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Front Line Manufacturing Manager (Bulk Drug Substance - Upstream) - Night Shift

  • Amgen
  • US - North Carolina - Holly Springs, United States of America
  • Full time
  • Salary not listed

About the role

Career Category Manufacturing Job Description   HOW MIGHT YOU DEFY IMAGINATION?   You’ve worked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills, experience, and passion to work toward your goals? At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies, reaching over 10 million patients worldwide. Come do your best work alongside other innovative, driven professionals in this meaningful role.    Be part of Amgen's newest and most advanced drug substance manufacturing plant. When completed, the Amgen FleX Batch facility will combine the latest in disposable technologies with traditional stainless-steel equipment to allow for maximum flexibility in operations. The FleX Batch facility will not only feature the best in-class drug substance manufacturing technologies with embedded industry 4.0 capabilities, but it will also integrate sustainability innovations to reduce carbon and waste, as part of Amgen's plan to be a carbon-neutral company by 2027.    Manager Manufacturing (Upstream) - Night Shift   What you will do     Let’s do this. Let’s change the world. In this dynamic role you will be the on-shift front line manager in manufacturing. The schedule is night shift (2-2-3, 12-hour rotation), 5:45PM to 6:15AM.  The successful candidate will be leading a team of experienced manufacturing associates responsible for the manufacture of GMP (Good Manufacturing Practices) drug substance. The manager will champion a safe and compliant production environment through structured on floor presence. The manager will be an active participant and role model in Lean culture and continuous improvement programs with responsibility to translate onto the manufacturing floor.    With minimal direction the manager is responsible for leading on the floor operations and staff in manufacturing. The successful candidate must demonstrate strong leadership skills and technical understanding of biotechnology production operations. This individual will be responsible for supervising, coaching, hiring, and development of floor staff.    The front-line manager will assist in defining area objectives, identifying improvement opportunities, and leading change efforts; effectively directing their team and delivering on short- and long-term Amgen Operational goals.    Responsibilities  Compliance:   Ensure safe working environment for all  Ensure Amgen policies are followed, including cGMP and CFR (Code of Federal Regulations) compliance of assigned areas  Evaluate and implement process improvements and optimizations, partnering with Quality, compliance, and EHSS (Environmental, Health, Safety and Sustainability) on change controls  Interact with regulatory agencies as needed  Assure proper gowning and aseptic techniques are followed    Staff Supervision:   Responsible for engaging staff and building relationships of trust and respect while driving team performance and continuous improvement  Responsible for selection, training, evaluation, staff relations and staff development  Mentor and coach staff members to live by the Amgen Values  Develop and implement trainings plans and programs, to ensure staff are prepared and compliant  Ensure adherence to production schedule and maintenance activities  Interacts with management in optimizing organizational structure and responsibilities  Ensure plant safety through auditing, evaluations, and cross functional walks  Process/Equipment/Facilities:   Demonstrate technical mastery of manufacturing processes  Collaborate with cross-functional teams (i.e., QA/QC, F&E (Facilities & Engineering), PPIC, Mfg, PD (Process Development), Regulatory, etc.) in completing production activities  Develop, implement, and assess CAPAs (Corrective Action Preventive Action) and solutions to complex problems  Responsible for elevating and resolving problems during daily operations  Oversees set up, execution, and completion of critical manufacturing processes/tasks  Administrative:   Interacts with management in planning, developing, and maintaining budget  Assist in developing and maintaining department goals  Other functional responsibilities may be assigned     Basic Qualifications   Doctorate degree   OR   Master’s degree and 3 years of Manufacturing and/or operations experience  OR   Bachelor’s degree and 5 years of Manufacturing and/or operations experience   OR   Associate degree and 10 years of Manufacturing and/or operations experience   OR   High school diploma / GED and 12 years of Manufacturing and/or operations experience   AND  Previous managerial experience directly managing people and/or experience leading teams, projects, programs or directing the allocation of resources    Preferred Qualifications   Bachelor’s degree in Life Sciences or Engineering  Experience in biotechnology or pharmaceutical plant start up   Basic understanding of upstream and/or downstream operations  Previous managerial experience directly managing people and/or experience leading teams, projects, programs or directing the allocation of resources  Knowledge and experience within a cGMP or other highly regulated 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    Thrive     Some of the vast rewards of working here   As we work to develop treatments that look after others, we also work to care for our teammates’ professional and personal growth and well-being.  Full support and career-development resources to expand your skills, improve your expertise, and improve your potential along your career journey  A diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act  Generous Total Rewards Plan—comprising health, finance and wealth, work/life balance, and career benefits—with compensation and benefits rated above 4 stars (out of 5) on Glassdoor    Apply now for a career that defies imagination  Objects in your future are closer than they appear. Join us.  careers.amgen.com     Ready to Apply for the Job?   We highly recommend utilizing Workday's robust Career Profile feature to complete the application process. A link to update your profile is available when you click Apply. You can then complete your Workday profile in minutes with the “Upload My Experience” functionality to upload an updated copy of your resume or you can simply edit the individual sections of your Career Profile.  Please note that you should be in your current position for at least 18 months before applying for internal positions. Staff must notify their current manager if invited for an interview. In addition, Staff are ineligible to apply for open positions if (a) their performance is currently being managed on a performance improvement plan (PIP) or other locally utilized formal coaching document or (b) their most recent performance rating was not a “Partially Meets Expectations” or higher. . Salary Range 106,148.00USD -143,612.00 USD