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Dr. Reddy’s Laboratories Mega Hiring 2026: 20 Openings in Quality Control (QC), Clinical & Pharma Operations, Medical Affairs & Review | Freshers & Experienced
Position Overview & Specifications
| Parameter | Official Specifications |
|---|---|
| Hiring Organization | Dr. Reddy’s Laboratories |
| Total Active Vacancies | 20 Verified Positions |
| Functional Domains | Quality Control (QC), Clinical & Pharma Operations, Medical Affairs & Review |
| Work Locations | Hyderabad, India, Amritsar, India & Multiple Locations |
| Target Qualifications | B.Pharm, M.Pharm, M.Sc Statistics, Mathematics, Computer Science, Life Sciences |
| Employment Type | Full-Time, Permanent Industry Placement |
| Application Procedure | Direct Official Online Submission / Verified HR Route |
Verified Vacancy Matrix & Hiring Tracks
Review all active hiring tracks below. Direct official application links for each position are provided at the bottom of this notification:
| # | Designation / Role | Functional Domain | Work Location | Experience | Application Mode |
|---|---|---|---|---|---|
| 1 | PV Specialist – EUG Operations | Pharmacovigilance (PV) | Hyderabad, India | 3-6 Yrs | Online Portal |
| 2 | Territory Manager | Clinical & Pharma Operations | Delhi, India | 6-10 Yrs (Mid-Senior Level) | Online Portal |
| 3 | Team Member Engineering Process | Clinical & Pharma Operations | Visakhapatnam, India | 1-3 Yrs | Online Portal |
| 4 | Territory Manager | Clinical & Pharma Operations | Ahmednagar, India | 6-10 Yrs (Mid-Senior Level) | Online Portal |
| 5 | Team Member – Warehouse | Packing & Warehouse | Visakhapatnam, India | 1-4 Yrs | Online Portal |
| 6 | Supply Planner | Clinical & Pharma Operations | Hyderabad, India | 1-4 Yrs | Online Portal |
| 7 | Medical Advisor-Haematology | Medical Affairs & Review | Hyderabad, India | 1-4 Yrs | Online Portal |
| 8 | Medical Advisor – Oncology | Medical Affairs & Review | Hyderabad, India | 1-4 Yrs | Online Portal |
| 9 | Territory Business Manager | Clinical & Pharma Operations | Amritsar, India | 6-10 Yrs (Mid-Senior Level) | Online Portal |
| 10 | Executive – Trade Marketing | Clinical & Pharma Operations | Mumbai, India | 1-3 Yrs | Online Portal |
| 11 | Team Lead – Engineering (Process Mechanical) | Clinical & Pharma Operations | Pydibimavaram, India | 6-10 Yrs (Mid-Senior Level) | Online Portal |
| 12 | Site Engineering Head | Clinical & Pharma Operations | Pydibimavaram, India | 12-18 Yrs (Leadership) | Online Portal |
| 13 | Team Member – QC Instrumentation | Quality Control (QC) | Pydibimavaram, India | 1-4 Yrs | Online Portal |
| 14 | Team Lead – Engineering (HVAC) | Clinical & Pharma Operations | Pydibimavaram, India | 6-10 Yrs (Mid-Senior Level) | Online Portal |
| 15 | Team Member – OSD production (Wurster Operation) | Production & Manufacturing | Baddi, India | 1-4 Yrs | Online Portal |
| 16 | HR Operations Partner | Clinical & Pharma Operations | Hyderabad, India | 1-4 Yrs | Online Portal |
| 17 | Medical Advisor-Grandera and Orion | Medical Affairs & Review | Mumbai, India | 1-4 Yrs | Online Portal |
| 18 | Medical Advisor – Vaccines | Medical Affairs & Review | Mumbai, India | 1-4 Yrs | Online Portal |
| 19 | Brand Manager | Clinical & Pharma Operations | Hyderabad, India | 6-10 Yrs (Mid-Senior Level) | Online Portal |
| 20 | Dr Reddy Hiring for Quality Control Associate – Bioassay | Quality Control (QC) | Hyderabad | 1-3 Yrs | Online Portal |
Key Roles & Detailed Responsibilities
- Execute daily operational mandates aligned with Dr. Reddy’s Laboratories’s standard operating procedures (SOPs) and cGMP/GCP compliance frameworks.
