Microbiologist - Biotechnology. Our client is a biotechnology company located in the Central Belt of Scotland and they require a microbiologist to work initially on initially a temporary contract possibly permanent, in their quality department.
The successful candidate will be responsible for QC testing of raw materials, intermediates and final products using a range of techniques including SDS PAGE, ELISA and carrying out environmental monitoring on site. You must have a degree in microbiology or similar qualification and ideally but not essential have proven experience bioburden and/or endotoxin testing gained within a GMP environment. This role would suit someone who has an interest in making a difference as the client encourages employees to make suggestions continuously improving the department.
CK Science is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
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. Please quote reference DH22686 in all correspondence.
Keywords: microbiology jobs, micro vacancies, biology jobs, scientific recruitment, pharmaceutical recruitment ckscience.co.uk
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Laboratory Team Leader - Scotland. Our client a pharmaceutical organisation located in Southern Scotland require a QC Laboratory Team Leader to cover maternity leave for one year.
The function of the role is to oversee routine performance of the^analytical department within Quality Control.
The main responsibilities of the role will include:
To supervise of a team of QC Scientists and Associates.
Review and approve documentation in support of product release.
To ensure all analyticalwork (Release, In-Process, Raw Materials & Stability) is performed and reported within agreed timelines and overview of calibration/maintenance of analytical equipment schedule.
Ideally, you will be qualified in a life sciences discipline and have demonstrable working experience in a GMP laboratory.
CK Science is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
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. Please quote reference DH22668 in all correspondence.
Keywords: science jobs, scientific recruitment, qc analyst, laboratory manager, laboratory supervisor, analytical jobs. ckscience.co.uk
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Senior Microbiologist - Scotland. Our client, a pharmaceutical organisation located in Southern Scotland, require a Senior Microbiologist on a fixed term contract to cover maternity leave.
The main duties of the role include being responsible for a team of microbiology staff within a Quality Control department, ensuring analytical work is performed and reported within agreed timescales and review and approve documentation in support of product release.
The ideal candidate will hold a science qualification and have demonstrable experience operating within a GMP analytical setting.
CK Science is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
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. Please quote reference DH22662 in allcorrespondence.
Keywords: science jobs, scientific recruitment, microbiologist, micro jobs, analytical jobs, qc, quality control, gmp, microbiologist ckscience.co.uk
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We are currently recruiting for a Packaging Technologist to join a Global Pharmaceutical company based in Hertfordshire.
You will be responsible for the provision of technical and operational support to packaging operations and will assist in the^implementation, qualification and validation of any processes and equipment used for the packaging of marketed drug products to comply with current GMP, company expectations and industry best practice. You will also provide support to the development, validation and commercialisation of new products and will review systems, procedures and operational practices to identify opportunities for improvements.
Main duties will include:
* Applying Good Manufacturing Practices in all areas of responsibility.
* Routine operational support of packaging operations
* Corrective Action & Preventative Action (CAPA) investigation for the department & third parties.
* Complaint investigation/root cause analysis.
* Assisting in the introduction and transfer of new products, materials and components into the department.
* Continuous improvement of processes, operations & systems.
* Technology transfer, optimisation and validation of new processes and products.
* Assisting with the planning^and execution of process development, comparison and demonstration batches.
* Technical support and trouble shooting for departmental packaging operations and supply chain.
* Supporting business development and commercialisation projects.
* Liaising with supply chain, packaging, Quality Control Quality Operations and others to ensure that schedules for the release of and distribution of products are met.
You will hold a Degree in a scientific/engineering related subject e.g. pharmacy/chemistry/chemical engineering/electrical engineering/mechanical engineering (or equivalent) and ideally will be a member of an appropriate technical body ( ISPE, IOP, IVT).
You will have relevant experience gained in the pharmaceutical industry, in^an operational or support role including qualification & validation along with practical hands on experience of packaging technology & equipment. It is essential that you have a knowledge and understanding of the packaging of pharmaceutical productsand a familiarity of MHRA guidance, cGMP and H&S regulations. Any experience of SAP would be a significant advantage.
CK Science is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
If youdonothear 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 theEEA is essential. Please quote reference^ST22650 in all correspondence.
Keywords: Packaging, Pharmaceutical, optimisation, development ckscience.co.uk
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Evaluation and assessment of individual case safety report (ICSRs)
Signal detection and evaluation
Periodic reporting
Preparation and update of Company Core Safety Information and risk management plans on authorized products.
Response to authority requests
Participation in other department functions, e.g. Clinical Trial Teams, Clinical Sub-Teams Education in life-science - preferable medical doctor or equvialent
Industry experience in drug development, drug safety or scientific www.nature.com
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