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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

This role is to supervise an experienced team in the packaging and labelling of clinical supplies.

This role also includes oversight of the GMP, safety and procedural aspects of producing the supplies in a cGMP production area.

Ideally the candidate will have pervious experience in pharmaceutical industry preferably 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 assessment, 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 mange tasks through teamwork .

• Working knowledge of computers using MS Office, MS Outlook and business software systems commonly used in 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, r equired

• Demonstrated experience in a 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/ (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.

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

Company: Bristol-Myers Squibb

Req Number: R1587840

Updated: 2024-12-12 03:42:05.343 UTC

Location: Moreton-GB

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.