Geforderte Skills
Jobbeschreibung
This contract Process Engineer role supports manufacturing processes and production equipment in a medical-device environment. The core requirements are engineering graduation, hands-on drafting or review of IQ/OQ/PQ process-validation documents, shop-floor equipment knowledge, and capability in continuous improvement, EHS&S, compliance, change management, a
Project overview
This contract Process Engineer role supports manufacturing processes and production equipment in a medical-device environment. The core requirements are engineering graduation, hands-on drafting or review of IQ/OQ/PQ process-validation documents, shop-floor equipment knowledge, and capability in continuous improvement, EHS&S, compliance, change management, audits, and QMS documentation. The structured experience band is 5–7 years; the description also accepts experience from pharmaceutical, consumer, or similar industries, although Medical Device industry is listed as mandatory.
Aurangabad is the stated location, while country and work mode are not specified. No named business or engineering software is provided; familiarity with relevant applications is mentioned generally.
Responsibilities
- Experience in the Medical Device industry or pharmaceutical or consumer or similar industry.
- Demonstrated knowledge of manufacturing principles and practices and procedures.
- Knowledge of specific business practices and software and software applications.
- Hands on exp in drafting/reviewing of IQ/OQ/PQ process validation documents for medical device production equipment in shop floor.
- Good knowledge on process excellence, Internal/External Audits, continuous improvement, EHS&S, Compliance, change management, QMS documentation.
Requirements
- Graduate qualification in Engineering
- Hands-on drafting or review of IQ/OQ/PQ process-validation documents
- Knowledge of production equipment used on the shop floor
- Knowledge of manufacturing principles, practices, and procedures
- Process excellence and continuous improvement
- EHS&S knowledge
- Compliance knowledge
- Change management
- QMS documentation
- Internal and external audit knowledge
- Medical-device industry experience, with related industries accepted as alternatives in the detailed description
- Knowledge of relevant business practices and software applications
Project details
- Start: flexible
- Remote: onsite
- Location: India, IN
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