Latest Science Jobs in the UK and Europe – 26/11/12

Here is a list of our latest science jobs in the UK and Europe. Click on the links below to find out more and be the first to apply!:

MScience Jobs of the weekidlands:

HR Administration Assistant – Wolverhampton

Analytical Chemist – Staffordshire

Quality Manager in Lincolnshire

Process Manager – Lincolnshire

Homecounties:

Senior QC Scientist – Pharmaceutical, Surrey

QC Microbiologist – Surrey

Senior Process Engineer – Water, Bedfordshire

Science Jobs of the weekSenior Electronics Engineer – Aerospace, Hampshire

Technical Support Chemist – Petrochemical – Berkshire

Quality Manager with QP Status – Hertfordshire

Shift QC Analyst – Berkshire

South West:

Microbiologist – Wiltshire

London:

Research Scientist, Assay – LondonScience Jobs of the week

Analytical Chemist – London

Yorkshire:

Food Technologist – Yorkshire

Process Technologist – Yorkshire

Humberside:

Pilot Plant Chemist – Polymers, Humberside

NScience Jobs of the weekorth East:

Synthetic Organic Chemist – North East England

NPD Manager in Newcastle

Technical Support Chemist in Middlesbrough

Wales:

EHS Compliance – Nuclear – Wales

South East:

API Plant Manger – South East

Europe:Science Jobs of the week

Mechanical Design Engineer – Water, Switzerland

Senior Process Engineer – Water, Switzerland

North West:

Senior GCMS Analyst – Headspace, Manchester

Not quite what you’re looking for? Click here to register your CV with us today.

Follow us on Twitter @CKScienceJobs to receive more industry news and CK jobs of the week updates

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Science Jobs in the UK and Ireland – 22/10/12

Here is a list of our latest science jobs in the UK. Click on the links below to find out more and be the first to apply:

South of the UK:

Sales Manager – Polymer, Chemical, South West

Polymer Chemist – Material Science, Hampshire

Home counties:

Analyst – Hertfordshire

Laboratory Analyst – Hertfordshire

Shift QC Analyst – Hertfordshire

PScience jobs in the UK and Irelandroduction Technicians – Clean Room, Surrey

Scientific Communications Officer – Hertfordshire

QC Scientist – Med Device, Pharmaceutical, Surrey

Process Engineer – Surrey

Senior QC Scientist – Pharmaceutical, Surrey

North East:

Purification Team Leader in Teesside

Process Chemist in Durham

Science jobs in the UK and IrelandScotland:

Molecular Biologist in Edinburgh

Midlands:

Trainee Recruitment Consultant – Chesterfield

Scotland:

Liquid Innovation Technologist in Glasgow

Science jobs in the UK and IrelandValidation Engineer in Irvine

North West:

Chemical Sales Representative – N.West

London:

Analytical Chemist – Petrochemical, East London

Ireland:

Science jobs in the UK and IrelandShift Manager – Manufacturing – N.Ireland

Yorkshire:

Shift Laboratory Technician – Bradford

 

Not quite what you’re looking for? Click here to register your CV with us today.

Follow us on Twitter @CKScienceJobs to receive more industry news and CK jobs of the week updates

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Our latest science jobs – 15th of October 2012

Here is a list of our latest science jobs in the UK. Click on the links below to find out more and be the first to apply:

Home based with in the UK:

Auditors & Document Reviewers – Medical Devices

Homecounties:

Medical Device Technologist – Hertfordshire

QC Officer – Food, Kent

Field Service Engineer – Mechanical, Electrical – Field based

Business Analyst – Oil & Gas, Surrey

Commercial Manager – Oil & Gas, Chemical, Surrey

Ireland:

Organic Chemist Technical Leader – APIs, N Ireland

Manufacturing Engineer, Medical Devices – Ireland

Formulation Development Scientist – N.Ireland

Group Leader – Formulation – N.I

East Anglia:

QA Auditor – Suffolk

QC Analytical Specialist – Suffolk

North East:

Organic Chemist in Cramlington

Laboratory Assistant in Teesside

Validation Engineer in Barnard Castle

Analytical Development Chemist in Newcastle

Glasgow:

Laboratory Technician in Glasgow

North West:

Scale Up Chemist, Chemicals, Greater Manchester

Quality Assurance Representative – N.West

Chemical Process Engineer – Chemicals, Merseyside

London:

QC Laboratory Assistant, Chemical – London

Scotland:

Qualified Person (QP) in Scotland

QA Officer in Central Belt

Offshore Chemist in Aberdeen

Midland:

NPD & Packaging Technologist – W. Midlands

 

Not quite what you’re looking for? Click here to register your CV with us today.

