GMP - Technical Training Expert

About Minapharm:

Minapharm Pharmaceuticals is a leading pharmaceutical company in Egypt and the Middle East and the largest end-to-end manufacturer of biological therapies in MEA with over 20 years of experience in cellular and bioprocess engineering.

Headquartered in Cairo, Minapharm commercializes over 100 life-saving and life-enhancing products ranging from small molecules to complex bioengineered proteins and viral vectors, with an impressive immunotherapy pipeline.

Together with its wholly-owned Berlin-based subsidiary, ProBioGen AG - a world-leading CDMO, Minapharm has established an integrated business model making it the only gene-to-market company in the region.

Consolidating its international platform of intelligent biopharmaceutical technologies with the longstanding process development and manufacturing expertise in the MEA, Minapharm, together with ProBioGen, have incorporated MiGenTra GmbH headquartered in Berlin and manufacturing in Cairo, to enhance the accessibility to critical healthcare transforming medicines through product development and commercialization of Biosimilar mABs, Cell, and Gene Therapies and vaccines, at affordable prices in Egypt, and MEA.

Minapharm Group of Companies employs a collective workforce of more than 1400 Individuals & continues to expand their workforce with Talented Human Capital.

Our Core Values:

Diversity & Respect

Integrity & Accountability

Collaboration

Leadership & Empowerment

Innovation & Continuous Learning

Job Summary:

The Technical Training Expert will facilitate the development of technical training activities including cGxP, lean and Six Sigma training programs. Follow up the implementation of training plan and facilitate its completion.

Duties & Responsibilities:

1. Follow up the implementation of annual GMP training plans for Quality / cGxP related training programs
2. Facilitate development of cGxP, lean and Six Sigma training programs
3. Conduct basic cGMP training programs.
4. Follow up the implementation of training programs to employees and provide necessary information about sessions
5. Gather data required for cGxP training needs assessment (TNA) to identify skills or knowledge gaps that need to be addressed
6. Order educational aids and materials
7. Gather data for instructional effectiveness to determine the impact of training on employee skills and KPIs
8. Gather feedback from trainers and trainees after each educational session
9. Maintain updated curriculum database and training records.

Qualifications (Educational Background & Preferred Experience)

• Bachelor Degree of Pharmaceutical Science.

Experience:

• 3 - 5 years of experience in Quality Assurance, validation or Production in pharmaceutical industry (has experience in training coordination is preferable)

Training:

• cGMP
• Lean manufacturing and six sigma

Knowledge:

• Knowledge of basic excel and word.
• Good capability to gather data from different sources including the internet
• Knowledge of Minitab and Visio software
• Good Knowledge of basic cGMP regulations and guidelines

Abilities:

• Communicate with all different levels.
• Facilitate cross functional teams.
• Plan and prioritize tasks
• Training & Presentation skills
• Certified TOT
• Good reporting skills

Behavioral Competencies:

• Adhering to principles and values.
• Deciding and initiating actions.
• Problem solving