QC Analyst

Alexander Mann Solutions (AMS) is the world's leading provider of Talent Acquisition and Management Services. We deliver award-winning solutions to over 65 outsourcing clients and consulting services to hundreds more. Our Contingent Workforce Solutions (CWS) service acts as an extension of our clients' recruitment team and provides professional interim and temporary resources.

Sanofi is a global life sciences company committed to improving access to healthcare and supporting the people we serve throughout the continuum of care. From prevention to treatment, Sanofi transforms scientific innovation into healthcare solutions, in human vaccines, rare diseases, multiple sclerosis, oncology, immunology, infectious diseases, diabetes and cardiovascular solutions and consumer healthcare. More than 110,000 people at Sanofi are dedicated to make a difference on patients' daily life, wherever they live and enable them to enjoy a healthier life.

On behalf of this organisation, AMS are looking for a QC Analyst for a 12 month contract based in Haverhill, Suffolk

Purpose of the QC Analyst Role:

Responsible for analysis (sample/equipment), review and collation of experimental data against specifications laid down by the Quality department

As a QC Analyst you will be responsible for:

Sampling and analysis of raw materials, drug substances and drug products.

Ensure stabilty testing is initiated and completed within the required time frame.

Documenting analytical data and results according to cGMP.

Collation of analytical data into release packs and generation of C of A's as required.

Review of raw data, where appropriate, ensuring all documented results are in accordance with the appropriate product/material specification and good documentation practice.

Responsible for first line troubleshooting.

Cross value stream working to support the QC function.

Training and support of coleagues where appropriate.

Supports projects on an as required basis.

May be required to support equipment requalifications, calibrations, services etc.

Ensure that equipment is maintained and fit for purpose against site procedures before use.

Carry out Risk/COSHH assessments and ensure that the laboratory is maintained in a safe and tidy manner at all times.

Raise Events, CAPA's & Laboratory investigations immediately or within the required time frame from detection.

Complete all corrective and preventative actions within the agreed timelines.

Maintain core training and prior to conducting any activity ensure you are trained in the current version.

Responsible for personal safety and that of others, reporting all accidents and unsafe acts and conditions.

Ensure that the laboratory is maintained in a safe and tidy manner and record all cleaning activities according to cGMP.

Identify and implement improvements to ways of working with an aim to standardise each working week.

Take responsibility for adhering to cGMP requirements during all activities performed, and seek clarification of requirements when they are unclear.

What we require from the candidate:

Demonstrated ability to work consistently to quality policies and cGMP

Proven, sustained competence in analytical techniques and skills relevant to group

A working knowledge of laboratory health and safety

Demonstrated ability to successfully manage own workload to meet departmental targets

If you are interested in applying for this position and meet the criteria outlined above, please click the link to apply and we will contact you with an update in due course...... click apply for full job details