Validation Associate

Resolute Workforce Solutions; Brantford; On-site; CAD 55,000 - 65,000; Full time

Job summary

Resolute Workforce Solutions is seeking a dedicated Validation Associate for an onsite engagement at a pharmaceutical manufacturing facility in Brantford, Ontario. The role focuses on cleaning validation, equipment, process, and computerized system qualifications within a GMP/cGMP environment.

The ideal candidate holds a science/engineering degree with 5+ years in Quality Engineering, QA/QC or Validation, and CQE is a plus.

Qualifications

• Bachelor's degree in Science, Engineering, or a related field from an accredited university.
• Minimum 5 years of experience in Quality Engineering, QA/QC, or Validation within a pharmaceutical manufacturing GMP/cGMP environment.
• Certified Quality Engineer (CQE) certification is an asset.
• Experience with GC, HPLC, laboratory equipment, and microbiological testing is preferred.
• Knowledge of GMP/cGMP, GLP, regulatory standards, and proficiency in MS Word, MS Excel, and electronic systems.
• Strong organizational, time management, multitasking, and problem-solving skills, with the ability to manage high workloads, work under pressure, and drive continuous improvement.
• Excellent interpersonal, verbal, and written communication skills.

Responsibilities

• Provide Quality support for New Product Development (NPD) and Existing Product Development (EPD) projects, including cleaning validation activities.
• Develop validation protocols and final reports for equipment, facility, cleaning, process, and computerized system qualifications.
• Maintain and update the Master Validation/Qualification Plan and manage calibration and preventive maintenance programs, coordinating with contractors to ensure compliance.
• Develop and implement SOPs and support the review and approval of QMS documents, including deviations, change controls, CAPAs, complaint investigations, and training records.
• Coordinate regularly with Production and QA teams to support operational planning and activities.
• Assist in preparing validation-related sections of Annual Product Quality Reports (APQRs).
• Follow all Occupational Health and Safety Act requirements, regulations, and safety procedures, and perform other duties as assigned by the Associate Manager, Quality.

Skills

Quality Engineering

QA/QC

Validation

GMP/cGMP

GLP

MS Word

MS Excel

Electronic systems

Interpersonal communication

Education

Bachelor's degree in Science/Engineering

Master's degree preferred

Tools

MS Word

MS Excel

Electronic systems

Job description

Brantford, Canada | Posted on 11/07/2026

• Work Experience Intermediate (5 to 8 years)
• Job Type Contract
• Date Opened 11/07/2026
• City Brantford
• Country Canada

Job Description

About Resolute

Resolute Workforce Solutions, a staff augmentation subsidiary of Brevitas Consulting Inc., provides qualified professionals to support the workforce requirements of organizations in the pharmaceutical and life sciences sectors.

We have been retained by a pharmaceutical manufacturing company to support its increased production demands through the provision of qualified resources at its manufacturing facility in Brantford, Ontario. All positions associated with this engagement are site-based and require personnel to work on-site. Please review the site location and associated logistics, including commuting arrangements, accessibility, and any site-specific requirements, when considering these opportunities.

Role Overview

We are looking for a highly motivated and energetic professional to join our team as a Validation Associate in Brantford,ON (Onsite). This role has a significant potential to extend to 1 year.

Responsibilities:

• Provide Quality support for New Product Development (NPD) and Existing Product Development (EPD) projects, including cleaning validation activities.
• Develop validation protocols and final reports for equipment, facility, cleaning, process, and computerized system qualifications.
• Maintain and update the Master Validation/Qualification Plan and manage calibration and preventive maintenance programs, coordinating with contractors to ensure compliance.
• Develop and implement SOPs and support the review and approval of QMS documents, including deviations, change controls, CAPAs, complaint investigations, and training records.
• Coordinate regularly with Production and QA teams to support operational planning and activities.
• Assist in preparing validation-related sections of Annual Product Quality Reports (APQRs).
• Follow all Occupational Health and Safety Act requirements, regulations, and safety procedures, and perform other duties as assigned by the Associate Manager, Quality.

Qualifications:

• Bachelor's degree in Science, Engineering, or a related field from an accredited university; Master's degree preferred.
• Minimum 5 years of experience in Quality Engineering, QA/QC, or Validation within a pharmaceutical manufacturing GMP/cGMP environment.
• Certified Quality Engineer (CQE) certification is an asset. Experience with GC, HPLC, laboratory equipment, and microbiological testing is preferred.
• Thorough knowledge of GMP/cGMP, GLP, regulatory standards, and proficiency in MS Word, MS Excel, and electronic systems.
• Strong organizational, time management, multitasking, and problem-solving skills, with the ability to manage high workloads, work under pressure, and drive continuous improvement.
• Excellent interpersonal, verbal, and written communication skills, with good judgment and the ability to collaborate effectively with internal teams and external contacts.
• Overtime may be required based on production needs and must be approved by Management.

Note: The annual salary range is $55,000–$65,000, depending on qualifications and experience.

We thank all applicants in advance; however, we will only contact the candidates whose qualifications match closely to the job requirements.

We welcome and encourage applications from people with disabilities. Accommodations are available on request for candidates taking part in all aspects of the selection process.