Senior QC Project Manager

Job summary

Manage analytical method transfer projects from initiation through close-out, ensuring compliance with applicable procedures and quality requirements. Coordinate project plans, documentation, risks, resources, analytical results, reporting, and stakeholder communication across multiple concurrent transfers.

Job details

Location: Remote, Canada Level: Mid-level to Senior Practice: Life Sciences, Quality and Compliance About the role Amaris Consulting is looking for an experienced Senior QC Project Manager to support the development of a potential nearshore delivery team for a major pharmaceutical client. The role will support the Analytical Method Transfer platform, which manages approximately 50 projects per year, with around 20 projects running in parallel and coordination across six Analytical Transfer Leads. You will be responsible for managing analytical method transfer projects from initiation through close-out, while ensuring compliance with procedures and quality standards. Key responsibilities Manage analytical method transfer projects from kick-off through close-out. Follow the GQSOP 078 process and ensure project activities remain aligned with applicable quality requirements. Create and maintain project Gantt charts, milestones, timelines and deliverable plans. Coordinate risk assessments, equipment and reagent requirements, training and testing activities. Contribute to the preparation and review of key project documentation, including TTP, AMTP, AMTR and close-out packages. Coordinate analytical results, statistical analysis and issue resolution. Support change controls, project reporting and communication with stakeholders. Track project progress, dependencies, risks and actions across multiple concurrent transfers. Identify opportunities to improve templates, planning processes and ways of working. Collaborate with international teams to ensure clear communication and timely delivery. Candidate profile We are looking for a mid-level to senior professional with: At least five years of experience in pharmaceutical quality control, analytical methods or analytical method transfer. Strong project management and coordination skills. A solid understanding of GMP and pharmaceutical QC processes. Experience reviewing analytical data and performing or coordinating statistical analysis. Experience with change controls, technical documentation and project planning. The ability to work comfortably in English with international stakeholders. Strong organisational skills and the ability to manage several projects in parallel. A proactive approach to issue resolution and continuous improvement. The following would be considered an advantage: Experience with analytical method transfer processes in a pharmaceutical environment. Experience improving processes, automating activities or creating project templates. Familiarity with analytical transfer documentation, including TTP, AMTP and AMTR. Working arrangement This is a fully remote position open to Canada-based candidates. If you have experience managing analytical method transfer projects and are looking to contribute to a high-impact pharmaceutical delivery programme, we would be pleased to hear from you. Why choose us An international community bringing together more than 110 different nationalities An environment where trust is central: 70% of our leaders started their careers at the entry level A strong training system with our internal Academy and more than 250 modules available A dynamic work environment that frequently comes together for internal events (afterworks, team buildings, etc.) Amaris Consulting promotes equal opportunities. We are committed to bringing together people from diverse backgrounds and creating an inclusive work environment. In this regard, we welcome applications from all qualified individuals, regardless of sex, sexual orientation, race, ethnicity, beliefs, age, marital status, disability, or other characteristics.

What you’ll do

Manage analytical method transfer projects from initiation through close-out, ensuring compliance with applicable procedures and quality requirements. Coordinate project plans, documentation, risks, resources, analytical results, reporting, and stakeholder communication across multiple concurrent transfers.

Requirements

Candidates must have at least five years of experience in pharmaceutical quality control, analytical methods, or analytical method transfer, along with strong project coordination skills and a solid understanding of GMP and pharmaceutical QC processes. Experience with analytical data and statistical analysis, change controls, technical documentation, and project planning is required; familiarity with transfer documentation and process improvement is an advantage.

Benefits

• Training and Development • Internal Academy • Team-Building Events

Listed skills

• Technical Documentation · Preferred
• issue resolution · Preferred
• Project management · Preferred
• Process Improvement · Preferred

Other relevant skills

Identified from the job description. Confirm important requirements above.

• Project Management
• Analytical Method Transfer
• Pharmaceutical Quality Control
• Good Manufacturing Practices
• Statistical Analysis
• Analytical Data Review
• Change Control
• Technical Documentation
• Project Planning
• Risk Assessment
• Stakeholder Communication
• Issue Resolution
• Quality Compliance
• Process Improvement
• Gantt Chart Management

Job areas

• Management & Leadership
• Healthcare
• Science & Research
• Consulting