GxP VSS Engineer

Urgent opening GxP VSS Engineer | In Remote

Interview Mode -Video Call

Salary - Standard

Work Delivery Mode : Remote

Exp Level: 2 + Yrs

Notice Period - Immediate Max 30 Days Joiner.

Commitment Type : Full time

Communication - Excellent

Job Title: GxP VSS Engineer

Qualification: B.E./B.Tech in Engineering, B.Pharm, M.Pharm, M.Sc. Life Sciences, or a related discipline

Industry: Pharmaceutical / Biotechnology / Life Sciences

Employment Type: Full-Time

Job Summary

We are looking for a detail-oriented GxP VSS Engineer to support validation activities, equipment qualification, compliance documentation, and quality assurance processes in a regulated environment. The ideal candidate should have a basic understanding of GxP guidelines, FDA regulations, validation protocols, and documentation practices.

Key Responsibilities

Develop, review, and execute Installation Qualification (IQ) and other equipment/system validation protocols as applicable.

Prepare and maintain validation documents, test records, reports, SOPs, and compliance documentation in accordance with GxP requirements.

Support validation activities for pharmaceutical, laboratory, manufacturing, and computerized systems.

Investigate deviations, non-conformances, and unexpected test results; assist in root cause analysis and CAPA implementation.

Perform data analysis and verify results against predefined acceptance criteria.

Collaborate with Engineering, Manufacturing, IT, Validation, and Quality Assurance teams to support project execution.

Respond to customer assurance requests, including security questionnaires, audit queries, and evidence collection.

Track customer audits and assurance deliverables, including assignment, review, approvals, deadlines, submission, and follow-up.

Ensure data integrity, traceability, and compliance with applicable regulatory requirements.

Required Skills

Basic knowledge of GxP, GMP, FDA regulations, and pharmaceutical quality systems.

Understanding of Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).

Familiarity with Computer System Validation (CSV), equipment qualification, or laboratory systems is an advantage.

Knowledge of deviations, CAPA, change control, and technical documentation.

Good analytical, problem-solving, communication, and technical writing skills.

Strong attention to detail and ability to work collaboratively across departments.

If you are interested than reply me back with your updated

resume and following detail:

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Thanks & Regards,

Manish Jha

Talent Acquisition Team | India Staffing

Net Connect Global

An ISO 9001: 2015 | ISO 27001: 2013 certified organization

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