Cambrex Production Engineer US-IA-Charles City Job ID: 2026-4911 Type: Regular Full-Time # of Openings: 1 Category: Engineering Cambrex - Charles City Overview 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 Equal employment opportunity, including veterans and individuals with disabilities. PI286256678

Cambrex Pharma 2 Operator US-IA-Charles City Job ID: 2026-4847 Type: Regular Full-Time # of Openings: 1 Category: Operations Cambrex - Charles City Overview Reporting to the shift supervisor, the Reactor Operator will be expected to successfully produce chemical and pharmaceutical products in our manufacturing environment. Responsibilities Operate batch and continuous type reactors, high pressure reactors, centrifuges, filters, solvent distillation equipment and supporting equipment involved in testing, all according to designated procedures. Monitor the equipment; setting controls on valves, vacuums, pumps, pressures, etc., according to designated procedures to achieve desired results. Monitors the process variables and makes process control adjustments to maintain the proper process control. Use manual and computer-controlled devices to monitor and control the process. Clean all equipment used (boil, scrape or scrub out) following designated procedures. Assist in training new Pharma Reactor Operators. Drum compounds and hazardous waste; label according to set standards; transport to assigned areas. Assure area is kept clean and all precautions are taken to prevent environmental spills and control discharge to WWTP at acceptable limits. Interpret results and monitor processes using computer-controlled devices. Responsible for safe handling of hazardous materials including loading/unloading trucks, processing, packaging and cleanup of equipment. Responsible for completion of all operation log books in Pharma area. Troubleshoot production line and equipment problems in a safe and effective manner. Assist lab personnel with implementing new processes or process changes Complete line entry, confined space, and hot work permits.  Assist in writing and updating process procedures and SOP’s. Adhere to all EPA, FDA and cGMP regulations as they relate to the operation of the chemical production facility. Take samples for in-process and Quality Control analysis. Perform laboratory tests on process samples and act on results. Assume duties of Reactor Operator Chem I/II Qualifications / Skills Good communication skills, both oral and written Strong mechanical aptitude/knowledge Qualifications High School Diploma or equivalent 3 or more years of experience in a manufacturing environment or related business Equal employment opportunity, including veterans and individuals with disabilities. PI286229708

Cambrex Chem 1 Operator US-IA-Charles City Job ID: 2026-4936 Type: Regular Full-Time # of Openings: 1 Category: Operations Cambrex - Charles City Overview Reporting to the shift supervisor, the Reactor Operator will be expected to successfully produce chemical and pharmaceutical products in our manufacturing environment. Responsibilities Operate batch and continuous type reactors, high pressure reactors, centrifuges, filters, solvent distillation equipment and supporting equipment involved in testing, all according to designated procedures. Monitor the equipment; setting controls on valves, vacuums, pumps, pressures, etc., according to designated procedures to achieve desired results. Monitors the process variables and makes process control adjustments to maintain the proper process control. Use manual and computer-controlled devices to monitor and control the process. Clean all equipment used (boil, scrape or scrub out) following designated procedures. Assist in training new Pharma Reactor Operators. Drum compounds and hazardous waste; label according to set standards; transport to assigned areas. Assure area is kept clean and all precautions are taken to prevent environmental spills and control discharge to WWTP at acceptable limits. Interpret results and monitor processes using computer-controlled devices. Responsible for safe handling of hazardous materials including loading/unloading trucks, processing, packaging and cleanup of equipment. Responsible for completion of all operation log books in Pharma area. Troubleshoot production line and equipment problems in a safe and effective manner. Assist lab personnel with implementing new processes or process changes Complete line entry, confined space, and hot work permits.  Assist in writing and updating process procedures and SOP’s. Adhere to all EPA, FDA and cGMP regulations as they relate to the operation of the chemical production facility. Take samples for in-process and Quality Control analysis. Perform laboratory tests on process samples and act on results. Assume duties of Reactor Operator Chem I/II Qualifications / Skills Good communication skills, both oral and written Strong mechanical aptitude/knowledge Qualifications High School Diploma or equivalent 3 or more years of experience in a manufacturing environment or related business Equal employment opportunity, including veterans and individuals with disabilities. PI286229425

