Are you ready to make a significant impact in the world of research As a QC Technologist III Lead at LGC you will play a pivotal role in ensuring the success of our research initiatives. This position is built for an exceptionally skilled individual who can manage complex tasks with a high degree of independence and judgment. You will be at the forefront of our mission using your expertise to achieve flawless results and drive world-class standards!
The job entails various functional duties including but not limited to the following:
- Operation routine and advanced maintenance of automated clinical analyzers
- Perform major troubleshooting of assay and analyzer issues with successful resolution or a call to service as needed
- Perform daily quality controls and calibrations as required
- Data entry as well as assessment interpretation and release of quality control results
- Testing production and research & development samples and assessing testing results
- Mentor/train junior staff in the operation of analyzers and department procedures and processes
- Assist with some Department administrative activities such as ordering data reviews etc.
Team duties consist of but are not restricted to the following:
- Focus on customer service
- Problem solving including ability to prioritize and adjust workload as needed
- Working with Production and R&D personnel to ensure efficient use of reagents and analyzers
- Able to evaluate processes for inefficiencies and suggest improvements
- Attention to detail
- Carry out and complete fresh assay validations following established protocols
- Build and conduct new instrument/analyzer validations
- Able to work independently and as part of a team
- May lead junior staff
- Participates in cross-functional meetings (i.e. Product Review Build teams Internal Audits etc)
- Lead all aspects of and coordinate department projects
Qualifications :
Minimum Qualifications:
- Bachelor degree or equivalent experience in a life science related field (such as biology chemistry biochemistry)
- Must be a certified medical lab technician (MLT) or ASCP certified medical technologist (MT C MLS CLS)
- Min 6 years working experience in a clinical lab or equivalent setting
- Strong organization and multitasking skills
- Experienced in use of various software programs (ex. MS Suite and MS teams)
- Previous working experience with mainstream clinical analyzers from Roche Siemens OrthoClinical Beckman Coulter or Abbott desired.
Preferred Qualifications:
- Bachelor degree or equivalent experience in Medical Technology
Additional Information :
All your information will be kept confidential according to EEO guidelines.
About LGC:
LGC a major player in the global life science tools industry supplies critical components in high-growth areas of human healthcare and applied markets. Its premium product lineup features essential tools for genomic analysis and quality assurance known for their performance and quality.
Our values:
- PASSION
- CURIOSITY
- INTEGRITY
- BRILLIANCE
- RESPECT
Equal opportunities
LGC is committed to ensuring that every potential applicant and employee is appreciated for their distinct abilities without any bias based on age disability race ethnicity gender sexual orientation gender identity marital status pregnancy parenthood religion or beliefs. The evaluation and selection of candidates will always be conducted without taking these aspects into account.
For more information about LGC please visit our website
#scienceforasaferworld
Remote Work :
No
Employment Type :
Full-time
Are you ready to make a significant impact in the world of research As a QC Technologist III Lead at LGC you will play a pivotal role in ensuring the success of our research initiatives. This position is built for an exceptionally skilled individual who can manage complex tasks with a high degree of...
Are you ready to make a significant impact in the world of research As a QC Technologist III Lead at LGC you will play a pivotal role in ensuring the success of our research initiatives. This position is built for an exceptionally skilled individual who can manage complex tasks with a high degree of independence and judgment. You will be at the forefront of our mission using your expertise to achieve flawless results and drive world-class standards!
The job entails various functional duties including but not limited to the following:
- Operation routine and advanced maintenance of automated clinical analyzers
- Perform major troubleshooting of assay and analyzer issues with successful resolution or a call to service as needed
- Perform daily quality controls and calibrations as required
- Data entry as well as assessment interpretation and release of quality control results
- Testing production and research & development samples and assessing testing results
- Mentor/train junior staff in the operation of analyzers and department procedures and processes
- Assist with some Department administrative activities such as ordering data reviews etc.
Team duties consist of but are not restricted to the following:
- Focus on customer service
- Problem solving including ability to prioritize and adjust workload as needed
- Working with Production and R&D personnel to ensure efficient use of reagents and analyzers
- Able to evaluate processes for inefficiencies and suggest improvements
- Attention to detail
- Carry out and complete fresh assay validations following established protocols
- Build and conduct new instrument/analyzer validations
- Able to work independently and as part of a team
- May lead junior staff
- Participates in cross-functional meetings (i.e. Product Review Build teams Internal Audits etc)
- Lead all aspects of and coordinate department projects
Qualifications :
Minimum Qualifications:
- Bachelor degree or equivalent experience in a life science related field (such as biology chemistry biochemistry)
- Must be a certified medical lab technician (MLT) or ASCP certified medical technologist (MT C MLS CLS)
- Min 6 years working experience in a clinical lab or equivalent setting
- Strong organization and multitasking skills
- Experienced in use of various software programs (ex. MS Suite and MS teams)
- Previous working experience with mainstream clinical analyzers from Roche Siemens OrthoClinical Beckman Coulter or Abbott desired.
Preferred Qualifications:
- Bachelor degree or equivalent experience in Medical Technology
Additional Information :
All your information will be kept confidential according to EEO guidelines.
About LGC:
LGC a major player in the global life science tools industry supplies critical components in high-growth areas of human healthcare and applied markets. Its premium product lineup features essential tools for genomic analysis and quality assurance known for their performance and quality.
Our values:
- PASSION
- CURIOSITY
- INTEGRITY
- BRILLIANCE
- RESPECT
Equal opportunities
LGC is committed to ensuring that every potential applicant and employee is appreciated for their distinct abilities without any bias based on age disability race ethnicity gender sexual orientation gender identity marital status pregnancy parenthood religion or beliefs. The evaluation and selection of candidates will always be conducted without taking these aspects into account.
For more information about LGC please visit our website
#scienceforasaferworld
Remote Work :
No
Employment Type :
Full-time
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