Lead Validation Engineer

3 weeks ago


Kalamazoo, Michigan, United States Verista Full time
Job Title: Lead Validation Engineer

Verista is seeking a highly skilled Lead Validation Engineer to join our team. As a key member of our commissioning and verification team, you will be responsible for ensuring the quality and integrity of our pharmaceutical manufacturing processes.

Responsibilities:
  • Lead the commissioning and verification process for our pharmaceutical manufacturing equipment and systems.
  • Develop and implement commissioning and verification plans and procedures.
  • Collaborate with cross-functional teams to ensure compliance with cGMP and industry standards.
  • Conduct risk assessments and develop mitigation strategies to ensure the safety and quality of our products.
  • Develop and maintain technical documentation and reports.
  • Provide training and support to colleagues on commissioning and verification procedures.
Requirements:
  • Bachelor's degree in a technical field (e.g. engineering, life sciences).
  • Minimum 4 years of experience in pharmaceutical manufacturing or a related field.
  • Strong knowledge of cGMP and industry standards.
  • Excellent communication and interpersonal skills.
  • Ability to work in a fast-paced environment and prioritize multiple tasks.
What We Offer:
  • Competitive salary and benefits package.
  • Opportunities for professional growth and development.
  • A dynamic and collaborative work environment.
  • Recognition and rewards for outstanding performance.

Verista is an equal opportunity employer and welcomes applications from diverse candidates. If you are a motivated and experienced professional looking for a new challenge, please submit your application.



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