Job Description
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!
Job 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 & Licensing Requirements
- 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
- Performs active work requiring the ability to exert up to 50 pounds of force occasionally and lesser amounts frequently to lift, carry, push, pull, or move materials
- Work is performed primarily in a production/manufacturing environment, with regular standing and walking throughout the shift
- May require climbing ladders and accessing elevated areas, including roof access as needed
- Requires visual acuity, manual dexterity (fingering/handling), and the ability to communicate effectively (verbal/written)
- Regular use of personal protective equipment (PPE), including but not limited to gloves, safety glasses, protective clothing, and respirators (e.g., supplied air and negative pressure)
- Work is conducted in a chemical manufacturing environment with exposure to typical hazards, including flammable and/or toxic materials, heavy material handling, and operation of large-scale process equipment
All requirements are subject to possible modifications to reasonably accommodate individuals with disabilities. Cambrex Corporation is an Equal Opportunity / Affirmative Action employer and will consider all qualified applicants for employment without regard to race, color, religion, sex (including pregnancy, sexual orientation, or gender identity), ancestry, national origin, place of birth, age, marital status, disability/handicap, genetic information, veteran status, or other characteristics protected by federal, state, and/or local law.
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