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Telix Pharmaceuticals (AMER)

Director, Product Development Quality

Telix Pharmaceuticals (AMER) · USA- Remote

Posted about 3 months ago

or apply directly on Telix Pharmaceuticals (AMER)'s site. We never take the application ourselves.

Is this posting real?

This role has been open
82 days
Telix Pharmaceuticals (AMER)'s roles stay open a median of 82 days
Reposted
No
Salary listed
No
0% of Telix Pharmaceuticals (AMER)'s roles list one
Ghost-job risk at Telix Pharmaceuticals (AMER)
high
41 stale, 6 reposted of 41 open
Hiring momentum
71 roles opened in the last 90 days
↑ up vs. the prior 90 days
Last confirmed on the employer's board
2026-10-24

Measured from postings appearing on and disappearing from Telix Pharmaceuticals (AMER)'s own greenhouse board since 2026-08-03. Full hiring picture for Telix Pharmaceuticals (AMER).

About this role

As the Director of Product Development Quality at Telix Pharmaceuticals, you will lead the Development Quality function, overseeing radiopharmaceutical development programs from early clinical stages to registration readiness. Your role involves establishing quality management systems, ensuring compliance with GMP regulations, and collaborating with cross-functional teams and external partners. You will also be responsible for leading a high-performing team and representing quality in regulatory interactions and inspections.

Our read on this posting2.6out of 5
benefits
3/5
freshness
1/5
career value
4/5
role clarity
5/5
pay transparency
0/5

Scored from the posting itself — how clearly the role is described, how much it says about pay and benefits, and how recently it was listed. Not a judgement of Telix Pharmaceuticals (AMER) as an employer.

What you need

  • Advanced degree (MS, PharmD, PhD) in a relevant scientific discipline or equivalent experience
  • 10+ years of progressive quality experience within the pharmaceutical, biotechnology, or radiopharmaceutical industry
  • 7+ years of leading and developing quality teams
  • Direct experience in radiopharmaceutical quality
  • Demonstrated experience with IND/CTA submissions and regulatory agency interaction
  • Comprehensive understanding of Good Manufacturing Practices (GMP) and regulatory requirements

Nice to have

  • Experience building greenfield or newly established quality functions
  • Oncology or targeted therapy development quality experience preferred

What you get

  • Competitive salaries
  • Annual performance-based bonuses
  • Equity-based incentive program
  • Generous vacation
  • Paid wellness days
  • Support for learning and development

Worth weighing

  • Role involves significant regulatory compliance responsibilities which may be stressful
  • Fast-growing environment may require adaptability and resilience
  • No specific salary range provided

Summarised from Telix Pharmaceuticals (AMER)'s posting. Read the full original.

Listed by Telix Pharmaceuticals (AMER) on their greenhouse job board, last confirmed open on 2026-10-24. PitchMeAI is not the employer.

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