Manager, Drug Product Operations & Engineering - Eurofins CDMO Alphora, Inc.

Eurofins•Mississauga, ON

19h•CA$120,000 - CA$120,000

About The Position

Eurofins CDMO Alphora Inc. develops and manufactures new therapeutics to improve the lives and health of patients. Eurofins CDMO Alphora provides contract research & development services to global pharmaceutical and biotech companies, developing their processes and manufacturing their bulk drug substances (Active Pharmaceutical Ingredients -“API’s”) as well as finished dosage products (tablets, capsules, suspensions) for supply to clinical trials and commercial requirements. Eurofins CDMO Alphora provides a rich and technologically challenging environment with a continuing flow of interesting projects. Our employees work in close concert with clients throughout the development process to achieve their program objectives. Eurofins CDMO Alphora Inc. is growing its state-of-the-art organization, with continued investments in modern facilities, equipment, and instrumentation while providing a rich environment for employees to develop their technical skills and careers paths. Lead Operations. Drive Innovation. Deliver Life-Changing Therapies. Are you a results-driven pharmaceutical operations leader with a passion for building high-performing teams, advancing manufacturing excellence, and delivering client success? We are seeking a Manager, Drug Product Operations & Engineering to lead our Drug Product Operations team and play a critical role in the successful development and manufacture of clinical-stage pharmaceutical products. This is an exciting opportunity to oversee a broad portfolio of operational, technical, engineering, and commercial activities while partnering with clients and internal stakeholders to bring innovative therapies to patients. As a key member of the leadership team, you will provide strategic direction for manufacturing operations, engineering initiatives, production planning, warehouse and materials management, and continuous improvement programs. You will also serve as a trusted technical and commercial partner, helping clients achieve their development milestones while ensuring operational excellence, regulatory compliance, and business growth.

Requirements

Minimum 10 years of experience within the pharmaceutical industry.
Minimum 5 years of leadership experience managing technical, operational, or manufacturing teams.
Strong experience in drug product development and manufacturing, particularly within solid dosage forms.
Demonstrated success leading GMP manufacturing operations and technical teams.
Strong business acumen with experience supporting commercial activities, quotations, forecasting, and client interactions.
Excellent verbal and written communication skills.
Proven ability to effectively manage multiple priorities in a fast-paced environment.
Proactive, hands-on leadership style with a focus on collaboration and accountability.

Nice To Haves

Strong problem-solving and decision-making capabilities.
Experience working within a contract development and manufacturing organization (CDMO) environment.
Passion for operational excellence, continuous improvement, and team development.
Ability to influence across functions and build strong relationships with clients and stakeholders.

Responsibilities

Lead all Drug Product manufacturing operations supporting client development programs and the production of cGMP clinical supply materials.
Oversee daily operations within production suites, warehouse activities, materials management, and associated support functions.
Ensure facilities, equipment, and manufacturing operations remain inspection-ready and compliant with GMP requirements.
Drive operational excellence through effective production planning, scheduling, resource allocation, and inventory management.
Provide strategic leadership to Drug Product Technical and Engineering teams.
Support client programs through process development, technology transfer, scale-up, and manufacturing activities.
Serve as the department's primary technical resource for existing and future manufacturing equipment and capabilities.
Partner with Engineering teams to maintain a robust equipment qualification and preventive maintenance program.
Identify, evaluate, and implement new technologies, capital projects, and continuous improvement initiatives.
Serve as the primary commercial lead for the department.
Support revenue forecasting and ensure accurate and timely revenue recognition.
Lead the development of competitive client proposals and quotations.
Build strong relationships with current and prospective clients, providing technical insight and program updates throughout development projects.
Collaborate with Formulation, Analytical, Quality, and other cross-functional teams to develop robust and scalable manufacturing processes.
Implement process improvements that enhance efficiency, productivity, quality, and cost performance.
Conduct pre-production batch reviews to ensure operational readiness and safety compliance.
Troubleshoot facility, equipment, and process issues using sound scientific and engineering principles.
Ensure compliance with all applicable GMP, Quality Systems, Environmental, Health & Safety, and regulatory requirements.
Develop, review, and maintain SOPs and operational procedures as required.
Provide leadership that fosters a strong culture of safety, quality, accountability, and continuous improvement.
Interface with regulatory agencies, auditors, inspectors, and external stakeholders as needed.