
Job Objective
The Manufacturing Training Manager is responsible for developing, implementing, and overseeing comprehensive training programs for the manufacturing team at the plasma derivatives manufacturing site. This role ensures that all employees are equipped with the necessary skills and knowledge to perform their roles effectively and safely. The Manufacturing Training Manager collaborates with various departments to create and maintain a robust training structure that supports the sites operational goals and regulatory compliance requirements
Key responsibility
Training Program Development:
Training Delivery
Competency Management
Assess employee competencies and identify skill gaps.
Create individual development plans to address identified training needs and enhance employee performance
Regulatory Compliance
Maintain accurate training records and documentation to support regulatory audits and inspections.
Collaboration and Coordination:
Collaborate with quality assurance, safety, and regulatory teams to integrate compliance requirements into training programs.
Coordinate with external training providers and consultants as needed.
Continuous Improvement
Conduct regular reviews and assessments of training materials and methods.
Incorporate feedback from trainees and stakeholders to refine training content and delivery
Reporting and Documentation:
Maintain comprehensive training records, including attendance, assessments, and certifications.
Prepare reports on training activities, outcomes, and progress for senior management.
Academic & Professional experience required
Bachelors degree preferred, preferably in an education or life sciences curriculum.
Advanced degree (MBA or MS) is preferred
Training certifications (e.g., Certified Professional in Learning and Performance, CPTM) are preferred.
Minimum of 5-7 years of experience in a training role within a manufacturing environment, preferably in the pharmaceutical or biotech industry.
Experience in developing and delivering technical training programs.
Computing Skills
Proficiency use of Microsoft Office.
Experienced in SAP environment.
Proficiency in using training software and e-learning platforms.
Familiarity with Documentum compliance systems for managing regulatory documents and ensuring compliance.
Personal Skills
Strong understanding of adult learning principles and training methodologies.
Excellent presentation and communication skills.
Ability to design and develop effective training materials.
Strong organizational and project management skills.
Familiarity with regulatory requirements and GMP standards.
Ability to assess training needs and develop competency frameworks.
Languages
Fluent written and spoken English and Arabic.

Grifols Egypt for plasma derivatives is a joint-venture (JV) company between the Egyptian Government, through the National Service Projects Organization (NSPO) and Grifols, the global leader in plasma medicines with more than 110 years of contribution to improving the health and well-being of people.
This joint venture is the first of its kind in the plasma industry and the first-ever Egyptian source member of the Plasma Protein Therapeutics Association (PPTA). GEPD is a groundbreaking global public-private alliance that will benefit the entire region.
GEPD is committed to developing the plasma medicines market and achieving self-sufficiency in these critical therapies, which is crucial for the Egyptian healthcare system.
We are combining the expertise of both shareholders to build and operate 20 plasma donation centers throughout Egypt, along with manufacturing facilities including fractionation, purification, and fill-and-finish plants with a processing capacity of up to 1 million liters of plasma annually that can double in the future.
The new manufacturing facility will include a plasma warehouse and a testing laboratory. It will occupy 105,000 square meters strategically located in the administrative capital’s medical city, adjoining various healthcare institutions.