REF 1836698
26.06.2025 | Dubai | full time
- General
- Location: Dubai
- Occupancy: full time
- To join : immediately
- Description
- Join an environment of excellence, where we’re backed by a belief that good can always be better. It means we search for opportunities to add value – harnessing science and evidence to foresee risk. A place to continuously innovate to find new and better ways to ensure we are improving outcomes for patients!
In this role you will ensure that all batch related activities are controlled while providing quality oversight and support at the source of key operational processes. Providing Quality Assurance support to an assigned area, including out of hours support. The job holder will have proven experience as a Quality Assurance Officer or equivalent.
Typical Accountabilities
Provide expert advice on Good Manufacturing Practice/Good Development Practice/ Good Laboratory Practice to Operations and ensure compliance with the associated quality standards.
Advise on deviations and use judgement to recommend approval or rejection of product within tight business deadlines.
Be able to perform product release activities and recommend batch disposition to the Qualified Person.
Collate the required documentation for product quality reviews within the required timescales.
Ensure compliance with change management processes and approval of associated documentation at a local level.
Apply risk management by using analytical skills and experience to make decisions, develop solutions, or more complicated judgements, within general operating guidelines.
Look for opportunities to identify change and make efficiency savings, influence decisions and deliver the results whilst ensuring an appropriate level of compliance.
Produce and deliver Good Manufacturing Practice training across site.
Drive out any non-value adding activities and support lean operations and support line management to develop a culture of continuous improvement.
Ensure plant readiness for any regulatory inspections. Plan and lead self-inspections to aid in developing follow-up improvement plans to ensure ongoing compliance
To review completed batch documentation for compliance with cGMP, product license and company requirements.
Support general BPD (Development), Manufacturing, QC, Engineering, Supply Chain and Manufacturing Excellence activities.
Support QC assay approvals (Including GQCLIMS).
- Requirements
- Associate degree or equivalent work experience
1 – 3 years’ experience in quality control of a manufacturing environment
Detailed oriented
Basic computer skills ( Microsoft office – Excel, Word, Outlook – )
Basic math skills.
- Provisions
- Salary: to be discussed
- Employment visa provided
- Medical insurance
- Accommodation provided
- Publisher
- direct employer
- up to 50 employees