At a Glance
- Tasks: Analyse and validate medical product samples to ensure quality control.
- Company: Join Orbia, a purpose-driven company focused on advancing life globally.
- Benefits: Enjoy a unique shift pattern with 8 days off and opportunities for growth.
- Why this job: Make a real impact in healthcare while working in a diverse and inclusive environment.
- Qualifications: A degree in Chemistry or related field is preferred; QC lab experience is a plus.
- Other info: Be part of a team that values every voice and embraces different perspectives.
The predicted salary is between 36000 - 60000 ÂŁ per year.
Direct message the job poster from Koura
Senior Recruiter, Fluor and Energy Materials, Polymer Solutions | MSc. Chemistry
You are purpose driven. Growth minded. Ready to stretch your potential. That’s the spirit of the community you’ll find at Orbia: where the purpose to advance life around the world drives our global team of over 23,000 every single day.
From creating solutions to deliver clean water, secure food supplies and reliable information to steering material advances that power the future of green and smart cities, transportation, and healthcare, we never settle for “good enough” when there’s an opportunity to make life better. Where purpose comes to life, it changes lives. This is what we live for.
Fluor and Energy Materials, an Orbia business, is looking for a Laboratory Shift Analyst to be based at Rocksavage, Cheshire, UK.
Main Purpose
To provide Medical Products manufacturing and packing operations and customers with a Quality Control and analysis service so that process control, product quality, and current Good Manufacturing Practice (cGMP) requirements are satisfied.
Shift pattern – 2 days, 2 nights (7-7) followed by 8 days off. Shift cover will be expected occasionally to ensure 24/7 support of the manufacturing operations.
Main Responsibilities
- To accurately analyse, validate and record results for samples from the medical products operation to ensure that production processes and final product quality is controlled within the agreed limits.
- To review and validate the analysis of other analysts in line with operating requirements.
- Prioritise work to ensure that business production, sales and customer support plans are achieved.
- Carry out investigation into any abnormal results and report to the Quality Control Team Leader, production personnel, and/or the Quality Assurance Team Leader as appropriate.
- Maintain the laboratory and analysis equipment in line with full requirements of current Good Manufacturing Practice.
- Ensure all sample, analysis and testing work is carried out in full compliance with cGMP and SHE standards.
Qualifications
- Desirable: Degree Chemistry or related subject.
Knowledge/ Experience Required
- Experience of working in a QC Laboratory, preferably one working to cGMP standards.
- Ability to work with a high level of independence.
Behaviours that can help you succeed at Orbia:
- Develop yourself & Others
- Drive Results
- Provide Vision & Direction
We welcome purpose-driven dreamers, doers, and builders, recognizing that it takes difference to make a difference. If you’re ready to bring your skills, talents, and perspective to moving your career, the company, people, and the planet forward, we’d like to hear from you.
We believe that every voice matters; every community deserves respect; and every challenge is an opportunity and united by empathy, we are stronger for our different perspectives. We are dedicated to building a more diverse, inclusive, and equitable workplace that supports the needs of all our employees regardless of their role, location, identity, and background.
Seniority level
-
Seniority level
Not Applicable
Employment type
-
Employment type
Full-time
Job function
-
Job function
Analyst
-
Industries
Chemical Manufacturing and Pharmaceutical Manufacturing
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Laboratory Shift Analyst employer: Koura Group
Contact Detail:
Koura Group Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Laboratory Shift Analyst
✨Tip Number 1
Familiarise yourself with cGMP standards and regulations, as this role heavily relies on compliance with these practices. Understanding the nuances of quality control in a laboratory setting will give you an edge during discussions.
✨Tip Number 2
Network with professionals in the chemical manufacturing and pharmaceutical industries. Engaging with current employees or recruiters can provide insights into the company culture and expectations, which can be beneficial during your application process.
✨Tip Number 3
Prepare to discuss your experience in a QC laboratory setting, particularly any specific instances where you ensured product quality or resolved abnormal results. Real-life examples can demonstrate your capability and fit for the role.
✨Tip Number 4
Showcase your ability to work independently and prioritise tasks effectively. This is crucial for the Laboratory Shift Analyst position, so think of ways to illustrate your organisational skills and decision-making abilities in your conversations.
We think you need these skills to ace Laboratory Shift Analyst
Some tips for your application 🫡
Understand the Role: Read the job description thoroughly to grasp the responsibilities and qualifications required for the Laboratory Shift Analyst position. Tailor your application to highlight relevant experiences that align with these requirements.
Highlight Relevant Experience: Emphasise any previous experience in a Quality Control laboratory, especially if it involved cGMP standards. Use specific examples to demonstrate your ability to analyse, validate, and record results effectively.
Showcase Your Skills: Include skills that are pertinent to the role, such as analytical skills, attention to detail, and the ability to work independently. Mention any relevant software or laboratory techniques you are proficient in.
Craft a Compelling Cover Letter: Write a cover letter that reflects your passion for the role and the company’s mission. Discuss how your values align with Orbia's purpose-driven approach and how you can contribute to their goals.
How to prepare for a job interview at Koura Group
✨Understand cGMP Standards
Familiarise yourself with current Good Manufacturing Practice (cGMP) standards, as this role heavily relies on compliance. Be prepared to discuss how you have adhered to these standards in your previous experiences.
✨Showcase Analytical Skills
Highlight your experience in analysing and validating results in a laboratory setting. Be ready to provide specific examples of how you've handled abnormal results and the steps you took to investigate them.
✨Demonstrate Independence
This position requires a high level of independence. Share instances where you successfully managed tasks or projects on your own, showcasing your ability to prioritise work effectively.
✨Emphasise Team Collaboration
While independence is key, teamwork is equally important. Discuss how you have collaborated with quality control teams or other departments to ensure product quality and operational efficiency.