Manufacturing Manager - 12-Hour PM Shift (Biotech)

BioSpace; New Albany (OH); On-site; USD 120,000 - 150,000; Full time

Benefits offered by this job

Health and welfare plans

Retirement plan

Stock-based long-term incentives

Generous time-off plans

Job summary

Amgen is seeking a Manager, Manufacturing for a 12 Hour PM shift (6:00pm - 6:30am) to lead a manufacturing area in an Inspection and Packaging facility. You will ensure production remains in full cGMP compliance, supervise staff, and maintain production schedules.

The role requires extensive leadership experience in pharma/biotech with a strong focus on regulatory compliance, cross-functional collaboration, and process optimization.

Qualifications

• Doctorate, or Master’s with 3 years in the pharmaceutical/biotech industry.
• Bachelor’s with 5 years in the pharmaceutical/biotech industry.
• Associate’s with 10 years in the pharmaceutical/biotech industry.
• High School Diploma/GED with 12 years in the pharmaceutical/biotech industry.
• Must have experience directly managing people and/or leadership experience leading teams, projects, programs, or directing resources.

Responsibilities

• Evaluate and approve reports and protocols.
• Ensure cGMP and CFR compliance of manufacturing areas.
• Revise, update, and review procedures.
• Coordinate the development and revision of SOPs.
• Evaluate current manufacturing procedures and recommend changes to management to optimize production.
• Assure all corporate change control procedures are followed, and Regulatory and QA are made aware prior to the changes.
• Interact with the FDA.
• Ensure Amgen policies are followed.

Skills

Leadership

People management

Project management

Education

Doctorate degree

Masters degree

Bachelor's degree

Associate's degree

High School Diploma/GED

Job description

Amgen is seeking a Manager, Manufacturing for a 12 Hour PM shift (6:00pm - 6:30am) to lead a manufacturing area in an Inspection and Packaging facility. You will ensure production remains in full cGMP compliance, supervise staff, and maintain production schedules.

The role requires extensive leadership experience in pharma/biotech with a strong focus on regulatory compliance, cross-functional collaboration, and process optimization.