Job Details: Validation Engineer


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.
Validation Engineer


Are you a Validation Engineer with Fill Finish experience in the biotech or pharma industries? Would you like to work for a multinational Biopharmaceutical companeny based in Waterford? If you have what it takes, send your CV to karen@jobcontax.com or call (01)7978720 for a confidential chat.



Validation Engineer - Fill Finish - Waterford



Employer

Our Client is one of the world's leading Biotech companies. Their Waterford plant is state-of-the-art facility for finishing of biopharmaceuticals and employs a high level of automation, including Manufacturing Execution Systems and was named one of Ireland?s top 10 best large workplaces by Great Place to Work Ireland.



Job Description



You will have a key role in ensuring the on-going validation compliance of equipment, systems and processes in both solid dosage forms and sterile products manufacturing



Accountabilities:

Capable of troubleshooting validation issues associated with projects, process development etc.

Designs, implements and executes validation studies for manufacturing and control equipment.

Provide technical assistance on current US FDA and EU validation requirements for Fill Finish manufacture and lyophilization.

Ensure that the validation status of equipment and systems are in compliance with c GMP at all times.





Requirements:



3rd level Science or Engineering qualification.

8-12 years? relevant experience in a highly regulated GMP environment.

Experience of Sterile Manufacturing Operations a must




Package:

Contract rate dependent on prior experience

Contract duration: 12 - 18 months



Contact:

Karen McHugh is the consultant managing this position. If you have any queries about this role, you can contact Karen by e-mail karen@jobcontax.com or phone +353-1-7978720

Click to connect with Karen on LinkedIn



Similar Jobs

Amgen Jobs in Ireland

Jobs in Waterford

Are you a Validation Engineer with Fill Finish experience in the biotech or pharma industries? Would you like to work for a multinational Biopharmaceutical companeny based in Waterford? If you have what it takes, send your CV to karen@jobcontax.com or call (01)7978720 for a confidential chat.



Validation Engineer - Fill Finish - Waterford



Employer

Our Client is one of the world's leading Biotech companies. Their Waterford plant is state-of-the-art facility for finishing of biopharmaceuticals and employs a high level of automation, including Manufacturing Execution Systems and was named one of Ireland?s top 10 best large workplaces by Great Place to Work Ireland.



Job Description



You will have a key role in ensuring the on-going validation compliance of equipment, systems and processes in both solid dosage forms and sterile products manufacturing



Accountabilities:

Capable of troubleshooting validation issues associated with projects, process development etc.

Designs, implements and executes validation studies for manufacturing and control equipment.

Provide technical assistance on current US FDA and EU validation requirements for Fill Finish manufacture and lyophilization.

Ensure that the validation status of equipment and systems are in compliance with c GMP at all times.





Requirements:



3rd level Science or Engineering qualification.

8-12 years? relevant experience in a highly regulated GMP environment.

Experience of Sterile Manufacturing Operations a must




Package:

Contract rate dependent on prior experience

Contract duration: 12 - 18 months



Contact:

Karen McHugh is the consultant managing this position. If you have any queries about this role, you can contact Karen by e-mail karen@jobcontax.com or phone +353-1-7978720

Click to connect with Karen on LinkedIn



Similar Jobs

Amgen Jobs in Ireland

Jobs in Waterford

We need : English (Good)

Type: Permanent
Payment: package
Category: Pharmaceutical

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