Packaging and Labelling Supervisor
Apply locations Moreton - GB time type Full time posted on Posted Yesterday job requisition id R1587840
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 Overview
Supervise an experienced team in the packaging and labelling of clinical supplies, including oversight of the GMP, safety and procedural aspects of producing the supplies in a cGMP production area. Ideally, you will have previous experience in the pharmaceutical industry, preferably in clinical trials packaging.
Key Responsibilities
* Demonstrates a thorough working knowledge of the technical aspects of cGMP’s as they relate to clinical supply packaging and labeling.
* Reviews the master production schedule and production orders, establishes production priorities and revises schedules according to production order specifications, establishing priorities for materials and staff.
* Supervises staff in all aspects of packaging and labeling of clinical supplies. Maintain employee records (attendance, vacation etc.).
* Assure all production orders are executed in accordance with cGMP's and SOP's, utilizing SAP for error-free technical documentation.
* Establish and support a work environment of continuous improvements that supports the Company’s Quality Systems and the appropriate procedures for the area.
* Utilizes technical writing skills to generate COSHH, Safety risk assessments, procedures and guidelines.
* Interacts and liaises with team members from Packaging & Labelling, Quality, Logistics and Quality Control.
* Oversees and/or conducts training of new or existing employees and ensures their training is up to date and documented.
* Ensures that health and safety guidelines are followed.
* Leads root cause investigations for process deviations and assigns Corrective/Preventative Actions.
Key Skills Required
* Prior supervision of production staff or leadership role within a production operation with demonstrated ability in scheduling, organizing and team building.
* Working knowledge of cGMP’s and regulatory (i.e. MHRA, FDA, EU CTR, etc.) requirements and their application within a clinical packaging and labeling production environment.
* Solid record of attention to detail and strict adherence to all procedures and regulations.
* Good understanding of the pharmaceutical development process and associated scientific principles.
* Demonstrated ability to communicate effectively with various support groups and able to lead in a team environment.
* Effectively manage competing priorities, adaptable to change, demonstrated ability to accept additional responsibilities and manage tasks through teamwork.
* Working knowledge of computers using MS Office, MS Outlook and business software systems commonly used in the pharmaceutical industry (i.e. SAP, Veeva).
* Demonstrates the ability to effectively schedule multiple jobs/orders.
Education and Experience Required
* Bachelor of Science or a Mechanical Engineering Degree, required
* Demonstrated experience in the pharmaceutical industry, required
* Experience in Pharmaceutical manufacturing with a focus on the production of Clinical Trial Supplies, preferred
* Extensive experience of progressive leadership or supervisory experience in the pharmaceutical industry, required.
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 science,” 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.
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