Senior Night-Shift GMP Manufacturing Lead

Biogen; Milwaukee (WI); On-site; USD 98,000 - 127,000; Full time

Benefits offered by this job

Medical, Dental, Vision, & Life ins.

Fitness & Wellness programs

Short- and Long-Term Disability

Vacation 15 days + shutdown

12 holidays + 3 personal days

Sick time 80 hours

Maternity/Parental Leave

401(k) with company match

Employee stock purchase plan

Tuition reimbursement up to 10000

Employee Resource Groups

Job summary

Biogen is seeking a Sr. Supervisor to oversee the 12-hour night shift for manufacturing of clinical and commercial products under GMP conditions.

You will supervise Manufacturing Associates, schedule tasks, ensure safety and GMP compliance, and coordinate with multiple departments to execute batch records and SOPs. The role requires a Parenteral Filling/Drug Product manufacturing background, strong leadership, and knowledge of GMP principles.

Qualifications

• Bachelor’s Degree (STEM) with 4+ years transferrable experience.
• Associates’ Degree with 6 years transferrable experience.
• High School Diploma with 8 years transferrable experience.
• GMP pharmaceutical manufacturing experience required.

Responsibilities

• Supervise Manufacturing Associates on night shift and develop staff.
• Oversee cGMP manufacturing activities and ensure proper documentation.
• Coordinate with QC, materials, and other groups to execute plans.
• Review batch records and SOP revisions for accuracy.
• Train staff on safety, cGMP, and process activities.

Skills

Leadership

Organization

Accountability

Tactical

GMP experience

Education

B.S.TEM degree

A.S. +6 years transferrable experience

High School Diploma +8 yrs transferrable

Tools

Oracle

CMMS

Trackwise

Job description

Biogen is seeking a Sr. Supervisor to oversee the 12-hour night shift for manufacturing of clinical and commercial products under GMP conditions.

You will supervise Manufacturing Associates, schedule tasks, ensure safety and GMP compliance, and coordinate with multiple departments to execute batch records and SOPs. The role requires a Parenteral Filling/Drug Product manufacturing background, strong leadership, and knowledge of GMP principles.