Pharmaceutical Technology Specialist II Biologics MPS Team
Pharmaceutical Technology Specialist II Biologics MPS Team
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Job Description
Youre driven by the science. By discovery. By the unknown. Take on the work that challenges you so you can challenge the status quo.
At our Westport site in Co. Mayo we are now hiring an Pharmaceutical Technology Specialist II to join our driven and ambitious team.
As our new Pharmaceutical Technology Specialist you will be responsible for the of biologics drug product batches at scale in support of commercial biologics manufacturing and process development. You will also be responsible for development studies and continuous process improvement initiatives. Its an exciting opportunity to develop your skills further in operations.
With an exciting pipeline of products and a great salary and benefits package this may be the ideal opportunity to develop your career with an industry leader.
So if you are interested in joining the Manufacturing Process Support team in AbbVie Westport read below to find out more
In your new role you will:
- Manufacture pharmaceutical products
- Support batch preparation activities
- Perform compounding sterile filtration and filling activities
- Accurately complete documentation on time accurately and legibly.
- Keep the Manufacturing area tidy and clean.
- Comply with Good Manufacturing Practices (GMP) and with Standard Operating Procedures (SOPs)
- Setup clean and maintain equipment
- Transfer of waste material out of the cleanroom areas
- Work with various vendors on the development/improvement of new and existing systems regarding single use technologies.
- Review and contribute to technical documents including protocols reports and batch manufacturing documents
- Adhere and support all EHS standard procedures and policies.
- Active contribution of functional area continuous improvement initiatives
Qualifications :
So does this role sound exciting then read on.....
To succeed in this role you will have the following Education and Experience:
- 3rd level qualification in relevant discipline and/or
- 1824 months minimum experience in the pharmaceutical or medical device industry
- Prior knowledge of aseptic practices in clean room environments
- Strong knowledge of GMP regulatory guidelines quality systems drug product manufacturing and validation is desirable
- Understanding of autoclave sterilization depryogenation and filter integrity testing is desirable.
- Knowledge of lyophilization and freeze dryer operations is desirable.
- Experience with single use technologies is desirable.
- Experience working with SAP within a similar industry is preferable.
- Experience working in project and teambased environments is essential.
- Strong communication documentation and IT skills.
- Proactive approach with proven problemsolving skills is desirable
Please note: Closing date for applications is the 28th March 2025.
Additional Information :
AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives serving our community and embracing diversity and inclusion. It is AbbVies policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race color religion national origin age sex (including pregnancy) physical or mental disability medical condition genetic information gender identity or expression sexual orientation marital status status as a protected veteran or any other legally protected group status.
US & Puerto Rico only to learn more visit & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:
No
Employment Type :
Fulltime
Employment Type
Full-time
