IPC Specialist - Pharmaceutical

PREVIOUS EXPERIENCE OF THE SAME ROLE IS ESSENTIAL

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Multicare Egypt for Pharmaceutical Industries is an equal opportunity employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, gender identity or expression, age disability, or other characteristics protected by prevailing regulations, practice or customs/traditions.

Multicare is a well-established Pharmaceutical Company with diversified scope in both manufacturing and marketing of pharmaceutical products, supplements, cosmetics and medical devices. Multicare has +20 years of prominent existence in the local market and has almost 35 products marketed and more to come through the pipelines. Multicare Egypt for Pharmaceutical Industries is the manufacturing facility of Pharmacare for Trading Agency, which located at the Industrial Zone – New Cairo and its HQ at New Cairo as well. We are one of the fast growing Pharmaceutical Companies in the market which has strong ambition and aspiration to be one of the key players not only in Egypt but also within the region.
Our international alliances are effective in different countries, including Saudi Arabia, United Arab of Emirates, India and New Zealand with future aspiration to extend more business associations and affiliations in near future to further markets. Recently Multicare Poland has been launched which will be the entry port of the business to the European Union (EU).

Job Purpose:

To check performed activities during production to monitor and, if appropriate, to adjust the process to ensure that the intermediate or API (drug substance) conforms to its specifications and/or other defined quality criteria

Designation: QA In-Process Control Specialist
Location: New Cairo HQ
Job Grade: qA1/qA02
Reporting: QA Section Head

A. Essential Duties and Responsibilities:

• Monitor, control and improve effectively the whole applied operations at every stage of the finished pharmaceutical products
• Work closely with manufacturing to address any production issues on shift and ensure appropriate documentation
• Perform sampling process for all manufacturing and packaging steps according to sampling plan for analysis
• Handle all required quality assurance functions, recommend and implement improvements for product manufacturing
• Apply in process tests to ensure product compliance with established specifications and provide vis-à-vis reports accordingly
• Inspection on the division of the warehouse release area, guarantee area and the reject area with the true identification labels
• Recording any complain from any customer from any product and investigate about the reason of the problem and solving
• Carry out the issuance and weighing process of raw materials to guarantee the conformity of specifications to quality standards, approving the release of materials to production, as well as ensuring compliance of raw material storage with regulatory guidelines
• Monitor GMP & system implementation on daily basis and providing related reports accordingly
• Documentation of validation steps according to the prevailing policies and procedures
• Ensure strict adherence to the relevant cGMP and ISO standards (ISO 9001, ISO 14001, OHSAS 18001