Manager, North America Quality Operations
Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing unique, accessible, and high-quality medications, Azurity leverages its integrated capabilities and vast partner network to continually expand its broad commercial product portfolio and robust late-stage pipeline. The company’s patient-centric products span the cardiovascular, neurology, endocrinology, gastro-intestinal, institutional, and orphan markets, and have benefited millions of patients. For more information, visit www.azurity.com.
Azurity Pharmaceuticals is proud to be an inclusive workplace and an Equal Opportunity Employer. Azurity's success is attributable to our incredibly talented, dedicated team that focuses on benefiting the lives of patients by bringing the best science and commitment to quality into everything that we do. We seek highly motivated individuals with the dedication, integrity, and creative spirit needed to thrive in our organization.
Brief team/department description:
Azurity is seeking a Quality Assurance Manager to lead batch release activities in Canada and ensure full compliance with Health Canada GMP and GDP regulations. In addition to core Canadian Quality Operation responsibilities, this role will support North American quality operations including CMO oversight, deviation assessment, change control, CAPA management, audits, and technical batch release.
Principle Responsibilities:
- Provide QA oversight for all quality aspects of assigned vendors based in US/CAN, including deviation/OOS/OOT investigations and assessment, change control, CAPA evaluation and complaint approvals.
- Establishment and maintenance of Quality Assurance Agreements with North American Vendors.
- Assess technical documentation for batch disposition (e.g., CoAs, investigation reports, stability data, transportation records) to support in-market product release.
- Batch disposition for commercial batches in accordance with Health Canada regulatory requirements (GMP and GDP), including those outlined in the Food and Drugs Act, Food and Drug Regulations (C.02 GMP) and applicable guidance.
- Ensure pharmaceutical Products are manufactured in accordance with current Good Manufacturing Practice (GMP) and specifications approved in Marketing Authorizations.
- Ensure pharmaceutical Products are distributed in accordance with Good Distribution Practices (GDP).
- Independently from Azurity’s Management, decides whether a batch can be released for distribution to Canadian market.
- Support regulatory inspections from Health Canada and manage follow-up actions.
- Establishment and maintenance of a compliant Canadian Quality Management System: deviation handling, CAPAs, change control, annual product quality reviews, stability programs, document control, training and risk assessments. Management of quality and compliance risks impacting Canadian batches.
- Conduct and support GMP/GDP audits of CMOs, 3PLs, and contract labs within North America.
- Drive continuous improvement and ensure training of QA personnel related to Canadian compliance requirements.
- Management and disposition of returned Products from the Canadian market.
- Management of Product recalls and involvement in periodic mock recalls for the Canadian market.
- Reporting of any Product defects to Health Canada.
- Maintain and ensure the validity of Azurity’s Drug Establishment License (DEL).
- Ensure accuracy of Certified Product Information Document (CPID) by periodic co-reviews.
- Collaborate cross-functionally with Supply Chain, Regulatory Affairs, Technical Operations, for the supply of medicinal products to the North American market.
- Conduct and/or review quality audits for facilities and service providers. Assure that the Vendors relevant to Canadian market have valid certifications and/or licenses issued by local authorities.
- Ensure quality processes align with international standards (e.g. ICH, PIC/S) and local market requirements.
- Ensure Product Master documents are available and in compliance with Marketing Authorization.
- Annual renewal of Unique ID Letter (if applicable).
- Collaborate cross-functionally with Supply Chain, Regulatory, Technical Operations, for the supply of medicinal products to the Canadian market.
Qualifications and Education Requirements
- Advanced University degree in pharmacy, chemistry, biology or other science-related field.
- Minimum 10 years in pharmaceutical QA.
- Thorough understanding of Health Canada GMP, GDP and Importation regulations, DEL requirements and compliance frameworks.
- Experience in interacting with regulatory agencies and supporting Health Canada inspections.
- Must be a permanent resident of Canada authorized to work in the country.
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Physical & Mental Requirements:
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
- Must be able to sit for long periods of time
- While performing the duties of this job, the employee is frequently required to stand; walk; sit; talk and/or hear
- May occasionally climb stairs and/or ride elevators
- The employee must occasionally lift and/or move up to 25 pounds
- Employee must be able to manipulate keyboard, operate a telephone and hand-held devices
- Other miscellaneous job duties as required
Benefits We Offer:
- Unlock Your Earning Potential: Join our team and be rewarded with a competitive compensation package, including an annual bonus based on company performance, that recognizes your exceptional talent.
- Sales - In lieu of annual bonuses, we offer an Incentive compensation program that allows you to earn more - even over plan.
- Fuel Your Success: *Sales Only* - We understand the value of your hard work and provide a car reimbursement program and gas card for both business and personal use as part of our commitment to supporting you.
- Comprehensive Health Coverage: We value your well-being and offer excellent medical, dental, vision, and prescription coverage to ensure you and your family are always taken care of.
- Flexibility for Your Lifestyle: Achieve work-life balance with our hybrid work model, allowing you to work two days from home and three days in the office. *Excludes Sales, Manufacturing, and some Operations positions*
- Start Your Week on a High Note: Indulge in our “Bagel Tuesday” perk, where you can enjoy a fresh bagel on us every Tuesday morning. **Only for On-site/Hybrid colleagues**
- Invest in Your Future: Our Retirement Savings Plan (401K) is designed to help you secure a comfortable retirement by matching dollar for dollar up to 5%.
- Time Off That Counts: Take advantage of our generous time off policy, which offers up to 15 vacation days annually + rollover (up to 40 hours) as well as five sick/wellness days. For new employees, vacation accrual will be prorated based on your start date.
- Meaningful Time with Your Loved Ones: We close between Christmas and New Year’s to give you an extra week off to spend quality time with your family and recharge.
- Enjoy the Holidays: Over the course of the year, Azurity recognizes 13 holidays.
- Summer Vibes: Embrace the summer season with our Summer-Hours perk, available between Memorial Day and Labor Day. **Excludes Sales Colleagues**
- Invest in Your Education: We support your professional growth with tuition reimbursement for undergraduate and graduate level courses or certifications.
- Recognize and Be Recognized: Our Azurity High Five peer recognition platform allows you to celebrate your colleagues' accomplishments and receive recognition for your own outstanding work.
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