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Production Specialist At Rameda Pharmaceutical

Production Specialist At Rameda Pharmaceutical

Production Specialist At Rameda Pharmaceutical
Production Specialist At Rameda Pharmaceutical

Rameda is the fastest-growing leading pharmaceutical company in Egypt, led by a team of professionals with extensive multinational experience. The Company develops and produces a wide range of branded generic pharmaceutical products.Rameda combines global standards with local insights, and you are allowed to gain experience professionally through an environment that supports and provides you with the tools you need to learn and move forward in your career. We are committed to attracting and retaining exceptionally talented employees; therefore, we are looking to hire the following post: –

“Production Specialist (Solid Area)”

Worksite: Plant/6th of October

Duties:-
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– Ensures that all activities in his unit or section are done according to the relevant cGMP and ISO standards (ISO 9001/2008, ISO 14001/2004, OHSAS 18001/2007).
– Supervise production line operations following the relevant SOPs and safety instructions.
– Ensure that all production line operators wear their protective equipment (PPE) during work.
– Ensuring that all required documents such as batch records, machine logs, cleaning records, identification labels … etc.. are filled on the spot and handled in a proper way as stated in the relevant SOPs.
– Participate in Issuing batch records and SOPs and keep them always updated as per business requirements
– Ensuring the commitment of all employees in his area to the cGMP standards.
– Deliver the required on-the-job training for production line operators to keep them qualified for doing their jobs properly.
– Conduct employee performance reviews.
– Responsible for shift schedule to include: workstation assignments, employee vacations, employee breaks, overtime assignments, back-up for absent employees, and shift rotations.
– Coordinate production startups, shutdowns, and changeovers.
– Participating in all validation activities as per business requirements.
– Reporting and handling of any violation of cGMP in a formal way as stated in the relevant SOP.

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Qualifications
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1- Bachelor’s degree in pharmacy, science or related discipline
2- Minimum 2 years experience in solid dosage form
3- Awareness of OEE&LEAN manufacturing
4- Outstanding communication skills

We offer:

· Competitive package
· Attractive incentive scheme
· Continuous training and development
· Promising Career Pathways

* Candidates that possess the above qualification kindly send your resume to: career@rameda.com with mentioning the job title in the subject

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