The Process Technician I supports the manufacture of active pharmaceutical ingredients (APIs) in a cGMP-regulated environment at the Cambrex High Point site. This entry-level role is responsible for executing batch operations, monitoring equipment and processes, and maintaining accurate documentation in accordance with standard operating procedures and regulatory requirements. Working as part of a highly collaborative production team, the Process Technician I contributes to safe, efficient, and high-quality manufacturing while gaining hands-on experience with chemical processing, equipment operation, and GMP compliance.
Responsibilities:
Execute batch manufacturing operations in accordance with approved batch records, SOPs, and cGMP requirements
Operate, monitor, and clean process equipment (e.g., reactors, filters, dryers) to support API production
Accurately document all manufacturing activities, observations, and data in real time following GDP (Good Documentation Practices)
Follow safety protocols and wear appropriate PPE to maintain a safe working environment; identify and report hazards or unsafe conditions
Support material handling activities, including charging raw materials and transferring intermediates and finished products
Assist in equipment setup, line clearances, and changeovers to support production schedules
Perform in-process checks and sampling as required to ensure product quality and process consistency
Collaborate with team members, supervisors, and cross-functional partners (e.g., Quality, Engineering) to resolve issues and maintain workflow
Participate in deviations, investigations, and continuous improvement initiatives as needed
Maintain a clean and organized production area in compliance with cGMP standards
Recognize, properly handle, and ensure compliant storage and disposal of hazardous materials in accordance with site procedures and regulatory requirements
Basic chemical processing skills: weighing, calculations, GMP documentation, vacuum and pressure operations
Forklift and other basic material handling experience
Qualifications:
High School Diploma or GED required
1–3 years of experience in a GMP chemical or pharmaceutical manufacturing or pilot plant environment preferred
3–5 years of experience in a chemical manufacturing environment preferred
Numbers & Facts
Location
High Point, North Carolina
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
Active Pharmaceutical Ingredient (API)unmatched
Application Programming Interface (API)unmatched
Check Processingunmatched
Continuous Improvementunmatched
Cross-Functionalunmatched
Current Good Manufacturing Practice (cGMP)unmatched
Documentationunmatched
Drug Manufacturingunmatched
Environmental Chemistryunmatched
Forkliftunmatched
GMP (Good Manufacturing Practices)unmatched
Hazard Analysisunmatched
Hazardous Materials Clean-Upunmatched
Hazardous Materials/Substancesunmatched
High School Diplomaunmatched
Manufacturingunmatched
Manufacturing Operationsunmatched
Organizational Skillsunmatched
Pilot Plantunmatched
Problem Solving Skillsunmatched
Procedure Developmentunmatched
Production Scheduleunmatched
Production Supportunmatched
Quality Engineeringunmatched
Regulatory Complianceunmatched
Regulatory Requirementsunmatched
Safety/Work Safetyunmatched
Standard Operating Procedures (SOP)unmatched
Team Playerunmatched
Writing Skillsunmatched
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