Piramal Pharma Apprentice QA Recruitment in Ahmedabad

Piramal Pharma Solutions Hiring Apprentice QA in Ahmedabad

Piramal Pharma Solutions is inviting applications for the Apprentice QA position in Ahmedabad, Gujarat. This full-time opportunity is within the Quality Assurance (QA) function and focuses on GMP documentation, document control, archival and retrieval of quality records, and monitoring retention sample storage. Candidates interested in pharmaceutical quality assurance and documentation management can review the eligibility details and apply through the official careers portal.

Company Overview

Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO) offering drug development and manufacturing services across the pharmaceutical product life cycle. Its services include drug discovery, pharmaceutical development, clinical trial supplies, and commercial manufacturing of active pharmaceutical ingredients (APIs) and finished dosage forms.

The company also provides specialized capabilities in highly potent APIs and antibody-drug conjugation, serving innovator and generic pharmaceutical companies worldwide.

Job Details

Job Role and Responsibilities

The Apprentice QA will support pharmaceutical quality assurance activities, particularly document control, Good Manufacturing Practice (GMP) documentation, and Quality Management System (QMS) record maintenance.

Key responsibilities include:

• GMP Document Control: Issue, control, maintain, and manage quality documents, including Standard Operating Procedures (SOPs), Batch Manufacturing Records (BMRs), Batch Packaging Records (BPRs), formats, logbooks, and laboratory notebooks (LNBs).
• Document Archival and Retrieval: Organize and archive controlled documents and retrieve records when required for operational or compliance purposes.
• QMS Record Maintenance: Update and maintain records associated with change controls, deviations, Out-of-Specification (OOS) events, and other quality-related activities.
• Retention Sample Monitoring: Monitor and record storage temperatures for retention samples to support proper storage conditions.
• Audit Preparation: Arrange relevant documents before audits and ensure records are available promptly during audit activities.
• Documentation Follow-up: Coordinate follow-ups to maintain updated and accessible quality records.

Eligibility and Relevant Qualifications

The supplied job listing does not specify the exact educational qualification or prior experience required for this apprenticeship. Candidates should verify these requirements in the official application before applying.

Relevant educational backgrounds to consider for a pharmaceutical QA documentation role may include:

• B.Pharm
• M.Pharm
• B.Sc. or M.Sc. in Chemistry
• Other relevant pharmaceutical or life sciences qualifications, if accepted in the official listing

Knowledge of GMP documentation, SOPs, document control, and pharmaceutical quality systems can be useful for this role. These are relevant skills rather than confirmed mandatory requirements from the supplied job description.

Key Skills for Apprentice QA

Candidates interested in pharmaceutical Quality Assurance should understand the importance of accurate documentation and controlled record management in regulated manufacturing environments.

Relevant skills include:

• GMP documentation and good documentation practices
• SOP issuance and document control
• Document archival and retrieval
• Quality Management System (QMS) records
• Change control and deviation documentation
• OOS record management
• Logbook maintenance
• Audit documentation and record retrieval
• Retention sample storage monitoring

How to Apply

Interested candidates can submit their applications through Piramal Pharma Solutions’ official recruitment portal.

Apply Online: Piramal Pharma Solutions Apprentice QA Recruitment

Review the official listing for the latest eligibility criteria and any additional application instructions before submitting your details.

Job Summary