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Manufacturing Supervisor; Pharmaceuticals

Job in Mundelein, Lake County, Illinois, 60060, USA
Listing for: Astrix Inc.
Full Time position
Listed on 2026-07-13
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Production Manager, Quality Engineering, Production QC/QA
Salary/Wage Range or Industry Benchmark: 70000 - 90000 USD Yearly USD 70000.00 90000.00 YEAR
Job Description & How to Apply Below
Position: Manufacturing Supervisor (Pharmaceuticals)

Manufacturing Supervisor (Pharmaceuticals)

Pay Rate Low: 70000 | Pay Rate High: 90000

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

  • 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.

Qualifications

  • 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!***

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