Supervisor, QC Analytical Sun to Wed 6:30 AM to 5:00 PM

PCI Services•Bedford, NH

42d

About The Position

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. Summary of Objective: 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.

Requirements

5+ years relevant Analytical Chemistry experience, preferably in Quality Control, in a pharmaceutical manufacturing company
Experience working in a cGMP laboratory required
Bachelor of Science in a scientific area of study
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

Nice To Haves

Experience working in a CMO (contact manufacturing/development organization) preferred
Prior leadership experience is preferred
Master of Science in a scientific area of study and 3+ years Analytical Chemistry experience, preferably in Quality Control, in a pharmaceutical manufacturing company

Responsibilities

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