Overnight QC Laboratory Supervisor

Overnight QC Laboratory Supervisor


Job ID: 9578933

Springfield, NJ, US

Scientific

Bachelors Degree

Full Time, Direct Hire

Experienced (Non-Manager)

On-site

Biotechnology/Pharmaceuticals

First Shift (Day)

Springfield, NJ, US

Experienced (Non-Manager)

Full Time, Direct Hire

Biotechnology/Pharmaceuticals

On-site

Scientific

Bachelors Degree

First Shift (Day)

Job details

Kelly Science is seeking an Overnight QC Laboratory Supervisor for a growing company located in Springfield, NJ.

Shift: Wednesday-Sunday 9pm-8am (1 hour lunch)
Employment Type: Full Time; Direct Hire

Responsibilities:

  • Managing QC laboratory operations including overseeing and performing QC testing, preparing and maintaining stability records and summaries.

  • Developing, training, and transferring methods to and from QC and contract manufacturers as assigned.

  • Modifying and validating analytical procedures to meet QC’s needs.

  • Performing design and development of experimental protocols, SOP’s, etc., consistent with cGMP/GLP.

  • Conducting all quality QC chemical tests for release of batches for patient use.

  • Leading special projects and department meetings via input, feedback, and execution of assigned tasks.

  • Performing timely radioactive and microbiological QC and record quality of product.

  • Reporting monthly on supplies for QC orders involving devices and reagents.

  • Leading laboratory investigations and root-cause analyses.

Essential Education and Qualifications:

  • Bachelors degree in Chemistry or Biochemistry required.

  • Minimum of 5 years GMP QC laboratory experience required, including people leadership experience.

  • Experience using analytical techniques, such as High-Performance Liquid Chromatography (HPLC) and radio-Thin Layer Chromatography (rTLC).

  • Excellent oral and written communication, organizational, and problem-solving skills while working under strict timelines.

  • Ability to convey complex ideas in a simple manner to management and customers, exercise independent judgement during method development/transfer processes.

  • Knowledge of analytical methods currently used for testing, release, and stability of sterile pharmaceutical products.

Interested? Please apply today for immediate consideration!
 

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