Production Support & Deviation Investigator (cGMP)

bimeda; Cambridge; On-site; GBP 35,000 - 40,000; Full time

Benefits offered by this job

Competitive salary

13 paid holidays

Vacation policy

Personal care days

Employee Assistance Program

Medical benefits

Job summary

Bimeda is seeking a Production Support Specialist for our Cambridge, Ontario site. The role focuses on investigations of production incidents, writing deviation reports, and implementing corrective actions to ensure cGMP compliance.

You will work with production and quality teams, perform root-cause analyses, and support regulatory inspections while maintaining meticulous documentation and adherence to FDA/Health Canada guidelines.

Qualifications

• 3–5 years of experience in aseptic manufacturing is required.

Responsibilities

• Coordinate investigations of production/manufacturing incidents and deviations.
• Lead deviation investigations and close CAPAs on time.
• Write SMART investigations and maintain regulatory compliance.

Skills

Regulatory compliance

Root cause analysis

Documentation

Quality systems

Analytical thinking

Education

Bachelor's degree in Life Sciences Microbiology

Job description

Bimeda is seeking a Production Support Specialist for our Cambridge, Ontario site. The role focuses on investigations of production incidents, writing deviation reports, and implementing corrective actions to ensure cGMP compliance.

You will work with production and quality teams, perform root-cause analyses, and support regulatory inspections while maintaining meticulous documentation and adherence to FDA/Health Canada guidelines.