I'm looking for...
close

Did you know that your Internet Explorer is out of date?

To get the best possible experience using our website we recommend that you upgrade to a newer version or download another web browser.
A list of the most popular web browsers can be found below. Just click on the icons to get to the download page.

crome
Google Chrome
IE
Internet Explorer
firefox
Mozilla Firefox
opera
Opera

Your browser will need to close to complete the installation and you will need to manually reload the site when finished
Contact Info
Avishek Singh
Life Science

00353872827991
[email protected]
Connect with me on
R&D Engineer
Galway
R&D Engineer
Galway
R&D Director
Galway
C&Q Lead
Tipperary
QA Engineer
Leitrim
Account Manager UK and Ireland
Republic of Ireland
R&D Engineer
Galway
Product Lead
Dublin
Senior Recruitment Consultant
Republic of Ireland
QA Manager
Canada
R&D Director
Galway
R&D Engineer
Galway
Process Chemist
Limerick
Project Engineer
Limerick
Head of R&D
Galway
Project Engineer
Republic of Ireland
R&D Manager
Athlone
Chemical Engineer
Tipperary
R&D Manager
Connaught
R&D Manager
Galway
Senior Microbiologist
Republic of Ireland
CQV Lead
Tipperary
R&D Engineer
Galway
Project Enginer
Dublin South
R&D Engineer
Galway
R&D Engineer
Clare
Project Engineer
Tipperary
R&D Engineer
Dublin
R&D Engineer
Galway
Senior Recruitment Consultant
Republic of Ireland
R&D Manager
Athlone
Quality Specialist
Tipperary
QA Manager
Canada
Senior Manufacting Engineer
Republic of Ireland
R&D Manager
Connaught
R&D Manager
Connaught
R&D Manager
Galway
R&D Manager
Connaught
Biostatistician
Dublin City Centre
R&D Manager
Galway
Process Engineer
Limerick
Recruitment Consultant
Republic of Ireland
Quality Specialist
Tipperary
R&D Engineer
Galway
R&D Manager
Galway
Project Manager
Limerick
Responsible Person (RP)
Republic of Ireland
Senior Quality Engineer-Remote
Republic of Ireland
R&D Director
Galway
R&D Engineer
Dublin
Apply for this job

Name:

Surname:

Email:

Phone:

Cv:

Salary Expectations:

Education:

Experience:

Current Location:

Notice Period:

Write here your cover note:


If you would like us to create a jobseeker account for you, giving you access to
account management, job alerts and one-click applications, then please tick this box

If you are having difficulty you can always email your cv to [email protected]
Details

Manufacturing Biotech Associate 24/7 Shift


Reference:AS20487 Location: Meath
Qualification:DegreeExperience:See description
Job Type:Fixed Term ContractSalary: Not Disclosed

Manufacturing Biotech Associate 24/7 Shift
AS20487
11 Months
Meath

We’re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Meath. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.

Duties:

  • Support operations team to consistently deliver on specific Key Performance Indicators (KPIs), e.g. Environmental Health and Safety (EHS) metrics, Production Plan, Overall Equipment Effectiveness (OEE), compliance and team training.
  • Execute commercial manufacturing processes according to established work instructions and
  • Standard Operating Procedures (SOPs).
  • Ensures that all assigned task related to manufacturing documentation support is in accordance with good manufacturing practices.
  • Routinely talk about any safety issues you are concerned about.
  • Work as part of a dedicated process team where flexibility and teamwork are a key requirement.
  • Generate SOPs/ Work Instructions (WIs) to ensure compliance with regulatory standards.
  • Maintain/ support a high standard of safety/ Good Manufacturing Practice (GMP) compliance at all times.
  • Determine solutions by referencing relevant past experiences as part of problem solving activities.
  • Get actively involved by participating in inspections, GEMBA’s and Go-See’s.
  • Act as a team member on process deviation reviews and Gemba walkdowns.
  • Mentor new members of staff in specific plant activities.
  • Be prepared to answer auditor questions during site walkdowns.
  • Engage in implementing innovative solutions that drive a high performance organisational culture that accommodates rapid growth and highly dynamic expectations ensuring attainment of site operational and development goals.
Education and Experience :
  • Level 7 qualification in a science or engineering discipline, or level 6 with a minimum of 4+ years’ experience in a GMP Manufacturing environment.
  • Experience of Upstream/ Downstream Processing.
  • Start-up experience in a large-scale commercial drug substance facility, or similar.
  • A proven ability to work with automated systems such as Manufacturing Execution System (MES), Systems Applications and Products (SAP), Delta V etc.
If interested in this posting please feel free to contactAvishek Singhon +353 (0)87 282 7991 or [email protected] for further information.