- Perform technical assessments, batch/case documentation, or analytical evaluations as assigned by department leadership.
- Collaborate cross-functionally across manufacturing, quality assurance, clinical data operations, and enterprise regulatory teams.
- Ensure full regulatory audit-readiness and adherence to global safety and compliance guidelines.
Eligibility Criteria & Candidate Profile
- Academic Background: B.Pharm, M.Pharm, M.Sc Statistics, Mathematics, Computer Science, Life Sciences from a recognized institution.
- Strong operational understanding of pharmaceutical workflows, regulatory standards (USFDA, EMA, CDSCO), and quality protocols.
- Demonstrated technical acumen, documentation discipline, and problem-solving skills.
- Both enthusiastic fresh graduates and experienced industry professionals are encouraged to review respective position criteria.
Core Technical Competencies & Instruments Matrix
Candidates possessing hands-on proficiency across the following analytical tools, software systems, and regulatory standards will receive priority evaluation:
HPLC (Waters Alliance / Agilent 1260 / 1290)Gas Chromatography (GC – FID / Headspace)Empower 3 / OpenLab Chromatography Data SystemsUV-Visible Spectrophotometry & Dissolution Testing (USP I/II)Karl Fischer & Potentiometric Auto-TitrationAnalytical Method Validation & Transfer (ICH Q2 R1)Finished Product, In-Process & Stability TestingALCOA+ Data Integrity & 21 CFR Part 11 Audit TrailsOut of Specification (OOS / OOT) Phase I/II InvestigationsLaboratory Information Management Systems (LIMS)
Daily Operational Workflow & Core Shift Duties
Detailed technical breakdown of standard shift activities, laboratory/plant floor execution, and daily operational deliverables for Multiple Positions (Quality Control (QC), Clinical & Pharma Operations, Medical Affairs & Review):
Duty 1Sample Intake, Allocation & LIMS Log-In
Receiving finished product, in-process, raw material, and stability samples; verifying physical integrity, batch numbers, and generating unique test tracking barcodes in LIMS.
Duty 2Mobile Phase Preparation & System Suitability (SST)
Preparing HPLC/GC mobile phases, buffer filtration, sonication, standard solution preparation, and running mandatory SST injections on Waters Empower 3 / Agilent OpenLab.
Duty 3Chromatographic & Wet Chemistry Analysis
Executing assay, related substances (RS), dissolution profile, residual solvents, or Karl Fischer titrations strictly per approved Standard Testing Procedures (STPs).
Duty 4Chromatographic Data Processing & ALCOA+ Audit Trails
Integrating peaks with validated processing methods, checking baseline separation, and reviewing audit trails to ensure 100% data integrity without manual overrides.
Duty 5OOS / OOT Escalation & Documentation
Contemporaneously recording raw data in analytical workbooks, verifying calculation formulas, and immediately logging Phase I lab investigations if any out-of-specification result occurs.
Regulatory & Quality Compliance Framework
Candidates must demonstrate operational awareness and rigorous adherence to the following regulatory chapters and international standards governing this role:
USFDA 21 CFR Part 211.160 / 211.194
General Laboratory Controls
Mandates scientifically sound laboratory controls, specifications, testing protocols, standards, and complete raw laboratory records.
ICH Q2 (R1)
Validation of Analytical Procedures
Provides global regulatory definitions and validation criteria for specificity, linearity, range, accuracy, precision, LOD, LOQ, and robustness.
ICH Q1A to Q1E
Stability Testing Guidelines
Regulates stability testing protocols across climatic zones, photo-stability, and mathematical evaluation of shelf-life data.
USFDA 21 CFR Part 11 & ALCOA+
Electronic Records & Data Integrity
Enforces strict user credentialing, automated immutable audit trails, and contemporaneous time-stamping for all chromatographic systems.
Tailored Resume Guidelines for Multiple Positions (Quality Control (QC), Clinical & Pharma Operations, Medical Affairs & Review)
- Highlight specific domain competencies relevant to Quality Control (QC), Clinical & Pharma Operations, Medical Affairs & Review directly within your professional summary.
