Qualified candidates must have:
At least 3 years quality control or manufacturing experience
Excellent cGMP knowledge
Microsoft Word and Excel knowledge/skills
Excellent written and verbal communications skills
Strong organizational skills
Ability to delegate and complete tasks in a timely manner
Ability to work independently and as part of the team
Ability to handle stressful situations and pressure
Ability to multi-task as priorities change frequently
Ability to follow Company SOPs
Willingness to accept and learn new responsibilities
Attention to detail
Flexibility (must be able to work overtime as needed)
Strong work ethic
Associate degree is preferred
QC Supervisor duties will include:
Supervision of QC lab personnel, ensuring all responsibilities of the department are performed in a timely manner.
This will include:
Coordination of incoming inspection, in-process testing, sampling/inspection/shipment of retention and stability samplesReview of documentation, including batch records, testing, inspection reports, etc.
Review/revision of SOPs
Preparation of protocol/experiment reports
Ongoing cGMP training of QC personnel
Position also entails acting as back-up for QC lab personnel and planning/developing/managing QC improvement projects. QC Supervisor will work closely with the QC Manager.
Hours are 2:25 p.m. to 12:55 a.m., with overtime as needed.
Pay rate is $37-40K/year (salaried position), depending on experience/education.