Manager (Shift), Sterile Drug Product, Qa Manufacturing Operations

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Bristol Myers Squibb Ireland
Bristol Myers Squibb has been in operation in Ireland since 1964, employing over 650 people across a range of activities and business units
Located in Dublin, Cruiserath Biologics Campus, a one billion Multi-Product Cell Culture Biologics Manufacturing facility plays a central role in the Global Product Development and Supply (GPS) network as the company's first European biologics manufacturing facility. This state of the art facility will produce multiple therapies for the company's growing biologics portfolio. Global Biologics Laboratory (GBL) responsible for the release testing of Biologics Drug product for the network, is also based on the Cruiserath Biologics Campus.
BMS Cruiserath has been awarded "Biopharma Company of the Year 2019" in the Irish Pharma Industry Awards and is certified as a Great Place to Work since 2017, including as a Great Place to Work for Women in 2020, 2021 and 2022.
Position Summary
BMS Cruiserath Biologics is seeking to recruit aManager, QA Manufacturing Operationsfor Sterile Drug Product.

Reporting to the Snr Manager, QA Manufacturing Operations for Sterile Drug Product, the Manager will support the start-up of a commercial drug product manufacturing facility for its biologic's commercial portfolio and clinical pipeline. This shall be achieved by working in conjunction with the project team to provide resolution on questions as they arise during project design, construction, and qualification. Providing quality assurance oversight for all phases of the project.

In addition, this role will support readying the facility for manufacturing operations on a 24/7 basis, supporting the Tech Transfer program for new products introduced into the facility.

Post start-up the successful candidate will support the execution and maintenance of the QA activities related to the commercial sterile drug product manufacture and release activities on shift in Cruiserath.

This position will beinitially on days but will move through various shift patterns as the project progresses to full commercial manufacture.

The start-up nature of this project will require adaptability & innovation due to the multiple project phases and multiple products onsite. The role will be both challenging & rewarding and will thus ensure that the successful candidate can seize a wide range of development opportunities within BMS. The Sterile Drug Product project scope includes construction and commissioning of new SDP product suite with parts prep, formulation, aseptic filling and capping of liquid & freeze-dried vials, aseptic filling of syringes, and Visual Inspection capabilities. The project also includes new and expanded clean utilities.

Key Responsibilities During Start Up
Responsible for hiring, coaching and development of staff and direct personnel to achieve operational goals and ensure the timely completion of tasks.
Provide QA oversight for Aseptic Sterile Drug Product processes such as Formulation, Filling, Lyophilization, Capping, and Visual Inspection
Work with the project design, CQV, & the Automation/CSV teams to facilitate the implementation of the project design and validation of the project for Drug Product Operations.
Prepare/Review/Approve documentation (SOPs, MBRs, Logbooks) required to enable manufacturing start-up and complete training on time.
Support CQV / Tech Transfer / Operational Readiness activities including but not limited to:New Product Introduction
SOP Development and Implementation
Training Material development
MES / MBR Design
CQV support as required

Participation in GMP reviews for new facility construction and new equipment support systems
Develop and execute training programs in support of multiproduct manufacturing.
Support establishment of Operational Excellence initiatives e.g., 5S / Std Work / LSW / Kaizen / Problem Solving etc.

Key Responsibilities During Commercial Operations
Manage team of QA Snr Specialists to provide direct QA on the floor support to manufacturing team for commercial and clinical sterile drug product
Responsible for hiring, coaching and development of staff and direct personnel to achieve operational goals and ensure the timely completion of tasks.
Provide Quality oversight for Batch record review activities to support the Disposition process for commercial and clinical drug product
Provide QA oversight for Aseptic Sterile Drug Product processes such as Formulation, Filling, Lyophilization, Capping, and Visual Inspection
QA Operations review of events and investigations
Authoring, review, and approval of QA-related procedures
QA support for implementation of Manufacturing Execution System (MES) and development of batch records
Change control assessment and CAPA evaluation/CAPA close-out.
Interface with relevant departments to ensure compliance with corporate policies, GMP and regulatory requirements.
Participation in internal, corporate, and regulatory inspections
Drives and supports culture of continuous improvement initiatives and safe working practices.
Designee for Snr Manager, Sterile Drug Product, QA Manufacturing Operations, when required.
Support Operational Excellence initiatives e.g., 5S / Std Work / LSW / Kaizen / Problem Solving etc.

Qualifications & Experience
The successful candidate must possess:
BSc in Science or related discipline with a minimum of 5 years' experience in Sterile Drug Product Manufacturing
Understanding and experience of the principles of Annex 1 and how they translate into a contamination control strategy for sterile manufacture.
The candidate will have proven success working well in a team environment, and the ability to manage people
A clear understanding of cGMP requirements for manufacturing and/or systems and compliance
Detailed knowledge of Sterile Drug Product would be a distinct advantage.
Required to work on his/her own initiative in addition to working as part of a team and must be open to shift work. Must be able to work across a team matrix to meet accelerated timelines.
Excellent communication and presentation skills are essential.
Excellent time management and organizational skills along with a proven ability to multi-task
Employees are expected to display the BMS Biopharma Behaviors, which enable them to be successful and perform at their highest level.

Why you should apply

You will help patients in their fight against serious diseases
You will be part of a company that encourages excellence and innovation, respects diversity, develops leaders and values its employees.
You'll get a competitive salary and a great benefits package including an annual bonus, pension contribution, family medical allowance, 27 days of annual leave, life assurance and on-site gym

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 workplaceaccommodations/adjustmentsand ongoing support in their roles. Applicants can request a reasonable workplaceaccommodation/adjustmentprior to accepting a job offer. If you require reasonableaccommodations/adjustmentsin completing this application, or in any part of the recruitment process, direct your inquiries ******. Visitcareers.bms.com/eeo-accessibilityto access our complete Equal Employment Opportunity statement.

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