Oversee pharmaceutical QA and QC operations in a cGMP manufacturing environment. Manage compliance programs including Change Control, deviations, CAPA, audits, product release, recalls, complaints, validation, and controlled documentation. Coordinate regulatory audits, quality reviews, calibration, preventive maintenance, staff supervision, training, and continuous improvement initiatives while ensuring GMP, safety, and documentation compliance.
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 QA Analyst in Brantford, ON (Onsite). This is a contract role.
Responsibilities:
- Prepare, review, and issue quality documentation, including batch records, packaging records, Certificates of Analysis (COAs), and product release documents.
- Ensure compliance with cGMP, GLP, FDA, Health Canada, and internal quality standards through document reviews, internal audits, and regulatory inspections.
- Coordinate Change Control, CAPA, deviation investigations, OOS/OOT investigations, and customer/vendor complaints, ensuring timely follow-up and closure.
- Develop, review, and maintain SOPs, controlled documents, master indexes, and quality records to support effective document control.
- Perform in-process inspections, production line clearances, and technical document reviews, including raw materials, finished products, stability, and validation records.
Support product launches, customer and label revisions, and preparation of Annual Product Quality Reports (APQRs).
Qualifications:
- Bachelor’s degree in Chemistry, Microbiology, or a related scientific discipline from a recognized accredited institution.
- Minimum 2 years of experience in Quality Assurance, Quality Control, and Validation within a pharmaceutical manufacturing cGMP environment.
- Strong knowledge of applicable regulatory and industry standards, particularly cGMP and GLP requirements.
- Ability to organize effectively, prioritize, and manage multiple tasks in a fast-paced environment.
- Valid WHMIS (Workplace Hazardous Materials Information System) training.
- Excellent organizational and time-management skills with strong attention to detail.
- Strong interpersonal skills with the ability to collaborate effectively with manufacturing personnel, administrative teams, and external contacts.
Note: The annual salary range is $50,000–$60,000, depending on skills and experience relevant to the role.
To Apply:
Click the “I’m interested” button below, or
E-mail your resume in MSWord or pdf format to [email protected] with the following details in the e-mail's Subject Line: QA Analyst : FIRST NAME, LAST NAME.
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.
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