Quality Assurance Specialist, Pfizer Newbridge, County Kildare
Please note, we may not have an active opening at this time. If your skills and experience match this position, our Talent Acquisition team will connect with you as soon as this opportunity becomes available. Please apply if you would like to be added to this pool of candidates for consideration for future vacancies.
*Due to high volume of applications we will be contacting successful candidates only.
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? If so, continue reading below………
About the role
The successful candidate will be joining a busy team with the opportunity to get involved in projects.
The site at Newbridge is a solid dose / packaging site and the Quality Specialist roles support a variety of aspects of the site operations including Quality Systems, Operations Support &; Projects. The role presents opportunity for exposure to many aspects of the QA organisations responsibilities in addition to being an integral part of a cross function production support team. Production operations at the Newbridge site utilise many specialised solid oral dose unit processes and advanced technologies.
What We Offer
Stability, Pfizer Newbridge was established in Co Kildare in 1992. Since then, successive expansions have seen the site grow to one of Europe's largest manufacturers of solid dose pharmaceuticals (tablets and capsules). Pfizer Newbridge is a rapidly expanding site in the Pfizer network.
Situated just 25 minutes from the M50, we are offering permanent positions with Competitive Salary & Bonus Schemes, Healthcare for you & your family, Pension & Share Scheme, Long term Income Protection, Life Assurance. Training & Opportunity for Career Progression.
Free parking and subsidized canteen
At Pfizer Newbridge we pride ourselves in our culture of high-performance team work and innovation which enables the business to deliver on its commitments. Pfizer Newbridge is the embodiment of how we behave, act, lead and engage with people every day. Our success is achieved through the commitment, engagement and excellence of all our colleagues. Working in a fast-paced environment where learning and personal development are actively encouraged, you will find the roles both challenging and rewarding.
• 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.
If your experience and skillset match the above, what are you waiting for?
How to apply
Make a difference today, all suitable candidates should apply though the link with CV provided. We are looking forward to hearing from you!
Please note there is no relocation support available for this position and a valid work permit is required.
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.Quality Assurance and Control