QA Technician - (Small Molecules) - New €250m site

Job content

An international pharma company is looking for a QA Technician to join their dynamic team! Our client is a Global leader in Pharmaceutical Grade Omega 3 Manufacturing. In this position you will be carrying out all activities in the area of small molecule API Quality Assurance in accordance with ISO and cGMP standards.

Our client is currently embarking on a new campaign, building their new plant in Stockton, U.K. Investing heavily to diversify their portfolio and give them a competitive advantage on the market. It is a personal office so this means that you will have closer contact with everyone which will give you faster decisions and you will not feel like a number.

You will work directly with a variety of stakeholders including; proposal manager, project manager, research & development technician and QC technician on every advancement and be able to directly make an impact on their new growth, while expanding your QA and communication skills.

Responsibilities:
Quality Assurance: Manage all types of Quality Assurance required audits - including all types of internal & client audits and regulatory inspections. Maintain the QA Systems. Act as Deputy Archivist.
Process Improvement: Support the operation in process improvement initiatives; develop Standard Operating Procedures (SOPs) to support the QMS.
Training: Maintain keen knowledge of Good Laboratory Practice (GLP), Good Clinical Practice (GCP), and appropriate regulatory standards to train and support the operation.
The QA of active pharmaceutical ingredients (API).

Requirements:
Bachelor’s degree required, Chemical or Chemistry.
Chemical background needed (Small molecules)
3 years of quality assurance experience required; experience in a laboratory, pharmaceutical or Clinical Research Organization (CRO) preferred.
Experience in a factory or plant production.
Experience with API’s
Knowledge of and demonstrated experience in Good Clinical Practice (GCP), Good Laboratory Practice, ISO15189, CAP, CLIA strongly preferred. Must have GLP experience.

Benefits
Be apart of their new strategic adventure.
New plant, new working equipment & atmosphere.
Diverse job activities and opportunity to develop, while working directly with senior management.
Structure and stability of a global pharma company.
Incredible growth opportunities.
Join a team with a good atmosphere and who organise after work activities.

Apply and send your CV to [email protected] or give me a call on Phone: +44 207 940 2105 Internal Extension: 3363. My name is Patrick Powell, Specialising in QA, in the Pharma industry in the United Kingdom and I’m responsible for hiring a new QA Specialist for this company.

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