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- Tasks: Conduct routine and non-routine analysis in a quality lab, ensuring compliance and efficiency.
- Company: Join a global biopharma leader dedicated to innovation and quality in healthcare.
- Benefits: Gain hands-on experience in a regulated environment with potential for career growth.
- Why this job: Be part of a high-performing team that values integrity and continuous improvement.
- Qualifications: Previous experience in a Quality Control lab and knowledge of analytical techniques preferred.
- Other info: This is a 9-month contract role based on-site in Montrose, Scotland.
The predicted salary is between 36000 - 60000 £ per year.
Location: Montrose, Scotland
Work type: On-site
Contract duration: 9 months
Payrate: TBC (PAYE/Umbrella, inside IR35)
Client: Global biopharma conglomerate
About your next role:
The quality team exists to deliver effective and efficient support services to the Montrose site. The Quality Laboratory team manages operational quality laboratory activities for the Montrose site in a safe, compliant and efficient way. The purpose of the quality analyst role is to ensure that:
- Day-to-day and routine analysis is completed in an effective and timely manner.
- There is a smooth and efficient flow of products from the site.
- Interfaces with other Montrose departments are effective for all parties.
- Significant quality or compliance issues are escalated through the appropriate management lines and/or management processes.
Utilization of all performance management to ensure continuous improvement to efficiency, safety and compliance.
Responsibilities include:
- Carrying out routine analysis on IPC, raw materials, manufactured and stability samples using classical and chromatographic techniques as appropriate.
- Using M-ERP and other IT systems to manage and report data.
- Providing an effective analytical service for the analysis of non-routine samples and assisting in troubleshooting production problems.
- Living the client’s values and meeting expectations to ensure tasks are carried out with integrity, a positive attitude and a willingness to work across boundaries to optimize efficiencies and reduce waste.
- Being actively involved in activities required for the effective running of the quality laboratory, including the review and preparation of procedures e.g. LSOP’s, validation reviews, COSHH and risk assessments, and GPS improvement activities.
- Working to current Good Laboratory Practice (cGLP) in a highly-regulated environment, following defined procedures (LSOP’s, GSOP’s and other applicable documentation).
- Being actively involved in various audit teams e.g. GMP, 5S and self-inspection audits.
- Supporting continuous improvement using GPS tools and value for every pound principles.
- Being involved in the capability building of staff, including training others in analytical techniques and being trained in new techniques.
- Working in a safe and compliant manner and supporting processes designed to ensure the safe, compliant operation of the laboratories as per order fulfilment requirements.
- Meeting requirements of site strategy including ZIP’s, ZAP’s and no overdue quality metrics.
- Owning, prioritizing and completing deviation management, planned and unplanned change management and improvement actions in a professional and timely manner.
Previous employment in a Quality Control lab or equivalent with a suitable level of competency in a range of analytical techniques e.g. chromatography and classical tests is preferred.
Quality Laboratory Analyst (Contract) employer: Allegis Global Solutions
Contact Detail:
Allegis Global Solutions Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Laboratory Analyst (Contract)
✨Tip Number 1
Familiarise yourself with Good Laboratory Practice (cGLP) and the specific analytical techniques mentioned in the job description, such as chromatography. This knowledge will not only help you during interviews but also demonstrate your commitment to quality standards.
✨Tip Number 2
Network with professionals in the biopharma industry, especially those who work in quality control labs. Engaging with them on platforms like LinkedIn can provide insights into the company culture and expectations, which can be invaluable during your application process.
✨Tip Number 3
Prepare to discuss your experience with performance management and continuous improvement initiatives. Be ready to share specific examples of how you've contributed to efficiency and compliance in previous roles, as this aligns closely with the responsibilities of the Quality Laboratory Analyst position.
✨Tip Number 4
Research the global biopharma conglomerate's values and mission. Understanding their core principles will allow you to tailor your conversations and show how your personal values align with theirs, making you a more attractive candidate for the role.
We think you need these skills to ace Quality Laboratory Analyst (Contract)
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in quality control and analytical techniques, particularly chromatography and classical tests. Use specific examples to demonstrate your competency in these areas.
Craft a Strong Cover Letter: In your cover letter, express your enthusiasm for the role and the company. Mention how your values align with those of the client and provide examples of how you've contributed to continuous improvement in previous roles.
Highlight Compliance Experience: Emphasise any previous experience you have working in highly-regulated environments and your familiarity with Good Laboratory Practice (cGLP). This will show that you understand the importance of compliance in the role.
Showcase Teamwork Skills: Since the role involves working as part of a high-performing team, include examples of how you've successfully collaborated with others in past positions. Highlight your ability to communicate effectively across departments.
How to prepare for a job interview at Allegis Global Solutions
✨Know Your Analytical Techniques
Make sure you brush up on your knowledge of analytical techniques, especially chromatography and classical tests. Be prepared to discuss your experience with these methods and how you've applied them in previous roles.
✨Understand Good Laboratory Practice
Familiarise yourself with current Good Laboratory Practice (cGLP) standards. Be ready to explain how you have adhered to these practices in past positions and how you would ensure compliance in this role.
✨Showcase Your Teamwork Skills
The role requires working as part of a high-performing team. Prepare examples of how you've successfully collaborated with others in the past, particularly in a laboratory setting, to achieve common goals.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving skills, especially regarding troubleshooting production issues or managing deviations. Think of specific instances where you've successfully navigated challenges in a quality control environment.
