Open Vacancies At Gypto Pharma
Gypto Pharma is looking for dynamic, innovative, and passionate individuals to join our team as a Raw Material Specialist.
Job Description:
1- Responsible for ensuring that raw and packaging materials meet the company's quality standards and comply with GMP.
2- Collecting and testing samples of raw and packaging materials, intermediates, and finished products according to approved protocols and specifications.
3- Implementing and maintaining Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and ISO requirements relevant to the role.
4- Preparing, standardizing, and maintaining reference standards, volumetric solutions, glassware, and reagents, ensuring proper handling and storage as per SOPs.
5- Ensuring that Environmental, Health, and Safety (EHS) requirements are fulfilled during work and supporting the implementation of the GYPTO Production System (GPS) for managing various analytical lab activities.
Qualifications:
- Bachelor's degree in Pharmaceutical Sciences, Vet Medicine, or Science.
- Proven experience in raw material analysis for at least 1-3 years.
- completed or exempted military service.
- Professional using computers & Microsoft Office.
- Organized and detail-oriented.
- Has good communication skills.
- Strong analytical skills.
If you meet the above requirements, Don’t miss this opportunity and
Send your Resume to HR Email: (hr@gyptopharma.com)
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Gypto Pharma is looking for dynamic, innovative, and passionate individuals to join our team as a Quality Compliance Section Head.
Job Description:
1. Review and ensure compliance of QMS policies, SOPs, and guidelines (EDA, WHO, EMA, FDA, etc.).
2. Oversee key policies related to customer complaints, recalls, sterile & non-sterile operations, risk management, supplier qualification, and change control.
3. Act as the process owner for change control, ensuring effective implementation of planned changes.
4. Lead and manage projects related to commercial, R&D, technical, and supply changes.
5. Ensure timely completion of PQRs in accordance with regulatory requirements.
6. Lead internal and external audits, including regulatory and toll manufacturer audits.
7. Ensure timely and effective closure of CAPA.
8. Deliver GMP, GDP, & data integrity training courses across the site.
Qualifications:
- Bachelor's degree in Pharmaceutical Sciences, Vet Medicine, or Science.
- Minimum of 10 years of experience in quality systems, with a strong preference for experience in sterile manufacturing.
- Proven track record in managing QMS, CAPA, change control, and quality risk management.
- Knowledge of global regulatory guidelines (EDA, WHO, EMA, FDA, etc.).
- Strong leadership and team management skills.
- Excellent communication and collaboration abilities.
- Action-oriented with strong problem-solving and decision-making skills.
- High level of integrity, self-discipline, and commitment to achieving targets.
If you meet the above requirements, Don’t miss this opportunity and
Send your Resume to HR Email: (hr@gyptopharma.com)