Industry: Medical Device / Pharmaceutical / Consumer / Similar Manufacturing Industry
Notice Period: Immediate to 15 Days Preferred
Employment: Contract Prospect with a Leading MNC
Customer Interview: Yes
Role OverviewWe are looking for an experienced Process Engineer with manufacturing industry experience, preferably in the Medical Device industry.
The candidate should have hands-on experience in drafting and reviewing IQ/OQ/PQ process validation documents for production equipment on the shop floor, along with knowledge of process excellence, continuous improvement, compliance, and QMS documentation.
Key Responsibilities
- Draft and review IQ/OQ/PQ process validation documents for medical device production equipment.
- Support process validation activities on the manufacturing shop floor.
- Apply manufacturing principles, practices, and procedures.
- Drive process excellence and continuous improvement initiatives.
- Support internal and external audits.
- Ensure EHS&S; and regulatory compliance requirements are followed.
- Manage and support engineering change management activities.
- Prepare, review, and maintain QMS documentation.
- Work with manufacturing teams to improve production processes and operational efficiency.
Mandatory Skills
- Hands-on experience in IQ/OQ/PQ process validation documentation.
- Experience with production equipment on the shop floor.
- Medical Device industry experience.
- Knowledge of manufacturing principles and practices.
- Continuous Improvement / Process Excellence.
- EHS&S; and Compliance.
- Change Management.
- QMS Documentation.
- Internal and External Audits.
Preferred Industry Experience
- Medical Device Manufacturing.
- Pharmaceutical Manufacturing.
- Consumer Manufacturing.
- Similar manufacturing industries.
QualificationGraduate in Engineering. Additional Requirements
- Strong documentation and analytical skills.
- Good communication and coordination skills.
📌 SMS Process Engineer (Aurangabad)
🏢 CSbusinesmgmt.in
📍 Aurangabad
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