Opening at Aneta Research Centre for Ph.D, M.Pharm, MSc candidates in AR&D, FR&D

Aneta Pharmaceuticals Incorporated in 2023 as an integrated private sector Pharmaceutical Manufacturer, with a WHO GMP Approved Production facility and GLP qualified stringent Quality Control. The path of success lies in its belief of creativity and no negotiation with the quality of work.

Opening at Aneta Research Centre for Below Position

Manager - Analytical Research and Development
Qualification : M.Pharm / MSC/ Ph.D
Experience : 10 to 18 years of relevant experience in Analytical Research and Development of finished product

Job Profile :
• Setting strategy for evaluating and implementing new technologies within the Analytical Development department, with a particular emphasis on state-of-the-art separation techniques (HPLC/GC/LCMS) and automation
• To develop the analytical method for Finished product - Oral Solids, Oral Liquids
• To develop and Validate Analytical method for Nitrosamines in Finished Product
• To prepare risk assessment for Elemental Risk Assessment / Nitrosamine Risk Assessment / Enivronmental Risk Assessment.
• Communicate with F&D, QC, QA and lead assist in method remediation/trouble shooting
• Authorize issuance and review of Laboratory notebook, SOPs and study reports etc.
• Develop new techniques two expand the analytical capacity
• Coordinate activities with QC, F&D and external contract research organizations / laboratories.
• Develop analytical methods that are accurate, precise, specific, and robust
• Author / review the method validation protocols
• Monitor / Execute method validation and prepare the necessary reports
• Reviews analytical documents / testing records of API, raw materials, stability, and product for accuracy and adherence to test methods.
• To develop the regulatory / QA support documents - FP Specifications, STP, RM Specs, PM Secs.

Trainee Research Scientist / Research Scientist - Analytical Research and Development
Qualification : M.Pharm / MSC / Ph.D
Experience : 01 to 08 years of relevant experience in Analytical Research and Development

Job Profile :
• To develop the analytical method for Finished product - Oral Solids, Oral Liquids
• Communicate with F&D, for testing of finished product / stability samples / API analysis
• To write / record Lab note books, write / review SOPs and study reports
• Coordinate for daily activities with QC, F&D
• Author the method validation protocols
• Execute method validation and prepare the necessary reports
• Prepare analytical documents / testing records of API, raw materials, stability, and product for accuracy and adherence to test methods.
• To prepare the regulatory / QA support documents - FP Specifications, STP, RM Specs, PM Secs.

Trainee Research Scientist / Research Scientist - Formulation Research and Development
Qualification : M.Pharm / Ph.D
Experience : 01 to 08 years of relevant experience in Formulation Research and Development of Oral Solid Dosage forms

Job Profile :
• To perform literature searches and prepare reports, RLD comparison study, development of product considering patent non-
infringing strategy.
• To develop the pharmaceutical oral solids / oral liquids / Semi-Solids Finished product for Regulated / RoW markets.
• To develop the manufacturing process - R&D Scale and Pilot Scale
• To execute product development trials and write / review and maintain Laboratory note books
• To write product development reports
• To prepare risk assessment for Elemental Risk Assessment / Nitrosamine Risk Assessment / Enivronmental Risk Assessment.
• Communicate with F&D, Manufacturing teams, QA and lead assist technology transfer /trouble shooting / process development for technology transfer
• To write Lab notebook, study protocols, reports, SOPs and study reports
• Technology transfer from F&D to pilot scale / manufacturing site.
• Willing to travel for client site visits, technology transfer.
• To work on project timelines.

Asst. Manager to Manager - Formulation Research and Development
Experience - 10 to 18 years of relevant experience in Formulation Research and Development of Oral Solid Dosage forms
Qualification - M.Pharm / Ph.D

Job responsibilities for this position include :
• Setting strategy for evaluating and implementing new technologies within the Formulation Development department, with a particular emphasis on development of Niche technologies / Platform technology / complex generics for Regulated Market
• To perform literature searches, RLD comparison, development strategy, development of product considering patent non-infringing strategy.
• To develop the pharmaceutical oral solids / oral liquids / Semi-Solids Finished product for Regulated / RoW markets.
• To develop the manufacturing process - R&D Scale and Pilot Scale
• To supervise / execute product development trials and write / review and maintain Laboratory note books write product development reports
• To review / prepare risk assessment for Elemental Risk Assessment / Nitrosamine Risk Assessment / Enivronmental Risk Assessment.
• Communicate with F&D, Manufacturing teams, QA and lead assist technology transfer /trouble shooting / process development for technology transfer
• Review / Write Lab notebook, study protocols, reports, SOPs and study reports
• Develop new techniques two expand the F&D technology base / capacity
• Coordinate activities with manufacturing and external contract research organizations / laboratories.
• Technology transfer from F&D to pilot scale / manufacturing site.
• Willing to travel for client site visits, technology transfer.
• To manage team of formulation scientists. Provide technical training and manage product deliverables on time as per project timelines.

Plant / Factory : Aneta Pharmaceuticals Pvt. Ltd
Survey No. 1008/3 & 1008/4, Kamod Preranapith road
Opposite Ashwamegh Industrial Park,
Tal: Daskroi, Dist : Ahmedabad; 382425 (India)