MSc Chemistry Job at Dr. Reddy’s | Quality Assurance Role
Looking for a strong Quality Assurance Job in a leading pharmaceutical company? This opportunity at Dr Reddy Career is ideal for candidates seeking MSc Chemistry Job roles in the QA QC Jobs domain. The position focuses on Analytical Quality Assurance, GMP compliance, OOS investigations, and laboratory data integrity. Candidates with Chemistry, Analytical Chemistry, or Pharmacy backgrounds can build a strong pharma career through this Dr. Reddy’s Careers opportunity in Andhra Pradesh.
About the Company
Dr. Reddy’s Laboratories is a globally recognized pharmaceutical organization committed to delivering affordable and innovative medicines. Dr Reddy Career opportunities are built on strong science, regulatory excellence, and quality-driven manufacturing systems. The company provides excellent exposure for professionals seeking Quality Assurance Job roles and MSc Chemistry Job opportunities in GMP-compliant pharmaceutical environments focused on global healthcare impact.
Job Overview
Dr. Reddy’s is hiring for the role of Team Member – Analytical Quality Assurance in Andhra Pradesh. This Quality Assurance Job focuses on ensuring GMP and GLP compliance in QC laboratory operations. The selected candidate will handle OOS/OOT investigations, CAPA management, stability data review, SAP transactions, and analytical documentation. This MSc Chemistry Job opportunity is ideal for
professionals seeking QA QC Jobs with strong exposure to regulatory and analytical systems in pharma manufacturing.- Job Post: Team Member – Analytical Quality Assurance
- Location: Andhra Pradesh, India
Roles & Responsibilities
- 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.
- Management of QMS notifications through DCMS.
- Monitor and ensure cGLP (current Good Laboratory Practices) in Quality control and Micro Lab, and implementation of standard operating procedures.
- Verification of audit trails for all the GxP computer systems at the Quality Control Laboratory.
- Preparation, Review, and approval of stability study protocols on LIMS.
- 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.
Requirements:
- Educational qualification: Graduation in Chemistry/Analytical Chemistry or Pharmacy is mandatory. A Master’s in Microbiology, Biochemistry, Biotechnology, Chemistry/Analytical Chemistry, or Pharmacy is preferred
- Minimum work experience: 2-4 years of experience
Skills & attributes & Critical exposures
Functional Skills
- Regulatory Compliance
- Regulatory Filings
- Technical Documentation
- Change Control
- Laboratory Information
- Risk Management
- Chromatography
Resident Skills
- Product Quality (QA/QC)
- Current Good Manufacturing Practices (cGMPS)
- Good Laboratory Practice (GLP)
- Quality Management Systems (QMS)
This Quality Assurance Job at Dr Reddy Career is an excellent opportunity for candidates seeking MSc Chemistry Job roles in the pharmaceutical QA QC Jobs domain. The position provides strong exposure to GMP systems, analytical compliance, and regulatory quality operations. Candidates with Chemistry backgrounds can build a stable and rewarding career in pharmaceutical quality assurance through this Andhra Pradesh opportunity at Dr. Reddy’s Careers.
