The Production Engineer will be a Operations technical expert and responsible for reviewing documentation for Operations to implement projects for the manufacture of APIs, bulk intermediates, and other products from development through piloting and/or commercial production.
Responsibilities:
Writing batch records and cleaning records for commercial products or simple revisions, campaign reports, as needed to support production operations.
Initiate SOPs and investigations/deviation reports/CAPAs for production operations and commercial products.
Reviewing and approving documentation (batch records, cleaning records, supplements, etc) for Operations as the area technical expert.
Troubleshoot equipment and coordinate with maintenance to monitor equipment for efficiency improvement.
Assist Process Engineers and Chemical Development teams when new processes are transferred into the area workcenter.
Work with Validation Engineering and Maintenance departments on developing and maintaining IQ, OQ and PQ documents and protocols. Ownership of equipment and facility change controls in their assigned area workcenter.
Generate product setups and cleaning memos as needed.
Troubleshooting, investigating process problems and deviations, and preparing appropriate reports on findings.
Participating in HAZOPs and providing guidance on corrective actions when needed.
Completing CAPAs and audit action items as assigned.
Train Operators or Technicians on equipment and process operations as needed to ensure safe and efficient manufacturing.
Additional job duties as assigned.
All employees are required to adhere to DEA, EPA, FDA and cGMP regulations as they relate to the operation of the Company; and to adhere to all company safety rules and procedures. All employees are expected to report to work regularly and promptly. Other duties relating to departmental mission, not specifically detailed in this section may be assigned.
Qualifications / Skills::
Knowledge of and/or direct experience in a cGMP environment is preferred
General knowledge of chemical operations equipment and manufacturing operations
Qualifications:
BS in Chemical Engineering or similar field, plus 1 – 3 years of experience in manufacturing environment, preferably in pharmaceutical manufacture; or equivalent education/experience
Numbers & Facts
Location
Charles City, Iowa
Job Type
Full-time
Industry
Biotechnology/Pharmaceuticals
Company Size
1,000 to 1,499 employees
Year Founded
1981
Website
http://www.cambrex.com
About Company
Cambrex is an innovative life sciences company with a refreshingly human approach. Driven by passion, our pharmaceutical products, expertise and technologies accelerate our customers’ small molecule therapeutics into markets across the world.
With over 35 years of active pharmaceutical ingredient (API) development and manufacturing expertise, a growing team of more than 1,200 experts and a strong presence in the USA and Europe, we are tried and trusted across branded and generic API markets.
Skills
Application Programming Interface (API)unmatched
Biotech and Pharmaceuticalunmatched
Campaignsunmatched
Change Controlunmatched
Chemical Engineeringunmatched
Chemical Processesunmatched
Corrective Actionunmatched
Current Good Manufacturing Practice (cGMP)unmatched
Documentationunmatched
Documentation Reviewunmatched
Environmental Protection Agency (EPA)unmatched
Equipment Maintenance/Repairunmatched
FDA Requirementsunmatched
Identify Issuesunmatched
Manufacturingunmatched
Manufacturing Operationsunmatched
Operational Auditunmatched
Operational Supportunmatched
Operations Processesunmatched
People Managementunmatched
Process Engineeringunmatched
Process Validationunmatched
Production Supportunmatched
Reporting Skillsunmatched
Safety Processunmatched
Safety/Work Safetyunmatched
Standard Operating Procedures (SOP)unmatched
Technical Operationsunmatched
United States Drug Enforcement Agency (DEA)unmatched
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