Start Date
Immediate
Expiry Date
24 Sep, 25
Salary
37.35
Posted On
23 Aug, 25
Experience
0 year(s) or above
Remote Job
Yes
Telecommute
Yes
Sponsor Visa
No
Skills
Good communication skills
Industry
Pharmaceuticals
Your Opportunity:
An exciting Quality Assurance (QA) opportunity! As a leader within the provincial Radiopharmaceutical Services of Alberta (RSA) Quality Assurance program, this Radiopharmacy Specialist II (QA) Lead position supervises, leads, organizes, and guides a high-functioning QA team at the Calgary Radiopharmaceutical Centre (CRC) site and provides leadership and guidance for the compliance and improvement of the quality management system (QMS). Reporting to the Provincial Radiopharmaceutical QA manager, this position is responsible for leading the day-to-day operations of the CRC QA team and is involved in the planning, coordination, implementation, and evaluation of RSA quality and GMP activities. As a QA Lead at the CRC, you will perform QA tasks to support GMP-compliant operations, maintain quality programs, and ensure regulatory compliance. The responsibilities include writing, reviewing and approving documents, validations and qualifications involved with GMP activities, leading and supporting continuous improvement initiatives, internal audits and external regulatory audits. We are looking for candidates with a strong technical understanding of regulatory and QMS elements in a parenteral drug product manufacturing facility. Ideal candidates will possess investigative and critical thinking skills, strong attention to detail, and effective written and verbal communication skills. Candidates should also be able to work independently within prescribed guidelines and promote good teamwork. Join us in ensuring the highest standards of quality and compliance in radiopharmaceutical manufacturing. Apply now to be a part of our dedicated team! Note: Please disregard the job descriptions and the CAMRT/CCRS certification requirements.
Description:
As a Radiopharmacy Specialist II, you will be responsible for the day-to-day coordination of an assigned area and/or quality control functions for the department. You will work to coordinate and prioritize daily assignments of staff, resolve complex issues, monitor the production of radiopharmaceuticals for regulatory compliance and ensure that operations are compliant with Radiation Safety and Production standards.
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