QA Data Reviewer Associate

AtomVie Global Radiopharma Inc.; Hamilton; On-site; CAD 60,000 - 100,000; Full time

Job summary

Join a forward-thinking company as a QA – Data Reviewer, Associate, where you will play a vital role in ensuring compliance and data integrity in the production of radiopharmaceuticals. This position involves reviewing analytical data, mentoring laboratory staff, and ensuring adherence to Good Documentation Principles. With a commitment to diversity and inclusion, this innovative firm offers a collaborative environment where your expertise will directly impact patient care and the advancement of healthcare solutions. If you are passionate about quality assurance and have a keen eye for detail, this opportunity is perfect for you.

Qualifications

• 5+ years of experience in analytical chemistry data review.
• Strong knowledge of GMP environments and data integrity principles.

Responsibilities

• Review data from various laboratory equipment ensuring integrity and compliance.
• Mentor and guide laboratory staff on data integrity and regulatory requirements.

Skills

Data Integrity

Good Documentation Principles (GDP)

Analytical Data Analysis

Communication Skills

Education

Post-Secondary Education in Engineering

Post-Secondary Education in Chemistry

Post-Secondary Education in Microbiology

Tools

HPLC

GC

TLC

pH meters

Job description

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AtomVie 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 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 the 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 reviews 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 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.
• Ensures compliance with Health and Safety for all policies, procedures, and regulations applicable to their work.

What You Bring to the Role

• Working knowledge and thorough understanding of data integrity, Good Documentation Principles (GDP), and the concept of 21 CFR Part 11 (and associated regulations).
• Working knowledge of laboratory equipment systems to perform audit trail reviews of testing.
• Familiarity with scientific principles pertaining to analytical records review.
• Understanding of 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.

Requirements

• 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.

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.

Seniority level

Not Applicable

Employment type

Full-time

Job function

Other

Industries

Pharmaceutical Manufacturing