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Supervisor, QC Analytical Wed to Sat

Job in Bedford, Hillsborough County, New Hampshire, 03110, USA
Listing for: PCI TRGR Penn Pharmaceutical Services Ltd
Full Time position
Listed on 2025-12-01
Job specializations:
  • Quality Assurance - QA/QC
  • Healthcare
    Data Scientist, Medical Science
Job Description & How to Apply Below
Position: Supervisor, QC Analytical Wed to Sat 6:30 AM to 5PM
* Prioritize and distribute work to the analysts working in the QC Analytical laboratory
* Conduct OOS and customer complaint investigations
* Complete peer review of work executed within the analytical laboratory
* Train new Employees
* Routine Analytical testing of samples supporting incoming raw materials, in-process production and finished product testing
* Performs analytical testing using HPLC, Karl Fischer, Particle Size Analyzer, UV Vis, Densitometer, Osmometer and other instrumentation as required
* Perform instrument calibrations and preventative maintenance as needed Documents laboratory work using laboratory worksheets/notebooks. Documentation must be detailed and meet CGMP requirements
* Write, review and revise SOPs as required
* Other duties as assigned or required
* Routine work requires walking, standing, bending, reaching, climbing stairs, lifting or carrying objects that typically weigh less than 50 lbs.
* Capacity to work on several tasks simultaneously.
* Able to organize and prioritize work activities.
* Must be able to walk and drive between locations
* Physically able to wear laboratory protective gowning and equipment, including but not limited to gowning, goggles, face shields, respirators, and protective gloves
* Comfortable with working/handling of hazardous materials
* 5+ years relevant Analytical Chemistry experience, preferably in Quality Control, in a pharmaceutical manufacturing company
* Experience working in a cGMP laboratory required
* Experience working in a CMO (contact manufacturing/development organization) preferred
* Prior leadership experience is preferred
* Bachelor of Science in a scientific area of study
* Master of Science in a scientific area of study and 3+ years Analytical Chemistry experience, preferably in Quality Control, in a pharmaceutical manufacturing company
* Ability to prioritize tasks for staff
* Ability to make informed decisions
* Detail oriented
* Strong oral and written communication skills
* Excellent organization skills
* Office Suite experience (Excel, Word, Access, and PowerPoint)
Bachelor of Science in a scientific area of study
* Excellent interpersonal skills and the ability to communicate well both orally and in in writing
* Ability to multi-task in a dynamic environment with changing priorities
* Resilient, can quickly move forward despite challenges
* A drive to achieve results for self, and the team, and is cable of working with limited supervision
* Positive attitude and strong team, cross team collaboration
* Honesty, integrity, respect and courtesy with leadership and peers
* Strong commitment to conducting PCI PHARMA SERVICES business according to the highest legal and ethical standards, and to continually pursue excellence in the manufacturing and delivery of PCI PHARMA SERVICES products and services
* undefined

At PCI, we have an uncompromising focus on providing quality and operational excellence and providing the industry leading customer experience. Our people make all of this happen, so providing an industry leading experience for our people is equally as important. By creating an authentic culture of purposeful work, we aspire to be an interesting and fulfilling place for talented individuals to grow careers.

We live a philosophy of intentional learning combined with real-life experience supported by a fair and competitive rewards program. We are individuals, teams and a company that believes in our purpose and our approach is simple, the people who work at PCI fuel our business; we don’t say no, we figure out how.
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