QA Coordinator

Recruiter
Consult Search & Selection
Location
Derbyshire
Salary
£24k-£28k
Posted
30 Sep 2017
Closes
03 Nov 2017
Contract Type
Permanent
Hours
Full Time
QA Coordinator
Salary £24k-£28k, depending on experience

The Company
My client is a successful pharmaceutical products contract testing company seeking a QA Coordinator to join their small friendly team in their accredited lab. Due to the location, private transport is essential. This is commutable from Stockport, Chesterfield and Sheffield.

The Job
This position is ideal for someone with existing Quality Assurance experience from a GMP manufacturing or ISO 17025 contract testing environment looking to take the next step and join a team with the opportunity for you to make it their own.
Although you will be solely responsible for management of the Quality Management system and is effectively a standalone role, this role requires you to work effectively with colleagues across all areas to achieve objectives whilst maintaining good working relationships.

Responsibilities:
Reporting directly to the Operations Manager, this role is focused on maintaining the QMS, which is in line with GMP guidelines and ISO17025 requirements. This would include:
  • Review, write, amend documentation, such as SOPs
  • Audit of GMP data, i.e. a review raw data prior to releasing a GMP CoA or CoP.
  • Co-ordination of quality issues investigation and CAPA.
  • Participation in the change control process to ensure changes to processes and systems are managed appropriately to maintain GMP compliance.
  • Track, trend and gathering data for meetings
  • Conducting training with staff in terms of quality matters, when needed.
  • Follow up on updates/changes and publications with regards to GMP.
  • Liaising with customers or regulatory representatives.
  • Responding to the external audit report findings, e.g. plan corrective actions, communicate with regulatory or customers.
  • Releasing necessary documentation externally in controlled manner. Obtaining and maintaining necessary external documentation, when needed.
  • Plan and conduct internal audits in line.
About You
To apply for this role you will have a scientific degree with some experience in a quality assurance position within a GMP environment.
This job was originally posted as www.totaljobs.com/job/76113956