10 Cambrex High Point Jobs Hiring Near You

Company Information

You Matter to Cambrex.

Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance, drug product, and analytical services across the entire drug lifecycle. With more than 40 years of experience and a growing team of over 2,000 professionals servicing global clients, Cambrex is a trusted partner in branded and generic markets for API and dosage form development and manufacturing.

Your Work Matters.

At Cambrex, we strive to build a culture where all colleagues have the opportunity to:

• engage in work that matters to our customers and the patients they serve
• learn new skills and enjoy new experiences in an engaging and safe environment
• strengthen connections with coworkers and the community

We're committed to attracting and nurturing a passionate team of valued professionals in our fast-paced and growing company.  We offer a competitive benefits package that includes healthcare, life insurance, planning for retirement, and more!

Your Future Matters.

Known for our customer-focused scientific and manufacturing excellence, as well as our strong commitment to quality and safety, we offer a range of career and growth opportunities across our global network of locations. Together with our customers, we aim to improve the quality of life for patients around the world. Start a career where You Matter by applying today!

Overview: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

Qualifications / Skills:

• Hazardous materials handling experience: flammable liquids, compressed gases, toxic solids.
• Writing skills for procedures and reports.
• Basic chemical processing skills: weighing, calculations, GMP documentation, vacuum and pressure operations
• Forklift and other basic material handling experience

Education, Experience, and Licensing Requirements: (Text Only)- 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  Employment Type: FULL_TIME