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Director, Technical Services

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Onsite

Director, Technical Services

Ladders

Director, Technical Services

Skills

Compliance

2 months ago

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Important information


Contract type:

Permanent

Location:

United States

Work mode:

Onsite

Published on:

31 August 2026

What they need


For our client, we are seeking a Director, Technical Services to join the team of a leader in the Healthcare space.

This leader will oversee technical operations across a distributed manufacturing network, with a strong focus on process validation, cleaning validation, and technology transfer. The role will partner closely with site teams and cross-functional stakeholders to drive technical consistency, resolve complex manufacturing issues, and strengthen quality and compliance in a regulated environment. This is a hands-on leadership opportunity for someone who can combine deep technical expertise with team development and network-level execution.

Location: Remote - US based candidates only, no visa sponsorship available

Compensation: $150,000 – $180,000 annually

Responsibilities

  • Lead technology transfer of products and processes across multiple manufacturing sites
  • Own the cleaning validation program, including protocol development and execution
  • Lead process validation activities, including documentation and ongoing verification
  • Troubleshoot technical issues and drive corrective and preventive actions across sites
  • Provide hands-on support for equipment-related problems and improvements
  • Set and oversee network-level strategies and standards for manufacturing processes
  • Manage and develop a team of Technical Services Managers, ensuring consistency and quality standards

Qualifications

  • Bachelor's degree in Engineering, Pharmacy, Chemistry, or a related field; advanced degree preferred
  • 12+ years of progressive experience in pharmaceutical manufacturing or sterile/nonsterile compounding with hands-on ownership of relevant processes
  • Expertise in 503A/503B compounding operations, sterile injectable manufacturing, or API/peptide manufacturing
  • Knowledge of USP standards and FDA guidelines for process validation and API manufacturing
  • Strong experience in root-cause investigation and CAPA in regulated environments
  • Ability to collaborate across geographically distributed sites with remote teams
  • Proficient technical writing skills for validation protocols and reports

Benefits

  • Unlimited PTO, company holidays, and quarterly mental health days
  • Comprehensive health benefits including medical, dental, vision, and parental leave
  • Employee Stock Purchase Program (ESPP)
  • 401k benefits with employer matching
  • Offsite team retreats

Our client is an equal opportunity employer. We encourage you to apply even if you don’t meet every qualification—your background could be exactly what this team needs.

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