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Quality Specialist


Newbridge, NY 13684
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Job Details

Do you want to make a difference in patients' lives each day?

Do you want to work with a dynamic, high performance team?

Do you want to have responsibility and get involved in exciting projects as soon as you join?

**About us**

We are situated in Newbridge, Co. Kildare, and manufacture and package life changing solid oral dosage products. We are an integral part of Pfizer's global solid oral dose network.

We pride ourselves in our culture of high performance team work and innovation which enables the business to deliver on its commitments.

We have approximately 30 colleagues on our Quality Assurance team. We work closely with operations and other functional areas to ensure products are manufactured to GMP standards, and quality systems are both compliant and operationally effective &; efficient.

We are committed and passionate with a strong focus on continuous improvement, structured problem solving and risk based approaches to ensure the best outcome for the Patient. The QA team have been and continue to be high contributors to site and network projects, consistently receiving recognition awards for varied initiatives.

**About the role**

We have an exciting opportunity for a QA Specialist to join the team. The successful candidate will be joining a busy team with the opportunity to get involved in projects.

If you are energised by a challenge and enjoy a diverse range of responsibilities, with a high degree of self-direction you may be the person we are looking for.

We are looking for a resilient, proactive and change agile individual who possesses the ability to guide and coach in Quality & GMP expectations and, through experience, has the confidence to make risk-based decisions when necessary.

This is an Individual Contributor role with ample opportunity to demonstrate initiative, leadership, and the ability to effectively deliver on varied projects/issues.

**About you**

Typically have a third level qualification in a science or technical background.

At least 3 years' experience in the Pharmaceutical industry.

Proven ability to work in a fast paced, dynamic environment as part of a team and self-directed as required.

Proactive approach and strong critical thinking skills.

Knowledge of GMP &; Regulatory requirements.

Experience with Quality Risk Management, Investigations, Pharmaceutical Manufacturing Operations, and Regulatory Processes are highly desirable.

Ability to positively influence and develop strong, effective peer relationships.

**And finally...**

If you would like to join this busy team, we would love to hear from you. Please submit your CV by Friday 23rd February 2018

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
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