Quality Control Laboratory Analyst - Liverpool, United Kingdom - Vitaflo (International) Limited
Description
Company description:
Vitaflo (International) Limited
For more than 25 years, Vitaflo has developed innovative specialised clinical nutritional products for inherited metabolic disorders, pediatric?kidney disease, and specialised diets such as the ketogenic diet.
We combine the latest medical research, together with insights on changing modern lifestyles to best support patients in the compliance of restrictive therapeutic diets.
Vitaflo continues its mission of Enhancing Lives Together with research and development at the heart of what we do.Job description:
We are part of Nestlé Health Science and continue to expand our global footprint with a worldwide presence in Clinical Nutrition.
Our employees are at the heart of what we stand for with 96% saying they are proud to work for us and 94% recommending Vitaflo as a good place to work.
We strive to be at the cutting edge of our industry sector with patient's needs being at the forefront of our mind.
We work collaboratively, share our knowledge and expertiseand above all love what we do and why we do it.Quality Control Laboratory Analyst
Are you meticulous about delivering high quality standards and exceeding customer expectations? Do you have a sound knowledge of quality control standards and legislation?
If so, we have the role just for you Vitaflo (International) Ltd are currently looking to recruit a Quality Control Laboratory Analyst on a full-time contract.
Working within the quality department, you will be responsible for conducting the analyticallaboratory tests required to ensure the safety and quality of Vitaflo products.
What will you do?
As a Quality Control Laboratory Analyst your responsibilities will consist of the following:
- Registration of samples for laboratory analysis
- Validation of ICP-OES method for UKAS ISO 17025 accreditation
- Statistical analysis of data
- Writing standard operating procedures
- Conducting ICP-OES analysis on finished product samples
- Conducting proficiency testing
- Calibration of laboratory equipment
- Validation of LC-MS/MS method for UKAS ISO 17025 accreditation
- Maintaining GLP standards
- Any other duties as requested
What skills and experiences should you have?
- Experience of working with ICP-OES & LC-MS would be highly desirable
- Experience of method validation for UKAS ISO 1702
- Results focused
- Excellent attention to detail that reflects thorough and accurate work
- Extremely organised with the ability to prioritise workload
- Proficient in IT packages inclusive of Microsoft Word, Excel, PowerPoint and Outlook
- Able to work independently and also as part of a team
- Enthusiastic and proactive with a cando attitude
- Excellent people skills with the ability to build relationships internally and externally
What we offer?
- Competitive salary
- 25 days annual leave (pro rata for part time) plus bank holidays and Christmas shut down
- Volunteering opportunities
- Hybrid Working
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