2nd shift Quality Assurance Senior Specialist (Contract) 25953, 25952

Job Description

The Sr. Quality 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

• Cell therapy / gene therapy quality assurance experience
• Commercial quality assurance operations experience
• Experience performing On the floor support as a QA
• Experience reviewing MBR’s and QC records as part of Lot disposition

Role will start off M-F for training (2 weeks).  After candidate is trained - the role will move to 4-10 hour shifts:

• Sunday - Wednesday 12:30pm est. - 11:00pm est.
• Wednesday - Saturday 12:30pm est - 11:00pm est.

REQUIRED KNOWLEDGE, SKILLS, AND COMPETENCIES

Key Leadership Skills

• Cross- functional collaborator
• Results Driver

Key Knowledge/ Skills and Competencies

• 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

KEY 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

REQUIRED EDUCATION AND EXPERIENCE:

• 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
• Experience with network-based applications such as Oracle, TrackWise
• 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.

Pay Range

$55-$65/hr

Requisition Disclaimer

This job posting is for a temporary role with a third-party agency partner on assignment at Vertex Pharmaceuticals (“Vertex”). The individual selected for this role will be offered the role as an employee of a third- party agency partner; compensation, medical benefits, fringe benefits and other terms and conditions of employment shall be presented by the third-party agency partner upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on a number of factors, including skills, competencies, experience, location and/or being pursued and other job-related factors permitted by law. In addition, this role will be eligible for overtime pay, in accordance with federal and state requirements

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