Senior Research Associate-AD

 Follow GLP, GDP and Data Integrity practices while working in laboratory To perform sampling of raw material and packaging materials as per SOP. Routine analysis of Raw materials, packaging materials, In-process, finished products, Cleaning swabs and Stability samples. To perform preventive maintenance and calibration of the analytical instruments as per calibration schedule. Preparation of technical documents like SOPs, specifications, COA, STP, Validation protocols/reports, Transfer protocols/reports etc. Archival and retrieval of system documents i.e. Instrument logbooks, Registers etc. Reference samples management. Validation and Verification of analytical methods. Reporting of analytical data and submit for review and release. Maintain hygienic condition in respective department. Column Management: Numbering, Issuance and Usage log maintenance of project specific column. Standard Management: Numbering, Issuance and Usage log maintenance of project specific standards. Review of logbooks. Ensure use of Personal Protective Equipment & attend EHS training & send waste to concerned person & comply EHS requirements.

Qualifications

Master in Pharmacy or Science

Required Skills

Data Integrity Expertise in HPLC, GC, UV, Dissolution, PSD, FTIR GLP Method Validation and Verification Preparation of Protocol, Reports, STP

About Us

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.

About The Team

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.Job Info

• Job Identification 9089
• Job Category Analytical Development
• Posting Date 07/18/2025, 05:06 AM
• Degree Level Master's Degree
• Job Schedule Full time
• Locations Plot No:-19,PHARMEZ, Sarkhej-Bawala NH-8A, Ahmedabad, Gujarat, 362001, IN