MPharma QA Jobs – Research Assistant Jobs, Research Associate Jobs at Accuprec Research Labs Pvt. Ltd.
Job Title: Research Assistant / Research Associate – QA Department
Company: Accuprec Research Labs Pvt. Ltd.
Location: Opp. Zydus Pharmez, Nr. Matoda Patiya, Post: Matoda, Ahmedabad, Gujarat – 382213
Department: Quality Assurance (QA)
Experience: 2–5 Years
Qualification: M.Pharm (QA) / M.Sc
Employment Type: Full-Time, On-site
Preference: Male candidates (as per department requirement)
Job Overview:
Accuprec Research Labs Pvt. Ltd. is looking for a motivated and detail-oriented QA professional to support quality assurance activities across GLP-regulated laboratory operations. The role involves documentation review, audits, compliance monitoring, and ensuring adherence to SOPs and regulatory standards.
Key Responsibilities:
-
QA Documentation & Review
• Review and maintain QA-related documents including SOPs, protocols, reports, and logs.
• Check batch records, raw data, and technical documents for accuracy and compliance.
• Ensure timely updating, issuance, and archival of controlled documents. -
SOP & Compliance Oversight
• Ensure all departments follow updated SOPs, guidelines, and internal quality procedures.
• Initiate, draft, revise, and assist in developing new SOPs as required. -
Internal Audits & Quality Checks
• Conduct internal audits to verify compliance with GLP and QMS standards.
• Identify deviations, non-conformities, and corrective actions.
• Follow up on CAPA implementation across departments. -
QMS Support & Monitoring
• Assist in maintaining and improving Quality Management Systems (QMS).
• Monitor laboratory operations to ensure adherence to data integrity and documentation practices.
• Support external audits, inspections, and regulatory assessments. -
Cross-Functional Coordination
• Coordinate with QC, QA, AD, Production, and other departments for document control and audit preparation.
• Provide QA guidance to lab personnel regarding compliance and documentation.
Required Skills & Competencies:
• Strong knowledge of QA documentation, SOP management, and GLP/QMS compliance.
• Good understanding of laboratory workflows (QC/AD).
• Excellent attention to detail and ability to review scientific documents.
• Strong communication and coordination skills.
• Familiarity with audit processes and regulatory expectations.
• Ability to work in a documentation-driven environment.
Preferred Candidate Profile:
• 2–5 years of experience in QA/GLP/QAU roles within pharmaceutical or research laboratories.
• Male candidate preferred as per department operational needs.
• Candidates familiar with regulatory audits (e.g., GLP, NABL) will have an advantage.
• Ability to join within a short notice period is preferred.
