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Cambrexposted 26 days ago
Full-time • Senior
Carrie Lane Chapman Catt Home, IA
1,001-5,000 employees
Chemical Manufacturing
Resume Match Score

About the position

The Senior Process Engineer 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 with minimal oversight to support production operations
  • Developing and maintaining IQ, OQ and PQ documents and protocols with minimal oversight
  • Providing mentorship and peer review for junior engineers during completion of documents and investigations
  • Identifying and monitoring KPIs and using process data to identify and execute improvements to new and existing products to achieve improved yields, quality or customer expectations
  • Identifying and executing Kaizen events with support from Process Improvement
  • Leading process improvement teams to further identify and execute larger scale process improvements on key products
  • 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
  • Leading efforts to troubleshoot and investigate process problems and deviations, and mentoring junior engineers on troubleshooting techniques; preparing appropriate reports on findings
  • Participating in HAZOPs and providing guidance on corrective actions when needed; leading HAZOPs when required
  • 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
  • Leading project teams and filling the role of project manager or key customer contact when required
  • Developing cost estimates and reviewing with accounting

Requirements

  • 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
  • BS in Chemical Engineering, plus 7 years or more of experience in manufacturing environment, preferably in pharmaceutical manufacture; or equivalent education/experience; advanced degree in Chemistry or Chemical Engineering preferred

Benefits

  • Healthcare
  • Life insurance
  • Planning for retirement
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