- Quantify your laboratory, clinical, or project experience (e.g., sample throughput, software tools like HPLC/GC/Argus/Rave, or batch volumes).
- Maintain clean single-column chronological layout with zero graphic elements for maximum enterprise ATS readability.
Technical Interview Assessment & Guidance
Q: What is the operational distinction between System Suitability Testing (SST) and Method Validation in HPLC analysis?
Authoritative Answer: System Suitability Testing (SST) is a mandatory daily verification conducted prior to sample analysis to confirm that the complete analytical system (instrument, column, mobile phase, and detector) operates with acceptable precision and resolution. Key SST parameters include Theoretical Plates (>2000), Tailing Factor (<1.5 or 2.0), and %RSD of peak areas across replicate injections (typically ≤1.0% or 2.0%). In contrast, Method Validation (per ICH Q2 R1) is a comprehensive, one-time documented validation proving that a test procedure is suitable for its intended regulatory purpose across parameters including Specificity, Linearity, Range, Accuracy, Precision, LOD, LOQ, and Robustness.
Authoritative Answer: System Suitability Testing (SST) is a mandatory daily verification conducted prior to sample analysis to confirm that the complete analytical system (instrument, column, mobile phase, and detector) operates with acceptable precision and resolution. Key SST parameters include Theoretical Plates (>2000), Tailing Factor (<1.5 or 2.0), and %RSD of peak areas across replicate injections (typically ≤1.0% or 2.0%). In contrast, Method Validation (per ICH Q2 R1) is a comprehensive, one-time documented validation proving that a test procedure is suitable for its intended regulatory purpose across parameters including Specificity, Linearity, Range, Accuracy, Precision, LOD, LOQ, and Robustness.
Q: How do you investigate and document an Out of Specification (OOS) result in accordance with USFDA guidance?
Authoritative Answer: An OOS investigation initiates with Phase I Laboratory Investigation prior to discarding any test solutions. The analyst immediately notifies the QC Supervisor and checks: calculation accuracy, instrument calibration, system suitability compliance, sample dilution/weighing errors, column performance, and chromatographic integration. If a clear laboratory assignable cause is identified with documented proof, the initial test is invalidated and re-testing is performed on the original sample. If no laboratory error is found, Phase II Manufacturing Investigation is launched with QA oversight to audit the batch manufacturing record (BMR), equipment cleaning, raw material lots, and environmental conditions.
Authoritative Answer: An OOS investigation initiates with Phase I Laboratory Investigation prior to discarding any test solutions. The analyst immediately notifies the QC Supervisor and checks: calculation accuracy, instrument calibration, system suitability compliance, sample dilution/weighing errors, column performance, and chromatographic integration. If a clear laboratory assignable cause is identified with documented proof, the initial test is invalidated and re-testing is performed on the original sample. If no laboratory error is found, Phase II Manufacturing Investigation is launched with QA oversight to audit the batch manufacturing record (BMR), equipment cleaning, raw material lots, and environmental conditions.
Q: How are ALCOA+ Data Integrity principles enforced across chromatographic workstations?
Authoritative Answer: ALCOA+ mandates that analytical data must be Attributable (unique user credentials with zero shared logins), Legible (permanent, readable electronic records), Contemporaneous (time-stamped at the moment of execution), Original (first raw data file without manual recalculation or suppression), and Accurate (validated integration methods). The ‘+’ criteria enforce that records must be Complete (including metadata, audit trails, and aborted injections), Consistent (chronological sequence), Enduring (secure archiving), and Available for regulatory inspection throughout the document retention period.
Authoritative Answer: ALCOA+ mandates that analytical data must be Attributable (unique user credentials with zero shared logins), Legible (permanent, readable electronic records), Contemporaneous (time-stamped at the moment of execution), Original (first raw data file without manual recalculation or suppression), and Accurate (validated integration methods). The ‘+’ criteria enforce that records must be Complete (including metadata, audit trails, and aborted injections), Consistent (chronological sequence), Enduring (secure archiving), and Available for regulatory inspection throughout the document retention period.
