MSc Chemistry Job at Dr Reddy’s Laboratories | API Jobs
Looking for an MSc Chemistry Job in the pharmaceutical industry? Dr. Reddy’s Laboratories is hiring for the position of Team Member – Manufacturing (Peptide) at Pydibimavaram, Andhra Pradesh. This opportunity is relevant to candidates exploring API Manufacturing Jobs and pharmaceutical production careers. Applicants with a B.Sc. or M.Sc. in Analytical or Organic Chemistry and 2–5 years of experience can explore this vacancy. Discover Dr Reddy’s Careers and take the next step in your professional journey.
- Job Title: Team Member – Manufacturing (Peptide)
- Job Location: Pydibimavaram, Andhra Pradesh 532409, India
- Qualification: B.Sc. / M.Sc. in Analytical or Organic Chemistry
- Experience: 2–5 years
About Dr Reddy’s Laboratories
Dr Reddy’s Laboratories Ltd. is a multinational pharmaceutical company established in 1984. With a global presence spanning 66 countries, the company focuses on improving access to affordable and innovative medicines. Its Global Manufacturing Organisation operates facilities across multiple locations and manufactures a portfolio of complex active pharmaceutical ingredients and other medicines. For candidates exploring Dr Reddy’s Careers, the company offers opportunities to work in pharmaceutical manufacturing and contribute to quality-focused production operations.
Job Overview
Dr Reddy’s Laboratories is recruiting for the position of Team Member – Manufacturing (Peptide) at its facility in Pydibimavaram, Andhra Pradesh. The role falls under the Manufacturing job family and Production – API sub-job family within the Global Manufacturing Organisation (GMO). This MSc Chemistry Job is suitable for candidates with a B.Sc. or M.Sc. in Analytical or Organic Chemistry and 2–5 years of relevant work experience.
Key Responsibilities
Candidates selected for this manufacturing position will be responsible for the following activities:
- Follow company safety norms, policies, and Standard Operating Procedures (SOPs).
- Execute batch manufacturing activities according to electronic Batch Manufacturing Records (e-BMR) and workflow instructions.
- Submit executed e-BMRs and workflows to the In-Process Quality Assurance (IPQA) department.
- Support trial, validation, and commercial batches in coordination with the MSAT and IPDO teams.
- Coordinate with the warehouse, Quality Control (QC), and other departments.
- Ensure timely equipment calibration and preventive maintenance in coordination with the shift-in-charge and the engineering department.
- Initiate quality and breakdown notifications as required.
- Participate in equipment commissioning and qualification activities.
- Ensure equipment qualification, validation, calibration, and process validation are completed according to schedules and requirements.
- Follow cleanroom practices and maintain the operating area in compliance with applicable regulatory requirements.
Educational Requirements
Candidates interested in MSc Chemistry Jobs in pharmaceutical manufacturing should meet the following requirements specified in the job posting:
- Educational qualification
- B.Sc. in Analytical or Organic Chemistry
- M.Sc. in Analytical or Organic Chemistry
- Work experience: 2–5 years of experience
Applicants should have relevant technical knowledge and experience in manufacturing operations, equipment handling, documentation, and quality compliance. Candidates should review the official vacancy details to confirm their suitability before applying.
Skills Required: Candidates applying for this role should have technical knowledge and behavioural skills relevant to pharmaceutical manufacturing.
Technical skills
- Operation of critical equipment, including reverse-phase chromatography, microwave reactors, and lyophilizers.
- Understanding equipment Overall Equipment Effectiveness (OEE) and utilisation.
- Proficiency in Manufacturing Execution System (MES) software for executing batch manufacturing activities.
- Knowledge of Quality Management Systems (QMS), SOPs, User Requirement Specifications (URS), and protocols.
- Familiarity with SAP software for initiating quality and breakdown notifications.
- Knowledge of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP).
- Experience in equipment qualification, validation, calibration, and process validation.
Behavioural skills
- Willingness to learn and apply knowledge while following safety and quality standards.
- Effective communication and coordination across departments.
- Ability to identify and address production-related issues promptly.
- Commitment to completing calibration, preventive maintenance, and operational activities on schedule.
- Focus on regulatory compliance, product quality, and workplace safety.
If you are searching for an MSc Chemistry Job that builds on your pharmaceutical manufacturing experience, this opportunity at Dr Reddy’s Laboratories is worth exploring. The role offers exposure to peptide manufacturing, batch operations, equipment qualification, and quality compliance. Candidates interested in API Manufacturing Jobs should review the eligibility requirements carefully and apply through the official careers portal. Explore Dr Reddy’s Careers to take the next step in your pharmaceutical career.