Job title: QC Laboratory Analyst
Location: Queenborough, Kent, ME11 5EL
We have a great people working with us and our success is driven by the quality and passion of each and every person. The mixture of experienced professionals combined with the fresh ideas of new talent makes us a great place to work whatever level you are in your career.
We are looking for an enthusiastic, organised and proactive QC Analyst to join our Quality Control Team in Queenborough, Kent.
About the role
Reporting to the QC Team Leader, you will test and analyse pharmaceutical drugs to determine their identify, purity and strength according GMP principles. The role will also involve:
• Undertake the analysis of incoming samples and finished products to documented specifications using conventional analytical techniques
e.g. HPLC, GC, FTIR, UV, Karl Fisher, Titrations etc.
• Ensure all activities are performed in compliance with customer and ICH procedures.
• Liaise with other professionals regarding the development, manufacturing and testing of pharmaceutical products.
Qualifications & Experience:
• Knowledge of analytical techniques HPLC/GC (including stability indicating methods) and ICH requirements essential.
• HNC/HND or Degree in relevant Science subject would be desirable
What we offer you
We want to provide an environment where our colleagues play an active part in the growth of our business. A challenging but supportive environment where talented people can really grow and take advantage of a wide range of diverse opportunities that we offer.
Above all, you can expect a safe, modern, friendly and collaborative working environment. We regularly benchmark ourselves against our industry and we are confident that we offer a competitive salary and benefits packages to all our colleagues including:
27 days plus statutory holidays
A defined contribution company pension scheme
Life assurance (equivalent to four times your salary)
All-employee share incentive scheme
Aesica is a leading pharmaceutical contract development and manufacturing organisation (CDMO) for developing both active pharmaceutical ingredient (API) and finished does forms.
Our state-of-the-art facilities are home to around 1,300 colleagues across six development, manufacturing and operational sites in the UK, Germany and Italy. We are particularly proud of the diverse workforce that we have built. It is this healthy mix of experienced pharmaceutical professionals and ambitious talent that helps us deliver on our business promises of expertise and innovation.
Our culture is driven by five core values.
Integrity > Respect > Team Work > Results Driven > Customer Focus
Integrity drives mutual Respect. Integrity and Respect are the basis for Team Work. Integrity, Respect and Team Work promote a Results Driven and Customer Focused culture.
To apply for this role please click the “apply online” button and you’ll be taken through our application system where you can quickly apply online by uploading your CV and a cover letter.