Research Scientist - ADL at Piramal

Navi Mumbai, maharashtra, India -

Full Time

Start Date

Immediate

Expiry Date

30 Apr, 26

Salary

0.0

Posted On

30 Jan, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Analytical Method Development, Method Validation, Method Transfer, Validation Protocols, Specifications, HPLC, GC, GC-Headspace, Amino Acid Analyzer, Team Management, Customer Interaction, Technical Discussions, Communication Skills, Documentation Skills, GLP Compliance

Industry

Financial Services

Description

Business: PPL Department: Analytical Development Location: Navi Mumbai Travel: Low Job Overview We are seeking an experienced analytical professional with strong expertise in analytical method development and validation for peptide molecules. The role involves independent execution of method validation, method transfer to the manufacturing plant, and preparation of validation protocols, reports, specifications, and STPs. Key and Responsibility: Strong expertise in analytical method development for peptide molecules Ability to independently perform analytical method validation Conduct and/or support method transfer activity to Plant Sound knowledge of preparation of validation protocols and reports Experience in preparing specifications and MOAs (STP) Hands-on experience with HPLC, GC, and GC–Headspace Working knowledge of Amino Acid Analyzer Ability to handle and mentor a team of 2–3 members Capable of handling customer interactions and technical discussions Good communication and documentation skills Conduct instrument calibration and maintain calibration schedules as per the calibration planner Provide technical support during customer audits, discussions, and project meetings Strictly follow departmental systems, safety practices, and discipline while working Complete assigned activities within stipulated timelines Ensure strict adherence to GLP compliance. Preferred candidate profile: Masters/bachelor’s degree in chemistry or a related field. Basic understanding of peptide synthesis principles is a plus. Strong attention to detail and commitment to quality. Ability to work in a team-oriented environment. Good communication and interpersonal skills. Willingness to learn and adapt to new processes. In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth. Driven by its core values, Piramal Group steadfastly pursues inclusive growth, while adhering to ethical and values-driven practices. Equal employment opportunity Piramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, ethnicity, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetics, or other applicable legally protected characteristics. We base our employment decisions on merit considering qualifications, skills, performance, and achievements. We endeavor to ensure that all applicants and employees receive equal opportunity in personnel matters, including recruitment, selection, training, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions, including reasonable accommodation for qualified individuals with disabilities as well as individuals with needs related to their religious observance or practice. Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our customers 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 such as the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products & services, and potent solid oral drug products. PPS also offers development and manufacturing services for biologics including vaccines, gene therapies, and monoclonal antibodies, made possible through Piramal Pharma Limited’s investment in Yapan Bio Private Limited. Our track record as a trusted service provider with experience across varied technologies makes us a partner of choice for innovators and generic companies worldwide.

Responsibilities

The role involves independent execution of method validation, method transfer to the manufacturing plant, and preparation of validation protocols, reports, specifications, and STPs. The candidate will also conduct instrument calibration and provide technical support during customer audits and project meetings.