Piramal Pharma

CDMO and hospital generics, consumer health

Senior Research Associate - AR&D

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours

Full-timeMedak, IndiaNo salary listedIn-person

About the Job

Requirements

Four to eight years of experience in API manufacturing in accordance with pharmaceutical Good Manufacturing Practice (GMP) requirements.
Ability to handle projects independently.
Experience handling high-performance liquid chromatography (HPLC), gas chromatography (GC), potentiometer, and polarimeter instruments.
Knowledge of API stability.
Ability to perform analytical method development, implementation, and validation.
Experience transferring analytical methods to quality control (QC).
Experience preparing method transfer protocols and reports, method validation protocols and reports, method development reports, specifications, and standard test procedures.
Awareness of Good Laboratory Practice (GLP) and 21 CFR Part 11.
Understanding of safety and environmental aspects.
Master of Science (M.Sc.) in Analytical Chemistry, Chemistry, or Organic Chemistry.

Responsibilities

Provide analytical testing support to the process development group synthetic group.
Coordinate with Quality Assurance (QA) regarding method transfer, CCF, and investigation reports.
Keep the work area clean and maintain the laboratory at controlled temperature.
Calibrate instruments according to the master calibration schedule and follow GLP and standard operating procedures (SOPs).
Maintain reagents and standardize volumetric solutions according to schedule.
Maintain laboratory journals and instrument logbooks online.
Ensure compliance with hazardous waste and chemical management.

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Job Description

Senior 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

About the Company

Piramal Pharma

CDMO and hospital generics, consumer health

Piramal Pharma is a diversified pharmaceutical group with three divisions: Piramal Pharma Solutions (PPS), Piramal Critical Care (PCC), and the Consumer Products Division (CPD). PPS operates as a contract development and manufacturing organization, providing development and manufacturing services across the drug lifecycle for clients in North America, Europe, and Asia through a globally connected network. PCC specializes in complex hospital generics, particularly inhaled anesthetics, serving markets in the USA, Europe, and over 100 countries. CPD leads consumer healthcare in India with brands such as Littles, Lacto Calamine, i-pill, Tetmosol, Polycrol, and Tri Activ, and the company serves pharmaceutical companies, hospitals, and consumers by leveraging its manufacturing scale and distribution network.

Company size: 1,001-5,000
Company stage: IPO
Headquarters: Maharashtra, India
Founded: 2020

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