Coordinator, Compliance
Edmonton, AB · On-site
... at our Biotechnology Business Development Centre. This role is responsible for creating and ... Collaborate cross-functionally with Production, QA, QC, Validation, and Engineering teams.
Edmonton, AB · On-site
... at our Biotechnology Business Development Centre. This role is responsible for creating and ... Collaborate cross-functionally with Production, QA, QC, Validation, and Engineering teams.
Edmonton, AB · On-site
... at our Biotechnology Business Development Centre. This role is responsible for creating and ... Collaborate cross-functionally with Production, QA, QC, Validation, and Engineering teams.
Edmonton, AB · On-site
One aspect of the project involves upgrading the Biotechnology Business Development Centre (BBDC ... Interface with Production, Quality Control, and Compliance functions for: * In-process support
Edmonton, AB · On-site
One aspect of the project involves upgrading the Biotechnology Business Development Centre (BBDC ... Interface with Production, Quality Control, and Compliance functions for: * In-process support
Edmonton, AB · On-site
One aspect of the project involves upgrading the Biotechnology Business Development Centre (BBDC ... Set up a contamination control strategy for the site. * Act as Alternate Biosafety Officer and ...
Edmonton, AB · On-site
One aspect of the project involves upgrading the Biotechnology Business Development Centre (BBDC ... Set up a contamination control strategy for the site. * Act as Alternate Biosafety Officer and ...
One aspect of the project involves upgrading the Biotechnology Business Development Centre (BBDC ... Work with Quality and Engineering to generate lifecycle CSV deliverables for each electronic system ...
One aspect of the project involves upgrading the Biotechnology Business Development Centre (BBDC ... Work with Quality and Engineering to generate lifecycle CSV deliverables for each electronic system ...
| Aspect | Qc Biotech | Qc Microbiologist |
|---|---|---|
| Required Credentials | Bachelor's in Biology, Biotechnology, or related field; GMP/GxP training | Bachelor's in Microbiology, Biology, or related; microbiology certifications |
| Work Environment | Biotech manufacturing labs, quality control departments | Microbiology labs, pharmaceutical or biotech settings |
| Employer & Industry Usage | Biotech companies, pharmaceutical manufacturers | Pharmaceutical firms, biotech research labs |
| Common Search & Comparison | Yes | Yes |
While both Qc Biotech and Qc Microbiologist roles involve quality testing in biotech and pharmaceutical settings, Qc Biotech focuses on overall product quality, including assays and validation, whereas Qc Microbiologists specialize in microbiological testing and contamination control. The roles often overlap but differ in specific expertise and focus areas.
For Qc Biotech jobs in Alberta, the most frequently searched job titles are:
The top searched job categories for Qc Biotech jobs in Alberta are:

Full-time
Medical, Retirement, PTO
Re-posted 7 days ago
Applied Pharmaceutical Innovation (API) brings life-saving research to the real world by helping life science innovators bridge the gap between academic research and commercial product development. We are driven, compassionate, and laser focused on making a dramatic positive impact with everything we undertake.
When you join API, you are part of a rapidly growing team that is creating collaborative opportunities to commercialize Canadian life sciences discoveries, increasing the amount of commercial research and development in the country, and supporting Alberta as a key pillar in Canada's life sciences sector.
We are seeking a detail-oriented Coordinator, Complianceto support pharmaceutical manufacturing operations at our Biotechnology Business Development Centre. This role is responsible for creating and managing GMP-compliant technical documentation, ensuring regulatory adherence, and supporting batch record review, audits, and quality processes. The successful candidate will be working cross-functionally with Production, Quality, and Engineering teams and will help maintain inspection readiness and uphold data integrity in a fast-paced, regulated environment, contributing to critical drug development and manufacturing initiatives.
** Please note this position requires full-time on-site presence.
Key Responsibilities, include but are not limited to:
Technical Documentation Management:
Compliance Coordination:
Batch Record Review:
Change Control & Deviation Support:
Audit & Inspection Readiness:
Training & Collaboration:
Qualifications - (Education, Certification, Degree, Skills, Knowledge, etc.)
Education
Experience:
Personal Competencies
Working Conditions:
Additional Required Documents to Support Application
Perks and Benefits at API
Comprehensive Health Coverage: At API, we prioritize the well-being of our employees. We offer a comprehensive health coverage plan. Our premiums are 100% covered, ensuring that you and your dependents receive the necessary healthcare support.
Retirement Savings: API offers a RRSP Matching Program. Employees may be eligible to participate, with API matching of contributions up to 1-3% of base salary, in accordance with program terms.
Professional Development Opportunities: We foster a culture of continuous learning and growth. API provides access to various professional development opportunities, including training programs, workshops, conferences, and certifications. We encourage employees to enhance their skills, broaden their knowledge, and stay updated with the latest advancements in the life sciences industry.
Collaborative and Inclusive Environment: At API, we believe in the power of collaboration and diversity. We foster an inclusive work environment that values and respects individuals from all backgrounds. We promote teamwork, open communication, and a supportive atmosphere where everyone's contributions are valued.
Generous Paid Time Off: We understand the importance of taking time off to recharge and maintain a healthy work-life balance. API offers a generous paid time off (PTO) policy that includes vacation days, medical/personal days, and holidays. We encourage our employees to prioritize their well-being and enjoy quality time away from work.
Green Transit Allowance: Employees based out of an office are eligible to enroll in our green transit program, which promotes the use of environmentally friendly modes of transportation. By participating in the program, you commit to making green transit your primary mode of transportation for at least 75% of your commute to and from work. Green transit includes walking, biking, carpooling, and public transportation.
Work From Home: Eligible employees are entitled to 20 Work from Home days, this is subject to job function, company needs, and manager approval.
How to Apply
Interested applicants must submit a resume and cover letter expressing their interest in the position and why they believe they are a strong candidate.
We appreciate all applicants' interest and will only contact those selected for interviews.
If you have any questions about the application process or require accommodations during the hiring process, please contact careers@appliedpharma.ca.
Our team, clients, and stakeholders come from a variety of backgrounds. In recruiting for our team, we welcome the unique contributions that all people bring to the workplace in terms of varied lived experiences, education, culture, gender, race, sexual orientation, religious or ethnic background, neurodiversity, and cognitive and physical ability.
Before employment, successful candidates will be required to meet the requirements of a pre-employment screening, which includes background reference checks, educational credential verification, and criminal reference checks.
This position will remain open until filled.