Quality Systems Officer – Grangemouth

Barney Smith is recruiting for a Quality Systems Officer to work for a pharmaceutical intermediates manufacturer in Grangemouth on a 12 month contract.

Working solely on New Process Introduction projects you will be responsible for preparing GMP batch records, generating GMP quality documentation for raw materials and equipment, and performing CAPA investigations.

To apply for this role you must have a proven track record of working in QA within a GMP environment.

For more information, or to apply, click here 

 

 

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QA Manager/QP – North Wales

Naynesh Mistry is recruiting for a QA Manager/QP to join a leading manufacturer of veterinary pharmaceutical and animal health products in North Wales on a permanent basis.

Main responsibilities in this role include leading the quality function to ensure all processes are carried out in compliance with internal, regulatory and statutory requirements. You will also be required to act as the primary QP and be responsible for the review of batch manufacturing records, process deviations, LIRs and disposition.

To apply for this position you should have extensive experience in quality assurance, quality control, compliance and/or manufacturing. The ability to work as on-site QP in accordance with Directive 2001/83/EC and Annex 16 of the Rules and Guidance for Pharmaceutical manufacturers and Distributors 2002 is also required.

For more information on this position, or to apply, click here 

 

 

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QA Officer – Teesside

Sarah Farrow is recruiting for a QA Officer to join a global pharmaceutical company at their site in Teesside on a permanent basis.

In this position your responsibilities would include, reviewing all GMP documentation from a QA angle, carrying out audits and providing support to the manufacturing team.

To apply for this position you should have QA experience, ideally in a GMP manufacturing environment.

If you would like to join a global pharmaceutical company that provides excellent opportunities and benefits, click here

 

 

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Shift QA Technician – South Lincolnshire

Hannah Oakley is recruiting for a Shift QA Technician to join a well known, privately owned beverages company in South Lincolnshire on a full time, temp to perm basis.

Responsibilities in this role include carrying out routine product testing, completing all record keeping and paperwork associated with quality measurements and conducting GMP and Hygiene assessments across the entire manufacturing operation to ensure continued improvement of site and operation.

This role requires a QA Technician with Level 2 Food Hygiene Training, understanding of HACCP and a commitment to working a 2pm to 10pm shift.

For more information or to apply for this role click here

 

 

 

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Are you looking for a QA job?

If so contact CK Science today! We currently have a number of junior and senior level QA roles based in London, Hertfordshire and Bedfordshire, such as:

  • QA Officers
  • QA Execs
  • QA Managers
  • QA Auditors
  • QA Validation experts
  • Qualified Person (QP)

So if you have experience in QA area and some of the following skills:

  • Batch review
  • CAPA
  • Continuous improvement
  • Auditing
  • ISO: 9001
  • ISO: 13485
  • ISO 17025
  • RCA:
  • Medical Device Directive MDD
  • In Vitro diagnostics directive IVDD
  • MHRA
  • FDA
  • UKAS
  • IQ, OQ, PQ
  • GMP, GLP
  • CMC
  • IMP
  • Specials

WIth a background in either pharma, biotech, chemical or med devices/diagnostics then call us on 01438 723 500 or click here to search our QA jobs

 

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Global Raw Material Compliance Coordinator

Jason at CK Science is recruiting for a Global Raw Material Compliance Coordinator to join a global pharmaceutical company at their UK Site in London/Kent on a full time, permanent basis.

Our client designs and supports advanced coating systems, modified release technologies and functional excipients for pharmaceutical dosage form and are looking for someone to manage the Raw Material Risk Assessment programme.

If you have experience in a QC, A or regulatory affairs at an intermediate level, and are competent at the day to day management of base raw material data and specifications in the Oracle Quality Module and Master items, our client would like to speak to you.

For more information on this role and to apply click here

 

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Quality Lead Manager – Hertfordshire

Julie Marshall is recruiting a Quality Lead Manager to join a global manufacturing and supply company on a contract basis.

This contract position lasts until June 2014 and requires a QP to provide effective leadership of a Operational Quality team to ensure that released products have been manufactured and packaged in accordance with cGMP and licensing requirements.

If this positions is of interest click here to read the full job description and to apply

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QA Specialist role based in Cork (12 month contract)

  • Reference: 27443
  • Salary: Competitive
  • Contract: 12 months initally

Hannah Milward at CK Science is recruiting for a QA Specialist working for a global healthcare organisation based at their offices in Cork on a 12 month contract.

Responsible for the Document Management System you will be skilled in quality assurance with previous experience working  in a GMP environment.

Click here for more information or to apply for this position

Pharmaceutical Jobs  Science Jobs

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QA Service Provider Strategy – Hertfordshire

Jason Johal at CK Science is currently recruiting for a QA Service Provider Strategy Lead to join one of the world’s leading research-focused healthcare groups for at their Hertfordshire site on a full time, permanent basis.

