Career Opportunity: IPQA Executive Walk-In Interview for Sterile Injectable Manufacturing
A rapidly expanding pharmaceutical company, a leader in the development and manufacturing of sterile injectable products, is actively seeking skilled professionals to join its dynamic team. With cutting-edge manufacturing facilities and a deep-rooted commitment to quality, strict regulatory compliance, and continuous innovation, this organization plays a significant role in both domestic and international markets. This presents an excellent career pathway for pharmaceutical experts eager to cultivate their proficiency in Quality Assurance, In-Process Quality Assurance (IPQA), and sterile manufacturing operations.
The company is pleased to announce a walk-in interview for the pivotal role of IPQA Executive.
Position and Company Overview:
- Company: Maiva Pharma Private Limited
- Position: IPQA Executive
- Department: IPQA (In-Process Quality Assurance)
- Experience: 1–5 Years
- Job Location: Hosur, Tamil Nadu
- Industry Focus: Pharmaceutical – Sterile Injectables
Required Educational Qualification:
Prospective candidates for the IPQA Executive position should hold one of the following academic qualifications: B.Pharm, M.Sc., M.Pharm, or B.Tech.
Core Responsibilities and Skills:
The chosen candidate will undertake various essential IPQA activities crucial to sterile injectable manufacturing. Key responsibilities include ensuring thorough line clearance prior to batch execution, conducting rigorous in-process quality checks, and real-time production monitoring, which encompasses both visual inspections and CCTV oversight. The role also involves granting clearance for the proper disposal of documents, meticulously preparing and reviewing Standard Operating Procedures (SOPs) and protocols, upholding stringent compliance with Good Manufacturing Practices (GMP) and overarching quality standards, and diligently verifying all documentation and batch records.
Eligibility Requirements:
Applicants must possess 1–5 years of pertinent pharmaceutical experience. Individuals with a proven track record in Production, Quality Assurance (QA), Quality Control (QC), or IPQA functions within a sterile injectable pharmaceutical manufacturing environment are particularly encouraged to attend. Candidates who can join immediately will receive preferential consideration. A robust understanding of GMP, accurate documentation practices, and in-process quality assurance principles is fundamental.
Walk-In Interview Schedule and Venue:
- Date: 23 July 2026 (Thursday)
- Time: 10:00 AM – 01:00 PM
- Venue: Maiva Pharma Private Limited, 32, SIPCOT Industrial Complex, Phase I, Hosur, Tamil Nadu – 635126
Documents Essential for Interview:
All attendees are required to bring a current resume, their latest increment letter, salary slips for the last three months from their present employer, relieving and service certificates from previous organizations, all relevant educational certificates, Aadhaar Card, and PAN Card.
Why Consider Joining This Organization?
This opportunity provides an excellent platform to contribute to a rapidly expanding sterile injectable pharmaceutical company. It offers valuable exposure to advanced IPQA and sterile manufacturing processes within a professional work environment dedicated to quality and compliance. Employees can expect significant career growth and continuous learning alongside experienced pharmaceutical manufacturing professionals.
Important Considerations for Candidates:
Candidates with direct experience in Production, Quality Assurance (QA), Quality Control (QC), or IPQA within a sterile injectable manufacturing facility are strongly advised to participate in the walk-in interview. Immediate joiners are highly preferred. Please ensure all necessary documents are brought for verification and arrive at the venue within the specified interview time.
Contact Information:
Email: sathishkumar.v@maivapharma.com
Mobile: 7708426169, 7550150702
