Vertex Pharmaceuticals
Senior Manager, Validation
Vertex Pharmaceuticals, Boston, Massachusetts, us, 02298
Job Description
General Summary:
The Validation Senior Manager position will be part of the Vertex Cell and Genetic Therapy Manufacturing Operations and Technical Operations group. The role will oversee Validation personnel and support managing day to day Validation operations at VCGT facilities for the T1D program at greater Boston location. This role will be involved in various aspects of validation including equipment, computerized systems and software, cleaning, sterilization, and shipping qualification. The incumbent will be responsible for managing and supporting personnel for validation of existing equipment and new capital projects (as required), enhancements and capabilities from conceptual to detailed design, installation, testing, commissioning, qualification, validation, periodic assessments, and revalidation.
Key Duties and Responsibilities:
Manage in-house staff and seasonal consultants supporting key CQV deliverables.
Manage periodic assessment and revalidation activities as part of Validation Maintenance activities.
Participate in design reviews for various capital projects and equipment with cost, efficiency and compliance always in mind, if required.
Lead IQ, OQ, PQ efforts for utilities, facility, and analytical equipment.
Coach and mentor reports to assure that team is attuned with changes in regulatory and industry standards.
Perform validation assessments for various projects (change controls, capital projects, etc.).
Provide SME support for regulatory inspections from Validation standpoint whenever required.
Assist in development of Validation KPIs and ensure they are appropriately monitored, tracked, and reported.
Work collaboratively with Manufacturing, Process/Analytical Development, R&D groups, EH&S, Capital Project Management, GIS, QA and others to support the consistent achievement of the company’s strategic objectives and meet aggressive timelines.
Manage the Site Validation Master Plan and Requalification Master Plans.
Cultivate change and innovation by seeking opportunities to strengthen and improve existing Validation program.
Serve as an advisor to reports and involve directly to resolve issues and/or meet timelines.
Support activities related to APS program.
Knowledge and Skills:
Expert knowledge of validation and system implementations in a GMP manufacturing environment
Direct experience with process equipment and systems qualification, sterilization qualification, critical utilities validation, cleaning validation, and temperature mapping is a must.
Strong Knowledge across technical areas
Has emerging competence in a supervisory role
Demonstrates strong aptitude helping to lead a group or team endeavor and building team unity
Communicates clearly and concisely (written and verbal) across levels of the company
Working knowledge of current applicable regulations, standards, and guidance like 21CFR 210, 211, Part11, ISO 14644, EU Annex 1, ATMP, EU Annex 15, USP
, GAMP, etc.
Must be able to establish strong working relationships with stakeholders (Quality, DPF, Tech Ops, Engineering, GXP Operations, and GIS) to ensure high quality deliverables meeting cGMP and Vertex validation requirements
Ability to perform complex assessments for automated processing systems against current industry compliance requirements
Demonstrable team leadership, problem solving, creative and critical thinking and project planning skills
Ability to navigate and be successful in a fast-paced, highly matrixed work environment
Displays high competence in the utilization of core quality systems such as change control, deviations, investigations, CAPA management and document control
Education and Experience:
Bachelor's or Master's degree in Biotechnology, Chemical, Industrial, or Biomedical Engineering, or a related discipline
Typically requires 6 years of experience in a related field and 1 year of supervisory/management experience or the equivalent combination of education and experience
#LI-onsite #LI-SV1
Flex Designation:On-Site Designated
Flex Eligibility Status:
In this On-Site designated role, you will 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 ApplicationAssistance@vrtx.com
#J-18808-Ljbffr
General Summary:
The Validation Senior Manager position will be part of the Vertex Cell and Genetic Therapy Manufacturing Operations and Technical Operations group. The role will oversee Validation personnel and support managing day to day Validation operations at VCGT facilities for the T1D program at greater Boston location. This role will be involved in various aspects of validation including equipment, computerized systems and software, cleaning, sterilization, and shipping qualification. The incumbent will be responsible for managing and supporting personnel for validation of existing equipment and new capital projects (as required), enhancements and capabilities from conceptual to detailed design, installation, testing, commissioning, qualification, validation, periodic assessments, and revalidation.
Key Duties and Responsibilities:
Manage in-house staff and seasonal consultants supporting key CQV deliverables.
Manage periodic assessment and revalidation activities as part of Validation Maintenance activities.
Participate in design reviews for various capital projects and equipment with cost, efficiency and compliance always in mind, if required.
Lead IQ, OQ, PQ efforts for utilities, facility, and analytical equipment.
Coach and mentor reports to assure that team is attuned with changes in regulatory and industry standards.
Perform validation assessments for various projects (change controls, capital projects, etc.).
Provide SME support for regulatory inspections from Validation standpoint whenever required.
Assist in development of Validation KPIs and ensure they are appropriately monitored, tracked, and reported.
Work collaboratively with Manufacturing, Process/Analytical Development, R&D groups, EH&S, Capital Project Management, GIS, QA and others to support the consistent achievement of the company’s strategic objectives and meet aggressive timelines.
Manage the Site Validation Master Plan and Requalification Master Plans.
Cultivate change and innovation by seeking opportunities to strengthen and improve existing Validation program.
Serve as an advisor to reports and involve directly to resolve issues and/or meet timelines.
Support activities related to APS program.
Knowledge and Skills:
Expert knowledge of validation and system implementations in a GMP manufacturing environment
Direct experience with process equipment and systems qualification, sterilization qualification, critical utilities validation, cleaning validation, and temperature mapping is a must.
Strong Knowledge across technical areas
Has emerging competence in a supervisory role
Demonstrates strong aptitude helping to lead a group or team endeavor and building team unity
Communicates clearly and concisely (written and verbal) across levels of the company
Working knowledge of current applicable regulations, standards, and guidance like 21CFR 210, 211, Part11, ISO 14644, EU Annex 1, ATMP, EU Annex 15, USP
, GAMP, etc.
Must be able to establish strong working relationships with stakeholders (Quality, DPF, Tech Ops, Engineering, GXP Operations, and GIS) to ensure high quality deliverables meeting cGMP and Vertex validation requirements
Ability to perform complex assessments for automated processing systems against current industry compliance requirements
Demonstrable team leadership, problem solving, creative and critical thinking and project planning skills
Ability to navigate and be successful in a fast-paced, highly matrixed work environment
Displays high competence in the utilization of core quality systems such as change control, deviations, investigations, CAPA management and document control
Education and Experience:
Bachelor's or Master's degree in Biotechnology, Chemical, Industrial, or Biomedical Engineering, or a related discipline
Typically requires 6 years of experience in a related field and 1 year of supervisory/management experience or the equivalent combination of education and experience
#LI-onsite #LI-SV1
Flex Designation:On-Site Designated
Flex Eligibility Status:
In this On-Site designated role, you will 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 ApplicationAssistance@vrtx.com
#J-18808-Ljbffr