Manufacturing Lead (Weekend Days)
On-site · Grand Rapids, Michigan, United States
Job Summary
Manufacturing Lead responsible for directing and coordinating routine production in a cGMP environment at the Butterworth Facility on shift B (Friday–Sunday, plus every other Thursday, 6:00 am–6:00 pm). Leads cleanroom and equipment cleaning, bulk drug formulation, and aseptic formulation duties under supervision; oversees cleanroom operations, allocates resources, and supports problem solving, quality events, and 1-on-1 meetings. Communicates with cross-functional teams, mentors staff on aseptic behavior in a Grade C environment, supports audits and client communications, and ensures accurate contemporaneous GMP documentation. Requires a Bachelor’s degree in life science or equivalent, 1–2 years of pharma experience, leadership ability, and proficiency with Microsoft Word, Excel, and Outlook; must be able to use a full-face respirator for hazardous chemical tasks. Preferred: experience in a CMO and sterile filling facility.
Required Qualifications
- Bachelor’s degree in life science or equivalent training/experience
- Minimum 1 to 2 years of relevant pharmaceutical experience
- Proven leadership experience and self-starter
- Professional and positive approach
- Leadership tendencies
- Strong in building relationships
- Excellent communication
- Team player, able to work on own initiative
- Well versed in cGMP and GDP
- Detail oriented
- Proficient computer skills in Microsoft Word, Excel and Outlook
- Qualification for use of a full-face respirator for hazardous chemicals
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