GMP C&Q Engineer - On-site Capital Projects (6-mo)

gloor & lang ag; Neuenburg; On-site; CHF 83,000 - 124,000; Part time

Job summary

gloor & lang ag is seeking an on-site specialist to deliver pharmaceutical capital projects from construction through qualification. You will coordinate C&Q activities for facilities, utilities, production equipment and computerized systems in a GMP environment.

Your responsibilities include driving commissioning, developing C&Q plans, reviewing qualification documentation, coordinating cross-functional teams, and supporting investigations and audit readiness.

Qualifications

• Degree in Engineering, Life Sciences or a related scientific discipline.
• At least 3 years of relevant experience in a pharmaceutical GMP environment.
• Experience in commissioning, qualification or validation; exposure to capital projects or oral solid dosage manufacturing is an advantage.
• Strong planning, communication and problem-solving skills, with the ability to work independently and collaboratively.

Responsibilities

• Drive commissioning and qualification activities in line with project milestones, GMP requirements and site procedures.
• Develop and maintain C&Q plans and schedules, particularly for construction and qualification phases.
• Prepare, review and approve qualification plans, protocols, reports and acceptance criteria.
• Coordinate colleagues, contractors and stakeholders across Engineering, QA, MS&T, suppliers and end-user teams.
• Support investigations, change controls, corrective actions and audit readiness.

Skills

GMP experience

Commissioning/qualification

Project coordination

Planning & communication

Education

Engineering or Life Sciences degree

Job description

gloor & lang ag is seeking an on-site specialist to deliver pharmaceutical capital projects from construction through qualification. You will coordinate C&Q activities for facilities, utilities, production equipment and computerized systems in a GMP environment.

Your responsibilities include driving commissioning, developing C&Q plans, reviewing qualification documentation, coordinating cross-functional teams, and supporting investigations and audit readiness.