 |
| Job Title |
|
QA Auditor: GMP/GCP/GDP/PPvp |
| Location |
|
Worthing, West Sussex |
| Job Number |
|
120249515 |
| Posted |
|
03/02/2012 (15:06) |
| Agency/Employer |
|
SLS SERVICES |
Description
|
|
QA Auditor Brand New Role!
Worthing, West Sussex
Permanent role with highly competitive salary (to be discussed on application)
Experience of Internal / External Auditing ESSENTIAL
Strong knowledge of Pharmaceutical regulations (preferably GCP, GDP, GMP) ESSENTIAL
Training provided in regulations where you may not have experience (e.g. GPvP)
Summary : A unique and exciting opportunity for a Pharmaceutical Quality professional with experience of organising and conducting audits, whether relating to clinical trial outsourcing, manufacturing, distribution or pharmacovigilance investigations.
The Company : A pioneering Pharmaceutical organisation specialising in the treatment and prevention of allergies. Their unique focus is on the vaccination and prevention of conditions such as hay fever and asthma, and their groundbreaking work has been in the UK press. The company prides itself on its staff development, training and morale, and this role is a fantastic, brand new opening for someone who is looking to be based on the South Coast and further their career in QA with a varied, dynamic and fun challenge.
The Role : Reporting directly to the Head of Science and QA, you will take a lead role in co-ordinating all global QA activities associated with GCP, GPvP, GDP and GMP. You will schedule and perform a range of audits, both of the Worthing facilities and external suppliers and CROs, and will be responsible for managing audit CAPA actions, monitoring clinical trials, writing and updating SOPs, training people across the business, investigating non conformances, updating technical agreements and assisting with customer complaint investigations.
This is a permanent position, based full-time on the Worthing site, though you will typically travel once a month to other locations, either UK-based or international. Being responsible for monitoring the internal and external auditing programme, your role will provide a fair amount of autonomy and you will therefore need to be hard-working individual with the ability to manage your own time effectively and handle several projects at once.
Benefits
25 days holiday
Private health cover
Life insurance
Discretionary annual bonus
Experience : The successful candidate will ideally have a relevant science degree (or equivalent background), with strong experience in a Quality Assurance capacity in the Pharmaceutical industry. You will ideally have a broad range of Auditing experience, covering GCP, Pharmacovigilance, GDP, GMP and other activities, and you must be a professional, hard-working individual with strong communication skills.
Candidates will be ideally have a lot of experience, though we will consider people at a relatively junior level as long as you can demonstrate at least some auditing experience and the desire to learn.
Keywords : QA audit, auditor, quality assurance, clinical, manufacturing, pharmacovigilance, GMP, GDP, GCP, PV, FDA, MHRA, non conformance, LIMS, root cause analysis, compliance, batch release, batch record, pharmaceutical, sterile, sterility, SOP
This is a permanent role
|
| Job Type |
|
Permanent |
| Contract Length |
|
N/A |
| Start Date |
|
ASAP |
| Contact Details |
|
 |
|
|
|
|
