Clicky

Skip navigation
Find us on Facebook Follow us on Twitter
You are here: Job Search - Quality Management

Quality Officer

Company Consort Medical Group Location Kent
Contract Permanent Position Salary Competitive
Sector(s) Quality Management

Job Description

HCMF is a purpose built, dedicated facility for type 2 diabetes drug manufacturing in high capacity. The facility is an advanced unit which contains highly technical and specialist equipment including state-of-the-art spray granulators, coaters, tablet presses, powder handling systems and large capacity blenders.

We have an exciting role for a Quality Officer to join our ambitious Quality team in HCMF department.  

If you are a confident communicator with a high attention to detail and previous experience in validation and internal auditing, then please apply now! 


About the role

You will be working closely to support QPs, QC audit team leader and production to ensure all Quality requirements are met and delivered on time and reviewing procedures and systems regularly for continuous improvement.

Some of the Key Responsibilities:

• Participate in internal/external audits to explain activities performed and systems managed
• Ensure that all methods and procedures held are current and that there is evidence that all relevant staff are trained accordingly in current and revised procedures upon re-issue as per the group document control process
• Undertake batch review, prior to QP batch release, operating within both company and regulatory requirements.
• Assist production to resolve quality issues identified during the manufacturing process.
• Ensure shop floor presence to drive a Quality Culture into manufacturing and packaging.

Requirements:

• Excellent verbal and written communication and interpersonal skills
• Good computer literacy and MS Office skills
• A good understanding of Regulatory requirements
• Knowledge in the pharmaceutical industry and GMP regulations is desirable
• Science degree or equivalent would be desirable
• ERP software experience would be desirable

• Previous experience working in the Quality role would be desirablePrevious experience working in the Quality role would be desirable


What 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. 

Competitive base salary
27 days plus statutory holidays
A defined contribution company pension scheme
Life assurance (equivalent to four times your salary)
Cycle-to-work scheme
All-employee share incentive scheme

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.

About Aesica

We are a leading pharmaceutical CDMO that delivers the high-quality active pharmaceutical ingredient (API) and finished dose formulation development and manufacturing services the industry demands.

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.

How to Apply

In order to apply for this job, please Sign In/Create Account.