Entry Level Jobs at Gilead Pharmaceutical Limited
Posted on: 9 February, 2016
30 March, 2016 Deadline:
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Gilead Pharmaceutical Limited is recruiting for qualified candidates to fill the position of:
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.
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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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
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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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.
Experience working in a clean room environment
Experience working as part of a team in a fast paced environment
Method of Application
To apply, send your applications and CV's to:
firstname.lastname@example.org Note: Only shortlisted applicants will be contacted.
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