Technical Scheme Manager

Eurofins-posted about 1 year ago
Full-time • Mid Level
Des Moines, IA
10,001+ employees
Professional, Scientific, and Technical Services
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The Technical Scheme Manager at Eurofins Scientific is responsible for the design, development, execution, and compliance with scheme and ISO 17065 accreditation requirements for certification activities in the United States. This role primarily focuses on dietary supplements good manufacturing practices certification and supplier auditing, while also managing relationships with external scheme owners and ensuring program compliance.

  • Serve as SME for assigned program area/s, including engagement with external scheme owners.
  • Develop and maintain scheme documents, policies, and procedures relevant to assigned program area/s.
  • Maintain knowledge of and assure program compliance with ISO 17065 independent third party assessment principles.
  • Govern competency requirements and perform scheme specific training for global audit and technical reviewer teams.
  • Offer robust and prompt support to clients and internal colleagues, addressing technical queries with clarity and precision.
  • Perform technical review of facility or product audits and assessments, ensuring all scheme specific KPIs are met.
  • Support and facilitate internal and accreditor audits of scheme records and procedures.
  • Collaborate with marketing and sales teams to produce engaging materials for trade events and webinars.
  • Maintain up to date technical expertise through continuing education.
  • Actively participate in and present at industry events to promote Eurofins certification services.
  • Engage in standards development activities for organizations like ANAB and ISO.
  • Contribute as an advisory role in guiding business program development strategy.
  • Bachelors or Master's degree in Food or Nutrition, Quality, Pharmaceuticals or other relevant scientific field required.
  • Minimum 3 years of experience in a manufacturing, quality or regulatory role, ideally in the dietary supplement or pharmaceutical industries.
  • Demonstrated ability to function in a collaborative environment with knowledge and capabilities to secure appropriate support resources to achieve business goals.
  • High proficiency and fluent in written and spoken English.
  • Out of the box critical thinker, self-motivated, result-driven and capable of working both independently and with a project team.
  • Authorization to work in the United States indefinitely without restriction or sponsorship.
  • Excellent full time benefits including comprehensive medical coverage, dental, and vision options.
  • Life and disability insurance.
  • 401(k) with company match.
  • Paid vacation and holidays.
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