- 经验
- 任何
- 薪水
- —
- 职位空缺
- 1
- 发布
- 页:1
- Work mode
- 在办公室
- 学历
- Diploma in Pharmacy
- Eligibility
- Candidates with a Diploma in Pharmacy, and preferably a Science or Pharmacy degree, who have entry-level to mid-level experience in pharmaceutical manufacturing or quality assurance, can apply.
- Resume
- Required to apply
Where you'll work
职位描述
Role overview
We are hiring an IPQA Engineer to manage in-process quality assurance across manufacturing activities. The position is focused on making sure products consistently satisfy quality, safety, and regulatory expectations. As a key quality checkpoint inside production, the role involves real-time monitoring, line clearance, inspections, and accurate documentation to help maintain compliant and efficient operations.
You will work closely with teams in Manufacturing, Quality Control, EHS, and Engineering to support right-first-time execution and ongoing improvement.
Location
Rewari, Haryana, India
What you will gain
- A practical role in a GMP-controlled manufacturing setup with direct influence on product quality and patient safety.
- Exposure to the full manufacturing flow, including Borsor, Printing, Inspection, and Packaging.
- Strong exposure to quality systems, SOP adherence, AQL requirements, and data-led decision making.
- Close collaboration with Manufacturing, Quality Control, Quality Assurance, and EHS teams.
- An opportunity to grow a long-term career in quality within a structured, compliance-driven environment.
Key responsibilities
- Carry out in-process quality assurance checks across manufacturing stages in line with approved SOPs and GMP standards.
- Complete line clearance tasks in the Borsor, Printing, and Inspection areas to confirm production readiness.
- Examine and validate the physical, dimensional, and visual characteristics of empty capsule shells at different stages such as Production, Printing, and Inspection.
- Perform AQL inspections and document the outcomes correctly in the approved formats and systems.
- Run PLF testing on retention samples and confirm capsule color, appearance, and overall conformity during production.
- Check batch documentation and ensure observations are recorded in real time with accuracy and compliance.
- Use data-based judgment to help improve productivity while protecting quality standards.
Requirements
- Diploma in Pharmacy is mandatory; a Science or Pharmacy degree is preferred.
- Entry-level to mid-level background in pharmaceutical manufacturing or quality assurance is preferred.
- Working knowledge of GMP, SOPs, AQL standards, and in-process inspection practices.
- Ability to carry out inspections, measurements, and documentation with strong attention to detail.
- Disciplined approach to process compliance and data integrity.
- Basic analytical and problem-solving ability to support improvements in quality and productivity.
- Good communication skills for working effectively with cross-functional teams.
About the company
Lonza operates with a global workforce across more than 30 sites on five continents, where teams collaborate to help manufacture the medicines of tomorrow. The company’s values center on Collaboration, Accountability, Excellence, Passion, and Integrity. It also emphasizes diversity and an inclusive workplace where ideas from people of all backgrounds can contribute to meaningful impact.
Additional information
Reference ID: R75500
The role is based in Haryana, India, with the job location specified as Rewari, India. This position is hands-on and embedded in a manufacturing environment. The source mentions no stipend or salary details, no vacancy count, and no start date.