Validation Specialist
Vor 6 Tagen
Validation Specialist for Pharmaceutical & Biotech Processes
About Us: Inova is a premier pharmaceutical consulting firm based in Switzerland, known for delivering cutting-edge solutions in the pharma industry. Our team of experts specializes in guiding pharma companies through complex regulatory landscapes and ensuring the highest standards of product quality and safety.
Job Description: We are seeking a skilled and experienced Validation Engineer to join our dynamic team. In this role, you will be instrumental in ensuring that all systems and processes meet the necessary specifications and regulatory requirements. Your expertise will contribute to the successful validation of biopharmaceutical processes and cleaning processes and systems in the pharmaceutical sector.
Key Responsibilities:
- Design and implement validation strategies for pharmaceutical processes and cleaning processes.
- Conduct risk assessments and ensure compliance with industry regulations and standards (e.g., FDA, EMA, GMP).
- Develop and execute validation protocols (IQ, OQ, PQ) and prepare detailed reports.
- Collaborate with cross-functional teams to resolve validation issues.
- Stay updated on industry trends and regulatory changes impacting validation processes.
Qualifications:
- Bachelor’s or Master’s degree in Engineering, Pharmacy, or related field.
- Minimum of 3 years of experience in validation engineering within the pharmaceutical industry.
- Strong understanding of GMP and regulatory requirements in pharma.
- Excellent analytical, problem-solving, and project management skills.
- Proficiency in English; German and/or French language skills are a plus.
We Offer:
- A competitive salary and benefits package.
- Opportunities for professional growth and development.
- A collaborative and inclusive work environment.
- Participation in cutting-edge projects in the pharma industry.
How to Apply: Interested candidates are invited to submit their CV through this form. Please include references and any relevant project details in your application.
Seniority levelMid-Senior level
Employment typeFull-time
Job functionQuality Assurance
IndustriesPharmaceutical Manufacturing
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