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Sr . Executive - IAS QA

Exclusive opportunity

Onsite

Sr . Executive - IAS QA

Indoco Remedies

Sr . Executive - IAS QA

Skills

Testing & QAInternal AuditCompliance

2 months ago

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Important information


Contract type:

Permanent

Salary:

₹800,000 – ₹1,300,000 / year

Location:

Navi Mumbai, Maharashtra, India

Work mode:

Onsite

Published on:

12 August 2026

What they need


Role & responsibilities

  • Preparing, Reviewing and/or implementing Standard Operating Procedures and department policies and procedures.
  • Maintaining updated Laboratory directory as and when changes takes place.
  • Issuance and archival of Protocols, Logbooks, Formats, etc.
  • Issuance of Training records, Incidence Investigation report, Change control form, Deviation form, OOS Investigation form, Customer complaint form, etc.
  • Preparing and checking laboratory schedules like Calibration Schedule, Preventive Maintenance Schedule, Training Schedule, Self-Inspection Schedule, and Data Backup Schedule etc.

Preparing Site Master File and System Manual.

  • Preparing Annual Review Report of the laboratory.

  • Reviewing Reports for analysis, as per the relevant Indian regulations/standards and Company policies/Standards.

  • Review and approval of Protocol, Report, Calibration certificate, Analyst qualifications and MOA, etc.

  • Review of DQ, IQ, OQ and PQ Files for Instruments/Equipments.

  • Review of audit trail.

  • Creation of User Id for various softwares of Instruments.

  • Review of External calibration certificates.

  • To assure the proper Induction and Training of employees.

  • To arrange and manage and perform Internal audits.

  • To indent logbooks and stationary.

  • To prepare calibration certificate of instrument.

  • To manage activities related to Internal and External audits.

  • Ensure that documents required by Customers are given to them (like Questionnaire, Organogram, Employee Profile, Equipment Master List, Certificates etc.)

  • To ensure that QMS like Change Control, Deviation Control, CAPA, Incidence Recordings, OOS, OOT, Customer complaints, etc. are raised as and when required and then closed at appropriate time.

  • Preparing Audit compliance reports.

  • To monitor and perform all the activities of QA In charge in his absence.

  • To ensure GLP compliance in laboratory.

  • Impart training to workmen and staff on GMP requirements and QMS requirements.

  • Handling of DMS, TRACKWISE and LIMS software.

  • Performs other related duties as required and directed.

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