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Manufacturing Supervisor; Pharmaceuticals

Job in Mundelein, Lake County, Illinois, 60060, USA
Listing for: Women Veterans Interactive
Full Time position
Listed on 2026-06-26
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Production Manager, Quality Engineering
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)

Manufacturing Supervisor (Pharmaceuticals)

Manufacturing

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.

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.

We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

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