Supplier Project Engineer Job at Katalyst Healthcares & Life Sciences, Acton, MA

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  • Katalyst Healthcares & Life Sciences
  • Acton, MA

Job Description

  • Katalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices.
  • We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field. We work with University hospitals, pharmaceutical companies and recruiting partners.

Job Description



Job Description

:

  • Strong written and verbal communication skills.
  • Possess strong analytical and problem-solving skills.
  • Familiarity with one of SAS, JMP, or Minitab is strongly desired.
  • Working knowledge of MS Office, including Office Project software.
  • Six Sigma Process Improvement Experience/Certification desirable.
  • Regulated industry experience preferred.
  • Familiarity with cGMP practices desired.
  • Outstanding team player who seeks and values diverse input to hone ideas, but who has the experience to develop strong starting proposals.
  • Highly motivated, self-starter.

Responsibilities:

  • Lead, plan, manage and implement supplier capital

    qualifications

    from kick-off to implementation into production. Collaboration
  • Generate or review supplier validation/qualification protocols and coordinate their execution and final reporting.
  • Lead with teamwork and drive for results; able to work in a borderless organization and across multiple functions including, programs, engineering, purchasing and suppliers.
  • Lead teams responsible for the procurement and installation of manufacturing equipment at global suppliers.
  • All other duties as assigned.

Requirements:

  • 3 years of relevant experience.
  • BS Engineering Degree (Plastics, Mechanical, Manufacturing/Industrial) or related field.
  • Ability to manage Supply Chain projects concept to production, including the authoring and oversight of IQ/OQ/PQ protocols for component manufacturing processes and secondary.
  • Experience within an FDA regulated industry.
  • Minitab is strongly desired or JMP.

Additional Information



All your information will be kept confidential according to EEO guidelines.

Job Tags

Contract work, Immediate start,

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