What are the responsibilities and job description for the Manufacturing Supervisor (Pharmaceuticals) position at Astrix?
We’re hiring a Manufacturing Site Supervisor to join a well-established company with over 50 years of industry experience and a growing international presence. This organization supports a diverse range of clients in the Pharmaceutical, Medical Device, and Life Sciences sectors.
If you’re looking to join a collaborative and expanding team, this is a great opportunity to gain hands-on experience with a broad portfolio of products and contribute to high-impact work in a regulated manufacturing environment.
Schedule: M-F 8a-5p
Salary: 70K-90K (not including annual bonuses!)
Location: Lake County, IL
Responsibilities
If you’re looking to join a collaborative and expanding team, this is a great opportunity to gain hands-on experience with a broad portfolio of products and contribute to high-impact work in a regulated manufacturing environment.
Schedule: M-F 8a-5p
Salary: 70K-90K (not including annual bonuses!)
Location: Lake County, IL
Responsibilities
- Train and supervise production staff on GMP procedures, safety rules, and quality standards.
- Assign tasks, check performance, and provide feedback.
- Handle employee concerns and help correct any issues related to GMP compliance.
- Perform routine quality checks during production to catch problems early.
- Investigate and document any issues or deviations from procedures.
- Keep accurate records, including batch documents and quality data.
- Report quality concerns to the appropriate team or leadership.
- Help prepare for and support internal and external audits.
- Create and follow production schedules to meet deadlines.
- Solve day-to-day production challenges.
- Oversee cleaning and sanitation in production areas to ensure hygienic conditions.
- Prepare regular reports on production performance, quality, and compliance.
- Use data to identify trends and suggest improvements.
- Bachelor’s degree in a science or engineering field.
- 3-5 years of experience in manufacturing operations within a regulated industry (e.g., pharmaceutical, food, cosmetics, personal care).
- Strong knowledge of cGMP standards and quality control practices.
- Proven leadership and team management experience.
- This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!***