Cambrex Pharma 3/4 Operator US-IA-Charles City Job ID: 2026-4876 Type: Regular Full-Time # of Openings: 1 Category: Operations Cambrex - Charles City Overview Reporting to the shift supervisor, the Reactor Operator will be expected to successfully produce chemical and pharmaceutical products in our manufacturing environment. Responsibilities Operate batch and continuous type reactors, high pressure reactors, centrifuges, filters, solvent distillation equipment and supporting equipment involved in testing, all according to designated procedures.  Monitor the equipment; setting controls on valves, vacuums, pumps, pressures, etc., according to designated procedures to achieve desired results.  Monitors the process variables and makes process control adjustments to maintain the proper process control. Use manual and computer-controlled devices to monitor and control the process.  Clean all equipment used (boil, scrape or scrub out) following designated procedures.  Assist in training new Pharma Reactor Operators.  Drum compounds and hazardous waste; label according to set standards; transport to assigned areas.  Assure area is kept clean and all precautions are taken to prevent environmental spills and control discharge to WWTP at acceptable limits.  Interpret results and monitor processes using computer-controlled devices.  Responsible for safe handling of hazardous materials including loading/unloading trucks, processing, packaging and cleanup of equipment.  Responsible for completion of all operation log books in Pharma area.  Troubleshoot production line and equipment problems in a safe and effective manner.  Assist lab personnel with implementing new processes or process changes  Complete line entry, confined space, and hot work permits.   Assist in writing and updating process procedures and SOP’s.  Adhere to all EPA, FDA and cGMP regulations as they relate to the operation of the chemical production facility.  Take samples for in-process and Quality Control analysis.  Perform laboratory tests on process samples and act on results.  Assume duties of Reactor Operator Chem I/II Qualifications / Skills Good communication skills, both oral and written Strong mechanical aptitude/knowledge Qualifications High School Diploma or equivalent 3 or more years of experience in a manufacturing environment or related business Equal employment opportunity, including veterans and individuals with disabilities. PI286229631

Cambrex Chem 2 Operator US-IA-Charles City Job ID: 2026-4747 Type: Regular Full-Time # of Openings: 1 Category: Operations Cambrex - Charles City Overview Reporting to the shift supervisor, the Reactor Operator will be expected to successfully produce chemical and pharmaceutical products in our manufacturing environment. Responsibilities Operate batch and continuous type reactors, high pressure reactors, centrifuges, filters, solvent distillation equipment and supporting equipment involved in testing, all according to designated procedures.  Monitor the equipment; setting controls on valves, vacuums, pumps, pressures, etc., according to designated procedures to achieve desired results.  Monitors the process variables and makes process control adjustments to maintain the proper process control. Use manual and computer-controlled devices to monitor and control the process.  Clean all equipment used (boil, scrape or scrub out) following designated procedures.  Assist in training new Pharma Reactor Operators.  Drum compounds and hazardous waste; label according to set standards; transport to assigned areas.  Assure area is kept clean and all precautions are taken to prevent environmental spills and control discharge to WWTP at acceptable limits.  Interpret results and monitor processes using computer-controlled devices.  Responsible for safe handling of hazardous materials including loading/unloading trucks, processing, packaging and cleanup of equipment.  Responsible for completion of all operation log books in Pharma area.  Troubleshoot production line and equipment problems in a safe and effective manner.  Assist lab personnel with implementing new processes or process changes  Complete line entry, confined space, and hot work permits.   Assist in writing and updating process procedures and SOP’s.  Adhere to all EPA, FDA and cGMP regulations as they relate to the operation of the chemical production facility.  Take samples for in-process and Quality Control analysis.  Perform laboratory tests on process samples and act on results.  Assume duties of Reactor Operator Chem I/II Qualifications / Skills Good communication skills, both oral and written Strong mechanical aptitude/knowledge Qualifications High School Diploma or equivalent 3 or more years of experience in a manufacturing environment or related business Equal employment opportunity, including veterans and individuals with disabilities. PI286229822