Follow us on Twitter @CKScienceJobs to receive more industry news and CK jobs of the week updates

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Interim Qualified Person, QP – Surrey

Reena Dhana at CK Science is currently recruiting for a Qualified Person (QP) to join a Global Pharmaceutical Company based in Surrey on a full time, 3 month contract.

Responsibilities:

As a Qualified Person you will be responsible for documentation control, sign off and batch release of over the counter drugs.

Qualifications:

The successful candidate for this Qualified Person role will hold a chemistry or pharmacy degree (or equivalent), will be on the register of eligible Qualified Persons and named in the appropriate Manufacturer’s Licence. You will also have experience ideally gained in the Pharmaceutical Industry.

Reena Dhana - Recruiter at CK ScienceHow to apply:

Apply online:

For more information or to apply for this role please contact Reena Dhana on 01438 723 500 or email rdhana@ckscience.co.uk.  Please quote reference ST25093 in all correspondence.

 

Are you looking for a new position in science? CK Science will help you.

Click here to search our current science jobs in the UK now.

       

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CPO Quality Unit Head – Surrey

Jason Johal at CK Science is currently recruiting for a CPO Quality Unit Head to join a global pharmaceutical company based in Surrey on a full time, permanent basis.

The job:

The CPO Quality Unit Head will ensure quality governance and quality planning in the Country organization through the implementation of quality systems and processes and the annual Quality Plan. They will also prevent significant quality issues or regulatory non-compliance which could lead to product stock-out or withdrawal, product approval delays or which would negatively impact the financial performance of the company as well as the reputation.

If successful, you will be joining a CPO Leadership Team that reports functionally to Global QA for a Global Pharma company. In return there is an attractive salary, coupled with excellent benefits and career progression opportunities.

Responsibilities:

As CPO Quality Unit Head you will:

  • Lead the local QA organization to ensure implementation, maintenance and upgrading of the local Quality System and Standard Operating Procedures in order to drive compliance of all cGXP and Pharmacovigilance related processes and tasks with local/International regulatory requirements and the Novartis Quality Manual
  • Ensure quality governance and quality planning in the Country organization through the establishment and implementation of the annual Quality Plan, the Country Quality Review Board, appropriate Key Quality Indicators, and Quality Risk Assessments.
  • Lead the country Quality Review Board
  • Ensure Good Clinical Practice (GCP) and Good Pharmacovigilance Practice (GPvP) oversight and quality & compliance of Development and Medical Affairs (MA) projects, products and programs (Phase I through Phase IV)
  • Ensure that co-ordinated contact is maintained with the local Regulatory Authorities, the local partners (suppliers, third parties, licensees, and distributors) and Pharma Global Quality Assurance
  • Ensure that all drug products are released in accordance with the registered specifications and are released to the market in accordance with local/international regulations and ensure that a respective Change control procedure is in place
  • Ensure CPO readiness for all GxP regulatory inspections.
  • Ensure management of external inspections, complaints, recalls, counterfeits and product tampering according to the Company Quality Manual and local written procedures.
  • Ensure that local audits are performed within the CPO organization and at 3rd parties, as appropriate.

Qualifications and skills:

The successful CPO Quality Unit Head will have the following qualifications, skills & experiences:

  • Extensive experience in the pharmaceutical industry in a relevant field such as quality assurance, quality control, registration, clinical development or production or a directly related area
  • Strong leadership skills
  • The ability to build the team according to requirements.
  • QP status would be advantageous
  • Strong knowledge of GMP and/or GCP
  • Degree in Life Sciences or related fields

Jason Johal  -  Manager at CK ScienceHow to apply:

Apply online:

For more information or to apply for this CPO Quality Unit Head role please contact Jason Johal via email jjohal@ckscience.co.uk or 01438 723 500.  Please quote reference ST24492 in all correspondence.

Click here to see our latest jobs in the pharmaceutical industry

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Microbiology Laboratory Supervisor Job – Surrey, UK

Our client, a leading Water Supplier and Testing organisation, are currently looking for a Microbiology Laboratory Supervisor to join their Microbiology & Cryptosporidium Testing Laboratory based in Surrey, UK.

This is an outstanding opportunity to join a leading Water Organisation in their growing Microbiology and Cryptosporidium laboratories. In return they offer an attractive salary and benefits package.

 

Responsibilities:

Working as a Microbiology Laboratory Supervisor, you will be responsible for the day-to-day management of teams of Analysts and Microbiologists within the Microbiology & Cryptosporidium divisions; ensuring sample turnaround including liaising with both internal teams and external customers regarding results as well as overseeing of quality systems in the laboratory (ISO, UKAS, DWI).

