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Qc analyst team lead

Limerick
Speedeck
Qc analyst
Posted: 8 May
Offer description

Job Description

We are seeking a QC Analyst Team Lead to join our Quality Control (QC) laboratory.

This role involves providing leadership and support to the QC team, overseeing laboratory operations, and ensuring compliance with Good Manufacturing Practice (GMP) standards.

The successful candidate will be responsible for managing daily QC activities, optimizing resources, and ensuring efficient testing processes to support pharmaceutical production.

* Lead and support the QC team in daily operations, ensuring tasks are completed efficiently and in compliance with regulatory standards.
* Monitor and report on Key Performance Indicators (KPIs) to track team and laboratory performance.
* Oversee the preparation of media, buffers, and analytical reagents for QC testing.
* Assign and delegate tasks within the team to maintain workflow efficiency.
* Ensure the proper operation, calibration, and maintenance of laboratory equipment.
* Maintain a clean, organized, and compliant laboratory environment.
* Manage inventory levels by ordering consumables and raw materials.
* Oversee sample receipt, handling, and shipping.
* Support and oversee analytical testing across various methodologies.
* Participate in bioreactor builds and equipment calibration processes.
* Conduct stock checks and ensure timely replenishment of laboratory supplies.
* Review and verify process data integrity to maintain compliance with quality and regulatory standards.


Qualifications

* Bachelor's degree in Biotechnology, Microbiology, Biochemistry, or a related scientific discipline.
* Minimum of 2 years of relevant experience in a QC, Microbiology, or Biochemistry laboratory.
* At least 1 year of supervisory or team lead experience in a GMP-regulated environment.
* Strong knowledge and practical application of GMP principles.
* Prioritization for candidates with an analytical background.
* Excellent organizational, problem-solving, and time management skills.
* Experience documenting and recording scientific studies, with a strong understanding of data integrity and electronic lab notebook systems.
* Demonstrated experience in maintaining laboratory safety and compliance standards.
* Strong leadership and communication skills.


About Us

* A dynamic pharmaceutical environment that prioritizes quality and innovation.
* A collaborative workplace that values continuous improvement.
* Competitive salary and comprehensive benefits package.
* Professional development and career growth opportunities.

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