Cambrex Pharma 1 Operator US-IA-Charles City Job ID: 2026-4895 Type: Regular Full-Time # of Openings: 1 Category: Operations Cambrex - Charles City Overview Reporting to the shift supervisor, the Reactor Operator will be expected to successfully produce chemical and pharmaceutical products in our manufacturing environment. Responsibilities Operate batch and continuous type reactors, high pressure reactors, centrifuges, filters, solvent distillation equipment and supporting equipment involved in testing, all according to designated procedures. Monitor the equipment; setting controls on valves, vacuums, pumps, pressures, etc., according to designated procedures to achieve desired results. Monitors the process variables and makes process control adjustments to maintain the proper process control. Use manual and computer-controlled devices to monitor and control the process. Clean all equipment used (boil, scrape or scrub out) following designated procedures. Assist in training new Pharma Reactor Operators. Drum compounds and hazardous waste; label according to set standards; transport to assigned areas. Assure area is kept clean and all precautions are taken to prevent environmental spills and control discharge to WWTP at acceptable limits. Interpret results and monitor processes using computer-controlled devices. Responsible for safe handling of hazardous materials including loading/unloading trucks, processing, packaging and cleanup of equipment. Responsible for completion of all operation log books in Pharma area. Troubleshoot production line and equipment problems in a safe and effective manner. Assist lab personnel with implementing new processes or process changes Complete line entry, confined space, and hot work permits.  Assist in writing and updating process procedures and SOP’s. Adhere to all EPA, FDA and cGMP regulations as they relate to the operation of the chemical production facility. Take samples for in-process and Quality Control analysis. Perform laboratory tests on process samples and act on results. Assume duties of Reactor Operator Chem I/II Qualifications / Skills Good communication skills, both oral and written Strong mechanical aptitude/knowledge Qualifications High School Diploma or equivalent 3 or more years of experience in a manufacturing environment or related business Equal employment opportunity, including veterans and individuals with disabilities. PI286229575

Cambrex Pharma 3 Operator US-IA-Charles City Job ID: 2026-4777 Type: Regular Full-Time # of Openings: 1 Category: Operations Cambrex - Charles City Overview Reporting to the shift supervisor, the Reactor Operator will be expected to successfully produce chemical and pharmaceutical products in our manufacturing environment. Responsibilities Operate batch and continuous type reactors, high pressure reactors, centrifuges, filters, solvent distillation equipment and supporting equipment involved in testing, all according to designated procedures. Monitor the equipment; setting controls on valves, vacuums, pumps, pressures, etc., according to designated procedures to achieve desired results. Monitors the process variables and makes process control adjustments to maintain the proper process control. Use manual and computer-controlled devices to monitor and control the process. Clean all equipment used (boil, scrape or scrub out) following designated procedures. Assist in training new Pharma Reactor Operators. Drum compounds and hazardous waste; label according to set standards; transport to assigned areas. Assure area is kept clean and all precautions are taken to prevent environmental spills and control discharge to WWTP at acceptable limits. Interpret results and monitor processes using computer-controlled devices. Responsible for safe handling of hazardous materials including loading/unloading trucks, processing, packaging and cleanup of equipment. Responsible for completion of all operation log books in Pharma area. Troubleshoot production line and equipment problems in a safe and effective manner. Assist lab personnel with implementing new processes or process changes Complete line entry, confined space, and hot work permits. Assist in writing and updating process procedures and SOP’s. Adhere to all EPA, FDA and cGMP regulations as they relate to the operation of the chemical production facility. Take samples for in-process and Quality Control analysis. Perform laboratory tests on process samples and act on results. Assume duties of Reactor Operator Chem I/II Qualifications / Skills Good communication skills, both oral and written Strong mechanical aptitude/knowledge Qualifications High School Diploma or equivalent 3 or more years of experience in a manufacturing environment or related business Equal employment opportunity, including veterans and individuals with disabilities. PI286229737

