Senior CQV Engineer – GMP Pharma Validation Leader

Anter Consulting; Singapore; On-site; SGD 55,000 - 75,000; Full time

Job summary

Anter Consulting is seeking a highly skilled CQV (Commissioning, Qualification, and Validation) Engineer to join our team for a significant pharmaceutical project in Singapore. The selected candidate will oversee the commissioning of pharmaceutical manufacturing equipment, ensuring all systems comply with regulatory requirements and GMP standards.

The role requires a Bachelor's degree in Engineering or Life Sciences and a minimum of 5 years of GMP experience. Strong analytical skills and attention to detail are crucial for success in maintaining compliance and ensuring seamless project execution.

Qualifications

• Bachelor's degree is required.
• Minimum of 5 years of GMP experience in the pharmaceutical industry.
• Strong understanding of pharmaceutical processes and equipment.

Responsibilities

• Oversee commissioning of pharmaceutical equipment and systems.
• Develop and execute qualification protocols for systems and utilities.
• Ensure all processes comply with GMP regulations.

Skills

GMP experience

Pharmaceutical manufacturing

Protocol development (IQ, OQ, PQ)

Analytical abilities

Communication skills

Attention to detail

Education

Bachelor’s degree in Engineering or Life Sciences

Job description

Anter Consulting is seeking a highly skilled CQV (Commissioning, Qualification, and Validation) Engineer to join our team for a significant pharmaceutical project in Singapore. The selected candidate will oversee the commissioning of pharmaceutical manufacturing equipment, ensuring all systems comply with regulatory requirements and GMP standards.

The role requires a Bachelor's degree in Engineering or Life Sciences and a minimum of 5 years of GMP experience. Strong analytical skills and attention to detail are crucial for success in maintaining compliance and ensuring seamless project execution.