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Supervisor Quality Control

Date Posted: 3/19/2019

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Job Description


  
Supervisor, Quality Control Analytical
 
Currently seeking an experienced Quality Control Supervisor that will be responsible for oversight and throughput of testing on their assigned shift.  The QC Supervisor will also perform data review functions, investigations and reporting of laboratory test results. This is an immediate Direct Hire opportunity for a candidate that is seeking an immediate position with a growing company.
 
Primary Responsibilities and Essential Functions of the Position:
 

  • Prioritize and coordinate completion of testing to meet timelines and budgetary commitments.
  • Solve complex analytical problems.
  • Follow cGMP, DEA and OSHA guidelines with regard to work practices and safety.
  • Review data and reports ensuring precise and accurate testing and information.
  • Carryout laboratory investigations.
  • Train laboratory employees in the use of equipment and analytical methods.
  • Qualify, calibrate, and maintain laboratory equipment.
  • Write, review, and revise Standard Operating Procedures (SOPs) as necessary.
  • Review and revise laboratory systems on an ongoing basis.
  • General laboratory maintenance.
  • Perform other duties as required and assigned.
 
Recruiter: Kim
Salary: 75K per year Direct Hire

How to Apply: Qualified candidates should forward their resume to kgorczynski@ultimatestaffing.com and enter QA DH Supervisor in the subject line of your email for immediate consideration.
 
Skills Required:
  • Capable of writing protocols, reports, investigations, and laboratory documents.
  • Excellent knowledge of computer systems and software.
  • Strong knowledge of cGMP and FDA regulations for method development, validation, and transfer.
  • Excellent communication skills both written and verbal.
  • Highly organized.
 
Minimum Education and Experience Required:
 
  • Bachelor's degree in a scientific field and ten (10) years of experience in the pharmaceutical industry.
  • One (1) to five (5) years in a supervisory or management role preferred.
Key words- QA,Quality Control Supervisor, QA Analytical, Pharmaceutical QA, Scientific Management                                                                                                                       

 

We are an equal opportunity employer and make hiring decisions based on merit. Recruitment, hiring, training, and job assignments are made without regard to race, color, national origin, age, ancestry, religion, sex, sexual orientation, gender identity, gender expression, marital status, disability, or any other protected classification. We consider all qualified applicants, including those with criminal histories, in a manner consistent with state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance.

Job Requirements

Skills Required:

-Capable of writing protocols, reports,
investigations, and laboratory documents.
-Excellent knowledge of computer systems
and software.
-Strong knowledge of cGMP and FDA
regulations for method development,
validation, and transfer.
-Excellent communication skills both
written and verbal.
-Highly organized.

Minimum Education and Experience Required:

Bachelors degree in a scientific field and ten (10) years of experience in the pharmaceutical industry.
One (1) to five (5) years in a supervisory or management role preferred.
Posted By: kgorczynski@ultimatestaffing.com

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Job Snapshot

  • Employee Type:Full-Time
  • Location:Fenton, MO
  • Job Type:Pharmaceutical
  • Experience:Not Specified
  • Education:Not Specified
  • Date Posted:3/19/2019
  • Contact: Kim Gorczynski (314) 994-7195
  • Pay Range: $75,000.00 - $75,000.00 Annually
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Job Reference: JO-1903-53614