Recruiting quality first

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IT job opportunities in Twickenham

St Mary's University

Job details

QC Manager

Location: Maidenhead

Salary/Rate: 48000

Type: Permanent

Closing Date:

Job Reference: 3074105

QC, CONTROL, QUALITY, GMP, Lab

LOOKING TO DEVELOP WITHIN THE QC INDUSTRY.

QC Manager

QC, Quality Control, GMP, HPLC

Your new company
This start up generics pharmaceutical company focuses on providing a wide variety of services and products. The company was founded in the past 5 years and began operating in 2016, their fresh focus is on IP and manufacturing of specific products that are aimed at a variety of therapeutic areas and operate worldwide. Some of the services they provide include R&D, IP licensing and manufacturing. They have an exquisite site that is newly built with fantastic facilities in Berkshire and are looking to strengthen their Quality Team through the appointment of a QC Manager at their manufacturing site based in Berkshire.

This company is willing to offer immense career and developmental opportunities to ambitious candidates who are willing to learn and enhance their skill set.

Your new role
Your new job role as QC Manager will be to support the manufacturing QC functions. You will ensure that the QC functions operate in a GMP compliant way organise the smooth operations of the QC Lab functions. You will have full responsibility and day to day management of QC Analysts and Senior QC Analysts. 

Other key responsibilities include:

  • Providing technical and analytical support for QC testing
  • Take part in documentation, lab systems and processes
  • Participate in various audits such as internal, safety and regulatory 
  • Support the QC instrument and qualification of equipment qualification
  • Managing the review and approval and implementation of SOPs, method validation, protocols and method development.

What you'll need to succeed
In order to be considered for this Senior QC Analyst position you will need the following:
  • Team lead and management experience is necessary 
  • Minimum of degree level or equivalent in a scientific discipline
  • Experience in GMP environment
  • Hands on experience of analysing, testing and developing instrumentation analysis 
  • Previous team lead or management experience in a QC environment 
  • At least 4 years of UK experience in QC
  • Method development and validation experience 
  • Outstanding written and oral skills are needed as well as the ability to work well within a dynamic team whilst using your initiative. You will also have knowledge of Microsoft tools. 

In return for this you will be given the opportunity to develop in a leading pharmaceutical company, along with a competitive salary and benefits package.

What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career.


Contact: Chandni Pankhania

Office: 107 Cheapside, London,EC2V 6DN

Phone: 02034650133

Email: chandni.pankhania@hays.com

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