Quality Control Supervisor - Carmel, IN

Only for registered members Carmel, IN, United States

1 day ago

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Quality Control Supervisor · 3rd SHIFT/$90-$110k/Full-Time · Carmel, IN · About the Company: · We are a bio medical manufacturer seeking a dedicated Quality Control Supervisor. · Your Impact · Guarantee adherence to all relevant regulatory standards, both in the US and internatio ...
Job description

Quality Control Supervisor

3rd SHIFT/$90-$110k/Full-Time

Carmel, IN

About the Company:

We are a bio medical manufacturer seeking a dedicated Quality Control Supervisor.

Your Impact

  • Guarantee adherence to all relevant regulatory standards, both in the US and internationally, encompassing FDA, EU, ISO, USP, NRC, and cGMP guidelines.
  • Collaborate across different departments to synchronize QC testing schedules with production timelines, ensuring all testing and maintenance tasks are completed promptly.
  • Conduct and oversee the testing of finished products, raw materials, components, stability samples, validation batches, and experimental samples.
  • Review, approve, and uphold controlled documents within your designated area of responsibility.
  • Spearhead and provide support for investigations pertaining to deviations, product failures, and customer feedback. Author and assess quality and safety reports, and facilitate timely corrective actions.
  • Ensure the secure handling of radioactive materials, maintaining exposure levels As Low As Reasonably Achievable (ALARA) to promote a safe environment.
  • Mentor, cultivate, and oversee team performance, aligning objectives with site goals and KPIs, while fostering team growth. Conduct daily meetings and relay performance metrics.
  • Control department overtime, uphold 5S standards, and guarantee adherence to training and qualification protocols.

What You'll Need

  • A bachelor's degree in Chemistry, Science, or a related field is essential. Equivalent experience may be considered as a substitute for a degree.
  • A minimum of 10 years of relevant experience is necessary, with prior supervisory experience being advantageous.
  • A solid grasp of cGMP laboratory operations and proficiency with major laboratory instrumentation is crucial.
  • The capacity to interpret laboratory data and arrive at well-informed compliance decisions.
  • Demonstrated skills in leadership, communication, coaching, and conflict resolution.
  • Exceptional analytical and problem-solving capabilities, coupled with the ability to effectively manage multiple priorities.
  • Capability to function within a radioactive manufacturing setting and fulfill physical requirements, including lifting up to 70 pounds, wearing PPE, standing for prolonged durations, and accommodating off-shift, weekend, or holiday work as required.


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