Trainee Bulk Analyst - Rosyth, Scotland

We are seeking candidates for a Trainee Bulk Analyst position to work towards undertaking analysis of materials for the identification of asbestos fibres. · Analysing bulk materials for asbestos content · Managing workload throughout the working day · Completing internal and exte ...

This is an opportunity for an experienced Asbestos Analyst to join a well established consultancy with a strong presence across Scotland and the wider UK. · ...

This role provides hands-on support with general quality control laboratory tasks and material management in a highly regulated pharmaceutical environment. · ...

The role involves assisting in the day-to-day maintenance and support of the University's enterprise resource planning (ERP) system. · Resolve day-to-day queries raised through helpdesk tickets, emails and calls. · Assist in the production of Statutory reports; collating data; co ...

We are one of the leading European contract manufacturers in the pharmaceutical, biotech and healthcare sectors. · This role reports to the QC Manager and provides hands-on support with general quality control laboratory tasks and material management. · You will also need a good ...

This is an opportunity for an experienced Asbestos Analyst to join a well established consultancy with a strong presence across Scotland and the wider UK. · The business has been operating for over 30 years and has built its reputation on technical quality, long term client relat ...

This role reports to the QC Manager and provides hands-on support with general quality control laboratory tasks and material management. · We are a highly regulated pharmaceutical environment, · so attention to detail accurate documentation · and clear written communication are ...

To supervise and execute defined and trained Quality Control department tests for the release of raw materials, in process products, bulk drug substance, final products and stability products according to defined procedures and proctocols and according with best cGMP work practic ...

The QC Team Leader position is responsible for managing analytical procedures and ensuring compliance with SOPs and protocols. They must apply best cGMP practices to manage testing and release of raw materials, in-process products, bulk drug substance, final products, and stabili ...

We are recruiting for a Part Time P401 Qualified Laboratory Analyst to join our team in Livingston. · ...

+This role provides hands-on support with general quality control laboratory tasks and material management. · + · ++A genuine passion for science and an eagerness to learn, · + · ++ ...

+We are one of the leading European contract manufacturers in pharmaceutical biotech healthcare sectors.We are looking for a Quality Specialist to join our team. · + · This role reports to QC Manager provides hands-on support general quality control laboratory tasks material mana ...

We are one of the leading European contract manufacturers in the pharmaceutical, biotech and healthcare sectors. · This role reports to the QC Manager and provides hands-on support with general quality control laboratory tasks and material management. · The Ideal Candidate Will B ...

The QC Analyst will perform batch disposition and stability activities in a proactive and timely manner which includes Quality Control testing and reporting of raw materials, in process, bulk drug substance, final products. · ...

This role reports to the QC Manager and provides hands-on support with general quality control laboratory tasks and material management. · We are a highly regulated pharmaceutical environment, so attention to detail, accurate documentation, and clear written communication are ess ...

The QC Team Leader will be responsible for managing analytical procedures, testing of raw materials, in process products, bulk drug substance, final products and stability products according to defined by SOP’s and protocols ensuring compliance with cGMP work-practices. · ...

To supervise and execute defined and trained Quality Control department tests for the release of raw materials,in process products,bulk drug substance,final products,stability products according to defined procedures protocols best cGMP work practices Quality standards metrics. · ...

The QC Team Leader will be responsible for managing analytical procedures, ensuring compliance with SOPs and protocols, and training the QC team in best cGMP practices. · ...

To supervise and execute defined and trained Quality Control department tests for the release of raw materials,in process products,bulk drug substance,final products and stability products according to defined procedures and proctocols and according with best cGMP work practices, ...

The QC Team Leader will be responsible for managing analytical procedures and ensuring compliance with SOPs. They will also lead the QC team and ensure they are trained and competent in their procedures. · Highly organized · Effective communication · ...