Job Description

Job Category: QUALITY
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ABOUT YOU
As the Quality Officer, you will have excellent communications skills and the ability to converse succinctly with key stakeholders, providing them with accurate information and progress reports on a consistent basis.
Required skills and experience:

• IT proficient
• Strong numeracy skills
• Clear written and verbal communications skills with the ability to clearly convey processes, results and key messages and able to build rapport, quickly and effectively
• Excellent interpersonal skills with the ability to network and build strong relationships to collaborate with key stakeholders
• The ability to effectively time manage workloads and work on multiple projects as required
• Ideally degree qualified in BioChemistry or Chemistry (or related scientific discipline)
• A sound working knowledge of GMP and other analytical related quality standards is preferable
• Proven industry experience of performing detailed experimental checks within the above regulatory framework
• Industry experience in analytical science (chromatographic methods e.g. HPLC, GC, LC etc. and/ or other pharmaceutical characterisation techniques)

ABOUT THE OPPORTUNITY
This opportunity will take place in an environment that has an extensive range of analytical instrumentation and that provides analytical services to customers in the pharmaceutical, biopharmaceutical, personal care and speciality chemical sectors in a GMP regulated laboratory. This role will review deviations, OOS and change control records, perform internal audits and review of equipment qualifications as well as perform checks GMP data as necessary in accordance with experimental checking procedures.
Key activities:

• Perform GMP and related quality system checks necessary to ensure that appropriate standards and effective working systems are employed to meet our company and customer requirements
• Assist the Quality Assurance Team Leader in the overall implementation of the Quality function
• Check analytical technical data, associated records, facility and operational systems, to monitor and assure management of the appropriate standard procedures being followed as required by relevant regulatory requirements
• Provide general support to all Quality Team activities relating to GMP, and other similar Quality Systems established to ensure that the appropriate standards and effective working systems and relationships are maintained and where necessary improved
• and completely reflect the raw data and meet current Good Clinical Practice standards and regulations
• Identify and contribute to areas for improvement within the quality management systems to ensure compliant and efficient systems
• Carry out internal audits and support in the hosting of client and regulatory audits
• Review and approval of Equipment Qualifications
• Review and Approval of QMS records such as Deviations, OOS Investigations and Change Controls.

WHAT WE OFFER
Join Intertek and become part of our global network of inspiring and entrepreneurial colleagues. We are a global family that values diversity and we thrive working together with precision, pace, and passion. We are working to make the world Ever Better, ensuring the quality, safety and sustainability of products and services used by millions of people around the world.

• Competitive salary/benefits
• Development and career opportunities around the Globe
• Working in a highly motivated team and dynamic working environment

We are an Equal Opportunity Employer who do not discriminate against applicants. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex or national origin.
Intertek operates a preferred supplier arrangement, and we do not accept unsolicited approaches from agencies.