Quality Control Analyst
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Application Details
In order to work in Ireland a non-EEA National, unless they are exempted, must hold a valid employment permit.Please review the Eligibility and requirements for an employment permit if you are unsure of your eligibility to apply for this vacancy.
Job Description- 6087188720703;-7.92410802841187;Co. Tipperary ,
Job Title: Quality Control Analyst Location: Co. Tipperary, onsite Position: Permanent
Job Summary: Our client is seeking an experienced Quality Control Analyst with a background in the pharmaceuticals industry. The successful candidate will have strong teamwork skills, excellent communication abilities, and proficiency in Laboratory Safety, Good Laboratory Practice (GLP), GMP, SOP, Invoice Processing, Purchasing, Calibrations, Physical Testing, and more.The Quality Control Analyst will play a critical role in ensuring customer satisfaction by monitoring, controlling, and improving all related customer processes.
Key Responsibilities:
Laboratory Operations:
Perform routine and non-routine analysis of raw materials, in-process samples, finished products, and stability samples according to SOPs, GLP, and GMP.
Ensure laboratory safety and compliance with regulatory requirements.
Maintain accurate and detailed laboratory records.
Conduct physical testing and calibrations of laboratory equipment.
Process Monitoring and Improvement:
Monitor, control, and improve all customer-related processes to ensure satisfaction.
Identify areas for process improvements and implement corrective actions.
Product Handling and Documentation:
Organise the shipment of products for sterilization and release products from quarantine.
Involve in the disposition of non-conforming products and manage CAPAs and temporary deviations.
Act as the point of contact for any problems in the Clean Room and Pack Line.
Liaise with Manufacturing, Production, and QE teams for day-to-day operations.
Sample Inspection and Environmental Monitoring:
Conduct routine sample inspections of products built in the clean room.
Address and resolve queried issues related to product samples.
Perform routine sampling of products based on company procedures.
Conduct environmental monitoring in a clean room environment, including sampling, tracking, and trending of tests.
Communication and Coordination:
Maintain effective communication with all relevant departments to ensure smooth operations.
Provide detailed reports and updates to management on quality control activities.
Qualifications:
Bachelor’s degree in Chemistry, Biology, or a related field.
Minimum of 3 years of experience in a Quality Control role within the pharmaceuticals industry.
Strong understanding of GLP, GMP, and SOPs.
Experience with laboratory safety protocols and physical testing methods.
Excellent teamwork and communication skills.
Detail-oriented with strong analytical and problem-solving abilities.
Proficiency in invoice processing, purchasing, and calibrations.
Skills and Competencies:
Knowledge of laboratory equipment and techniques.
Ability to work effectively in a clean room environment.
Strong organisational and time management skills.
Proficiency in using quality management software and tools.
Ability to adapt to changing business environments and handle complex situatio- This vacancy is suitable for Remote/Blended working
- Sector:
- Entry Level
Candidate Requirements
Essential- Minimum Experienced Required (Years):
- Minimum Qualification:No Qualification
- Ability Skills:Skilled Trade(s), Technical IT
- Competency Skills:Teamwork, Time Management