Packaging and Labelling Supervisor page is loaded
Packaging and Labelling Supervisor
Apply locations Moreton - GB time type Full time posted on Posted 15 Days Ago 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. Maintains employee records (attendance, vacation etc.).
* Assures all production orders are executed in accordance with cGMP's and SOP's, utilizing SAP for error-free technical documentation.
* Establishes and supports 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 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 in 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.
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/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.
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
Bristol Myers Squibb is Disability Confident – Employer
A UK Government scheme.
We’re creating innovative medicines for patients fighting serious diseases. We’re also nurturing our own diverse team with inspiring work and challenging career options. No matter the role, each one of us makes a contribution. And that makes all the difference.
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