Microbiologist – Blackpool

Hannah Oakley is recruiting for a Microbiologist to be based in Blackpool at a leading medical device organisation.

In this role, your main function will be to carry out microbiological and environmental tests to ensure that the ongoing production is up to standard. You will also need to ensure that the cGMP principles and that all procedures comply with the appropriate industry directives.

This role requires you to have a BSc within a scientific discipline as a minimum, alongside experience within the microbiological field.

For more information on this role, please click here

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Engineering Compliance Manager – London

Reena Dhana at CK Science is currently recruiting for an Engineering Compliance Manager to join a Global Pharmaceutical Organisation at their site in London, on a full time, 6 month contract.

Responsibilities:

As an Engineering Compliance Manager the main purpose of your role will be:

  • To ensure that all Manufacturing Sites are supported with documented technical standards
  • To ensure that the necessary systems, processes, procedures and training is in place so that line managers in Manufacturing Engineering can ensure their staff remain compliant with the cGMP and Engineering standards.

Qualifications and skills:

As an Engineering Compliance Manager you will have the following qualifications, skills and experience:

  • Previous experience in an operational or managerial engineering role would be ideal.
  • You will have technical expert in all areas of Engineering ideally in the Pharmaceutical industry.

As an Engineering Compliance Manager, you will be joining a Global Pharmaceutical Organisation who in return are offering a competitive salary

Reena Dhana - Recruiter at CK ScienceHow to apply:

For more information or to apply for the role of Engineering Compliance Manager please contact Reena Dhana on 01438 723 500 or email rdhana@ckscience.co.uk. Please quote reference ST24933 in all correspondence.

 

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NPI Project Manager Job (Medical Device) – UK

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.

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

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

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.

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Process Development Technologist Job – Oxfordshire

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.

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Quality Assurance Officer Jobs, Pharmaceutical

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.

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Quality Assurance Officers (Pharmaceutical Product Release) – County Durham, UK

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.

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