QC Analyst

Recruiter
Key People Limited
Location
Berkshire, UK
Salary
Competitive
Posted
16 Jul 2019
Closes
25 Jul 2019
Ref
1194691745
Sector
Healthcare
Contract Type
Permanent
Hours
Full Time
My client, a start up Generics Pharmaceutical company in the Berkshire area is looking for a QC Analyst with a minimum of 2 years of experience on a permanent basis. Salary is paying up to £26,000 plus benefits. Please find below an outline of the role and responsibilities associated; 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 oHPLC oGC oDissolution oUV oFTIR 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. If this role is of interest, please apply and get in touch at rwilson@keypeople.co.uk

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