Front Line Manufacturing Manager (Bulk Drug Substance - Downstream) - Night Shift
About The Position
Amgen is seeking a Front Line Manufacturing Manager for their newest and most advanced drug substance manufacturing plant, the Amgen FleX Batch facility. This facility combines disposable technologies with traditional stainless-steel equipment for maximum flexibility. It features industry 4.0 capabilities and sustainability innovations to reduce carbon and waste, aligning with Amgen's goal of being a carbon-neutral company by 2027. The Manager Manufacturing (Downstream) - Night Shift role is a vital and dynamic position supporting critical 24/7 manufacturing operations. The working schedule is a 12-hour night shift rotation (5:45pm to 6:15am) on a 2-2-3 schedule. The manager will oversee teams of manufacturing associates responsible for the manufacture of GMP drug substances, championing a safe and compliant production environment. This role is active in a Lean and continuous improvement culture, embedding these principles on the manufacturing floor. The manager will oversee technical, on-the-floor operations in a biotechnology production setting and support staff development through coaching, hiring, and mentorship. The Front-line Manager will assist in defining area objectives, identifying improvement opportunities, leading change efforts, directing their team, and delivering short- and long-term Amgen Operational goals.
Requirements
- Doctorate degree OR Master’s degree and 3 years of Manufacturing or Operations experience OR Bachelor’s degree and 5 years of Manufacturing or Operations experience OR Associate’s degree and 10 years of Manufacturing or Operations experience OR High school diploma / GED and 12 years of Manufacturing or Operations experience
- Previous managerial experience directly managing people and/or experience leading teams, projects, programs or directing the allocation of resources
Nice To Haves
- Bachelor’s degree in Life Sciences or Engineering
- Demonstrated strong leadership skills and technical understanding of biotechnology production operations
- Experience in biotechnology or pharmaceutical plant start up
- Understanding of downstream purification operation (Column Chromatography, TFF, Viral Filtration, Viral Inactivation)
- Previous knowledge and experience within a cGMP environment
- 5+ years process experience in a cGMP manufacturing facility
- 3+ years of experience in a production Area Lead, Specialist or Manager role
- Strong leadership and teambuilding skills (coaching, mentoring, counseling)
- Experience with performance management including performance reviews
- Conflict Resolution, analytical problem solving, and project management skills
- Thorough understanding of regulatory requirements
- Excellent verbal and written communication (technical) skills
- Excellent computer skills with Microsoft, EBR/MES, Delta V, Electronic quality systems
Responsibilities
- Ensure a safe working environment.
- Ensure Amgen policies are followed, including cGMP and CFR compliance of assigned areas.
- Evaluate current operating procedures and recommend changes to management to optimize production.
- Assure all corporate change control procedures are followed, and Regulatory and QA are notified prior to changes.
- Interact with regulatory agencies as needed.
- Assure proper gowning and aseptic techniques are followed.
- Engage staff and build relationships of trust and respect while driving team performance and continuous improvement.
- Recruit, train, evaluate, coach, and develop staff.
- Mentor and coach staff members to live by the Amgen Values.
- Develop and implement training plans and programs to ensure staff are prepared and compliant.
- Ensure adherence to production schedule and maintenance activities.
- Interact with management in optimizing organizational structure and responsibilities.
- Ensure plant safety through auditing, evaluations, and cross-functional walks.
- Ensure gowning and aseptic techniques training programs are maintained.
- Demonstrate technical mastery of manufacturing processes.
- Collaborate with cross-functional teams (i.e., QA/QC, F&E, PPIC, Mfg, PD, Regulatory, etc.) in completing production activities.
- Develop, implement, and assess CAPAs and solutions to complex problems.
- Responsible for elevating and resolving problems during daily operations.
- Oversee set up, execution, and completion of critical manufacturing processes/tasks.
- Interact with management in planning, developing, and maintaining budget.
- Assist in developing and maintaining department goals.
Benefits
- Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.
- A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
- Stock-based long-term incentives
- Award-winning time-off plans and bi-annual company-wide shutdowns
- Flexible work models, including remote work arrangements, where possible
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Full-time
Career Level
Manager
Education Level
No Education Listed
