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Pharmaceutical Technologist Apprenticeship - Accord

Employer
Cogent Skills
Location
Fawdon, Newcastle Upon Tyne
Salary
£15,000
Closing date
16 Jun 2023

This is a fantastic opportunity to embark on a career in science and technology with a leading global company in the life sciences sector. Accord Healthcare Ltd is seeking an Apprentice Pharmaceutical Technologist, who will provide technical support in all aspects of the New Product Introduction (NPI) process.

Qualification requirements: Minimum 5 GCSEs (or equivalent) at Grade 4 or above, including English, mathematics and science

TRAINING TO BE DELIVERED

Apprenticeship standard:Level 3 Science Manufacturing Technician

Training provider: Cogent SSC

Qualification: Pearson BTEC Level 3 National Certificate in Applied Science

Delivery model: Blended, through online and on-site learning, plus two short residential courses – 3 days at York Stem Cell Centre to undertake practical work within the labs; 2 day residential to Cogent Head office in Warrington for invigilated examinations in either January or June (cohort dependant)

JOB DESCRIPTION

Cogent Skills is working with Accord Healthcare Ltd to recruit an Apprentice Pharmaceutical Technologist for its busy manufacturing site in Fawdon, Tyne & Wear. The successful candidate will be employed by Cogent Skills Services but will undertake all on-job learning with Accord Healthcare.

Reporting to the Principal Pharmaceutical Technologist, the Pharmaceutical Technologist will provide technical support in all aspects of the New Product Introduction (NPI) process, focusing on the preparation and support for the manufacture of initial scale up batches at both pilot and commercial scales through to complete Process Validation, ensuring validation lifecycle approach is followed.

This will include:

helping to manage product development and inter-site transfers of solid oral dose products from laboratory to pilot and commercial scales applying scientific techniques for experimental design and process scale up performing all physical analysis during the oral solid dose manufacturing process protocols/reports, batch manufacturing records and technical document creation and review co-ordinating circulation and approval of master records compiling CMC documentation packages and aid regulatory submissions improving process/quality/costs by applying scientific principles and logical methodologies liaising with other teams to ensure NPI plan is implemented in a timely manner

This is a fantastic opportunity to embark on a professional science career with a leading global company

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