Mandatory Documents Checklist for Interview & Verification
Ensure you organize the following original credentials and self-attested photocopies for technical interviews and HR onboarding verification:
Curriculum Vitae (2 Hard Copies)
Updated, clean chronological CV featuring core instrumentation, software tools, and role-relevant achievements.
Updated, clean chronological CV featuring core instrumentation, software tools, and role-relevant achievements.
Academic Certificates & Marksheets
Original and self-attested copies of 10th, 12th, Graduation, and Post-Graduation marksheets and degree certificates.
Original and self-attested copies of 10th, 12th, Graduation, and Post-Graduation marksheets and degree certificates.
Government Photo Identification
Original Aadhaar Card and PAN Card (mandatory for statutory PF/ESI registration) plus Passport or Driving License.
Original Aadhaar Card and PAN Card (mandatory for statutory PF/ESI registration) plus Passport or Driving License.
Past 3 Months Salary Slips & Bank Records
Official payslips and corresponding bank statement records validating salary credits (for experienced candidates).
Official payslips and corresponding bank statement records validating salary credits (for experienced candidates).
Relieving & Appointment Letters
Appointment letter and latest increment letter from current firm, plus relieving letters from all prior employers.
Appointment letter and latest increment letter from current firm, plus relieving letters from all prior employers.
Passport Photographs & Professional Registration
4 recent passport-size color photographs, plus State Pharmacy Council registration certificate (where applicable).
4 recent passport-size color photographs, plus State Pharmacy Council registration certificate (where applicable).
Frequently Asked Questions (FAQ)
Q: What is the recruitment mode for these 20 positions at Dr. Reddy’s Laboratories?
Answer: All positions are verified active openings accepting direct candidate submissions through Dr. Reddy’s Laboratories’s official ATS or authorized HR channels.
Answer: All positions are verified active openings accepting direct candidate submissions through Dr. Reddy’s Laboratories’s official ATS or authorized HR channels.
Q: Are freshers eligible to apply for any of these roles?
Answer: Yes, entry-level openings accept recent graduates (0 years experience). Please review the specific experience tag in the table above.
Answer: Yes, entry-level openings accept recent graduates (0 years experience). Please review the specific experience tag in the table above.
Q: Is there any fee or payment required to apply?
Answer: No. Pharma Speed Post and all featured enterprise recruiters operate strictly 100% free recruitment with zero candidate charges.
Answer: No. Pharma Speed Post and all featured enterprise recruiters operate strictly 100% free recruitment with zero candidate charges.
Related Career Pathways & Functional Specializations
Associated functional specializations and recruitment tracks for Multiple Positions (Quality Control (QC), Clinical & Pharma Operations, Medical Affairs & Review) at Dr. Reddy’s Laboratories:
Dr. Reddy’s Laboratories Recruitment 2026Dr. Reddy’s Laboratories Careers IndiaDr. Reddy’s Laboratories Multiple Positions (Quality Control (QC), Clinical & Pharma Operations, Medical Affairs & Review) VacancyMultiple Positions (Quality Control (QC), Clinical & Pharma Operations, Medical Affairs & Review) Jobs in Hyderabad, India, Amritsar, IndiaPharma Quality Control ChemistHPLC GC Dissolution Testing JobsAnalytical Method Validation ChemistPharma QC Walk In Interview 2026Finished Product Testing QC AnalystB Pharmacy Jobs 2026M Pharmacy Pharmacology CareersMSc Chemistry Jobs Pharma IndustryBSc Life Sciences CareersPharma Freshers Jobs 2026Entry Level Clinical Research VacanciesPharma Jobs in Hyderabad, India, Amritsar, India
Application Procedure
- Carefully review the functional eligibility criteria, academic qualifications, and key duties specified for Multiple Positions (Quality Control (QC), Clinical & Pharma Operations, Medical Affairs & Review) at Dr. Reddy’s Laboratories above.
- Calibrate your resume to highlight relevant instrumentation, software platforms, or cGMP/GCP regulatory compliance.
- Ensure your contact details, active mobile number, and email address are up to date in your CV.
- Click the official application button below to access the direct employer recruitment portal or HR email channel with zero intermediary charges.
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