Quality Assurance Project Manager

Reposted Yesterday
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Houston, TX
In-Office
Mid level
Pharmaceutical
At Lonza, we enable A Healthier World by supporting our healthcare customers on the path to commercialization.
The Role
The role involves leading QA projects for new Cell & Gene Therapy clients, managing risks, and coordinating across teams to ensure project success.
Summary Generated by Built In

 

Quality Assurance Project Manager

Location: Houston, Texas – Onsite

Lonza is seeking a Quality Assurance Project Manager to support the onboarding of new Cell & Gene Therapy clients. In this role, you will lead internal QA projects from initiation through closeout, ensuring seamless execution and alignment across cross‑functional teams.

What You Will Get

A competitive compensation. In addition, below you will find a comprehensive summary of the benefits package we offer:

  • Performance-related bonus.

  • Medical, dental and vision insurance.

  • 401(k) matching plan.

  • Life insurance, as well as short-term and long-term disability insurance.

  • Employee assistance programs.

  • Paid time off (PTO)

Compensation for this role will be determined by the candidate’s qualifications, skills, experience, and relevant knowledge.

What You Will Do

  • Lead QA projects related to onboarding new Cell & Gene Therapy clients from initiation through closeout.

  • Develop project scope, define guidelines, and secure necessary cross‑functional approvals.

  • Identify project risks and conduct regular status meetings to review progress and challenges.

  • Communicate major project milestones to the Head of Quality Assurance Operations.

  • Generate and issue meeting minutes for all relevant project meetings.

  • Manage internal resource demands and resolve conflicts to keep projects on track.

  • Provide performance feedback on internal project team members to their supervisors.

What We Are Looking For

  • Bachelor’s degree preferred, ideally in a scientific discipline.

  • Advanced experience in biotechnology, with strong knowledge of cGMPs.

  • Experience in Quality Assurance within a regulated environment.

  • Advanced experience in project management or a proven track record managing large/complex projects.

  • Strong analytical and problem‑solving skills; able to work independently and collaboratively.

  • Familiarity with pharmaceutical cGMP, regulatory standards, and biotech processes (preferred).

  • Ability to manage multiple projects simultaneously with strong organizational and time‑management skills.

About Lonza

At Lonza, our people are our greatest strength. With more than 30 sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values—Collaboration, Accountability, Excellence, Passion, and Integrity—guide how we work and grow together. Every idea, big or small, has the potential to improve millions of lives, and that’s the kind of work we want you to be part of.

Innovation thrives when people from all backgrounds bring their unique perspectives. We value diversity and are committed to fostering an inclusive environment for all employees. If you're ready to help turn breakthrough ideas into life‑changing therapies, we look forward to welcoming you.

Ready to shape the future of life sciences? Apply now.

Top Skills

Biotechnology
Cgmp
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The Company
HQ: Basel
0 Employees
Year Founded: 1897

What We Do

At Lonza, we enable A Healthier World by supporting our healthcare customers on the path to commercialization. Our community of 16,000 talented employees work across a global network of more than 30 sites to deliver for our customers across the pharma, biotech and nutrition markets.

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