2nd Shift -Quality Assurance Senior Specialist (Contract) 27517

Atrium Works•Boston, MA

9d•$55 - $65

About The Position

The GMP Operational Quality Sr. Specialist is recognized as an expert internally in the principles and application of quality assurance and compliance. The Sr. Quality Specialist coordinates GMP activities in support of clinical and commercial Drug Product disposition. This position reports to Manager GMP Quality - Cell & Gene. Ideal candidate will have strong experience in deviation, QC data review, quality events, QA operations, documentation and batch review. Sr Specialists will be executing disposition and Quality on the Floor (including walkthroughs) activities per the Quality Ops task list Shift: Sunday - Wednesday - 2nd shift

Requirements

Strong leadership skills with the ability to thrive in a high throughput environment
Collaboration / Teamwork
Ability to independently lead cross-functional teams and represent the Quality unit
Communication Ability to communicate effectively across all organizational levels
Critical Thinking / Problem Solving Ability to evaluate quality matters and make decisions utilizing risk-based approach
Attention to detail
Knowledge in the following areas: Expert knowledge of GMP requirements governing oral drug products manufacturing practices
Proven experience supporting GMP manufacturing either via experience in manufacturing and /or experience providing QA operational support of GMP manufacturing
Demonstrated success by independently leading cross-functional teams
Experience providing QA support and oversight of GMP manufacturing operation including batch release
Experience with ATMP drug product development and manufacturing with proficient knowledge of the following in a pharmaceutical setting: Cell and gene therapy cGMP’s and associated CMC regulatory considerations
Aseptic processing
Experience successfully leading event investigations, Root Cause Analysis and CAPA
Master’s degree with 2-3 years of relevant work experience, or Bachelor’s degree in a scientific or allied health field with minimum 3-5 years of relevant work experience, or relevant comparable background.

Responsibilities

As part of the GMP Operational Quality group primarily responsible with providing quality oversight and support to Vertex Cell and Gene Therapy operations in the following key areas/activities; support of manufacturing operations across all phases of development and commercial, support of analytical laboratory, materials management, and facility/engineering groups.
Lead QA efforts to establish new programs to support Drug Product facility including start-up of assembly, packaging and label operations
Responsible for batch disposition activities. Review batch data, including batch records, deviations, in-process data, EM data, QC release testing and other quality systems as applicable to determine acceptability of product disposition.
Responsible for review and approval of COAs, and product release
Provide production floor support and provide guidance for GMP product quality and compliance for product release, including resolution of product quality investigations and quality issues of a significant nature, and provides direction for product disposition decisions including shipment.
Review and approval of manufacturing documents.
Develop and deliver technical training programs
Supports drafting and revising Quality Agreements between CMOs/Suppliers and Vertex, as needed
Provide QA support of change controls, GMP investigations and CAPAs. OOS and OOT investigations and ensuring appropriate CAP actions are identified.
Provides experienced technical advice for fill finish related program decisions
Provides project support involving technical transfers, engineering projects and similar activities
Participate in compliance walkthroughs and help drive the closure of any observations
Responsible for identifying risks and communicating gaps for GMP process/systems
Responsible for identifying risks and communicating any gaps for quality processes optimization for area/equipment release, material disposition, quality systems etc.
Participate in continuous improvements of department processes.
Participate in inspection readiness and support activities
Participate in process improvement initiatives (as necessary).
Act as a trusted advisor to the site by providing compliance guidance through collaborative review and working with the business owners to gain a better understanding of their needs and facilitate resolution of quality issue in a timely manner
Experience on product complaints investigations and recalls