Manager, Technology Transfer - API Manufacturing - Eurofins CDMO Alphora, Inc.

Eurofins; Oakville; On-site; CAD 80,000 - 120,000; Full time

Job summary

An established industry player in life sciences is seeking a Manager for their Technology Transfer department. This role involves strategic leadership in overseeing cGMP manufacturing processes, ensuring compliance with industry standards, and managing a team of skilled professionals. The successful candidate will design and implement scalable chemical processes while fostering collaboration with various stakeholders. With a strong emphasis on continuous improvement and adherence to safety protocols, this position offers a unique opportunity to contribute to a recognized leader in the field. Join a dynamic team and make a significant impact in a growing organization.

Benefits

Health Insurance

Dental Insurance

Life Insurance

RRSP with 3% match

Paid Holidays

Time Off

Qualifications

• Over 10 years of experience in pharmaceutical manufacturing.
• Proven leadership and team management skills in a cGMP environment.

Responsibilities

• Lead a team of Process Specialists and manage departmental activities.
• Design scalable processes and ensure compliance with SOPs and EHSPs.

Skills

Leadership

Project Management

Communication

Multitasking

Interpersonal Skills

Education

MSc in Chemistry

PhD in Chemical Engineering

Job description

Manager, Technology Transfer - API Manufacturing - Eurofins CDMO Alphora, Inc.

Job Description

Eurofins CDMO Alphora is seeking a Manager, Technology Transfer to oversee our cGMP manufacturing facilities. The role reports to the Director of Operations and provides strategic leadership for the Technology Transfer department, aligning with Manufacturing Business Unit goals. Responsibilities include designing, implementing, and executing chemical processes safely, complying with cGMP, EHS, and company standards.

This position is onsite.

Key Duties and Responsibilities:

1. Lead a team of 5-10 Process Specialists.
2. Manage departmental activities such as planning, training, performance, recruitment, and budgeting.
3. Support production schedules and collaborate with Manufacturing BU stakeholders.
4. Design scalable processes from gram to multi-kilo scale, generate Master Batch Records, and oversee batch meetings and record reviews.
5. Coordinate exception management to meet deadlines.
6. Ensure compliance with CAPA, audits, and training commitments.
7. Establish process workflows and departmental KPIs.
8. Participate in project meetings and promote continuous improvement initiatives.
9. Lead training efforts and facilitate seamless process transfers.
10. Interact with clients, auditors, and regulatory agencies as needed.
11. Adhere to SOPs and EHSPs.

Qualifications:

• MSc or PhD in Chemistry or Chemical Engineering (preferred).
• Over 10 years’ experience in pharmaceutical manufacturing.
• Proven leadership and team management skills.
• Experience in a cGMP environment.
• Excellent communication, multitasking, interpersonal, and project management skills.

Additional Information:

Eurofins offers comprehensive benefits including health, dental, life insurance, RRSP with 3% match, paid holidays, and time off. Accommodations are available for persons with disabilities. Join a recognized global leader in life sciences with a strong growth trajectory. Only local applicants within the GTA will be considered. No agency inquiries.