Reference Number: JO-2311-526139
QC Analyst
Rate: Negotiable
Job Type: Permanent
Location: Maidenhead

QC Analyst


Up to £26,000

Permanent employment

An exciting opportunity for a Quality Control Analyst to join an expanding team in a newly established and evolving generic IP focused pharmaceutical company. The successful candidate will be undertaking the testing of materials, components and finished products, gaining a great insight into the business area of Quality.


• Carry out Quality Control analysis on Incoming Materials, Components and Products (including stability and other samples) as well as data in support of the onsite manufacturing and QC functions

• Help to ensure that QC functions operate in a fully current GMP compliant manner and in compliance with the filed regulatory dossiers for the products supported.

• You will have involvement 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. 

• Participate in documentation, laboratory systems and processes to include updating existing ones as required.

• The successful candidate will be involved in various 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 partake in ensuring all housekeeping and work safety operations within the QC laboratory take place in the correct and proper manner

• 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 at last 1 years QC Analyst.

• Strong hands-on experience of undertaking testing, analysis of Raw Material, Packaging Material and Finished Product using instrumentational analysis such as 


o Dissolution

o UV 

• Good knowledge of GMP, MHRA and, ICH guidelines, with an understanding of Quality Assurance processes and methodologies.

• Experience of LIMS or equivalent system is desirable.

• Good understanding of FDA guidelines and other governing bodies is desirable but not essential

Upload your CV and any other relevant file.
I would like to be contacted via SMS
I have read and agree to the Clinical Professionals Group Privacy Policy

Find our privacy policy here