CDMO Technical Specialist

Responsible for coordinating and monitoring CDMO operations, covering production planning, project and contract management, cross-functional coordination for customer order fulfillment, and business development initiatives to ensure timely execution and achievement of company targets.

Qualifications:

• Must be a licensed pharmacist (Apoteker)

• Minimum 2–3 years of experience in the pharmaceutical industry, particularly in Validation or Quality Assurance (QA)

• Strong knowledge of GMP/CPOB, pharmaceutical manufacturing processes, validation, and applicable regulations

• Experienced in pharmaceutical project management, cross-functional coordination, and project monitoring

• Strong ability to manage technical documentation and CDMO project requirements

• Strong leadership, analytical, problem-solving, and organizational skills

• Excellent English communication and coordination skills with internal teams and customers

• Possess a valid SIM A

• Willing to work in a fast-paced environment and support CDMO business development and service expansion