QA Specialist (4m Contract | Up to $3800 | No Exp needed) #HAC
Summary
Manage GMP document lifecycle, training records, and support day-to-day QA activities in a cGxP contract manufacturing facility using a Documentation Management System.
Job Responsibilities
- Management of GMP document lifecycle in Documentation Management System including archiving and inactive records
- Management of documents within onsite archive room
- Support DMS Migration activities
- Management of training records including processing and data entries of form
- Support day-to-day Quality Assurance activities in accordance with approved SOPs / Policies for a multi-product, cGxP contract manufacturing facility
- Display a good level of problem solving ability by analyzing and interpreting data and puts forward new ideas based on scientific knowledge or field experience
- Detect non-compliance with cGxP and cGDP requirements and provide guidance on GDP corrections
- Generally provide basic compliance support to staff in all departments
- Demonstrate appropriate interpersonal skills that encourage collaboration of
- individuals or teams to meet objectives
- Uphold data integrity principle in accordance to company policies. Proactively evaluate, identify and improve data integrity process.
- Any other tasks as and when assigned by Supervisor
Key Requirements
- Diploma / Degree in a related Science or Engineering discipline such as Biotechnology, Biological Science, Chemistry, Biomedical Engineering, Chemical Engineering
- Able to start within a short notice period
All interested candidates are invited to email your resume in MS Word format to:
anna.chen@recruitexpress.com.sg
Please include your full working experience, education background, notice period, and expected salary.
Anna Chen jiaxin
CEI No: R25157621
Recruit Express Pte Ltd
EA License: 99C4599