Join Our Team: Validation Specialist
2 weeks ago
At our company, we are seeking a Validation Specialist to join our team.
The Validation Specialist will be responsible for performing risk-based commissioning, qualification and validation of pharmaceutical and biopharmaceutical equipment, utilities, facilities and processes.
This includes developing validation protocols and reports that fulfill regulatory requirements and industry best practices. The candidate will also assist in developing User Requirements Specification documents.
A strong understanding of GxP, GDP, CQV approaches including Validation Lifecycle approach (URS, DQ, FAT/SAT, IOQ, CSV, Cleaning/ Thermal Validation etc.) is required.
RequirementsWe are looking for a candidate with a degree and/or diploma in engineering/science or related studies. A minimum of 3-5 years' experience in pharmaceutical/biopharmaceutical manufacturing facility is preferred.
The ideal candidate will have good knowledge of technical writing and presentations. Proficiency in MS Office Suite (Microsoft Word, PowerPoint, Excel) is also necessary.
Additionally, the candidate must be able to work independently, be self-motivated and task-oriented. Good communication skills and ability to openly communicate and escalate any relevant issues are essential.
As a Validation Specialist, you will play a critical role in ensuring the success of our business by validating our equipment and processes to meet regulatory requirements.
What We OfferWe offer a competitive salary and benefits package, as well as opportunities for career growth and professional development.
Our company is committed to providing a safe and healthy work environment, and we are an equal opportunity employer.
If you are a motivated and detail-oriented individual with a passion for validation and quality assurance, we encourage you to apply for this exciting opportunity.
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