Posts Tagged ‘auditing’

QA Auditor Job in Sussex

Wednesday, May 23rd, 2012

Julie Marshall at CK Science is currently looking for a QA Auditor to join the Quality Auditing team of a successful pharmaceutical company based in Sussex.

This QA Auditor role is a full-time, temporary role. If successful, you will be joining a global company and in return there is an attractive salary, coupled with career progression opportunities.

To be considered for this Quality Assurance Auditor position, you will have the following qualifications, skills and experience:

  • Experience in performing and maintaining compliance audits in line with Regulatory and QMS requirements
  • Experience in leading Audits, including scheduling, planning, executing, reporting and CAPA management
  • A degree (or equivalent) in an appropriate discipline or related experience
  • Knowledge of GMP regulations and in-depth knowledge of Quality Management Systems
  • Certified Auditor/Internal/External
  • Experience within a quality function or from a quality based role within manufacturing

How to apply:

Julie Marshall - Scientific Recruitment Consultant at CK Science

Please contact Julie for more details.

Click here to apply online now.

For more information regarding this QA Auditor position, please contact Julie Marshall at CK Science on 01438 723500 or email jmarshall@ckscience.co.uk. Please quote reference ST24342 in all correspondence.

Not quite right? Click here to search our other Quality Assurance jobs online now.

Associate Director Job (Pharmaceuticals, Quality Auditing) – Suffolk, UK

Tuesday, June 28th, 2011

We are currently looking for an Associate Director to join a global pharmaceutical company in the Suffolk region.

As Associate Director, you will be responsible for developing and managing audit programs for healthcare compliance and privacy at the company’s facilities to ensure they are meeting the relevant company and regulatory standards.

 

As Associate Director, you will also:

  • Develop and introduce a process for carrying out healthcare compliance audits. This will include the auditing procedure and the reporting of audit results and metrics to senior management. 
  • Train company auditors in healthcare compliance auditing.
  • Auditing company facilities including country offices and relevant business units for healthcare compliance.
  • Develop and introduce a process for carrying out privacy audits. This will include the auditing procedure and the reporting of audit results and metrics to senior management.  The audits will check that the organization can both meet the requirements of the company and the relevant regulatory requirements.
  • Train auditors in privacy auditing.
  • Auditing facilities for privacy.

 

Person specification:

The ideal candidate for this Associate Director position will have the following qualifications, skills and experience:

  • Possess a Bachelors degree (or equivalent) with related industry experience.
  • Extensive experience in auditing
  • Expert knowledge of healthcare compliance and/or privacy requirements for the pharmaceutical and/or medical device industries
  • Strong written and oral communication skills.

 

How to apply

For more information or to apply for this Associate Director position, please contact Jason Johal at CK Science on 01438 723 500 or email jjohal@ckscience.co.uk. Please quote reference ST22200 in all correspondence.

 

Click here to apply online!

Not quite what you’re looking for? Search our current pharmaceutical jobs online now.

Senior QA Officer Job – Cambridgeshire, UK

Tuesday, August 31st, 2010

Our client, is a leading global biotechnology company based in the Cambridgeshire/Suffolk area, looking for a Senior Quality Assurance Officer to join their QA team.

As Senior QA Officer, you will be responsible for reviewing documentation in accordance to in-house specifications as well as cGMP. You will also provide QA advice for deviation investigation, root causing and change management. Part of the role will include internal auditing and supervision of less experienced staff.

To be successful for this Senior QA Officer role you will have a BSc in a scientific discipline (or equivalent). Previous experience with deviation investigation, batch release of API and dealing with customer complaints is essential. Experience in auditing or documentation review within a Quality Management System is also essential.

This is a fantastic opportunity to join a biopharmaceutical company within an easy commuting distance from Cambridge.

Apply Now

For more information, or to apply for this Senior QA Officer position, please contact Reena at CK Science on 01438 723 500 or email rdhana@ckscience.co.uk. Please quote reference ST20411 in all correspondence.

Meet Reena – Our Specialist Environmental and Food Recruitment Consultant (South, UK)


EHS Specialist (Chemicals) – North West, UK

Friday, June 18th, 2010

An EHS Specialist is required to join a speciality chemicals company based in the North West of England.

