Quality Assurance Job at Piramal Pharma Solutions | Apply Now
A unique opportunity in Piramal Pharma careers has arisen for an Executive – Quality Assurance at Piramal Pharma Solutions in Turbhe, MH. This role offers a chance to ensure compliance with quality systems and regulatory standards within a dynamic manufacturing environment.
About The Company
Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. The organization serves clients through a globally integrated network of facilities in North America, Europe, and Asia. This enables Piramal to offer a comprehensive range of services, including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, and the commercial supply of APIs and finished dosage forms. The company also specializes in the development and manufacture of Highly Potent APIs and Antibody Drug Conjugation.
- Job Title: Executive – Quality Assurance
- Location: Turbhe, MH
- Division: Piramal Pharma Solutions
- Job Requisition ID: R00004310
Piramal Pharma Careers: Job Description
The Executive – Quality Assurance is responsible for ensuring compliance with quality systems, cGMP requirements, and regulatory standards within the manufacturing environment. The role involves the review of production and quality control documentation, validation activities, annual product reviews, quality management system processes, and cross-functional coordination to maintain product quality and compliance. This Executive Quality Assurance role supports continuous improvement initiatives, documentation management, regulatory readiness, and adherence to Environmental Health & Safety (EHS) requirements.
Key Responsibilities
- Review of executed BMR, ECR and Analytical Raw Data.
- Review of BMR, ECR and MMF in Ensur Software.
- Preparation of Process validation protocol & report and Monitoring of process validation activities.
- Dispatch and line clearance activity.
- Preparation and review of SOPs.
- Preparation of Annual Product Review.
- Handling Cleaning Validation.
- Review of Analytical data, Audit Trail and Batch release.
- Initiation of Deviations, Change controls whenever required.
- Issuance, archival and retrieval of documents in R&D and ADL.
- Management of quality-related activities in R&D and ADL.
- Review and approval of R&D and ADL documents.
Eligibility Criteria
Qualification: M.Sc (Chemistry) / B. Pharm / M. Pharm
Experience: 1-3 years
Skills and Competencies:
- Good knowledge of cGMP, GDP, and pharmaceutical quality systems.
- Experience in BMR, ECR, MMF, and analytical data review.
- Understanding of Quality Control analytical documentation and data integrity requirements.
- Familiarity with Annual Product Review (APR/PQR) preparation and documentation.
This Piramal Pharma careers opportunity at Piramal Pharma Solutions presents a significant opportunity for qualified candidates to contribute to the quality assurance processes in a leading pharmaceutical organization. Interested individuals are encouraged to apply before the deadline to seize this opportunity.
