Laboratory Analyst
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Job Location:
Midrand - South Africa
Monthly Salary:
Not Disclosed
Posted on:
11 hours ago
Vacancies:
1 Vacancy
Job Summary
A pharmaceutical client is looking for a Laboratory Analyst To ensure timeous sample testing and release.
RESPONSIBILITIES AND TASKS:
Strict adherence to Laboratory Standard Operating Procedures
Sampling testing reporting and trending of results
Performing and or assisting in Annual Product Reviews
Ensures control to the storage of retention samples.
Supports validations
- Ensuring a smooth and efficient operation of the QC laboratory
- Testing and release of samples according to test methods
- Ensuring sample traceability-Interprets data-Reporting of results-
- Complete and review batch release specifications in accordance with approved requirements.
- Generate and issue the Certificate of Analysis (COA) for finished products.
- Ensure that documents are properly archived and where required shared with customers or otherstakeholders.
- Where required send finished product samples to customers.
Strict adherence to Laboratory Standard Operating Procedures
- Maintaining a clean and organized laboratory environment
- Monitoring and documenting of environmental conditions
- Compliance with GLP requirements.
- Operation and maintenance of laboratory instruments.
- Data integrity
Sampling testing reporting and trending of results
- Water
- Swabs and settle plates
- Raw Material Packaging Materials Finished products
Performing and or assisting in Annual Product Reviews
- Pest control and Halaal/ Koscher management
- Performing pest control weekly and monthly inspections
- Halaal/Koscher document management and participating in inspections
Ensures control to the storage of retention samples.
- Controlling sample entry and exit from the stores
- Monitors and recording of storage conditions
- Removal and destruction of expired samples
- Reporting of all non-conformances and OOS and supporting investigations
Supports validations
- Testing of samples and reporting of results.
- National Diploma in Analytical Chemistry or equivalent qualification.
- Proficiency in Microsoft Office (MS Word Excel and Outlook).
- Knowledge of GMP standards and GLP requirements.
- Minimum of 1 year experience in a GMP-regulated environment.
- Ability to work independently and willingness to work overtime when required.
- Good communication skills (Written & Spoken)
- Strong attention to detail.
- Ability to multitask.
- Self-motivated
Required Experience:
IC
Key Skills
- Bidding
- Jpa
- E Learning
- Fire And Safety Engineering
- Assembling
