Process Project Engineer

Role & responsibilities

Job Title: Project Engineer

Overall exp-6-8 Years

Location- Aurangabad

Domain-Medical Device industry or pharmaceutical or consumer or similar industry

Qualification-Bachelors degree with minimum 6 to 8 years of experience in Engineering/Industrial/Electrical/Biotechnology Engineering (related stream).

Mandatory Skills: Medical Device industry, manufacturing principles, Six Sigma tools for process improvements, Statistical Data Analysis, critical path, capacity modeling, time and motion studies.

Shift Timings-Candidates should be flexible for any shift based on project criteria.

Detailed JD:

• 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.
• Knowledge of Six Sigma tools for process improvements
• Statistical Data Analysis: Utilizes analytical approach to evaluate product/process data
• Demonstrates good knowledge of Quality and Compliance.
• Knowledge of Financial systems, ROI Analysis, Standard costs and planning values
• Demonstrates sound knowledge of cycle time modelling covering critical path, capacity modeling, time and motion studies.
• Good knowledge of vacuum technology, PLC programming, electrical and mechanical engineering, packaging process and package design. .

Job Title: Process Engineer

Location- Aurangabad

Experience Level-5-7 Years

Domain-Medical Device industry

Qualification- Graduate in Engineering

Mandatory Skills: IQ/OQ/PQ process validation documents, production equipment in shop floor, continuous improvement, EHS&S, Compliance, change management, QMS documentation. Medical Device industry

Detailed JD:

• 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.