Transport Validation Specialist
Zentiva is hiring a Transport Validation Specialist to oversee pharmaceutical transport validation in compliance with regulatory standards. The role involves defining validation approaches, executing protocols, managing data, and ensuring quality compliance across supply chain processes. Candidates must possess significant experience in validation or quality assurance and deep knowledge of GMP/GDP standards. This is an onsite role based in Ankleshwar focused on maintaining regulatory rigor.
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Experience
5+ years
Function
Quality Assurance
Work mode
Onsite, India
Company
Tier 2
What you will work on
Zentiva is hiring a Transport Validation Specialist to oversee pharmaceutical transport validation in compliance with regulatory standards. The role involves defining validation approaches, executing protocols, managing data, and ensuring quality compliance across supply chain processes. Candidates must possess significant experience in validation or quality assurance and deep knowledge of GMP/GDP standards. This is an onsite role based in Ankleshwar focused on maintaining regulatory rigor.
TAL's take
Solid industry-specific role at a stable pharmaceutical firm with clearly defined quality assurance and validation responsibilities.
Very clear, well-defined responsibilities for a validation specialist in the pharma industry.
Must haves
- University degree in Engineering, Life Sciences, or related field
- Minimum 5 years experience in validation or quality assurance roles
- Strong understanding of regulatory requirements (EMA, FDA, ICH, ISO)
- Familiarity with GMP and GDP
- In-depth knowledge of validation principles and practices
- Proficiency in statistical analysis and data interpretation
Tools and skills
About the company
Established pharmaceutical company, not in tier 1 global/India list.