Stability Analyst

Kedrion Biopharma GmbH; United Kingdom; On-site; GBP 30,000 - GBP 40,000; Full time

Job summary

A reputable biopharmaceutical company is seeking a dedicated Stability Analyst to join their Quality Department at the Elstree site. The ideal candidate will have a degree in Science or Mathematics, experience in a laboratory, and strong analytical skills. Responsibilities include setting up stability trials, analyzing samples, and ensuring accuracy in reporting. This full-time position is on-site and offers benefits such as pension, life insurance, and employee assistance programs.

Benefits

Pension

Life insurance

On-site parking

Employee assistance programme

Virtual GP

Cycle to work scheme

Subsidised canteen

Employee discounts and cash back

Family friendly policies

Employee recognition programme

Qualifications

• Experience of working in a laboratory environment is essential.
• Understanding of GMP/GLP is desirable.
• Experience in writing reports.

Responsibilities

• Set up stability trials, collect and distribute stability samples.
• Update stability spreadsheets and records.
• Perform stability specific testing in accordance with SOPs and BPL policies.

Skills

Attention to detail

Communication skills

Experience in analytical equipment

Education

Degree level qualification in Science or Mathematics

Tools

Microsoft Office (Word, Excel)

Job description

Kedrion Biopharma is recruiting a dedicated and detail-oriented Stability Analyst to join the Quality Department at our site in Elstree, Hertfordshire, and act as a key member of Quality’s data evaluation and reporting function.

This role will suit someone who enjoys practical hands on work in setting up and sampling product for stability analysis but also working with data, spotting trends, and ensuring accuracy in reporting, and who has experience evaluating and reporting on samples or working in a role with a strong focus on data handling and analysis. It would be well suited to a graduate with a science or mathematics degree, or someone who may have already worked in a similar role.

The successful candidate will be responsible setting up stability trials, taking samples for analysis by other analytical testing sections and also some sample testing, also coordinating the shipment of samples to external testing laboratories. Additionally you will be evaluating and reporting on a range of data samples. You will also be responsible for tracking samples and coordinating the receipt and review of results when they are returned, ensuring accuracy, consistency, and reliability in all findings.

This position is full time, Monday to Friday, and is fully on-site.

Our site is not easily accessible by public transport, so please take this into consideration when applying.

Duties & Responsibilities -

• Set up stability trials, collect, pull and distribute Stability samples.
• Update Stability spreadsheets and records.
• Ship samples to outside testing laboratories (OTLs) and coordinate receipt of results back.
• Perform stability specific testing in accordance with Standard Operating Procedures, BPL policies and GMP.
• Provide practical and administrative assistance to the laboratories testing stability samples.
• Be responsible for preparing reagents, standards and control samples and contribute to general laboratory housekeeping duties.
• Promptly report deviations, out-of-specification / limits results. Assist where required with investigations.
• Read, collate, report and archive results using defined documentation and computer systems.
• Ensure equipment used is clean, calibrated and maintained. Perform system suitability checks where required
• Assist with the calibration or validation of laboratory equipment and automated systems.
• Ensure good stock control.

Skills & Education to help you in the role -

• Degree level qualification in Science discipline or equivalent such as Mathematics is desirable
• Experience in using analytical equipment and pipettes
• Experience in writing reports
• Experience of working in a laboratory environment is essential
• Understanding of GMP/GLP is desirable
• Computer literate – competent in the use of Microsoft Office, in particular word and excel at an intermediate level.
• Attention to detail – Able to ensure high levels of quality are achieved.
• Communication skills – Able to communicate clearly and persuasively with your team, managers peers and clients.
• Ability to understand and follow written instructions

In return we offer -

If you are confident in your ability to work with laboratory software and possess strong computer skills, we encourage you to apply for this role. Join our team and contribute to our mission of delivering accurate and reliable data analysis.

• Pension
• Life insurance
• On-site parking
• Employee assistance programme
• Virtual GP
• Cycle to work scheme
• Subsidised canteen
• Employee discounts and cash back
• Family friendly policies
• Employee recognition programme

Please apply today for immediate consideration.