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Cambrex Production Engineer US-IA-Charles City Job ID: 2026-4910 Type: Regular Full-Time # of Openings: 1 Category: Engineering Cambrex - Charles City Overview 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 Equal employment opportunity, including veterans and individuals with disabilities. PI286210875

Cambrex Mechanical Integrity Engineer US-IA-Charles City Job ID: 2026-4958 Type: Regular Full-Time Category: Maintenance Cambrex - Charles City Overview The Mechanical Integrity Engineer is responsible for managing and executing the mechanical integrity and inspection programs for applicable equipment at the Charles City site. This role focuses on ensuring the integrity, reliability, and regulatory compliance of pressure vessels, piping systems, and storage tanks through the implementation of OSHA Mechanical Integrity inspection standards. The Mechanical Integrity Engineer will support and oversee activities in accordance with Code of Federal Regulations Title 29 Subtitle B, Chapter XVII, Part 1910, Section 119, Subpart H, § 1910.119, Clause j, that will serve to prevent or minimize the consequences of catastrophic releases of toxic, reactive, flammable, or explosive chemicals. These releases may result in toxic, fire or explosion hazards. This role will work closely with operations, maintenance, and inspection personnel to monitor equipment condition, evaluate damage mechanisms, and implement corrective actions that support safe and reliable plant operation. The ideal candidate will bring strong knowledge of equipment inspection, corrosion management, and industry codes, along with the ability to analyze inspection data and drive improvements in asset integrity and reliability. Responsibilities Develop, implement, and maintain the mechanical integrity program to ensure the safety and reliability of equipment such as pressure vessels, pipelines, storage tanks, and heat exchangers. Plan, coordinate, and oversee inspections of critical equipment, including non-destructive testing (NDT), visual inspections, pressure tests, and thickness gauging. Ensure compliance with inspection schedules and regulatory requirements in alignment with industry codes (e.g., OSHA, ASME, API). Review and analyze inspection data to identify trends, anomalies, and areas of concern. Evaluate and manage corrosion rates, wear, material degradation, and life expectancy of equipment. Collaborate with regulatory bodies and internal/third-party auditors during inspections and certifications. Maintain comprehensive documentation on mechanical integrity programs, inspection records, repairs, and certifications for audits and legal compliance. Collaborate with Maintenance Dept. to plan and execute repairs, modifications, or upgrades for mechanical equipment and systems. Make recommendations on appropriate materials, repairs, or replacements to improve safety and longevity. Monitor repair quality and verify compliance with engineering specifications and standards. Maintain updated records of inspections, repairs, and asset integrity assessments in computerized maintenance management systems (CMMS). Develop reports on mechanical system performance, risks, and integrity management activities for internal use and external stakeholders. Analyze data to drive improvements in asset integrity and performance. Work closely with engineers, maintenance and operations teams, reliability experts, and management to ensure proper integration of mechanical integrity efforts within overall operations. Provide technical guidance and training to operations and maintenance personnel on mechanical integrity standards, processes, and best practices. Actively participate in incident investigations related to mechanical equipment and provide engineering input to improve safety systems. Facilitate failure analysis investigations to determine root causes and recommend corrective or preventive actions. Track advancements in mechanical integrity practices, standards, and technologies, and recommend updates to programs and methods accordingly. Identify opportunities for cost savings and process optimization without compromising safety or compliance. Improve asset reliability and availability by implementing advanced engineering solutions such as condition monitoring and predictive maintenance techniques. Other duties as assigned. Qualifications / Skills Proficiency with ASME, ANSI, and OSHA standards. Qualifications Bachelors Degree in Engineering with applicable experience in mechanical integrity. 5 years experience with NDE methods and techniques used to support mechanical integrity programs. Equal employment opportunity, including veterans and individuals with disabilities. PI285944654