Entry Level Jobs at Gilead Pharmaceutical Limited

Job Details

• To manage the design, development, testing and support of data gathering and data processing systems / tools
• To provide training and support on data capture and processing tools.
• To monitor and manage the quality of data tools and systems.
• To capture, process and collate data for use in databases
• To generate reports using database and assist in their analysis.

Candidate Requirements

• A Bachelors Degree in a IT based subject
• Excellent communication skills (both written and oral)
• A concern for quality, attention to detail and accuracy
• Ability to analyse and think logically
• Ability to work independently in a fast-paced environment
• Good working knowledge of Excel
• Knowledge of database systems
• Not essential but any experience with Visual Basic, Web application development would be advantageous.
• Good organizational and administrative skills

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Job Details

• As a Quality Assurance Pharmacist you are responsible of the quality processes especially in API according to CROs
• Preparation and implementation of SOPs
• Document management and change control management.
• Responsible for employee trainings
• Competence for internal and external audits, as well as their proper implementation
• Responsibility for the complaint management in GMP.
• Responsible for all relevant process optimizations and validation

Requirements

• Degree in Pharmacy preferred
• 1-3 years professional experience in the pharmaceutical Industry
• Good knowledge in GMP
• Experienced in all EDV-Systems
• Excellent English skills in speaking and writing
• Flexible and a team player.

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Job Details

• Manufacturing chemotherapy, total parenteral nutrition (TPN) and antibiotic pharmaceuticals in a clean-room environment using barrier isolator technology in accordance with procedures and regulations;
• Operation of gas sterilization units for the sterilization of isolators;
• Environmental monitoring of the clean-room facility;
• Assisting in process and equipment validation in accordance with procedures and regulations;
• Observation and active promotion of Good Manufacturing Practices;
• Liaising with Customer Services and Warehousing on goods inwards and delivery related issues;
• Facility Monitoring (fridges, isolator physical parameters, pressure differentials, incubators);
• Stocking and maintenance of changing rooms and other ancillary areas;
• Stock maintenance in Grade D preparation areas;
• Tray assembly (assembly of products required for manufacture);
• Tray assembly checking (verification of assembled items for manufacture);
• Transfer sanitization to Grade D and Grade C clean-rooms;
• Cleaning of isolators, integrity checking and pressure gauge checking;
• Transfer sanitization into Isolators
• Volume and in-process checking;
• Environmental monitoring of isolators;
• Liaising with the Quality department on quality-related issues including maintaining and development of GMP within the manufacturing area.

Qualifications and Experience
Essential:

• Diploma or Degree in Science or a Healthcare-related discipline;
• Previous experience in a GMP healthcare production environment or experience of aseptic pharmaceutical production gained in a hospital or industrial setting.

Preferred:

• Experience working in a clean room environment
• Experience working as part of a team in a fast paced environment