Quality Control Analyst

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.

Noumed Life Sciences is an emerging pharmaceutical company based in Maidenhead, Berkshire focusing on cGMP, solid dosage generic pharmaceuticals. The company has been officially trading since April of 2017 and is able to offer all employees an exceptional insight into the development of a new pharmaceutical company, giving them autonomy and broad learning. A once in a career opportunity to be actively involved in the start-up of an aspiring global organisation.

Responsibilities

• 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 HPLC

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

Additional Experience

· Strong Microsoft Office Suite experience.

· Attention to detail and quality of documentation

· Effective oral and written communication skills

· Excellent organisational and planning skills

· Ability to work independently

· Ability to interpret data

Job Types: Full-time, Permanent

Salary: £23,000.00-£26,000.00 per year

Benefits:

• Casual dress
• Company pension
• Cycle to work scheme
• Employee discount
• Free parking
• Gym membership
• On-site gym
• On-site parking
• Referral programme

Schedule:

• 8 hour shift
• Day shift
• Monday to Friday
• Overtime

Work Location: In person