Job Description
We are looking for an experienced CSV / Automation Consultant with a strong background in the pharmaceutical or life sciences industry to support a 5-6-month project in Massachusetts.
Required Skills & Qualifications
- Experience in Computer System Validation (CSV) and/or automation within the pharmaceutical industry.
- Strong knowledge of cGMP/GxP regulations and regulated manufacturing environments.
- Experience preparing and executing validation documentation, protocols, test scripts, and compliance activities.
- Ability to troubleshoot automation systems and validation-related issues.
- Strong documentation, communication, analytical, and problem-solving skills.
- Willingness to relocate to Massachusetts for the 5-6-month assignment.
Rate:
£38,500/year
Location:
United States
IR35 Status:
Outside
Remote Status:
Not specified
Industry:
IT
Seniority Level:
Mid-Level