hirly

Pciservices

Supervisor, Qc Analytical (Sun-Wed)

Bedford, NH, USA

See how you match this job — and similar ones. Free.

Upload your resume and hirly scores it against this role at Pciservices first, then against similar open jobs, and shows where you fit and why.

PDF or DOCX, up to 12MB. No sign-up to see your matches.

Get past the screening software and onto a recruiter's desk

hirly rewrites your resume for this job — matching the keywords and skills in the posting, moving your most relevant experience to the top, and writing a cover letter to fit. About 30 seconds.

  • Keywords matched to this posting
  • Fit score before you apply
  • Cover letter included

Matched against 2.3M live jobs from 200,000+ employers in 200+ countries.

Tailor my resume for this job →

hirly's read of this role

Seniority
Mid level
Country
US
Work mode
On-site / unstated
First seen by hirly
27 Sept 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.

We are PCI.

Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.

The QC Analytical Supervisor will have responsibility for supporting all activities in the Quality Control Laboratory including completing the majority of the peer review in the department and approving the majority of procedures used in the analytical department. The work includes the testing of in-process samples, finished product samples and raw materials. The QC Analytical Supervisor will communicate with clients regarding Out of Specification and other Quality System Events. The person in this position has knowledge of commonly-used analytic concepts, practices, and procedures within the field of his/her responsibilities. Also, must be familiar with cGMPs as they relate to analytical test methodologies and practices.

Essential Duties and Responsibilities: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The essential duties and responsibilities include the following but other duties may be assigned.

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

Special Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. The employee must be physically capable to perform the duties listed below with or without reasonable accommodations which may be made to enable individuals with disabilities to perform the essential functions.

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

Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Works closely with Quality Assurance and Quality Control staff in performing varied work procedures and activities.

Interacts with Operations staff, Research and Development staff and clients on a regular basis.

Supervises the employees in the QC Analytical departmen

TRAVEL –

Qualifications: The requirements listed below are representative of the knowledge, skill, and/or ability required for the stated position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

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

#LI-RS1

Join us and be part of building the bridge between life changing therapies and patients. Let’s talk future

  • Equal Employment Opportunity (EEO) Statement:
  • PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

At PCI, Equity and Inclusion are at the core of our company’s purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity – at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.

Original posting on Pciservices's site ↗

Want this one?

Upload your resume and hirly rewrites it for this job and writes the cover letter — in about thirty seconds, before you sign up.

Tailor my resume for this job