Technical Manager-Global Annual Product Quality Review (APQR)

F. Hoffmann-La Roche AG; Mississauga; On-site; CAD 90,000 - 120,000; Full time

Job summary

A leading company in healthcare is seeking a Technical Manager for the Global Annual Product Quality Review (APQR) process. This role involves ensuring product quality throughout its lifecycle, conducting reviews, and collaborating with teams to resolve issues. The ideal candidate will have a background in Life Sciences and experience in the pharmaceutical industry. Join us to innovate and improve global health.

Qualifications

• 3-5 years of experience in cGMP pharmaceutical or biopharmaceutical industries.
• Technical expertise in drug manufacturing processes.

Responsibilities

• Conduct annual site and end-to-end reviews for APQR reports.
• Collaborate with stakeholders to resolve product quality issues.
• Develop and maintain global APQR systems.

Skills

Leadership

Data Collection

Problem Solving

Education

B.A., B.S., or higher in Life Sciences

Tools

Enterprise Databases

Collaboration Tools

Analytics

Job description

Technical Manager - Global Annual Product Quality Review (APQR)

Location:

Mississauga

Type:

Full-time

Posted:

2 days ago

Application deadline:

May 23, 2025 (8 days remaining)

Job ID:

202505-110865

About Roche:

At Roche, we embrace diversity and encourage personal expression, open dialogue, and genuine connections. Our culture values you for who you are, fostering an environment where you can thrive both personally and professionally. Our mission is to prevent, stop, and cure diseases, ensuring access to healthcare for all, now and in the future. Join Roche, where every voice matters.

The Position

12-Month Contract

We are driven to innovate and advance science to create a healthier future, providing more time with loved ones. As the Technical Manager for the APQR process, you will support and drive the process per GSP037, identifying trends, issues, and implementing actions to maintain product quality throughout its lifecycle.

Key Responsibilities

1. Conduct annual site and end-to-end reviews to produce APQR reports as per GSP037 requirements.
2. Support data collection and visualization for APQR reports across Roche's network.
3. Collaborate with stakeholders to identify, escalate, and resolve product quality issues, proposing action items as needed.
4. Develop, maintain, and execute global APQR systems, projects, and administrative activities.
5. Ensure timely, accurate, and compliant delivery of cross-functional team deliverables related to APQR and quality oversight activities.

Qualifications

1. B.A., B.S., or higher in Life Sciences or related field, with 3-5 years of experience in cGMP pharmaceutical or biopharmaceutical industries, or equivalent.
2. Strong leadership skills in cross-functional teams, with the ability to resolve complex technical, quality, and business issues.
3. Technical expertise in small and large molecule drug manufacturing processes, control, and documentation systems. Knowledge of medical devices is a plus.
4. Experience with enterprise databases, collaboration tools, analytics, and metrics reporting is preferred.

Additional Information

Relocation benefits are not available for this position.

About Us

Roche is committed to innovation and improving global health. With over 100,000 employees worldwide, we have treated over 26 million people and conducted more than 30 billion tests. We foster a creative environment to deliver impactful healthcare solutions. Join us in building a healthier future.

Roche is an Equal Opportunity Employer.