Document Control Specialist (Pharma) (SG)
Date Posted: August 29, 2024
Job Description
We seek a Document Control Specialist to manage critical document transfers. You’ll migrate documents between systems, ensuring accuracy and compliance.
Key Responsibilities
- Efficiently transfer and organize documentation.
- Conduct technical reviews and maintain document integrity.
- Develop certification traceability matrices.
- Collaborate with QA to drive document approval.
- Utilize the Kneat platform for document management.
- Coordinate project deliverables and system handovers.
Required Qualifications and Skills
- Bachelor’s degree in Engineering or related field.
- 5+ years’ GMP experience with document control.
- Pharmaceutical industry expertise.
- Strong analytical and problem-solving skills.
- Excellent communication and teamwork.
- Kneat platform proficiency.
If you are keen to grow your career with this job, apply with us and send us your resume now. All shortlisted candidates will be contacted shortly.
Reference no.: 122-4948-2918-NW
Registration no.: 968446516E
