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Posts Tagged ‘cGMP’

NPI Project Manager Job (Medical Device) – Oxfordshire, UK

Tuesday, December 7th, 2010

CK Science are currently searching for a NPI Project Manager to join a global Medical Device company based in Oxfordshire, UK.

Key Responsibilities:

Your key responsibilities of this NPI Project Manager will include providing technical support to the NPI (New Product Introduction) for the diabetes strip-manufacturing unit and supporting the unit to maintain production output and yields. Ensuring the analysis and interpretation of measurements in process and release test data, identify potential areas of inefficiency to drive continuous process, product, cost and quality improvements in the manufacturing unit. You will also ensure all work carried out in compliance with the correct processes and procedures and take ownership of assigned ER’s CAPA’s and VMP activities.

Person Specification:

For this NPI Project Manager role you will be degree qualified in a scientific/Engineering discipline (or equivalent) with previous experience in Validation. Previous knowledge of relevant processes, test methods, analytical techniques, experimental design, data analysis and statistical process control would be advantageous. You will have a good understanding of cGMP in Design Control and Validation. Understanding the principals behind Six Sigma and Continuous Improvement methodologies is essential and have excellent communication and IT skills. Previous experience in a highly regulated industry would be advantageous.

Apply Now

For more information, or to apply for this NPI Project Manager job, please contact Reena Dhana at CK Science on 01438 723 500 or email rdhana@ckscience.co.uk. Please quote reference ST20816 in all correspondence.

Alternatively, click here to apply for this NPI Project Manager online now.

Tags: CAPA, cGMP, ER, lean manufacturing, medical device, NPI, NPI Project Manager job, Oxfordshire, Six Sigma, uk, VMP
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NPI Project Manager Job (Medical Device) – Oxfordshire, UK

Thursday, December 2nd, 2010

CK Science are currently searching for a NPI Project Manager to join a global Medical Device company based in Oxfordshire.

Responsibilities:

Your key responsibilities will include:

Providing technical support to the NPI (New Product Introduction) for the diabetes strip-manufacturing unit and supporting the unit to maintain production output and yields.
Ensuring the analysis and interpretation of measurements in process and release test data, identify potential areas of inefficiency to drive continuous process, product, cost and quality improvements in the manufacturing unit.
You will also ensure all work carried out in compliance with the correct processes and procedures and take ownership of assigned ER’s CAPA’s and VMP activities.

Person Specification:

For this role you will be degree qualified in a scientific/Engineering discipline (or equivalent) with previous experience in Validation. Previous knowledge of relevant processes, test methods, analytical techniques, experimental design, data analysis and statistical process control would be advantageous. You will have a good understanding of cGMP in Design Control and Validation. Understanding the principals behind Six Sigma and Continuous Improvement methodologies is essential and have excellent communication and IT skills. Previous experience in a highly regulated industry would be advantageous.

Apply Now

Tags: CAPA, cGMP, ER, lean manufacturing, medical device, NPI, NPI project manager, oxfordshire UK, senior technologist, Six Sigma, VMP
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Process Development Technologist Job (Medical Device) – Oxfordshire, UK

Thursday, November 11th, 2010

CK Science are currently searching for a Process Development Technologist to join a global Medical Device company based in Oxfordshire, UK.

Responsibilities:

As a Process Development Technologist, your key responsibilities will include providing technical support to the NPI (New Product Introduction) for the diabetes strip-manufacturing unit and supporting the unit to maintain production output and yields. Ensuring the analysis and interpretation of measurements in process and release test data, identify potential areas of inefficiency to drive continuous process, product, cost and quality improvements in the manufacturing unit. You will also ensure all work carried out in compliance with the correct processes and procedures and take ownership of assigned ER’s CAPA’s and VMP activities.

Qualifications and Experience:

For this Process Development Technologist role you will a degree in a scientific discipline (or equivalent) with previous experience in a similar discipline. Previous knowledge of relevant processes, test methods, analytical techniques, experimental design, data analysis and statistical process control would be advantageous. You will have a good understanding of cGMP in Design Control and Validation. Understanding the principals behind Six Sigma and Continuous Improvement methodologies is essential and have excellent communication and IT skills.

Apply Now

For more information, or to apply for this Process Development Technologist position, please contact Reena Dhana at CK Science on 01438 723 500 or email rdhana@ckscience.co.uk. Please quote reference ST20816 in all correspondence.

Alternatively, click here to apply for this Process Development Technologist position online now.

Tags: CAPA, cGMP, ER, medical device, medical devices jobs, NPI, Oxford, Oxfordshire, process development technologist jobs, VMP
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Quality Assurance Officer Jobs (Pharmaceutical Product Release) – Country Durham

Wednesday, September 8th, 2010

Our client, a major pharmaceutical company located in County Durham, has a number of long term temporary vacancies for Quality Assurance Officers with relevant experience in product release and cGMP compliance. Some but not all of the positions may involve shift working, for which there is a generous shift allowance.

As a Quality Assurance Officer, you will ensure that all products released for sale or further processing comply with cGMPstandards, product quality specifications and regulatory requirements. You will also generate and review product related technical documents, and collate and interpret data such as analytical results/trends and regulatory, validation and engineeringinformation. Working as a Quality Assurance Officer you will also lead and direct investigative work into products failing to meet requisite standards (and regulatory issues). You will also lead investigative work and develop and agree corrective actions.
Our client is looking for individuals with a strong background in Quality Assurance, good knowledge of cGMP and regulatory requirements and the ability to manage multiple activities concurrently within high volume, complex areas. Excellent communications skills are also required, togetherwith demonstrable leadership and decision-making abilities.

Apply Now

For more information, or to apply for this Quality Assurance Officer position, please contact Graeme on 0191 384 8905 or email gpallas@ckscience.co.uk.

Tags: cGMP, compliance, investigations, pharmaceutical jobs, product release, QA jobs, quality assurance jobs
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Quality Assurance Officers (Pharmaceutical Product Release) – County Durham, UK

Thursday, July 15th, 2010

Our client, a major pharmaceutical company located in County Durham, has a number of long term temporary vacancies for Quality Assurance Officers with relevant experience in product release and cGMP compliance. Some but not all of these Quality Assurance Officer positions may involve shift working, for which there is a generous shift allowance.

As a Quality Assurance Officer you will have the following responsibilities:

You will ensure that all products released for sale or further processing comply with cGMP standards, product quality specifications and regulatory requirements.
You will also generate and review product related technical documents, and collate and interpret data such as analytical results/trends and regulatory, validation and engineering information.
To lead and direct investigative work into products failing to meet requisite standards (and regulatory issues).
You will also lead investigative work and develop and agree corrective actions.

Our client is looking for individuals with a strong background in Quality Assurance, good knowledge of cGMP and regulatory requirements and the ability to manage multiple activities concurrently within high volume, complex areas. Excellent communications skills are also required, together with demonstrable leadership and decision-making abilities.

Apply now

For more information, or to apply for these Quality Assurance Officer roles, please contact Graeme at CK Science on 0191 384 8905 or email gpallas@ckscience.co.uk. Please quote reference DH20139 in all correspondence.

Tags: cGMP, compliance, Country Durham, investigations, north east, pharmaceutical jobs, product release, QA jobs, quality assurance jobs, Quality Assurance Officer, science jobs, scientific recruitment, uk
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