QA Specialist, I

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. JOB DESCRIPTION: Position Title : QA Specialist I Location: Bedford, New Hampshire Department: Quality Assurance Reporting To: QA Supervisor, External QA Responsible For (Staff): No The QA Specialist will work with other departments to ensure the quality of products and compliance to  internal procedures and external standards. Primary responsibilities for this role includes Batch Record  Review, Lot Disposition, and Quality System review. This position will also be responsible for evaluating deviation incidences and determining which warrant escalation to an investigation, quality review and approval of investigations, and creating and monitoring the associated CAPAs. In this role, the opportunity exists to shape and transform GxP programs by providing QA expertise and guidance to  the manufacture of both clinical and commercial products.  ESSENTIAL DUTIES AND RESPONSIBILITIES: Perform review of batch documentation for release of internal and external clinical  products/commercial products, while ensuring compliance with cGMPs, site SOPs, and regulatory requirements. Prioritize batch record review in support of business needs including maintaining batch  status and communicate release needs throughout the organization  Review and approve master batch records for the timely initiation of GxP manufacturing activities  Responsible for quality oversight and administration of the deviation/investigation and CAPA programs  Review and approve Manufacturing, Quality Control, and other investigations in support of batch release and GMP compliance  Provide direction for complex investigations and CAPAs  Ensure timely, accurate and complete execution and documentation of quality system events: deviations, and CAPAs  Review, develop, and approve quality system procedures, specifications, and test methods  Review and approve CAPAs to prevent recurrence of deviations  Review and approve Change Control documentation  Responsible for tracking investigations and change control for timely completion. Provide status reports, including relevant quality metrics and participates in the management review process  Establish collaborative relationships with internal and external customers to ensure all quality and compliance matters and any issues that arise are addressed in an open and timely manner.  Monitor, identify and propose quality process and system improvements. Lead improvement projects and communicate status to management  Serve as QA representative to cross functional project teams such as tech transfer, process validation, and process improvement  Coordinate change control review meetings  Monitor status of change controls and facilitate the approval process  Perform risk assessments to comply with internal procedures and external guidelines  Provide training on department specific procedures and systems  Interface with clients to address any documentation and compliance concerns  Initiate, revise, and review controlled cGMP documents including SOPs, Material Specifications, Investigation protocols/reports, validation protocols/reports as applicable  Ensures site readiness for regulatory inspections  Performs other duties as assigned. QUALIFICATIONS: Required: Experience performing RCA, technical writing, and working with quality related investigations Knowledge of laboratory and production equipment and IQ/OQ/PQ  Knowledge of FDA regulations (i.e., 21CFR Part 210, 211 & 820) and some experience working with international regulations such as ICH  Experience using Risk Management Tools (FMEA, HACCP, PHA, etc.) and familiarity with ICH Q9  Bachelor’s Degree in a relevant scientific discipline preferred with a minimum of 5-7 years of  pharmaceutical or biotech industry experience with 3+ years of experience in a QA Operations  role supporting late stage clinical and/or commercial production  Exceptional organizational skills and attention to detail  Ability to make risk based decisions and resolve issues with minimal guidance  Excellent interpersonal skills and the ability to communicate well orally and in writing  Proficiency in MS Office including Word, Excel, Access and Visio  Excellent verbal and written communication skills required  Ability to work in a dynamic, fast-paced work environment  Honesty, integrity, respect and courtesy with all colleagues     Creative with the ability to work with minimal supervision and balanced with independent thinking  Resilient through operational and organizational change  Preferred: Bachelor’s Degree in a relevant scientific discipline preferred with a minimum of 5-7 years of  pharmaceutical or biotech industry experience with 3+ years of experience in a QA Operations  role supporting late stage clinical and/or commercial production  ASQ certification preferred  #LI-CW1 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