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Associate Director of QC and Technical Support

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Recruiter: Real Staffing
Listed on: 21st May
Location: Dublin
Type: Permanent
Start Date: ASAP

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My Client a Dublin based Biopharmaceutical company have ambitious plans and have an exciting opportunity for a permanent full time Associate Director, Quality Control and Technical Support.

The Company

Biopharmaceutical company focused on improving patients' lives by identifying, developing, acquiring and commercialising differentiated and accessible medicines that address unmet medical needs. The company has a portfolio of medicines through its orphan and inflammation groups. The company's global headquarters are in Dublin, Ireland. The company also has offices in the US and Europe.

The Position

Reporting to the Quality Control Director, this position is responsible for the technical transfer, troubleshooting and technical documentation related to all Quality Control (QC) activities. This is to support new product commercialisation and the consistent delivery of commercial products to meet regulatory, quality, supply volume, timing and cost objectives.

The position holder will be an analytical expert for both biological and small molecule drug substance and drug product analytical test methods, test method validation and test method transfers both internally and externally. This position is responsible for quality control (QC) tasks such as drug product quality complaints handling from a QC perspective and QC management of assigned critical vendors for the companies products.

The Associate Director, Quality Control and Technical Support, furthermore executes QC related activities deviations, investigations, CAPA, method transfer, scheduling of expeditated testing, trending data and change control tasks as needed. As a key member of the Quality Operations team, this position will be working within the Technical Operations organisation and its partners to collaborate on the different quality topics and relevant QC projects assigned.

Qualifications and Skills Required:

  • Proven track record of working in a virtual organisation.
  • At least 10 years of experience within manufacturing or technical operations in Quality Control and/or Quality Assurance in the pharmaceutical industry (solid oral dose, small-molecule and biologics, with the majority of the experience in Biologics)).

The company offers a competitive salary and benefits package. Interviews will take place remotely. For immediate consideration please reply with an up to date CV.

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Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Agency in relation to this vacancy| Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England and Wales