Jobs in Macclesfield

Up to £30,764.28 per annum (pro rata)

Macclesfield

Part-time

Our Maxim Department are excited to announce that we are looking for a team member to join us as a Coach Mentor AAT.

£23,088 FTE (Actual salary - £20,308.56)

Macclesfield

Full-time

Our Art Department are excited to announce that we are looking for a team member to join them as a Art Technician.

£24.59 per hour

Macclesfield

Part-time

Our Social Science Department are excited to announce that we are looking for a team member to join as an PTHP A Level Lecturer in Psychology.

£24.59 per hour

Macclesfield

Part-time

Our Social Science Department are excited to announce that we are looking for a team member to join as an PTHP A Level Lecturer in Sociology.

£24.59 per hour

Macclesfield

Part-time

Our Social Science Department are excited to announce that we are looking for a team member to join as an PTHP A Level Lecturer in Criminology.

£24.59 per hour

Macclesfield

Part-time

Our Art Department are excited to announce that we are looking for a team member to join the us as a Evening Lecturer in Photography.

DOE

Macclesfield

Full-time

Experienced window/ door installer required for rapidly expanding company in Macclesfield.

Premium
Journalist

DOE

Full-time

Nub News is looking for journalists to come on board to help expand its coverage in Cheshire.

Pharmiweb

Annual

Macclesfield (SK101)

Permanent

Proclinical is seeking a dedicated Senior Scientist to join our client's team in England, focusing on the development of small molecule drug products for early clinical phases. This role is crucial for ensuring the analyt. aspects of drug product devel. and supply are met with precision and innovation.

CK Group

Annual

Macclesfield (SK101)

Permanent

Lead the analytical development activities to support development and supply of drug product during the early clinical phases.Identify and develop the analytical methodologies that support project progression through early development.Conduct lab-based experimental work to generate data to support progression of your own and other projects. This will include compliance with Good Manufacturing Practice where appropriate.Author the relevant sections of regulatory submissions and prepare responses to regulatory questions.Interpret analytical data and draw reliable conclusions and recommendations to influence project progression.Develop the risk assessments and stability and control strategies that ensure our patients receive a safe and efficacious drug product.

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