At Hikma we put better health within reach, every day in more than 50 countries around the world. For more than 40 years, we've been creating high-quality medicines and making them accessible to the people who need them. Headquartered in the UK, we are a global company with a local presence across the United States (US), the Middle East and North Africa (MENA) and Europe, and we use our unique insight and expertise to transform cutting-edge science into innovative solutions that transform people's lives. We're committed to our customers, and the people they care for, and by thinking creatively and acting practically, we provide them with a broad range of branded and non-branded generic medicines. Together, our 8,600 colleagues are helping to shape a healthier world that enriches all our communities. We are a leading licensing partner, and through our venture capital arm, are helping bring innovative health technologies to people around the world. For more info Disclaimer: EMPLOYMENT RECRUITMENT FRAUD ALERT Please be advised that the Hikma Pharmaceuticals Group does not ask its employees or prospective employees to wire any money either to its bank accounts or to any third party, and does not conduct employment interviews via any social media platform, Google Hangouts, Yahoo! Messenger, text message, or e-mail. Unfortunately, employment scams are increasingly common and it is important to remain vigilant when conducting a job search. For more information about these scams, see the UK National Fraud Intelligence Bureau’s website and the US Better Business Bureau’s article on the subject. If you receive a request to send money through any means or a request for personal information from anyone claiming to be a Hikma recruiter, DO NOT REPLY. Instead, please forward the communication(s) to us at vacancy@hikma.com so that we may provide it to relevant law enforcement agencies, as appropriate.
Website
http://www.hikma.com Job Purpose:To supervise the manufacturing of solid dosage forms (tablets, capsules) ensuring full compliance with GMP requirements, achieving production targets, and maintaining product quality, safety, and efficiency throughout all production stages
Duties & Responsibilities:
- Supervise dispensing, granulation, blending, compression, coating, and encapsulation processes.
- Ensure production activities are executed according to approved SOPs and BMRs.
- Monitor critical process parameters (CPPs) such as blending time, compression force, coating parameters.
- Verify line clearance before starting any batch activity.
- Ensure proper documentation of all production activities in batch records and logbooks.
- Review Batch Manufacturing Records (BMR) for completeness and accuracy.
- Maintain environmental conditions (temperature, humidity, differential pressure) within limits.
- Ensure compliance with GMP, hygiene, and safety standards in production areas.
- Investigate and report deviations, incidents, and non-conformities and participate in CAPA implementation.
- Coordinate with QA, QC, and Engineering for smooth production operations.
- Ensure proper cleaning and sanitation of equipment and production areas.
- Participate in validation activities (process validation, cleaning validation).
- Monitor equipment performance and report any malfunction or maintenance needs.
- Optimize production processes to improve yield, reduce waste, and increase efficiency.
- Ensure adherence to production schedules and achieve planned targets.
- Train and supervise operators on SOPs, GMP, and safety practices.
- Job Location: Bady City, Cairo
Qualifications:
- * Bachelor’s degree in Pharmacy.
- Fresh Graduate.