Manager, QP Operations (Pharma)

Beschreibung:

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. 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.

If you're a quality assurance professional with a passion for operational excellence and a strong grounding in pharmaceutical GMP, this is your opportunity to make a real difference at a global biopharmaceutical leader.

As Manager, QP Operations (Pharma), you'll play a key role within BMS's QP Operations team, working at the heart of our batch certification and QP release activities across our Dublin and Utrecht sites. Reporting to the Senior Manager, QA Lead - Pharma QP Operations, you'll collaborate closely with internal sites, external vendors, and supply chain partners to ensure the efficient and compliant operation of the QP function.

This is a 12-month fixed term contract and a role where your work directly supports the quality and integrity of the medicines we deliver to patients every day.

What You'll Do
* Support the Qualified Person with the batch certification function, including preparation and review of batch documentation packages for QP release
* Communicate and collaborate with BMS Supply Chain to support the QP release schedule
* Complete activities associated with new product introductions
* Author, review, and approve QA-related procedures and relevant controlled documents
* Prepare quality documents supporting batch certification, including QP declarations, Product Quality Reviews, and Risk Assessments
* Act as functional lead for QMS activities such as Change Control assessments, Investigations, and Quality Agreement updates
* Support the site inspection readiness program for corporate and regulatory inspections, acting as SME when required
* Provide training to new team members as required
* Support Opex programs and champion continuous quality improvement initiatives
* Interface with relevant departments to ensure compliance with corporate policies, GMP, and regulatory requirements

What You'll Bring

Education

* BSc in Science or a related discipline with 2-3 years of QA experience in a pharmaceutical environment, preferably operations-based

Experience & Skills
* A clear understanding of cGMP requirements for manufacturing and/or systems and compliance
* Demonstrated ability to communicate and collaborate effectively at a variety of levels and across divisions
* Proven ability to recognise issues, highlight risks, and prioritise workload based on schedule requirements
* Proven success working well in a team environment with the flexibility to react to changing business needs
* Strong interpersonal, oral, and written communication skills
* Proactive in resolving issues and escalating to management when necessary
* QP Eligible - desirable

Why BMS?

* At BMS, we don't just offer a job - we offer a purpose. You'll join a company that.
* Operates in more than 40 countries with a truly global footprint.
* Delivers transformative therapies for oncology, immunology, hematology, cardiovascular disease, and beyond
* Is consistently recognised as a top employer for diversity, inclusion, and employee wellbeing
* Invests in your growth - with access to world-class development resources and a culture of innovation
* Puts patients first - in every decision, at every level

You'll get a competitive salary and a great benefits package including, but not only, an annual bonus, pension contribution, family health insurance, 27 days of annual leave, access to BMS Cruiserath on-site gym and life assurance.

We believe that the diverse experiences, perspectives, and expertise of our people are our greatest strength. Here, you can be bold, be yourself, and do your best work.

Ready to Take the Next Step?

If you're ready to bring your quality and pharmaceutical expertise to a company where the stakes truly matter, we'd love to hear from you. Apply now and take the next step in a career defined by meaningful impact.

#LI-Hybrid

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 a supportive culture, promoting global participation 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 an 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.

Supporting People with Disabilities
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.

Candidate Rights
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/

Data Protection
We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at TAEnablement@bms.com. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.

R1603724 : Manager, QP Operations (Pharma)