Biopharma CQV Manager: Lead Process Validation

MMR Consulting; Toronto; On-site; CAD 95,000 - 120,000; Full time

Benefits offered by this job

Equal opportunity employer

Inclusive environment

Job summary

A consulting firm in the pharmaceutical industry is seeking a CQV Manager to lead commissioning and qualification activities in bioprocess systems. The ideal candidate will have over 8 years of experience in the pharmaceutical/biotech sectors, strong leadership and project management skills, and a relevant engineering degree. This role requires direct management of a team and oversight of various validation projects to ensure compliance with industry standards. Occasional travel may be required.

Qualifications

• 8+ years of experience in commissioning and qualification within the pharmaceutical/biotech industry.
• Some previous leadership experience is required.
• Experience with developing validation projects is an asset.

Responsibilities

• Directly manage and lead a team of CQV engineers and specialists.
• Provide technical guidance on commissioning and qualification.
• Lead development and execution of qualification deliverables.

Skills

Leadership skills

Commissioning and qualification experience

Knowledge of regulatory requirements

Project management skills

Education

Engineering degree (Mechanical, Electrical, or Chemical)

Tools

cGMP process equipment

PCS, SCADA, Historians

Job description

A consulting firm in the pharmaceutical industry is seeking a CQV Manager to lead commissioning and qualification activities in bioprocess systems. The ideal candidate will have over 8 years of experience in the pharmaceutical/biotech sectors, strong leadership and project management skills, and a relevant engineering degree. This role requires direct management of a team and oversight of various validation projects to ensure compliance with industry standards. Occasional travel may be required.