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Senior QC Analyst

Salary:
£26000 - £32000 per annum
Location:
Maidenhead
Company:
Key People

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An excellent opportunity has arisen for a Senior QC Analyst to join a growing organization based in Maidenhead, Berkshire.An excellent opportunity has arisen for a Senior QC Analyst to join a growing organization based in Maidenhead, Berkshire.

Responsibilities

Execute Quality Control analysis on Incoming Materials, Components and Products including stability and other samples alongside data in support of the onsite manufacturing and QC functions
Assist in making sure that QC functions operate in a fully current GMP compliant manner and in compliance with the filed regulatory dossiers for the products supported.
Participating in the writing, reviewing and implementing of SOP's, methods, protocols and reports as required.
You must be able to follow and understand specifications for sample analysis.
The successful candidate will need to be able to provide technical support/advice for QC testing whilst ensuring that the test methods are followed correctly.
Assisting with documentation, laboratory systems and processes to include updating existing ones as required.
The successful candidate will be involved in a range of audits as and when required.
You will need experience in identifying out of specification as well as atypical results and trends.
The successful candidate will always seek best practice process and should share this to all relevant stakeholders.
You will be expected to make sure all housekeeping and work safety operations within the QC laboratory take place in the correct way
Any other task given to you by relevant stakeholder in order for you to be
able to perform your role

Required Skills:

Degree in Chemistry, Pharmaceutical Science, analytical or related
Proven experience of 2-4 years as QC Analyst.
Strong hands-on experience of undertaking testing, analysis and development using instrumentational analysis such as:
- HPLC
- GC
- Dissolution
- UV
- FTIR in a cGMP environment.

Good knowledge of GMP, ICH guidelines, BP/EP/USP methods with an understanding of QA processes and methodologies.
Experience of LIMS or equivalent system is desirable.
Sound understanding of MHRA guidelines
Good understanding of FDA guidelines and other governing bodies is desirable but not essential

Additional Experience:

Strong Microsoft Office Suite experience.
Attention to detail and quality of documentation
Good interpersonal skills
Effective oral and written communication skills
Excellent organizational and planning skills
Ability to work independently
Ability to interpret data
Ability to demonstrate calm objectivity in a pressurised, results driven environment, whilst successfully dealing with often changing and conflicting priorities.

For further details, please contact Tim Barratt on +4401727 817 626 or email tbarratt@keypeople.co.uk

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