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An independent tech consulting firm is seeking an experienced validation specialist to ensure compliance and quality oversight in pharmaceutical projects. This role involves collaborating with cross-functional teams and maintaining adherence to cGMP and regulatory standards. The ideal candidate will have over five years of validation experience and strong analytical and communication skills. Join a dynamic environment where your expertise will contribute to impactful projects in the life sciences and engineering sectors.
Our client is an independent tech consulting firm offering solutions across Information Systems & Digital, Telecom, Life Sciences, and Engineering.
Key Responsibilities:
Requirements:
Interested applicants are welcome to apply or reach out for more information.
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