 

Person Specification:

To be considered for this Microbiology Laboratory Supervisor role, you will be educated to degree level (or equivalent) including strong experience in Microbiology and/or Cryptosporidium and demonstrated Laboratory Supervisor / Team Leader experience including knowledge of quality standards (ISO, UKAS, DWI) gained in the Water, Analytical Testing or a related industry.

 

Apply Now

For more information or to apply for this Microbiology Laboratory Supervisor position, please contact Andrew Bolton at CK Science on 01438 723 500 or email abolton@ckscience.co.uk. Entitlement to work in the EEA is essential. Please quote reference ST21162 in all correspondence.

 

Alternatively, click here to apply for this Microbiology Laboratory Supervisor position online now.

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

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Quality Director Job (Pharmaceutical) – Surrey, UK

Our client, a world leading Pharmaceutical organisation, are currently looking for a Quality Director to join their Drug Development Group based from their state-of-the-art facilities in Surrey, UK.

 

Responsibilities:

Working as a Quality Director, you will be responsible for managing quality systems across the European arm of the group. Your duties will include maintaining GCP, GLP and GMP quality systems including development of SOPs for the group; development of function specific training maps for employees; selection and relationship management of contract research firms; management of audits for both internal and 3rd party partner sites / systems as well as coordinating and approving the final release of clinical products. With full responsibility for the Quality Department, you will also be responsible for full management of the division including recruitment, development and training of staff.

This is an outstanding opportunity to join an early phase drug development group that manages a broad portfolio of new molecular entities from candidate selection through clinical Proof of Concept (PoC).

 

Person Specification:

To be considered for this role, you will meet the following criteria:

 

Qualifications:

  • A Degree
  • MSc
  • PhD in a relevant Scientific subject
  • A QP license would be advantageous.

 

Experience:

  • Proven practical experience managing GCP, GLP and/or GMP requirements at a Pharmaceutical or similar organisation.
  • A working knowledge of large & small molecule drug substance manufacturing, analytical laboratories, drug product solid dosage forms manufacturing, parental manufacturing, extemporaneous preparation, PET studies and clinical packaging / labelling operations.

 

Apply Now

For more information, or to apply for this Quality Director position, please contact Jason Johal at CK Science on 01438 723 500 or email jjohal@ckscience.co.uk. Please quote reference ST20896 in all correspondence.

 

Alternatively, click here to apply for this Quality Director role online now.

 

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

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Preclinical Toxicology Scientist Job (ADME) – Surrey

Our client, a world leading Pharmaceutical organisation, are currently looking for a Preclinical Toxicology Scientist to join their Drug Development Group based from their state-of-the-art facilities in Surrey, UK.

This is an outstanding opportunity to join an early phase drug development group that manages a broad portfolio of new molecular entities from candidate selection through clinical Proof of Concept (PoC).

Working as a Preclinical Toxicology Scientist, you will be responsible for all phases of the toxicology and ADME plans for a product portfolio ranging from large biologics (antibodies, proteins and peptides) to small molecules.

 

Responsibilities:

Your duties will include creation and implementation of preclinical toxicology/ADME plans; development of safety assessment plans; approval of methodology, protocols and final study reports; project management activities related to preclinical work product (timeline, scope, budget, risk mitigation, contingency plans) as well as working closely with quality and regulatory to prepare nonclinical ADME safety pharmacology and toxicology sections of IB, INDs, CTD, IMPDs and other regulatory documentation.

As part of the role, you will also be required to build, establish and communicate a network of preclinical toxicology/ADME content experts as well as a network of external contract vendors to support activities.

 

Person Specification:

To be considered for this role, you will meet the following criteria:

Qualifications:

  • Degree / MSc / PhD in Toxicology
  • Veterinarian Medicine
  • Occupational Health
  • Health Sciences or a related discipline (or equivalent)

 

Experience:

  • Ability to identify structural/chemical class problems that will guide preclinical activities around specific identified issues with a compound.
  • Extensive experience working in Toxicology/ADME or equivalent.
  • Proven practical experience working across multiple phases of drug development.
  • Demonstrated experience preparing GLP regulatory documentation: ICH, FDA, and EMEA non clinical safety, toxicology and ADME guidance.

 

Apply Now

For more information, or to apply for this Preclinical Toxiciology Scientist position, please contact Jason Johal at CK Science on 01438 723 500 or email jjohal@ckscience.co.uk. Please quote reference ST20902 in all correspondence.

 

Alternatively, click here to apply for this Preclinical Toxicology Scientist position online now.

 

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

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