Senior Executive at Piramal Pharma Ltd

, , India -

Full Time

Start Date

Immediate

Expiry Date

14 Aug, 26

Salary

0.0

Posted On

16 May, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Stability Analysis, cGMP, HPLC, Dissolution Testing, Karl Fischer (KF), UV-Vis Spectroscopy, IR Spectroscopy, Data Integrity, GLP, Physical Testing, Documentation, Laboratory Management

Industry

Pharmaceutical Manufacturing

Description

Be the First to Apply Division Piramal Pharma Solutions Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia. This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation. Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide. For more details, please visit : www.piramalpharmasolutions.com Job Title Senior Executive Job Description Analysis of stability sample, finished product and related documentation as per cGMP. Analysis of stability sample, finished product and related documentation as per cGMP. Responsible for only run the method in the KF Instrument , Dissolution Instrument , UV Instrument , HPLC, does not access to change the method, report format and method configuration. Responsible to perform Dissolution testing, KF apparatus, IR, UV, Friability, DT, pH and physical testing etc. Maintenance of stability incubators & chamber. Preparation of stability monthly planner. Receipt/Inward/Storage of QC samples. Concurrent documentation of analytical records and storage of raw data, online entries in Instrument/ Equipment’s usage log books. Instant reporting in case of any deviation, incident, OOT or OOS to Section Head/ Head QC. Any additional responsibility assigned by section head. Maintenance of Bin Card of chemical store. Follow of GLP / GMP requirements. maintain QC Laboratory Records. (Like Laboratory note Book, COA and SSR etc.). Support to site DICO (Data Integrity Compliance Officer) for monitoring and implementation of actions related to Data Integrity awareness at site. 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

Perform analysis of stability samples and finished products using various laboratory instruments such as HPLC and UV. Maintain stability incubators, manage QC sample storage, and ensure all analytical records comply with cGMP and GLP standards.