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Director of Technical Services & Application Development

Job in Holland, Lucas County, Ohio, 43528, USA
Listing for: Tekni-Plex
Full Time position
Listed on 2026-02-28
Job specializations:
  • Engineering
    Biomedical Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below
Location: Holland

The Director of Technical Services & Application Development is responsible for leading customer-facing technical support, application development, and product implementation activities for pharmaceutical and medical packaging solutions. This role serves as the technical authority bridging customers, sales, manufacturing, quality, and R&D, ensuring packaging systems meet regulatory, functional, and performance requirements across sterile, non-sterile, and medical device applications.

The position requires deep expertise in pharmaceutical and medical packaging materials, processing technologies, validation practices, and global regulatory expectations, combined with strong leadership and cross-functional collaboration skills.

Key Responsibilities Technical Services Leadership
  • Lead and develop a multidisciplinary technical services and application development team supporting pharmaceutical, biotech, and medical device customers.
  • Provide expert technical guidance on packaging system selection, material compatibility, barrier performance, sterilization compatibility, and processing robustness.
  • Serve as the escalation point for complex technical issues, deviations, complaints, and field performance concerns related to packaging applications.
  • Establish standardized technical service processes, documentation, and response protocols aligned with GMP and quality system requirements.
Application Development & Product Implementation
  • Oversee application development activities for new and existing packaging solutions, including customer trials, line qualifications, and scale-up activities.
  • Partner with customers to define packaging requirements and translate them into validated, manufacturable solutions.
  • Support new product introductions (NPI), including design for manufacturability, performance testing, and lifecycle management.
  • Ensure alignment between application development, manufacturing capabilities, and quality/regulatory expectations.
Regulatory, Quality & Compliance Support
  • Provide technical input for regulatory submissions, including DMFs, technical dossiers, and customer filings.
  • Support audits, inspections, and customer assessments by serving as a subject matter expert for packaging systems, materials, and processes.
  • Ensure technical services activities comply with applicable standards and regulations, including FDA, EMA, ISO 11607, ISO 15378, USP, and relevant pharmacopeial requirements.
Cross-Functional Collaboration
  • Act as the primary technical interface between Sales, Marketing, Manufacturing, Quality, and R&D teams.
  • Support commercial teams with technical presentations, customer meetings, and proposal development.
  • Drive alignment between customer needs and internal technology roadmaps.
Strategy & Continuous Improvement
  • Contribute to the long-term technical and application strategy for pharmaceutical and medical packaging platforms.
  • Monitor industry trends, emerging technologies, and evolving regulatory requirements to inform innovation and service offerings.
  • Lead continuous improvement initiatives related to application development efficiency, technical risk reduction, and customer satisfaction.
Required Qualifications Education
  • Bachelor’s degree in Engineering, Materials Science, Polymer Science, Chemistry, or a related technical discipline required.
  • Advanced degree (Master’s or PhD) preferred.
Experience
  • Minimum of 10–15 years of progressive experience in pharmaceutical or medical packaging, with significant exposure to customer-facing technical roles.
  • Demonstrated leadership experience managing technical, engineering, or application development teams.
  • Proven track record supporting pharmaceutical, biotech, and/or medical device customers in regulated environments.
Technical Expertise
  • Strong knowledge of pharmaceutical and medical packaging systems (e.g., primary packaging, barrier materials, closures, flexible and rigid packaging).
  • Experience with sterilization methods (e.g., EtO, gamma, e-beam, steam) and material compatibility considerations.
  • Familiarity with packaging validation, performance testing, and risk management methodologies.
  • Working knowledge of global regulatory and quality standards relevant to…
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