Director, Combination Product Development

McDermott Laboratories Limited Viatris

Competitive salary; bonus scheme available; health...
Not specified (assumed to be hybrid or onsite based on company culture).
Manage multidisciplinary scientific and engineering teams
Oversee device control strategies for manufacturing
Lead regulatory inspection readiness and audits
McDermott Laboratories Limited Viatris is seeking a Director of Combination Product Development to lead a multidisciplinary team focused on developing innovative device and combination products in the pharmaceutical sector. The ideal candidate will have a strong background in engineering or a scientific discipline, experience in regulatory submissions, and leadership skills to drive team performance and compliance

Job Summary

  • The role involves leading a multidisciplinary team of scientists and engineers to develop safe and effective combination products for injectable, respiratory, and transdermal therapies.
  • Candidates must provide technical leadership to ensure robust evidence generation for product safety, efficacy, and regulatory compliance across global markets.
  • Viatris offers competitive salaries, bonus schemes, health insurance, pension plans, and an inclusive environment dedicated to diversity and sustainability.

Matching Summary

Match Score: 85

McDermott Laboratories Limited Viatris is seeking a Director of Combination Product Development to lead a multidisciplinary team focused on developing innovative device and combination products in the pharmaceutical sector. The ideal candidate will have a strong background in engineering or a scientific discipline, experience in regulatory submissions, and leadership skills to drive team performance and compliance.

Salary

Competitive salary; Bonus scheme available; Health insurance and pension included

Skills & Requirements

Must-have

  • Manage multidisciplinary scientific and engineering teams
  • Oversee device control strategies for manufacturing
  • Lead regulatory inspection readiness and audits
  • Ensure ISO 13485 and FDA 21 CFR Part 820 compliance
  • Support design verification and stability studies

Nice-to-have

  • Strong stakeholder management and communication skills
  • Experience with complex generics and biologic therapies
  • Ability to perform effectively in fast-paced environments
  • Demonstrated problem-solving and organizational skills

Key Requirements

  • Degree in Engineering or relevant scientific discipline
  • Proven experience managing technical teams in pharmaceutical R&D
  • Experience supporting regulatory submissions and leading inspections
  • Working knowledge of ISO 13485 and FDA 21 CFR Part 820

Work Rights

Not specified

Tailored Resume

Cover Letter