This role monitors activities outsourced to Service Providers through periodic risk assessment, risk-based routine audits and provides ongoing support to mitigating actions. It also provides actionable data to Senior Procurement/Outsourcing functional management based on analysis of data (audit/inspection/risk) and identification of trends.

Responsibilities

Joining the international Product Development Quality Assurance (PDQA) team, this position will be assigned to the Laboratory service category (GLP, GCP). Reporting to the Principal Team Lead for Service Provider QA Strategy the ideal candidate will be responsible for the design and implementation of the Service Provider risk management and audit strategy across the GLP, GCP, GPVP areas. The role works in partnership with Procurement/Outsourcing Functions and the PDQA GLP, GCP, PV Strategy Leads to ensure that Risk Assessments are maintained across the inventory of Service Providers engaged globally (gRED, pRED, PD, GPS/gMED) and at Affiliate Level.

As QA Service Provider Strategy Lead you will:

  • Design and implement the PDQA Service Provider risk-based strategy for risk management and audit activities
  • Define/maintain the “audit/risk universe” of Service Providers based on input from Procurement/Outsourcing functions and PDQA GxP Strategy Leads
  • Partner closely with the GxP Strategy Leads, Procurement/Outsourcing Functions to ensure that risk assessments are maintained for Service Providers to determine which audits will be conducted and where risk mitigation activities should occur.
  • Develop and implement a GxP risk based strategy to deliver an audit program and quality oversight model for service providers within service category areas.
  • Assess specific risk areas on an on-going basis, communicate to PDQA senior leadership and propose modifications to PDQA strategy where necessary
  • Assess data/metrics from audits, inspections and risk management activities for compliance trends and risks
  • Develop communication tools (reports/dashboards) for audit and inspection metrics and trends
  • Support regulatory authority GCP inspections at service providers

Qualifications

The successful QA Service Provider Strategy Lead will have the following qualifications, skills & experiences:

  • Bachelor’s degree or equivalent in a scientific or quality related field or equivalent combination of education, training and experience
  • Extensive experience in the pharmaceutical industry and/or quality assurance with excellent knowledge of a GLP or Pharmacovigilance Service Provider Quality role
  • Demonstrated knowledge of GLP, GCP, CSV, PV / drug safety and regulatory requirements
  • Project management experience with proven leadership, mentoring and coaching skills
  • Experience supporting Service Provider sourcing initiatives and/or representing QA on Service Provider Strategic Alliance or Category governance teams
  • Proficiency in the conduct of GxP related audits of Service Providers
  • Experience supporting regulatory authority inspections

Benefits

If successful, you will be joining a QA Service Provider Strategy Lead. In return there is:

  • Attractive salary
  • Excellent benefits
  • Career progression opportunitiesJason Johal - Scientific Recruitment at CK Science

How to apply

Apply online now

To apply for this QA Service Provider Strategy Lead position contact Jason Johal via email: jjohal@ckscience.co.uk or telephone: 01438 723 500. Please quote reference ST25997 in all correspondence. Entitlement to work in the EEA is essential.

Are you looking for a QA job?

Click here to view all CK Sciences QA jobs

 

Healthcare Recruitment - CK Science   Healthcare Recruitment - CK Science

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Regional Quality Assurance Consultant – Berkshire

Reena at CK Science is currently recruiting for a Regional Quality Assurance Consultant to join a Global Consumer Healthcare Organisation. Based in Berkshire, this role is a full time on a 12 month contract

Responsibilities

As a Regional Quality Assurance Consultant you will:

  • Providing QA governance and approval of key deliverables for regional validation.
  • Producing regulation and GxP assessments for the regional validation project.
  • Identifying opportunities for continuous improvement mitigation key risks and resolving issues where key decisions are actually required.
  • Driving regionalisation of business processes
  • Holding monthly regional governance board sessions with key leads.
  • Providing QA oversight and support for Change Management function

Qualifications

The successful Regional Quality Assurance Consultant will have the following qualifications, skills & experiences:

  • BSc or equivalent in a life Science subject
  • Proven experience of operating at senior leadership levels within a quality function 
  • Regional Quality Assurance background
  • Proven track record of driving continuous business improvement and change resulting in benefits being achieved
  • Evidence of working at all levels of the organisation
  • Ability to mentor and provide guidance
  • Team management experience essential

 Benefits

As a Regional Quality Assurance Consultant this is an excellent opportunity to join a Global Consumer Healthcare Organisation, which in return offers a competitive salary.

Reena Dhana - Scientific Recruitment ConsultantHow to apply

Apply online now 

For more information or to apply for the role of Regional Quality Assurance Consultant please contact Reena Dhana on 01438 723 500 or email rdhana@ckscience.co.uk. Alternatively please click on the link below to apply online now.  Please quote reference ST25975 in all correspondence.

Entitlement to work in the EEA is essential.

Are you looking for a job in QA?

Click here to view all CK Sciences QA jobs

Science jobs     Science jobs

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