Quality Assurance Senior Specialist - Compliance (Contract) 23271-2
Company: Vertex
Location: Boston
Posted on: February 23, 2025
Job Description:
Job DescriptionThe Sr. Quality Specialist - Compliance is
recognized as an expert internally in the principles and
application of quality assurance and compliance. The Sr. Quality
Specialist will coordinate GMP activities in support of clinical
and commercial Drug Product disposition. This position reports to
Manager GMP Quality - Cell & Gene.REQUIRED KNOWLEDGE, SKILLS, AND
COMPETENCIESKey Skills
- Cross-functional collaborator
- Results DriverKey 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
- 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 manufacturingKEY 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.
- Leads from a Quality perspective root cause analysis and
product impact assessments for investigations resulting from
deviations. Assure appropriate correction, interim controls and
CAPAs are in place to mitigate risks.
- Liaises with cross-functional teams and support quality
partners to ensure GMP manufacturing and testing activities,
including disposition timelines are met.
- Leads/executes continuous improvement activities.
- Provide QA support of change controls, GMP investigations and
CAPAs. OOS and OOT investigations and ensuring appropriate CAP
actions are identified.
- Provides project support involving technical transfers,
engineering projects and similar activities.
- Participate in compliance walkthroughs and help drive the
closure of any observations as needed.
- 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.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
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Keywords: Vertex, Boston , Quality Assurance Senior Specialist - Compliance (Contract) 23271-2, Other , Boston, Massachusetts
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