Quality Control Officer

Peters Surgical India (Advanced Medical Solutions)

Gurugram District

On-site

INR 450,000 - 650,000

Full time

44 hours ago
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Job summary

Peters Surgical India (Advanced Medical Solutions) is seeking a detail-oriented Quality Control Specialist to support product testing and quality monitoring in the medical device sector. The role emphasizes GMP compliance, laboratory practices, in-process testing, and robust documentation control across manufacturing operations.

Key duties include in‑process control at production areas, daily in‑process testing, pre‑shipment checks, calibration of laboratory equipment, testing of raw materials

Qualifications

  • GMP knowledge and familiarity with quality systems.
  • Hands-on experience with laboratory processes and testing.
  • Experience in maintaining controlled documentation.

Responsibilities

  • In-process control at production area.
  • Execution of daily in-process testing.
  • Pre-shipment checks of consignments.
  • Maintain the management of control samples room.
  • Calibration of daily instrument and equipment of laboratory.
  • To perform the testing of Solution and preparation of test reports.
  • Review of proof check, artwork & printing records.
  • Provide data for quality trends and annual product report.
  • Day to day activities related to stability chamber and stability studies.
  • Preparation and review of test certificates.
  • Execution of daily testing of incoming raw material.
  • Execution of testing of finished goods inspection including the sampling.
  • Approve & release of batch production record.
  • Preparation of quality procedures, QSPs, work instructions.
  • To perform the moisture testing of the samples.
  • Support in the failure investigation of raw material, finished products and complaint samples

Skills

GMP knowledge
Laboratory practices
In-process testing
Documentation control

Job description

We are seeking a detail-oriented Quality Control Specialist to support product testing and quality monitoring within the medical device industry. The ideal candidate will have strong knowledge of GMP, laboratory practices, in-process testing, and documentation control, ensuring product quality, regulatory compliance, and continuous improvement across manufacturing operations.

Key Responsibilities
  • In-process control at production area.
  • Execution of daily in-process testing.
  • Pre-shipment checks of consignment.
  • Maintain the management of control samples room.
  • Calibration of daily instrument and equipment of laboratory.
  • To perform the testing of Solution and preparation of test reports.
  • Review of proof check, artwork & printing records.
  • Provide the data for preparation of quality trends of sealing strength, annual product report, in process testing etc.
  • Day to day activities related to stability chamber and stability studies.
  • Job responsibility may be change as required and allocated by Quality Manager.
  • Preparation and review of test certificates.
  • Execution of daily testing of incoming raw material.
  • Execution of testing of finished goods inspection including the sampling.
  • Approve & release of batch production record.
  • Preparation of quality procedures, QSPs, work instructions etc.
  • To perform the moisture testing of the samples.
  • Support in the failure investigation of raw material, finished products and complaint samples
Pay range and compensation package

Full time

Equal Opportunity Statement

We are committed to diversity and inclusivity.

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