Job Details: QA Specialist


jobContax

104 Upper Drumcondra Road,
Dublin 9
http://www.jobcontax.com
Please contact: Karen
JobContax was founded in 2001 by Karen McHugh, an engineer passionate about offering quality opportunities to the jobseeker and an intelligent service to the client. Jobcontax has successfully operated as a global market leader and technical specialist within the following sectors:

Construction and Infrastructure

Engineering and Design

Mining - Oil and Gas

Biotechnology and Pharmaceutical

During the past 10 years Jobcontax have expanded our international network across 5 continents. In 2005 we began recruiting for the Australian market and in 2011 we set up our first strategic partnership in WA. In March 2010, we opened our Shanghai office to strengthen our presence in the rapidly expanding Chinese market for highly skilled professionals. JobContax has a strong presence in Canada, Europe and the Middle East.

Jobcontax has built its reputation on its consultative approach. Our understanding of the industries and the businesses and individuals within these industries enables us to facilitate the perfect match between client and jobseeker. From global multinationals to SME?, Jobcontax has become the trusted recruitment partner.
QA Specialist
Job Description




This position involves day-to-day QA production activities, production batch documentation review, execution of line clearances, document initiation request / document change request review, on-line quality impact assessments, participation in quality risk assessments, support problem solving, internal/external auditing, house-keeping inspections, customer compliants and project work, as required. The position will also involve the assessment of compliance with GMP regulations (EU, FDA, Japan) within the Company and the Development of Regulatory Systems/Standards.

Coaching and advising line operating personnel on compliance requirements and best practice is a daily requirement.




Requirements:



Third level degree in a relevant scientific discipline.

Quality Assurance and Compliance experience in a pharmaceutical environment is essential.

Knowledge of Trackwise would be an advantage.

The successful candidate must have excellent communication skills, proven leadership skills, report writing skills, good attention to detail and also be a team player, including cross functional teams.

Shift work is a requirement of this position




Package:

Contract rate - Negotiable based on experience

Minimum Contract duration: 6 months



Job Description




This position involves day-to-day QA production activities, production batch documentation review, execution of line clearances, document initiation request / document change request review, on-line quality impact assessments, participation in quality risk assessments, support problem solving, internal/external auditing, house-keeping inspections, customer compliants and project work, as required. The position will also involve the assessment of compliance with GMP regulations (EU, FDA, Japan) within the Company and the Development of Regulatory Systems/Standards.

Coaching and advising line operating personnel on compliance requirements and best practice is a daily requirement.




Requirements:



Third level degree in a relevant scientific discipline.

Quality Assurance and Compliance experience in a pharmaceutical environment is essential.

Knowledge of Trackwise would be an advantage.

The successful candidate must have excellent communication skills, proven leadership skills, report writing skills, good attention to detail and also be a team player, including cross functional teams.

Shift work is a requirement of this position




Package:

Contract rate - Negotiable based on experience

Minimum Contract duration: 6 months





We need : English (Good)

Type: Permanent
Payment: package
Category: Pharmaceutical

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