Allergy Therapeutics are a market leading, pioneering immunology business with specialist experience in the research and development of allergy treatments.
We believe that transformational outcomes for patients are achieved by directly treating the cause, rather than just managing symptoms. Our vaccines are aluminium free. Driving convenience; our ultra-short course treatments make life easier and increase adherence.
Our adjuvant technologies not only advance the results of allergy immunotherapy but also drive beneficial immune responses in cancer and infectious disease.
We are a proud and passionate team with a vision that delivers growth and transforms the way we think about immunology.
We are continuing to grow and it's an exciting time to be joining us. You will contribute to our ongoing success and be part of our future which is looking very bright!
You'll join a team of like-minded people who are passionate about what they do and providing positive outcomes for our patients.
We are looking for a QC Scientist Level III to work as part of the team delivering QC testing activities. This is a 12-month fixed term contract working on a shift basis - Sunday to Wednesday (33 hours per week with a salary plus shift premium)
About you
You will have a relevant qualification in Microbiology or a science related subject and have practical experience within a lab environment.
You will have a real GMP focus and be able to adapt to changing priorities whilst ensuring quality and maintaining lab compliance.
We are looking for a real team player who is happy to help develop the skills of others in the team.
The role
You will be involved in the following:
Performing environmental monitoring of the Classified Areas to support manufacturing
Performing routine analytical testing on raw and source materials following Pharmacopeia
Preparing and testing samples in support of in process monitoring for production
Preparing reagents and solutions for use in analysis
Performing routine analytical testing of finished products for the purposes of release in accordance with the standard analytical methods and the weekly test schedule
Performing any additional analysis in support of development projects or as part of investigations for out of specifications/out of expectations
Entering data onto the LIMS system
Act as checker for analyst methods and test results and validate in LIMS
Laboratory support
Supporting and training colleagues in analytical methods as required
Assisting with laboratory equipment validation
Assisting with investigation of OOS and deviations after undertaking the appropriate training.
Appropriately raising and reporting any potential or confirmed OOS and deviations and notify the relevant departments
Undertaking and completing tasks such as Root Cause Analysis, NC report writing or laboratory Hypothesis investigation in order to determine a suitable root cause for a deviation or OOS (if applicable)
Performing bench freeze on all carried out analysis/testing
Performing and reporting assay and product trending
To undertake the drafting, completion and checking of SAMs, risk assessments or SOPs as and when required, which aid in the training of personnel in the laboratory
To liaise with various departments within the company, such as Production and Planning to deliver updates on testing and raise any concerns or issues that arise that may affect scheduling and product release
Please note that this role is based on-site in Worthing.
Job Types: Full-time, Permanent
Pay: 26,500.00-31,000.00 per year
Benefits:
Company pension
Cycle to work scheme
Free flu jabs
Health & wellbeing programme
Life insurance
On-site parking
Private medical insurance
Referral programme
Application question(s):
Do you have experience in a lab role in a GMP environment?
Do you live within commutable distance of Worthing, West Sussex?
Are you happy with a 12 month fixed term contract?
Are you happy with the working hours (Sunday to Wednesday - 33 hours per week)
Work authorisation:
United Kingdom (required)
Work Location: In person
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