Manager, Clinical Supply Chain and Packaging

Thryv Therapeutics Inc.; Brampton; On-site; CAD 90,000 - 120,000; Full time

Job summary

A leading pharmaceutical company in Canada seeks a Manager of Clinical Supply Chain and Packaging. The role involves overseeing packaging, labeling, and distribution for clinical trials, ensuring inventory levels, and managing logistics vendors. Candidates should have a relevant degree and at least 8 years of experience in the pharmaceutical industry, preferably with GMP and FDA knowledge. Excellent communication and organizational skills are essential.

Qualifications

• Minimum of 8 years’ experience in the pharmaceutical or related industry.
• Experience in GMP and FDA environment preferred.

Responsibilities

• Responsible for Clinical Packaging, Labeling and Distribution to clinical sites.
• Ensures availability of intermediates and drug products in the supply chain.
• Manages storage and logistics vendors for shipments.

Skills

Project management skills

Excellent oral/written communication

Organizational skills

Education

Bachelors/Master’s degree in a scientific discipline

Job description

Thryv Therapeutics Inc. is a privately owned company based in Montreal, Quebec, Canada. Thryv Therapeutics is pioneering a precision medicine approach to treat indications including Congenital Long QT Syndrome (LQTS), atrial fibrillation and heart failure with potent and selective inhibitors of Serum Glucocorticoid inducible Kinase (SGK1).

Opportunity Summary

The Manager of Clinical Supply Chain and Packaging will be responsible for clinical labeling, packaging and distribution as well as for planning and implementing activities related to the timeline, cost-effective procurement, inventory and quality control of reference standard and production intermediates. They will develop, implement and maintain policies, procedures and material control systems to reduce costs, streamline procedures and implement solutions. This role will report directly to the Senior Director, Product and Process Development.

Key Responsibilities

• Responsible for Clinical Packaging, Labeling and Distribution to clinical sites.
• Ensures the availability of intermediates, drug substance and drug product in the supply chain and the maintenance of inventory at minimum acceptable levels.
• Responsible for tracking expiry/retest dates and scheduling retesting for all reference and internal (cold-labeled) standards, intermediates, drug substance and drug product.
• Manages storage and logistics vendors for domestic and international shipments.

Education & Work Experience

• Bachelors/Master’s degree in a scientific discipline is required. Equivalent experience may be accepted.
• A minimum of 8 years’ experience in the pharmaceutical or other related industry is required, with GMP and FDA environment experience preferred.

Technical Knowledge & Skills

• A thorough understanding of cGMPs is preferred.
• Experience in clinical packaging and labeling.
• Project management skills are a plus.

Non-technical Skills & Competencies

• Exudes the highest level of integrity and an acute sense of ethics.
• Operates with a sense of urgency and perseverance to achieve results.
• Ability and enthusiasm to work in a cross-functional team environment.
• Superior organizational skills and the ability to multi-task and prioritize competing assignments.
• Excellent oral/written communication, interpersonal, organizational and presentation skills.
• Proactive and self-motivated with the ability to work independently with minimal supervision.
• Ability to work under pressure to meet deadlines.

EQUAL OPPORTUNITY WORKPLACE

Thryv Therapeutics Inc. is proud to be an equal opportunity employer. We are committed to equal employment opportunity regardless of race, colour, religion, sex, sexual orientation, gender identity, age, national origin, disability, and any other characteristic protected by law.

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Please send your resume and cover letter to [e-mail]

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