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Immediate Opening For QC Position

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Onsite

Immediate Opening For QC Position

Vimta Labs

Immediate Opening For QC Position

Skills

ComplianceRegulatory Compliance

20 days ago

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Important information


Contract type:

Permanent

Location:

Hyderabad, Telangana, India

Work mode:

Onsite

Published on:

6 October 2026

What they need


Dear All,

Greeting From Vimta Labs.

Company Name: Vimta Labs

Location: Shamirpet, Hyderabad

Experience: 8 to 12 Years

Education: M.Sc. / B.Pharmacy / M.Pharmacy

Key Responsibilities Core QMS & Investigations

  • Investigate quality issues: Lead and participate in QMS investigations concerning Incidents, Out of Specification/Expectation (OOS/OOE/OOX), Occurrences, and Deviations.
  • Review documentation requests: Serve as a designee for authorizing procedural document issuance.
  • Monitor environmental conditions: Record and witness temperature monitoring protocols within the biopharma department.

Documentation & Compliance Review

  • Author and review SOPs: Prepare and review Standard Operating Procedures, instrument qualification protocols, raw data, and final reports.
  • Audit logbooks: Perform periodic reviews of instrument usage and maintenance logbooks across the department.
  • Manage standards: Review the usage, maintenance, and tracking of reference standards.

Equipment Qualification & Data Integrity

  • Ensure instrument compliance: Review analytical instrument software user roles, privileges, project-related protocols, and raw data to ensure data integrity.
  • Oversee maintenance schedules: Review equipment lists, calibration schedules, and preventive maintenance (PM) timelines.
  • Verify equipment safety: Review periodic calibrations, PM, and electrical safety protocols for all biopharma equipment.

Training & People Management

  • Deliver training: Provide technical training on system-related procedures and quality management systems to the team.
  • Authorize training records: Act as a designee for the review and authorization of Training Documentation Forms (TDF) and Training Assessment Forms (TAF).

Required Technical Skills & Competencies

  • Deep understanding of regulatory compliance (GxP, FDA, MHRA) in a biopharma or analytical testing environment.
  • Strong expertise in Data Integrity principles and software user-privilege management for analytical instruments.
  • Proven track record in handling complex root cause analysis (RCA) for OOS and deviations.

Interested Candidates Please share Profiles to [email protected]

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