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

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.

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Salary Range

106,148.00USD -143,612.00 USD