Qa Jobs in Burlington on
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Qa • burlington on
- Promoted
QA Data Reviewer Associate
AtomVie Global Radiopharma Inc.Hamilton, ON, CanadaHACCP Coordinator (6-Month Contract)
Stampede Culinary PartnersOntario, ON, CANSenior Analyst, Quality Assurance
Ontario HealthOntario Health, OntarioQA Manager / Welding Engineer
Walters IncHamilton, ON, CAFSQA Pre-Op Inspector
Maple Leaf FoodsHamilton, ON, CanadaSr. Quality Assurance Auditor GCP GXP
ParexelRemote, Ontario, CanadaManager Quality Assurance
Sotera HealthON, CanadaQA Specialist
CB CanadaBurlington, Ontario, Canada- Promoted
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The Mason Group - Strategic Search PartnersBurlington, ON, Canada- Promoted
Construction Manager
Executive Integrity | B CorpOntario, Canada, CanadaLab Technician-Quality Management System
BungeHamilton, ON, CAComputer System Validation (CSV) Specialist
Innomar StrategiesRemote, ON- Promoted
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The Mason Group Incburlington, ontario, CanadaQA 6264-22
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N. Harris Computer Corporation - CADOntario, CanadaSenior Developer
Arctic WolfRemote, OntarioQA analyst, TSYS
Emonics LLCOntario, Canada- Promoted
Quality Assurance Specialist
eInfochips (An Arrow Company)Ontario, Canada, CanadaJPC - 1414 - Senior Project Manager
ITS GlobalOntarioQA Data Reviewer Associate
AtomVie Global Radiopharma Inc.Hamilton, ON, Canada- Full-time
AtomVie Global Radiopharma Inc. is a global leading GMP manufacturer and distributer of clinical and commercial radiopharmaceuticals. We work with our partners to transform patients’ lives by advancing high quality drugs for the treatment and diagnosis of diseases.
We are a community that challenges ourselves professionally, takes pride in what we can accomplish together and values the impact we can make with our partners and patients across the globe. Start your career with AtomVie today and help us achieve our vision : to transform lives by revolutionizing healthcare.
About the Role
The QA – Data Reviewer, Associate is responsible for ensuring GMP compliance and data integrity through verification of records generated in sampling, preparation, instrumental analysis, data evaluation and calculation of reportable results related to radiopharmaceuticals at AtomVie. This role is critical in sustaining data integrity principles in Analytical Development and Quality Control laboratories operating at AtomVie.
What You Will Do
- Reviews data carried out using a wide variety of equipment including but not limited to HPLC, GC, TLC, and pH meters
- Reviews the completeness of the records generated in sampling, preparation, instrumental analysis, data evaluation and calculation of reportable results to verify integrity of all data generated and reported
- Ensure the test methods, protocols and Standard Operating Procedures (SOPs) were followed by chemists, scientists and biochemists
- Conducts and documents periodic review of audit trails in the variety of equipment as prescribed by internal SOPs
- Contributes to laboratory investigations of Out of Specification and / or Out of Trend results
- Works collaboratively with stakeholders to ensure the data meets ALCOA+ integrity
- Provide guidance and support to laboratory staff and management, ensuring the data is maintained to AtomVie standards and regulatory requirements, mentoring and coaching these staff members to understand the importance and implications GDP and data integrity in the laboratory has at AtomVie.
- Ensure compliance with Health and Safety for all policies, procedures and regulations applicable to their work.
What You Bring to the Role
Requirements
AtomVie Offers
AtomVie is committed to fostering a workplace that values diversity, equity, and inclusion. We believe that a diverse and inclusive workforce enhances our ability to innovate, collaborate, and better serve our clients and patients. We thank you for considering a career with AtomVie. Only those candidates selected for an interview will be contacted. Accommodations are available upon request for candidates taking part in all aspects of the recruitment and selection process. We are dedicated to ensuring that every qualified applicant has an equal opportunity to thrive within our organization.