Job Description
Celogen Lanka (Pvt) Ltd is Sri Lanka’s largest pharmaceutical manufacturing facility with manufacturing capacity for tablets, hard gelatin capsules, soft gelatin capsules & suppositories
WE ARE HIRING!
Responsibilities
- Ensure that Quality systems are maintained as per cGMP and Eu GMP requirement.
- Issuance, mastering and controlling of the documents.
- Review of quality management system documents of all departments.
- Preparation and compilation of documents related to cGMP requirements.
- Preparation and review of Protocols and Reports of Studies and Non- Routine validations.
Skills Required
- Communication Skills: Ability to communicate fluently in Sinhala and English languages.
- Strong interpersonal skills and should be a good team player.
- Ability to work under pressure and extended hours when required.
Medical Knowledge: Understanding of pharmaceutics, pharmaceutical chemistry, pharmacology and pharmacovigilance.
- Regulatory Knowledge: Familiarity with ph23armaceutical regulations (e.g., NMRA, EMA guidelines).
- Data Analysis Skills: Comprehensive knowledge of MS Office package.
- Problem-Solving Skills: Identify and assess and determine appropriate actions.
Key Requirements
- Bachelor’s Degree: Fresh graduate in pharmacy (B. Pharm)/ Science (BSc.) or a related field.
If you are interested, please forward your CV to HR@celogen.lk on or before 31st December 2024
Celogen Lanka (Pvt) Ltd Lot No. 07A, Industrial Park-BOI, Pallekele, Kandy 081-2424821,081-2424831,081-2424841
WWW.CELOGEN.LK