RESPONSIBILITIES
Responsible for regulatory affairs.
Responsible for organizing product licenses
Responsible for authorization of production, Batch Manufacturing Record (BMRs) and document review
Responsible for Marketing Authorization
Responsible for supervising Quality Management System (QMS)
Ensures Good Manufacturing Practise (GMP) is adhered
Ensure customer complaints are resolved
Liaison with Government and Statutory Agencies and Medical Institutions
Conduct training to Pharmacists on QMS, CGMP and Job related aspects
Attends to any incidental work that may be required by the Factory Manager
REQUIREMENTS:
Bachelors degree in Pharmacy
Minimum of 5 years experience in Pharmaceuticals manufacturing
Knowledge of Drug Rules and manufacturing of Pharmaceutical Dosage Forms.
Leadership skills
Time Management
Team Spirit
Interpersonal skill
Safety adherence
Attention to details
Punctuality and Discipline
Perseverance
Compliance with GMP
Forward updated resume to jobtrain@es-africa.com for consideration
Apply via :
jobtrain@es-africa.com
