Validation Technologist

Nanz Pharma; Pickering; On-site; CAD 65,000 - 70,000; Full time

Job summary

A leading pharmaceutical company is seeking a Validation Technologist responsible for the qualification and validation of various systems and processes. The ideal candidate will have a Bachelor’s degree and 3-5 years of relevant experience in validation within the pharmaceutical or medical device industries. This role involves ensuring compliance with safety standards and participating in investigations related to validation.

Qualifications

• 3 to 5 years of experience in validation or QA within the Pharmaceutical industry.

Responsibilities

• Perform activities according to SOPs, cGMP, and safety standards.
• Prepare, review, and execute validation protocols.
• Participate in investigations for deviations and product incidents.

Skills

Knowledge of cGMP

Strong communication skills

Team player

Education

Bachelor of Science Degree

Tools

Word

Excel

Job description

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Nanz Pharma is a globally respected pharmaceutical entity with a passion for innovation, excellence, and commitment to deliverables. Our vision is to provide high-quality hygiene and wellness products that improve people's lives through trust, quality, and brilliance.

Job Summary:

As a Validation Technologist you will be responsible for qualification/validation of equipment, computerized systems, utilities, facilities, cleaning methods, analytical methods and manufacturing / packaging operations and support investigations.

Job Responsibilities:

• Perform all activities according to the SOP’s, cGMP, and all other established safety standards.
• Prepare, review, and execute Qualifications / validation protocols.
• Prepare reports (endorsement, interim, validation/verification reports) based on the data gathered/ results from the execution of Qualifications / validation protocols.
• Collect samples and submits for laboratory testing as stipulated in the protocols.
• Participate in investigations for deviations and product incidents that impact validation.
• Review investigations related to validation and support to identify root cause and implement CAPAs.
• Assess all changes related to equipment, computerized systems, utilities, facilities, cleaning methods, analytical methods, and manufacturing / packaging .
• Assist in responding validation queries from regulatory authorities and clients in a timely manner.
• Assist in reviewing SOPs related to validation such as but not limited to Cleaning, Environmental Monitoring, Sampling, Systems, Equipment, and others.
• Perform other duties as required and instructed by the Supervisor/Manager.

Job Requirements:

• Education: Minimum Bachelor of Science Degree or college diploma (or equivalent) in a related discipline.

Knowledge, Skills and Abilities:

• Knowledge of cGMP and understanding of pharmaceutical manufacturing/packaging processes.
• Knowledge of pharmaceutical validation principles.
• Highly motivated, conscientious, self-managed team player, with experience working in a team environment.
• Strong communication skills, both verbal and written.
• Computer skills such as Word and Excel.

Experience: 3 to 5 years of experience in validation, qualification, or QA within the Pharmaceutical or Medical Device industries.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

• Industries

  Pharmaceutical Manufacturing

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