Why This Role Stands Out
Elevate your career in the pharmaceutical sector as a CSV/Automation Consultant, where you'll leverage your expertise in compliance and validation to make a significant impact on critical projects. This hybrid role offers a competitive hourly rate and the chance to expand your skills within a dynamic, regulated environment, making it an ideal opportunity for experienced professionals seeking impactful work and professional growth. Apply now to join a leading client and contribute to groundbreaking advancements.
Quick Overview
Job Description
Location: Massachusetts (Relocation Required/Accepted)
Duration: 5-6 Months
Start Date: November 2, 2026
Industry: Pharmaceutical / Life Sciences
Client: Pharma-related
Rate: $50/hr on W2
Visa: /
Mode of Interview: Skype
PV: Oxford Global
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.
The ideal candidate will have hands-on experience with Computer System Validation (CSV), automation systems, and compliance requirements in regulated pharmaceutical manufacturing environments.
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.
Interested candidates: Please share updated resumes along with current location, visa status, pharmaceutical industry experience, and relocation availability.
Vodala Shruthi
Lead Technical Recruiter
StratEdge IT Consulting Inc.
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