Team Member Analytical QA

qvents.in · Baddi

  • Experience2–3 yrs
  • SalaryNot disclosed
  • Work modeonsite
  • Levelmid
  • Posted30 Aug 2026
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About qvents.in

qvents.in is hiring in Baddi in pharma biotech. This role looks for around 2+ years of experience.

Skills

  • pharmaceutical quality control
  • analytical chemistry
  • laboratory investigations
  • analytical instrumentation
  • Quality Management System
  • Good Manufacturing Practice
  • SAP
  • Laboratory Information Management Systems
  • method validation
  • method transfer
  • Change Control
  • CAPA
  • data integrity

The role

An analytical quality assurance professional at a pharmaceutical manufacturing company investigates laboratory deviations, reviews Good Manufacturing Practice compliance and analytical data, and manages Quality Management System documentation. Expertise includes pharmaceutical quality control, analytical chemistry, and laboratory investigations, with additional capability in SAP transactions and Laboratory Information Management Systems.

Full job description

Designation : Team Member

Function : Quality Assurance

Functional Area : QC, Analytical

Job Role Summary : Investigation of Laboratory incidents, OOS, OOT, QMS documents, Change management, Reviewing Analytical documents

Job Profile

You will be responsible for participating in investigations of Quality Management System (QMS) documents such as OOS, OOT, and laboratory deviations, and ensuring timely closures as per SOP timelines.

You will be responsible for preparing trending reports for OOS, OOT, and laboratory incidents, using analytical insights to support CAPA identification and process improvements.

You will be responsible for evaluating Change Controls and CAPA action plans, verifying their effectiveness to ensure resolution of root causes and prevention of recurrence.

You will be responsible for reviewing all analytical data generated in the Quality Control laboratory—including electronic and raw data—ensuring accuracy and compliance with relevant SOPs.

You will be responsible for reviewing instrument and equipment calibration records and audit trails to confirm reliability, data integrity, and GMP adherence.

You will be responsible for preparing and reviewing documentation related to stability samples and ensuring that reference standards, impurity standards, working standards, and related records are maintained per applicable procedures.

You will be responsible for performing and verifying SAP transactions related to laboratory workflows and data entries as outlined in SOPs, ensuring traceability and accuracy.

You will be responsible for reviewing and approving method validation and method transfer protocols and reports, as well as LIMS master data and control limit updates, ensuring analytical consistency across platforms

Job Requirements

2+ years experience in Pharma Quality control, Analytical QA functions

Experience handling Laboratory investigations, Laboratory Document review, Analytical Instrumentation

Work / Job Experience : 2+ Years

Type of Experience : Pharma QC, Analytical QA experience

Academic Qualifications

Graduation in Chemistry/Analytical Chemistry or Pharmacy is mandatory

Masters in Microbiology, Biochemistry, Biotechnology, Chemistry/Analytical Chemistry or Pharmacy is preferred

Additional Certifications like CQA, CPGP, CBSP, Six Sigma, ICH Q5/Q6, Advanced Biologics Manufacturing or RAC are preferred

Job Post Link : https://tinyurl.com/4axdn3ep

Full Time

India | HImachal Pradesh | Baddi

Posted 5 hours ago

Website Linkedin Dr.Reddys Laboratories

To apply for this job please visit careers.drreddys.com.