The main duties of the EHS Specialist will be to ensure environmental, health and safety regulations are complied with and to assist the EHS Manager.

For this EHS Specialist position the responsibilities will be as follows:

  • You will conduct audits and keep procedures up to date as well as performing incident investigations and reporting H&S metrics as required.
  • Compliance: You will support the EHS Manager in compliance issues and this support is primarily related to the conduction of risk assessments, job safety analysis, environmental compliance such as emission monitoring, waste disposal and all related inspections from authorities.
  • You will develop proposals for improvement and follow-up corrective actions.
  • You will implement corporate EHS initiatives and identify opportunities for improvement as an advisor for the plant employees.
  • Responsible care management system: You will write, implement and keep the EHS procedures up to date and inform employees as appropriate. Reporting of accidents, incidents and hazards/near misses will be ensured by yourself and you will provide adequate tools to the site. You will carry out incident investigation with appropriate root cause analysis and identify corrective actions.
  • Auditing and inspection: You will be responsible for performing the necessary EHS inspections at the site related to work permits, the workplace and good house keeping practices. Regular safety tours on the plants will be conducted to ensure visibility and awareness to EHS. Internal audits will be required under ISO/RC 14001 certification as well as reporting and identifying opportunities for improvement. You will manage the internal safety observation programme and report results and support observers in their role.
  • Reporting and communication: Your will report performance indicators related to EHS for the site and prepare and submit reports coming from audits, inspections, training and monitoring activities. Ensurance of H&S communication by issuing safety information as appropriate to the employees.

The requirements for this EHS Specialist role are as follows:

  • Bachelors degree or equivalent in chemistry or a related subject desired.
  • NEBOSH/ IOSH qualified or part qualified.
  • Previous work experience in a chemical manufacturing facility essential.
  • Prior management experience is a preference.
  • Thorough knowledge of H&S laws, regulations, standards and permitting requirements.
  • Fact-based analysis and reporting skills; strong technical, interpersonal and communication skills; Assertive and persuasive
  • Knowledge of ISO/RC 14001 principles and auditing.
  • Good basic working IT knowledge of Microsoft Office Professional.

 

Apply Now

For more information, or to apply for the EHS Specialist job, please contact Victoria Walker at CK Science on 0114 283 9956 or email vwalker@ckscience.co.uk. Please quote reference SH19982 in all correspondence.

Alternatively, click here to apply for this EHS Specialist job online now.

QA Manager (GCP) – London, UK

Tuesday, June 8th, 2010

A QA Manager is required to join a CRO based in London, UK.

 

As QA Manager, the main aim of your role will be to implement and manage the CRO’s Quality System and to develop and implement QA GCP audit strategy in line with the overall QA strategy. You will also be responsible for ensuring the compliance of their clinical trials in accordance with business and statutory regulations and reporting critical GCP non-compliance.

Working as a QA Manager, your main responsibilities will include:

  • Acting as the source of advice and guidance on GCP and SOP related quality issues and will determine the effectiveness of the Company’s quality systems and procedures.
  • Delivering the SOP Management System.
  • Assessing GCP non-conformities and non-compliant findings.
  • Supporting the implementation of technical training within the Company.
  • Co-ordinating with the GCP regulatory inspectorate client auditors and customers.
  • Ensuring compliance of the quality documentation related to Clinical processes and studies through audit and review.

The ideal candidate for this QA Manager position will be degree qualified (or equivalent) and will ideally hold a  qualification in Quality or QA.  This QA Manager job also demands a candidate with experience and knowledge in the following:

  • Industrial experience within QA.
  • Proven auditing experience across full range of clinical audit types including CROs, investigator sites, protocol, clinical study reports, systems and submissions.
  • Proven management experience.
  • A good knowledge of phase I – IV studies, bioanalytical, PK, skin, blood and urine laboratory analysis an experience auditing.

Apply Now

For more information, or to apply for this QA Manager job, please contact Jason Johal on 01438 723 500 or email jjohal@ckscience.co.uk. Please quote reference ST19921 in all correspondence.

 

 

Alternatively, click here to apply for this QA Manager job online now.

Not quite what you’re looking for? Click here to search our current science jobs online now.

 

 

If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential.

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