Job Description
General Summary:
The Quality Manager is a technical resource on the principles and application of quality assurance and compliance. The Quality Manager coordinates or executes activities on a wide range of projects and participates in the design and execution of new projects.
Key Duties and Responsibilities:
- Collaborate with internal and external business partners to resolve quality issues to ensure compliant solutions.
- Lead root-cause analysis and product impact assessment for investigations as a result of deviations, OOS, and OOT investigations ensuring appropriate CAPA actions are identified.
- Perform change control assessments and closure approvals.
- Establish and revise Quality Agreements between CMOs/Suppliers and Vertex, as needed.
- Collect data and report on metrics.
- Represent Vertex Quality on cross-functional working teams, applying strong communication and collaboration skills.
- Lead continuous improvement projects.
- Author SOPs to support commercial quality functions.
- Assist with regulatory agency inspections.
- Identify and facilitate continuous improvement efforts.
Knowledge and Skills:
- Good understanding of both the conceptual and practical application of cGMPs in a pharmaceutical setting.
- Proven experience leading various straightforward projects/teams within stated objectives and timelines.
- Ability to communicate effectively with cross-functional team members, exchanging complex information and influencing/guiding others to understand a stated viewpoint.
- Ability to manage own workload to achieve goals and seek opportunities to share information and help others understand technical processes.
- Formal project management experience.
- Strong communication skills (written and verbal) with the ability to communicate to a variety of audiences.
- Able to integrate activities with other groups, departments, and project teams as needed.
- Demonstrated ability to evaluate quality matters and solve problems leveraging technical experience and advanced judgment to select appropriate solutions.
- Excellent team player and collaborator.
- Highly proficient in leading event investigations, Root Cause Analysis (RCA), and CAPA.
- Experience with electronic document management systems (e.g., QDoccs, Trackwise, Veeva).
Education and Experience:
- Bachelor's degree in scientific or allied health field (or equivalent degree).
- Typically requires 4 years of experience or the equivalent combination of education and experience.
Flex Designation:
Hybrid-Eligible Or On-Site Eligible
Flex Eligibility Status:
In this Hybrid-Eligible role, you can choose to be designated as:
- Hybrid : work remotely up to two days per week;
- On-Site : work five days per week on-site with ad hoc flexibility.
Note: The Flex status for this position is subject to Vertex's Policy on Flex @ Vertex Program and may be changed at any time.
Company Information
Vertex is a global biotechnology company that invests in scientific innovation.
Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.
Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at .
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