: Bachelor's degree