C&Q Engineer GMP Projects

gloor & lang ag; Neuenburg; In loco; CHF 83.000 - 124.000; Part-time

Descrizione del lavoro

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.

Competenze

• 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.

Mansioni

• 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.

Conoscenze

GMP experience

Commissioning/qualification

Project coordination

Planning & communication

Formazione

Engineering or Life Sciences degree

Descrizione del lavoro

5–6-month assignment | French and English required |Equipment, Utilities and CSV

Help deliver pharmaceutical capital projects from construction through qualification. In this on-site assignment, you’ll coordinate C&Q activities for facilities, utilities, production equipment and computerized systems in a GMP environment.

Your 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.

Your profile

• 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.