Quality Engineer

at  Scitex Recruitment

Hamilton, Waikato, New Zealand -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate01 Aug, 2024Not Specified05 May, 2024N/AAnalytical Skills,Iso Standards,Regulatory RequirementsNoNo
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Description:

  • Play a critical role in ensuring the safety and efficacy of life-saving products
  • Development and growth potential within a cutting-edge industry.
  • Based in Te Rapa with flexibility in working hours.
    Are you passionate about ensuring the quality and safety of life-changing pharmaceutical and medical device products? Join this dynamic team as a Validation Engineer, where you will play a crucial role in bringing new products into production and shaping the future of healthcare.

KEY QUALIFICATIONS AND EXPERIENCE:

  • Bachelor’s degree in Engineering, Pharmacy, or related fields.
  • Proven experience in validation activities within the pharmaceutical or medical device industry.
  • Familiarity with regulatory requirements such as FDA, cGMP, and ISO standards.
  • Strong analytical skills and attention to detail.
  • Excellent communication and team collaboration abilities.

Responsibilities:

  • Conduct validation activities for pharmaceutical / medical device production processes.
  • Develop and execute validation protocols, including URS/IQ/OQ/PQ, to ensure compliance with regulatory standards.
  • Analyze and interpret validation data, identifying areas for improvement and implementing corrective actions.
  • Collaborate with cross-functional teams to integrate validation requirements throughout the product development lifecycle.
  • Stay up to date with industry regulations and best practices, applying them to enhance validation processes.


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Graduate

Engineering pharmacy or related fields

Proficient

1

Hamilton, Waikato, New Zealand