Documentation Officer at Willers Solutions

Sector: Pharmaceutical
Remuneration: 90k to 120k

Responsibilities

• Responsible for document and data control activities 
• Performs QA document control function, including login,tracking,processing, approval distributing and archiving in compliance to internal and external requirement.
• Co-ordinates the revision, review and approval by SOPS and GMP documents 
• updates and maintenance Quality Assurance operations logs and database
• Responsible for developing and keeping copies of required BMR/BPR for production 
• Participate in internal audits and supporting external audits.
• Preparationof quarterly departmental reports for the managing director. 

Requirements

• Minimum of BSc/HND in PURE/APPLIED CHEMISTRY, MICROBIOLOGY
• Minimum of 1 to 2 years of experience in a pharmaceutical or manufacturing settings 
• Solid knowledge of laboratory analysis 
• Excellent Knowledge of Raw materials, laboratory samples.
• A team player.