Manager, Manufacturing Planner, Sterile Drug Product

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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.

Position Summary
BMS Cruiserath Sterile Drug Product is seeking an experienced individual for the role of Sterile Drug Product (SDP) Manufacturing Planner.
Reporting to the Associate Director of Operations, the SDP Manufacturing Planner will play a key role within the overall program to deliver the new Sterile Drug Product facility and operational capability at Cruiserath.
The SDP Manufacturing Planner will work in close collaboration with the Project Manager responsible for the Site Start-Up Readiness and process Technology Transfer programs in the new facility. The SDP Manufacturing Planner will generate and manage both the individual and rolled-up schedules for the portfolio of projects which integrate the Site Start-Up Readiness charters.
The SDP Manufacturing Planner will manage the Operational Readiness Schedule and Weekly Work Plan Process for SDP Operations in collaboration with the Manufacturing Leadership Team.
Post project phase SDP Manufacturing Planner will execute detailed planning and scheduling for manufacturing activities to ensure the safe and on-time delivery of manufactured drug product.
The start-up nature of this project will require adaptability and innovation due to the multiple project phases and multiple products onsite. The role will be both challenging and rewarding and will thus ensure that the successful candidate can seize a wide range of development opportunities within BMS.

Key Responsibilities

Start-up / Project Phase
* Support the Site Start-Up Readiness Project Manager in developing an integrated schedule and detailed resourcing plan for the operational start-up and technology transfer program for the commercial assets identified for the project.
* Partner with Site Start-Up Readiness and process Technology Transfer workstreams to ensure alignment to the integrated master schedule.
* Work closely with Workstream Leads across multiple functions/departments to plan, assign, and amend scheduled activities (including Weekly Work Plans) as required.
* Work closely with the CAPEX Project Scheduler to ensure the Site Start-Up Readiness schedule is linked with the CAPEX schedule and meets overall SDP project needs.
* Support coordination of stakeholder activities in the Post-OQ schedule period to maximize efficiency and plant start-up time.
* Provide weekly metric reports on overall delivery of the Site Start-Up and Technology Transfer Readiness schedule for review by the Leadership Team in tiered meetings.
* Identify and escalate key project schedule risks and communicate them to the Project Manager and other relevant stakeholders.
* Provide input into Capacity Modelling and development of Finite Scheduling Systems.
Operational / Business-as-Usual Phase
* Develop and maintain the detailed manufacturing schedule to meet plan-of-record output from the facility.
* Partner with cross-functional stakeholders (e.g., Supply Chain, Shift Manufacturing Leads) to plan, assign, and amend scheduled activities as required.
* Coordinate with Supply Chain to ensure raw materials and consumables are available for all planned work.
* Maintain awareness of short-term business priorities and objectives through regular communication with key stakeholders (Project Manager, leadership, functional teams).
* Provide regular schedule adherence updates to relevant stakeholders (Project Manager, functional managers, Workstream/Shift Leads).
* Follow up on completed work and track variances/lost time as required.
* Drive continuous improvement of planning tools, processes, and SOPs to optimize schedule performance.
* Use planning tools to keep a complex operation on schedule and coordinate parallel activities, including coordination with Facilities, EHS, QA, and other functions. Manage external factors such as planning and inspections.

Qualifications & Experience

* A degree qualification in engineering, project management or science discipline with relevant experience in the regulated manufacturing industry is advantageous.
* Proficiency or working knowledge of scheduling software systems such as Primavera and/or MS Project is essential.
* Advanced user skill of standard software applications e.g. MS Excel, MS Word, MS PowerPoint, SharePoint etc.
* Excellent communication and presentation skills and experience interfacing with multiple stakeholders and partner functions are essential.

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

#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
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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.

R1602771 : Manager, Manufacturing Planner, Sterile Drug Product