• Manufacturing Supervisor (Pharmaceuticals)

    Astrix Technology (Mundelein, IL)


    Manufacturing Supervisor (Pharmaceuticals)

     

    Manufacturing

     

    Mundelein , IL, US

    Pay Rate Low: 70000 | Pay Rate High: 90000

    + Added - 03/10/2025

     

    Apply for Job

     

    _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).

    + 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!***_

    INDBH

    \#LI-DNP

    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.