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Job Details

Project Engineer pharmaceutical/biopharmaceutical

Location
Ridgefield, NJ, United States

Posted on
Aug 13,2019

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Experience in pharmaceutical/biopharmaceutical industry.
Experience in cGMP environment, including commissioning, qualification and validation.
Well-develop.
Experience in cGMP environment, including commissioning, qualification and validation.
Well-developed communication skills, both verbal and written.
Based on level, should have demonstrated experience managing teams consisting of internal staff, supervising engineering and construction activities, and preparing turnover documentation from C execution and as-built drawings.
Based on level, demonstrated project controls skills such as estimating, scheduling and cost reporting.
Larger projects may require earned value/progress tracking systems.
Leadership skills.
Proficient with Microsoft Office products (Excel, Word, PowerPoint, stc.)
Skills: Knowledgeable in auto CAD, PLC, and HMI programming.
Job Types: Full-time, Contract Experience: commissioning, qualification and validation: 3 years (Preferred)
Cost Reporting: 1 year (Preferred)
cGMP environment: 3 years (Preferred)
Education: Bachelor's (Required)
Location: Ridgefield, NJ 07657 (Preferred)
Work authorization: United States (Required)
Contract Renewal: Likely
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Project Engineer (pharmaceutical/biopharmaceutical)
**MEMBERS ONLY**SIGN UP NOW***.
Ridgefield, NJ
11 hours ago
Full-time | Contract
Estimated: $65,000 - $89,000 a year
&partnerApiToken=3104322b831a591659ae09f5428af3cc9663a7cb28ac7a65daecf96494dc4549&
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Education
Bachelor's Degree
Skills
Mechanical Engineering Experience
Construction Estimating
Microsoft Word
AutoCAD
Microsoft Office
Job Title: Project Engineer I
Job Location: Ridgefield, NJ
Duration: 06+ Months Contract
Duties:
BS in chemical or mechanical engineering, or related degree supplemented with relevant experience.
Experience in pharmaceutical/biopharmaceutical industry.
Experience in cGMP environment, including commissioning, qualification and validation.
Well-develop.
Experience in cGMP environment, including commissioning, qualification and validation.
Well-developed communication skills, both verbal and written.
Based on level, should have demonstrated experience managing teams consisting of internal staff, supervising engineering and construction activities, and preparing turnover documentation from C execution and as-built drawings.
Based on level, demonstrated project controls skills such as estimating, scheduling and cost reporting.
Larger projects may require earned value/progress tracking systems.
Leadership skills.
Proficient with Microsoft Office products (Excel, Word, PowerPoint, stc.)
Skills:
Knowledgeable in auto CAD, PLC, and HMI programming.
Job Types: Full-time, Contract
Experience:
commissioning, qualification and validation: 3 years (Preferred)
Cost Reporting: 1 year (Preferred)
cGMP environment: 3 years (Preferred)
Education:
Bachelor's (Required)
Location:
Ridgefield, NJ 07657 (Preferred)
Work authorization:
United States (Required)
Contract Renewal:
Likely
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data-indeed-apply-joburl=****data-indeed-apply-coverletter=optional>
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