Latest Pharma Job Opportunity 2026 | Intas is hiring for Assistant Manager -Quality Assurance Role | Apply Now
Looking for promising Quality Assurance Jobs in the pharmaceutical industry? Intas Pharmaceuticals is offering an excellent Pharma Job opportunity for professionals seeking career growth in global regulatory compliance and audit management. This Quality Assurance Jobs opening allows candidates to work in a highly regulated biopharma environment with exposure to international standards like USFDA and EMA, making it an ideal Pharma Job for experienced QA professionals.
- Job Title: Assistant Manager – Quality Assurance
- Job Requisitions No.: 16028
- Location: Biotech, Ahmedabad, Gujarat, India – 382213
About the Company
Intas Pharmaceuticals does not request or accept any fees during the recruitment process. If someone asks for payment on their behalf, it is a scam. Candidates are advised to report such incidents to local police or cybercrime authorities.
Intas is a leading global pharmaceutical company specializing in the development, manufacturing, and marketing of pharmaceutical formulations. The mission of the company is to address unmet medical and societal needs through a fully integrated pharmaceutical value chain spanning across the world.
Job Description
Competencies
- Intas – Problem Solving
- Intas – Action Oriented
- Intas – Dealing with Ambiguity
- Intas – Customer Focus
- Intas – Time Management
Purpose of Job
- Audit and Compliance, Quality Technical Agreement, Gap Assessment, Extended CAPA
Key Responsibilities
- Drive the self-inspection program at the Intas-Biopharma site. Ensure the self-inspection program runs as per the defined schedule.
- Perform a risk assessment to determine the frequency of the self-inspection. Ensuring the appropriate CAPAs are identified and implemented appropriately.
- Management of external quality audits. Responsible for facilitating the management of backroom, coordinating the auditors’ requests, working as a scribe during audits, and preparing responses.
- Tracking and follow-up of internal and external audit CAPA.
- Verification of the effectiveness of internal and external audit CAPAs.
- Provide the necessary information/support to the health authority, business partner, and customer as per regulations and agreement, respectively.
- Preparation and review of the Quality Technical Agreement with the business partner/Customer. Follow up and track the renewal of the Agreement with stakeholders.
- Gap assessment of corporate guidelines, other site audit observations, and regulatory guidelines.
- Gap assessment of extended CAPA from the other site and tracking of CAPA.
- Responsible for the preparation, review, and revision of SOPs related to audit and compliance.
Qualification
- Post Graduate in Pharmacy, Biotechnology, Microbiology, or Biochemistry.
Relevant skills
- Having exposure to USFDA and EMA Audits.
