QA Data Reviewer Associate

Atom Vie Global Radiopharma Inc. is a global leading GMP manufacturer and distributor 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 Atom Vie today and help us achieve our vision: to transform lives by revolutionizing healthcare.

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 s role is critical in sustaining data integrity principles in Analytical Development and Quality Control laboratories operating at Atom Vie.

• Reviews data carried out using a wide variety of equipment including but not limited to HPLC, GC (including headspace), 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
• Ensures 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
• Provides guidance and support to laboratory staff and management, ensuring the data is maintained to Atom Vie 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 Atom Vie.
• Ensures compliance with Health and Safety for all policies, procedures and regulations applicable to their work.

• Working knowledge and thorough understanding of data integrity, Good Documentation Principles (GDP) and concept of 21 CFR Part 11 (and associated regulations)
• Working knowledge of laboratory equipment systems to perform audit trail of testing
• Familiarity with scientific principles pertaining to analytical records review
• Understanding or principles and requirements for analytical methods qualification, validation and verification
• Aptitude for analytical data analysis and interpretation
• Flexibility in schedule to support a 24/7 operational environment

• Post-Secondary Education in Engineering, Chemistry, Microbiology or a related field.
• Minimum 5 years of experience conducting testing or reviewing analytical chemistry data in the pharmaceutical, radiopharmaceutical or biotechnology field.
• Experience working in a GMP environment is required.
• Proficiency in the English language both written and oral, and excellent communication skills; detail oriented.
• Group Health & Dental Benefits (from day
  1)
• RRSP Matching Program
• Employee Assistance and Wellness Programs

Atom Vie 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 Atom Vie. 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.

• Seniority level:
  Associate
• Employment type:
  
  Full-time
• Job function:
  Quality Assurance and Other
• Industries:
  Pharmaceutical Manufacturing