NPI QC Bioassay Trainer
NPI QC Bioassay Trainer
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Job Description
We are now hiring an NPI QC Bioassay Trainer into our team in Westport for a Fixed Term Contract for 23 months FixedTermContract. This person will join the Westport Bioassay department and the role centres on providing an efficient training programme to all personnel working in the QC Bioassay labs. The trainer role will be responsible for developing and managing training of all new hires for NPI QC Bioassay and will be responsible for updates to key stakeholders on training timelines to support analyst training completion on time.
The trainer role will also include supporting NPI drug product stability testing adhoc investigational & development testing. There may be a requirement to execute/assist on new method transfers and validations. To support this volume of testing ancillary laboratory duties including critical reagent screening/qualifications laboratory housekeeping review of paperwork and procedural updates are required.
- Design and deliver comprehensive training program to meet all job requirements of laboratory personnel.
- Understand regulations and business processes required to maintain laboratory data integrity.
- Responsible for updates to key stakeholders on training timelines to support analyst training completion on time or highlighting challenges to the timeline or training gaps.
- Measure and continually improve effectiveness of training in the journey to become best in class.
- Keep informed on best practices within the industry with regards to Laboratory training and work to implement best practices on site.
- Support testing for NPI QC Testing via Cell Based Potency Assay and related ELISA methods.
- Review of testing records and all associated documentation.
- Routine lab duties including critical reagent qualifications inventory management and equipment maintenance.
- Provide input on assay performance monitoring and trending
- Supporting Root Cause Analysis Investigations
- Attend departmental and Tier meetings
Qualifications :
- Bachelors of Science Masters Degree or Ph.D in a Biological Science13 years QC GMP experience
- Practical experience of mammalian cell culture and basic techniques (Passaging freezedown drug treatments) is an advantage
- Train the Trainer qualification is advantageous.
- Sound scientific/practical understanding of ELISA based methods.
- Proven problem solving is advantageous.
- Clear communication skills required.
- Good organizational skills and interpersonal skills required.
- Willingness to upskill and collaborate.
- Ability to support priority projects to meet timelines.
- Focus on Right First Time (RFT).
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.
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Remote Work :
No
Employment Type :
Fulltime
Employment Type
Full-time
