Process Engineer 1 at Cambrex
Charles City, IA 50616, USA -
Full Time


Start Date

Immediate

Expiry Date

05 Dec, 25

Salary

0.0

Posted On

06 Sep, 25

Experience

3 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Word Processing, Chemical Engineering, Windows

Industry

Mechanical or Industrial Engineering

Description

Overview:
The Process Engineer I will be responsible for implementation of projects for the manufacture of APIs and bulk intermediates and other products from development through piloting and/or commercial production.

Responsibilities:

  • Writing batch records, cleaning records, SOPs, campaign reports, supplements, and investigation/deviation reports as needed to support production operations
  • Monitoring KPIs and using process data to identify and execute improvements to new and existing products to achieve improved yields, quality or customer expectations
  • Working with process improvement to identify and execute Kaizen events
  • Providing training and process support to production areas including training on new processes and on-site oversight of key processing steps
  • Working in a team environment that includes cross-departmental participation from Engineering, Research and Development, Regulatory, Quality Control, Analytical Development and Operations
  • Developing plans for production of pilot and commercial volumes of product
  • Developing and maintaining IQ, OQ and PQ documents and protocols
  • Troubleshooting, investigating process problems and deviations, and preparing appropriate reports on findings
  • Participating in HAZOPs and providing guidance on corrective actions when needed
  • Providing PFD and P&ID generation, energy balances, material balances, environmental calculations and other calculations and formulations as needed
  • Working with appropriate departments to set up codes, label requests, and MSDS revisions
  • Completing CAPAs and audit action items as assigned

Qualifications / Skills::

  • Knowledge of and/or direct experience in a cGMP environment is preferred
  • General knowledge of chemical operations equipment and manufacturing operations
  • Proficient in windows based environment including word processing, spreadsheet and data base programs

Qualifications:

  • BS in Chemical Engineering, plus 1 – 3 years of experience in manufacturing environment, preferably in pharmaceutical manufacture; or equivalent education/experience

How To Apply:

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Responsibilities
  • Writing batch records, cleaning records, SOPs, campaign reports, supplements, and investigation/deviation reports as needed to support production operations
  • Monitoring KPIs and using process data to identify and execute improvements to new and existing products to achieve improved yields, quality or customer expectations
  • Working with process improvement to identify and execute Kaizen events
  • Providing training and process support to production areas including training on new processes and on-site oversight of key processing steps
  • Working in a team environment that includes cross-departmental participation from Engineering, Research and Development, Regulatory, Quality Control, Analytical Development and Operations
  • Developing plans for production of pilot and commercial volumes of product
  • Developing and maintaining IQ, OQ and PQ documents and protocols
  • Troubleshooting, investigating process problems and deviations, and preparing appropriate reports on findings
  • Participating in HAZOPs and providing guidance on corrective actions when needed
  • Providing PFD and P&ID generation, energy balances, material balances, environmental calculations and other calculations and formulations as needed
  • Working with appropriate departments to set up codes, label requests, and MSDS revisions
  • Completing CAPAs and audit action items as assigne
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