Associate Director Quality Assurance CMO Management Hybrid
Associate Director Quality Assurance CMO Management Hybrid
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$ 152200 - 228300
1 Vacancy
Job Description
Job Description
The Associate Director Quality Assurance CMO Management is responsible for supporting the daytoday Quality Operations of Contract Manufacturing Organizations (CMOs) for Cell & Genetic Programs through the management of quality management system (QMS) events. The role will assure Quality oversight for technical and operational CDMO activities from clinical throughout product commercialization activities postapproval process monitoring and deviation management. The role is also responsible for the development and maintenance of relationships with the internal and external partners to drive compliance monitor performance and support continuous improvement activities.
The role will closely partner with operational stakeholders and participate in associated governance for the successful planning and of the QMS. The successful candidate will be a key member of the Vertex Cell & Genetic Therapy Quality Team and the Virtual Product Team.
Key Duties & Responsibilities
- Lead execute and oversee the deviation management process across all stages of manufacturing from identification to closure. Ensure proper investigation documentation and resolution of all deviations in accordance with internal policies and regulatory requirements.
- Provide quality and technical expertise in the investigation of deviations including OOS/OOTs conduct thorough root cause analysis to identify underlying issues and oversee efficient and effective implementation of corrective and preventive actions (CAPA) to prevent recurrence.
- Partner closely with other departments including CDMOs External manufacturing QC MSAT Regulatory Affairs and other Quality functions to ensure timely and effective resolution of deviations and alignment with patient safety and product compliance.
- Ensure that all deviation investigations comply with relevant regulatory standards (such as FDA EMA cGMP) and company policies. Maintain awareness of and ensure compliance with industry best practices and regulatory guidelines.
- Establish and maintain deviation tracking systems ensuring that all deviations are properly documented categorized and monitored for timely resolution. Prepare and present regular reports on deviation metrics to senior leadership.
- Lead and execute continuous improvement activities and drive quality remediation.
- Identify potential risks and trends related to deviations and work proactively to mitigate such risks with preventive measures.
- Support risk assessments to evaluate the impact of deviations on product quality safety and regulatory compliance.
- Ensure that all deviation records are maintained in a compliant and auditready manner. Lead or support internal and external audits related to deviation management ensuring all required documentation is available and accurate.
- Participate in Business Review Meetings to ensure Quality issues are raised and addressed as necessary.
- Provide guidance and support through Quality representation in relevant geographies at periodic intervals on site at the CDMOs.
- Participate in Cell & Genetic Program and Quality projects.
Knowledge and Skills:
- Indepth global regulatory agency knowledge and experience across GXP life cycle in Cell & Gene therapy and/or Biologics.
- Experience in product life cycle from discovery to commercials product development
- Broad understanding of regulatory environment including quality systems compliance and strategy.
- Broad technical knowledge in Cell technology aseptic manufacturing technology analytical assays cell & genetic therapies/Biologics processing fill/finish and testing.
- Indepth knowledge of deviations root cause analysis CAPA and change control processes
- Ability to lead improvement projects experience with Root Cause Analysis data analytics and other Operational Excellence experience such as LEAN DMAIC Six Sigma.
- Substantial experience with electronic document management systems (e.g. QDoccs Trackwise Veeva)
- Excellent communication skills with the ability to present complex information and a proven track record Influencing/building/promoting a culture of Quality and Excellence.
- Ability to apply risk management principles to decisionmaking and operational priorities.
- Substantial background in managing complex projects/teams within stated objectives and timelines and with a strong understanding of the underlying business drivers.
- Critical Thinking and ProblemSolving skills
- Strong leadership and an innate ability to collaborate and build relationships.
Education and Experience:
- Bachelors degree in a biotech/life sciences field.
- Masters degree or relevant comparable background.
- Typically requires 8 years of relevant industry experience such as manufacturing quality assurance and/or quality control in biotechnology/regulated pharmaceutical environment.
Were enabling flexibility and choice between individuals and their managers to maintain our strong culture of collaboration and ensure a daily vibrancy within our sites globally. In this Hybrid or OnSiteEligible role you canchoose to work:
1.Hybridand work remotely up to two days per week;or select
2.OnSite andwork 5 days per week with ad hoc flexibility.
#LIAR1 #LIHybrid
Pay Range:
$152200 $228300Disclosure Statement:
The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors including skills competencies experience and other jobrelated factors permitted by law.
At Vertex our Total Rewards offerings also include inclusive marketleading benefits to meet our employees wherever they are in their career financial family and wellbeing journey while providing flexibility and resources to support their growth and aspirations. From medical dental and vision benefits to generous paid time off (including a weeklong company shutdown in the Summer and the Winter) educational assistance programs including student loan repayment a generous commuting subsidy matching charitable donations 401(k) and so much more.
Flex Designation:
HybridEligible Or OnSite EligibleFlex Eligibility Status:
In this HybridEligible role you can choose to be designated as:
1. Hybrid: work remotely up to two days per week; or select
2. OnSite: work five days per week onsite with ad hoc flexibility.
Note: The Flex status for this position is subject to Vertexs 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 nondiscrimination for all employees and qualified applicants without regard to a persons 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 EVerify 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
Required Experience:
Chief
Employment Type
Full-Time
