Piramal QA Job as Senior Executive in DQA, Pharmacy candidates – Apply Online!
Looking for a rewarding Quality Assurance career in the pharmaceutical industry? Piramal Pharma Solutions is hiring a Senior Executive – DQA at its Medak, Telangana location. If you’re a qualified Pharmacy or Science graduate with a passion for quality systems in R&D, this is your chance to join a global leader in contract development and manufacturing.
About the Piramal:
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.
- Job Posting: Senior Executive – DQA
- Location: Medak, Telangana, India
Job Description:
Key Roles & Responsibilities:
- Oversee and support the overall activities during the product development life cycle from quality perspective in R&D (API and intermediates).
- To understand the site needs with respect to system establishment and sustainability.
- Author/ Review and approve the SOPs/work directions required for implementing the Quality systems in R&D activities as per GLP and regulatory requirements. Ensure effective implementation of SOPs/ work directions.
- Review and approve Lab Familiarization Reports (LFR), Product development reports (PDR), Technology transfer, product specifications & STPs, analytical method validation, method transfer, qualification, calibration, process validation protocol and reports. Ensure effective execution of these activities.
- Periodic audits of R&D laboratory. Ensure online documentation and review lab notebooks, PDR/LFR documents, analytical documents and stability data.
- Effective maintenance of R&D records, distribution and archival systems.
- Perform cGMP audit of R&D facilities and operations. Assist the team in auditing contract manufacturers/ vendors/ contract testing laboratory.
- Ensure R&D team is trained for their relevant job function and GMP/GLP training.
- Provide quality related inputs to new projects, existing project, upgradations etc.
- Participate in identification of key starting material (KSM)/registered starting material (RSM) and ensure that it is correctly identified.
- Participate in handling of OOS, OOT, Deviations, Batch failures, investigations and CAPA implementation at site.
- Establish raw material standards by studying manufacturing/R&D requirements-conferring with suppliers.
- Responsible to follow the safety and environmental procedures deployed in the site.
Qualifications:
Graduation and above in Science / Pharmacy
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. PPS also offers development and manufacturing services for biologics including vaccines, gene therapies, and monoclonal antibodies.
Equal Employment Opportunity
Piramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer. We base our employment decisions on merit considering qualifications, skills, performance, and achievements.
If you are interested in joining our team, please apply for the Senior Executive – DQA position here.
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