Associate Director, Operational Area Quality, Materials Management (Hybrid)

Vertex Pharmaceuticals Incorporated; Boston, Auburn (MA, ME); On-site; USD 95,000 - 140,000; Full time

Job summary

An established industry player is seeking an Associate Director in Materials Management to ensure quality oversight in drug product manufacturing. This pivotal role involves collaborating with external vendors, maintaining compliance with cGMP requirements, and leading quality initiatives across the product lifecycle. The successful candidate will be instrumental in driving continuous improvement and ensuring the integrity of materials management processes. Join a dynamic team where your expertise will shape the future of innovative therapies and contribute to meaningful advancements in patient care.

Benefits

Medical benefits

Dental benefits

Vision benefits

Generous paid time off

Educational assistance programs

Student loan repayment

Commuting subsidy

401(k) matching

Annual bonus eligibility

Annual equity awards

Qualifications

• 8+ years of experience in quality oversight in Cell & Gene therapy.
• Strong understanding of regulatory compliance and quality systems.
• Experience managing complex projects and teams.

Responsibilities

• Oversee material management program and systems across CDMOs.
• Partner with vendors to ensure compliance and address quality issues.
• Lead quality process monitoring and reporting on performance metrics.

Skills

GXP life cycle knowledge

Root Cause Analysis

Data analytics

LEAN

Six Sigma

Communication skills

Critical Thinking

Problem Solving

Education

Bachelor's degree in relevant field

Tools

Electronic document management systems

Job description

Job Description

The Associate Director in Materials Management is responsible for quality oversight of all materials used in drug product manufacturing, and associated materials management controls to meet cGMP requirements. This includes providing quality oversight to inventory management, and consumption controls to assure accurate lot genealogy and traceability throughout the drug product manufacture.

The role is also responsible for the development and maintenance of relationships with the external material and manufacturing vendors, to drive compliance, monitor performanceand support continuous improvement activities.

The quality role will closely partner with operational stakeholders and participate in associated governance for the successful planning and execution of the product life cycle Management. The successful candidate will be a key member of the Vertex Cell & Genetic Therapy Quality Team and the Operational Product Teams.

Key Duties & Responsibilities

• Be the Quality expert for all regions on material management.
• Partner with material vendors and CDMOs within the Quality organization and participate in Business/Quality Review Meetings to ensure Quality issues are raised and addressed, as necessary
• Oversight of material management program and systems across CDMOs and Component manufacturers network
  • Assure processes are compliant for the release and usage of all materials including critical components at the CDMOS to assure lot genealogy and traceability of materials in drug product manufacture.
• Lead quality process monitoring of the drug product materials through establishment of proactive monitoring and indicators for compliance oversight
• Report on CDMO/vendor performance metrics at Quality/Governance meetings.
• Partner with CMSC to provide Quality oversight for evaluating, implementing and maintaining systems including performance monitoring to optimize the procurement and maintenance of all product materials.
• Liaise with material suppliers to identify Quality / compliance issues and partner with them to align on the risk and mitigation plans.
• Negotiate and maintain Quality Agreements with clear and tangible metrics with Vertex owned material suppliers.
• Assess critical components / raw materials traceability across the CDMOs network for effective lot genealogy. Work with CDMOs to Identify and execute mitigation plans to close gaps.
• Participate in mock lots' traceability sessions with the component suppliers and CDMOs.
• Act as the Quality SME for root-cause analysis and material impact assessments for investigations resulting from deviations at the CDMOs.
• Act as the Quality SME for any corrective actions identified from investigations to implement viable, permanent solutions to materials related issues. Work with both internal and external customers to develop solutions which meet company-wide needs and objectives.
• Establish oversight and consistency on Bill of Materials across the network.
• Risk Management:
  • Identifying and mitigating gaps and risks associated with the material management program
  • Ensure the risk register is kept updated and communicated across Quality teams and other stakeholders.
• Continuous Monitoring:
  • Stay up to date with industry developments and best practices to guide business partners and assure the Materials Management Quality oversight program remains compliant and effective.
• Training and Development:
  • Providing training and guidance to materials management staff on quality assurance procedures

Required Knowledge/Skills

• In-depth 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.
• 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
• Excellent communication skills and a proven track record Influencing/building/promoting a culture of Quality and Excellence.
• Ability to apply risk management principles to decision making 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 Problem Solving skills
• Strong leadership and an innate ability to collaborate and build relationships.

Education and Experience:

• Bachelor's degree in relevant field is required
• Typically requires 8 years of experience in addition to 2 years of management experience or the equivalent combination of education and experience

We're 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 On-Site-Eligible role, you canchoose to work:

1.Hybridand work remotely up to two days per week;or select

2.On-Site andwork 5 days per week with ad hoc flexibility.

#LI-AR1 #LI-Hybrid

Pay Range:

$0 - $0

Disclosure 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 job-related factors permitted by law.

At Vertex, our Total Rewards offerings also include inclusive market-leading 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 week-long 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:

Hybrid-Eligible Or On-Site Eligible

Flex Eligibility Status:

In this Remote-Eligible role, you can choose to be designated as:
1. Remote: work remotely five days per week and come into the office on occasion - you're always welcome on-site; or select
2. Hybrid: work remotely up to two days per week; or select
3. 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 [e-mail]