Shift Supervisor – Pharmaceutical Manufacturing (cGMP / API / Leadership Opportunity)
Location: Grafton, Wisconsin | Company: Siegfried USA | Industry: Life Sciences / Pharmaceuticals
About Siegfried
Siegfried is a global life sciences partner providing integrated pharmaceutical development and manufacturing solutions. With a dynamic and international environment, we bring together a highly professional and motivated team working on the cutting edge of API manufacturing and drug product development.
We value diversity, flexibility, and inclusion, creating an environment where every employee can grow professionally, contribute to innovation, and deliver superior performance.
Position Overview
The PM Shift Supervisor provides leadership and direction for manufacturing operations at our Siegfried Acceleration Hub in Grafton, specializing in early-phase development and highly potent API manufacturing.
This role ensures that all production activities are executed safely, efficiently, and in compliance with cGMP, SHE, and FDA regulations. The Shift Supervisor acts as the primary management representative during off-shifts and weekends — overseeing personnel, production, and site safety.
Key Responsibilities
- Lead and supervise manufacturing operations to ensure compliance with GMP, SHE, and company policies.
- Act as Incident Commander and ensure site safety during all shifts.
- Assign, train, and mentor operators to meet production, quality, and safety goals.
- Collaborate with Maintenance and Quality Assurance teams to resolve process and equipment issues.
- Lead troubleshooting and continuous improvement initiatives to increase efficiency.
- Review production schedules, track performance metrics, and investigate variances.
- Support deviation investigations, change control, and CAPA processes within the Siegfried Quality System.
- Manage shift scheduling, overtime, and coverage planning.
- Promote a culture of teamwork, accountability, and operational excellence in alignment with Siegfried’s Code of Conduct.
Qualifications
- Associate’s or Bachelor’s degree in Chemical Engineering, Life Sciences, or related field (or equivalent experience).
- 3+ years’ experience in pharmaceutical manufacturing, chemical processing, or regulated production environment.
- Strong knowledge of cGMP, SHE, and FDA regulatory requirements.
- Demonstrated leadership and team development skills.
- Excellent problem-solving, communication, and decision-making abilities.
- Willingness to work rotating shifts, weekends, and off-hours as needed.
What We Offer
- Opportunity to work in a global, innovative, and future-oriented company.
- A diverse, inclusive, and flexible work environment that values personal and professional growth.
- Competitive compensation and benefits, including performance-based incentives.
- Career development and advancement opportunities across Siegfried’s international network.
Join Our Team
Be part of a company that’s transforming pharmaceutical manufacturing through innovation, teamwork, and excellence. At Siegfried, your leadership helps shape the future of medicine.
Apply now to start your journey with us.
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Job Type: Full-time
Pay: $35.00 - $40.00 per hour
Benefits:
- 401(k)
- Dental insurance
- Health insurance
- Paid time off
- Vision insurance
Work Location: In person
