مطلوب ضابط أول لدى أدوية الحكمة في القاهرة ,مصر

Sr. Officer, Validation

About the job
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 [email protected] so that we may provide it to relevant law enforcement agencies, as appropriate.

إقرأ أيضا:وظائف شركة Oceaneering النفط والغاز بابوظبي ودبي

Website

http://www.hikma.com Job Summary:

Responsible for performing basic tasks and some standardized routine testing and maintaining a high level of quality section services by monitoring and recommending solutions to quality-related issues. Job holders also train lower-level jobs to ensure continuity of work and compliance to set standards.

Job Description

Follows all relevant Quality instructions so that work is carried out in a controlled and consistent manner.
Follows the day-to-day operations related to own jobs in the function to ensure continuity of work.
Participates as a team member, under close supervision, and receives and carries out detailed instructions in order to grow professional capability.
Applies standard quality techniques to provide solutions to problems involving a limited number of variables.
Applies technical knowledge, following established procedures and/or standard practices, to perform basic analyses.
Preparation and reviewing of the validation documents, systems, SOPs, protocols & reports preparation.
Preparation and reviewing of the qualification documents, systems, SOPs, protocols & reports preparation.
Preparation and reviewing of the documents related to pharmaceutical premises, utilities, equipment & software validation & qualification.
Preparation and reviewing of the documents related to pharmaceutical premises, utilities, equipment calibration, and the related documents, systems, SOPs, protocols & reports preparation & implementation as per the latest requirements.
Preparation and reviewing of the pharmaceutical laboratories equipment’s validation, qualification, calibration, and the related documents, systems, SOPs, protocols & reports preparation & implementation.
Preparation and reviewing of the thermal mapping and internet of things implementation and reporting.
Preparation and reviewing of the pharmaceuticals process validation documents, systems, SOPs, protocols & reports preparation & implementation as per the latest requirements.
Preparation and reviewing of the pharmaceuticals cleaning validation documents, systems, SOPs, protocols & reports preparation & implementation as per the latest requirements.