Current Job Positions at Gilead Pharmaceutical Limited, February 2016


Gilead Pharmaceutical Limited, is currently seeking to employ suitably qualified candidates, to fill the positions below:


Job Title: Quality Assurance Pharmacist
Location:
Lagos
Role / Descriptions

  • 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.

Job Title: Graduate Clinical Data Specialist
Location:
Lagos
Job Description

  • 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


Job Title: Pharmacy Technician

Location:
Lagos

Job Description
  • 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


How to Apply

Interested and qualified candidate should forward their CV's to: [email protected]

Note: Only shortlisted applicants will be contacted.

Application Deadline  30th March, 2016.