Senior Research Associate - AR&D

Piramal Pharma Ltd; Medak; On-site; INR 600,000 - 1,000,000; Full time

Job summary

Piramal Pharma Ltd invites applications for a Senior Research Associate - AR&D at Digwal. The role focuses on supporting API development and analytical testing under GMP and safety guidelines, with responsibilities spanning method development, validation, and transfer to QC.

The ideal candidate holds an MSc in Analytical Chemistry or related fields with hands-on experience in HPLC, GC, and analytical instrumentation, and is familiar with GLP and 21 CFR Part-11.

Qualifications

• MSc in Analytical Chemistry or related discipline required.
• Hands-on experience with HPLC/GC and analytical instrumentation.
• Familiarity with GLP and 21 CFR Part-11 compliance preferred.

Responsibilities

• Capable to handle independent projects.
• Analytical testing support to PDG synthetic group.
• Coordinate with QA regarding method transfer, CCF and investigation reports.
• Experience with HPLC, GC, Potentiometer, Polarimeter instruments.
• Analytical method development, validation and transfer to QC.
• Prepare method transfer protocol and reports, as well as validation reports.
• Maintain GLP practices and SOPs; ensure compliance with safety.

Skills

HPLC

GC

Method development

Method validation

Method transfer

Polarimeter

Potentiometer

GLP

21 CFR Part-11

QA coordination

Education

MSc in Analytical Chemistry / Chemistry

Job description

Job DescriptionSenior Research Associate - AR&DJob Description Business: PPL Digwal Department: PTS Location: Digwal Job Overview: To perform AR&D actives as per GMP & Safety Travel Requirements: NA Reporting Structure: Reports to Research Scientist - AR&D (Service) Key Stakeholders: Internal: QC, QA, SCM & Safety External: NA Experience:

• 4-8 Year Experience in manufacturing (API) as per Pharma Manufacturing GMP requirements.
• Responsibilities for Internal Candidates Key Roles & Responsibilities 1. Capable to handle independent projects 2. Analytical testing support to PDG synthetic group. 3. Coordinate with QA regarding method transfer, CCF and investigation reports. 4. Experience of handling of HPLC, GC, Potentiometer, Polarimeter instruments. 5. API Stability knowledge. 6. Capable to handle analytical method development, Implementation, Validation as per requirement. 7. Should have experience of Analytical method transfer to QC. 8. Experience of making documents like method transfer protocol & report, method validation protocol & report, method development report, specification, standard test procedure etc. 9. Should aware about GLP practices and 21 CFR part-11. 10. Keep the work area clean and the laboratory under controlled temperature. 11. Calibrate the instruments according to the master calibration schedule and follow GLP and SOPs. 12. Understand the safety and environmental aspect. 13. Maintain the reagents and standardize the volumetric solutions as per schedule. 14. Maintain the laboratory journals and instrument log books online. 15. Ensure compliance to Hazardous waste and chemical management. Essential Qualification Qualification : M.Sc (Analytical Chemistry), (Chemistry) & (Organic Chemistry)Full time