Manufacturing Engineer

Company Description

A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Job Description

Description:

Designs, specifies and installs new equipment and provides engineering technical support and troubleshooting for all cell culture, purification and processing equipment. Provides project engineering as required for new processing equipment installations and modifications to existing equipment. Able to manage small engineering projects with little direction. Works with and provides some direction to contractors. Participates in multi-function teams to implement change and improve on existing processes. 

Job Duties: 

• Provides responsible engineering support for a single area of a manufacturing facility containing processing & support equipment 

• Troubleshoots equipment systems and supports associated automation system troubleshooting efforts. 

• Identifies and leads equipment related projects, including technology transfers, capital projects, and modifications. 

• Develops and supports equipment commissioning and qualification (validation) activities. 

• Maintains personal training, goal development / completion, compliance workflow tracking, & progress tracking. 

• Assesses equipment needs and generates equipment user requirement specifications for fabrication or purchase 

• Helps implement new manufacturing processes and technology transfers as needed for new products or modifications to existing products. 

• Investigates process or equipment failures and implements changes to avoid future occurrences. 

• Manages and tracks completion timelines for compliance tasks (change controls, deviation investigations, corrective & preventive actions) 

• Supports creation of new procedures for equipment and systems in Engineering and Manufacturing. 

Experience Requirements:

• 2 – 3 years’ experience in pharmaceutical or biotech manufacturing environment 

Skills and Qualifications: 

• Practical knowledge and application of GMP and EMEA regulations. 

• Two to three years’ experience in pharmaceutical or biotech manufacturing environment 

• Competency in Delta V, MS Word, MS Excel, MS Power Point and MS Project. 

• Excellent oral and written communication skills. 

• Ability to work rotating shifts, extended shifts and weekends as needed. 

• Assignments are moderately complex in nature where ability to recognize deviation from accepted practice is required. Judgment is required in resolving problems & making routine recommendations. 

• Broad understanding of the detailed aspects of the job. 

• Applies job skills and company policies and procedures to complete a variety of tasks.

Qualifications

Education Requirements:

• Bachelor’s Degree with a minimum of 2 - 3 years related industry experience, or an MBA/MS 

Additional Information

Ankita Teja

Technical Recruiter

Integrated Resources Inc.

IT REHAB CLINICAL NURSING

Inc. 5000 – 2007-2014 (8th Year)

Certified MBE I GSA - Schedule 66 I GSA - Schedule 621I I GSA - Schedule 70

Tel: 732-429-1919

Fax: 732-549-5549