Associate Director,CQV Workstream Job Tustin area,California USA,Business

Looking to join a passionate team dedicated to developing and manufacturing life-saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes.

Your Role:

The Associate Director, CQV Workstream provides owner-side leadership for commissioning, qualification, and validation scope within identified projects. The role establishes and integrates the CQV strategy, execution plan, dependencies, documentation, and readiness requirements across project and operating teams. The position is accountable for workstream scope, schedule, cost, risk, quality, and handover while coordinating Quality, Validation, Engineering, Automation, Manufacturing, and external partners. The role operates with substantial day-to-day independence and escalates material commitments or changes through the appropriate project governance channels.

Key Responsibilities:

Own the integrated CQV workstream strategy, plan, milestones, dependencies, risks, and deliverables through operational handover.
Align commissioning, qualification, validation, and startup activities with project sequencing and business-readiness requirements.
Coordinate Quality, Validation, Engineering, Automation, Manufacturing, vendors, and contractors to support compliant execution.
Monitor workstream scope, schedule, cost, quality, documentation, and readiness, escalating material issues with clear options and recommendations.
Provide oversight of CQV deliverables, acceptance criteria, issue resolution, and turnover documentation.
Lead readiness planning for systems, procedures, training, documentation, and transition to the operating organization.
Maintain workstream governance, decision records, risk documentation, and concise stakeholder reporting.
Support inspection-ready execution and successful transition of qualified systems and processes to operations.

Minimum Qualifications:

Bachelor’s degree in engineering, life sciences, quality, or a related field, or equivalent relevant experience.
10 or more years of relevant experience in commissioning, qualification, validation, quality, engineering, or capital-project delivery in a regulated environment.
Demonstrated ownership of complex cross-functional CQV or validation initiatives.
Working knowledge of GxP requirements, risk-based validation, documentation, and operational readiness.

Preferred Qualifications:

Experience supporting biotechnology or pharmaceutical manufacturing facility startup.
Experience with integrated commissioning and qualification delivery models.
Project management or validation-related certification.

Position Type/Expected Hours of Work:

This role is a full-time onsite position. Schedule flexibility may be required to support project milestones, commissioning, startup, and operational-readiness activities. The employee must also have the ability to work overtime and/or weekends when necessary.

Compensation:

We offer competitive compensation packages for this role, including a base salary, performance-based bonuses, and comprehensive benefits such as health, dental, and vision insurance, 401(k) matching, and paid time off.

The compensation range for this role is $147,200 - $184,000 annually depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment.

Who you are:

You have a bring it on! team player approach and an unshakable positive attitude, always ready to tackle anything that comes your way.
Your written and verbal skills are out of this world, and you communicate with clarity and confidence.
You have exceptional multitasking skills and an…