#NEW#CSV Specialist - Contract to Perm
About the Role:
We are seeking a skilled and motivated CSV Specialist to join our Automation team on a 1-year contract, with potential for conversion to a permanent position.
The ideal candidate will play a key role in ensuring compliance with QA standards, supporting internal/external audits, managing system reviews, and contributing to technical documentation within the pharmaceutical industry.
Key Responsibilities:
- Handle and support work involving QA and compliance requirements, including addressing internal/external audit findings.
- Assist in writing technical reports as required.
- Review SOPs/WIs for technical accuracy and provide recommendations.
- Conduct periodic system reviews and generate compliance reports as needed.
Key Requirements:
- A degree in Chemistry, Engineering, or another Science-related discipline.
- A minimum of 2–3 years of experience in a CSV role within the pharmaceutical industry.
- Experience in compliance or validation is advantageous.
- Strong written and oral communication skills, with technical report-writing experience being an added advantage.
- Demonstrated personal leadership, accountability, and organizational skills, with the ability to operate independently with minimal supervision.
Anyone with relevant experience is welcome to chat. For more details, please email [email protected].
Business Registration Number : 200611680D | Licence Number : 10C5117 | EA Registration Number : R1768258
