Executive - Quality Control at Piramal Pharma Ltd

, , India -

Full Time

Start Date

Immediate

Expiry Date

20 Jun, 26

Salary

0.0

Posted On

22 Mar, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality Control, Raw Materials Analysis, Finished Products Analysis, Stability Samples Analysis, cGMP, HPLC, GC, UV, IR, GLP, Data Entry, Solution Preparation, Standardization, Training

Industry

Pharmaceutical Manufacturing

Description

Be the First to Apply Job Description Executive - Quality Control• Timely analysis of Raw Materials / Finished Products / Stability Samples and completion of related documentation for release of Raw Materials / Finished Products / Stability Samples for use in Production and compliance/ HPLCJob Description • Analysis of Raw Materials / Finished Products / Stability Samples and related documentation as per cGMP requirement. • Ensure analysis of Raw Materials / Finished Products as per requirement from Outside Commercial Lab. • Analysis of Vendor Approval samples. • Preparation and Standardization of Solution, as and when required. • Implementation of GLP / GMP requirements. • Allocate works to workmen and trains them. • Review of laboratory chemicals. • Entry of data in system. • Responsible for only run the method in the HPLC , GC , UV and IR , does not access to Change the method , report format , cancellation of any run, or system and method configuration Key Responsibilities • Analysis of Raw Materials / Finished Products / Stability Samples and related documentation as per cGMP requirement • Entry of data in system. • Ensure analysis of Raw Materials / Finished Products as per requirement from Outside Commercial Lab. • Analysis of Vendor Approval samples. • Review of laboratory chemicals. • Responsible for only run the method in the HPLC, GC, UV and IR, does not access to Change the method, report format, cancellation of any run, or system and method configuration. • Preparation and Standardization of Solution, as and when required. • Implementation of GLP / GMP requirements. • Allocate works to workmen and trains them. Essential Qualification Qualification:- Minimum Graduate / Post Graduate with chemistry background, having technical background is preferred. Experience:- More than 5 years in manufacturing operations Introduce yourself to our recruiters and we'll get in touch if there's a role that seems like a good match. Piramal Pharma Limited, offers a portfolio of differentiated products and services through its 17 global development and manufacturing facilities and a global distribution network in over 100 countries. PPL includes Piramal Pharma Solutions (PPS), an integrated Contract Development and Manufacturing Organization; Piramal Critical Care (PCC), a Complex Hospital Generics business; and the India Consumer Healthcare business, selling over-the- counter products. In addition, one of PPL’s associate companies, AbbVie Therapeutics India Private Limited is a JV with AbbVie Inc. and has emerged as one of the market leaders in the ophthalmology therapy area. Further, PPL has a minority investment in Yapan Bio Private Limited. In October 2020, PPL received a 20% strategic growth investment from the Carlyle Group. PPL provides equal employment opportunities to all employees and applicants for employment. It prohibits discrimination and harassment based on race, color, age, sex, religion, national origin or ethnicity, disability status, genetics, protected veteran status, sexual orientation, gender identity, or expression, or any other characteristic protected by applicable law. Our employment decisions are based on merit considering qualifications, skills, performance, and achievements. Equal employment opportunity applies to all terms and conditions of employment, including recruitment, selection, training, social programs, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions.

Responsibilities

The Executive - Quality Control is responsible for the timely analysis of Raw Materials, Finished Products, and Stability Samples according to cGMP requirements, including completing all necessary documentation for product release. Key duties involve running methods on analytical instruments like HPLC, GC, UV, and IR, and allocating and training workmen.