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Details
Senior Associate Scientist (Shift)
Reference: | RK3443 | Location: |
Dublin |
Qualification: | Degree | Experience: | 2-3 Years |
Job Type: | Fixed Term Contract | Salary: | Not Disclosed |
May be suitable for:
Scientist
Senior Associate Scientist (Shift)
RK3443
12 Months
Dublin
We’re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Dublin. 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:
- Leads / assists forensic investigation and identification of defects arising from drug product manufacture and write up of these investigations to cGMP standards.
- Be accountable for the maintenance, distribution and upkeep of extensive defect panels used for the set-up, training and characterisation of automated / semi-automated / manual finished drug product visual inspection equipment at.
- Working as part of the PD laboratory team be expected to contribute to upkeep / maintenance of a GMP laboratory environment.
- Provide process development expertise for commercial drug product particle / defect identification and contribute to the maintenance of local and global particle / defect libraries.
- Perform experiments, organise data and analyse results with minimal supervision (in a GMP laboratory environment) to evaluate product impact due to process variables encountered during drug product manufacture.
- Creation, Management and Maintenance of Inspection defect panels / sets.
- Execution of Knapp studies and data analysis.
- Establish experimental design, develop and implement protocols, obtain reproducible and reliable results and communicate data to cross functional groups.
- Ensuring all aspects of laboratory activity adheres to required policies and procedures, including safety and training.
- Ensure that the laboratory and site meet the quality requirements of its customers and applicable regulations (FDA, EU & international standards).
- Participate in cross functional teams at the site to ensure adherence to required policies and procedures and be responsible to deliver against organisational goals and project milestones.
- Assist in deviation and exception resolution and root cause analysis.
Education and Experience :
- Bachelor’s degree in a Science related field is required.
- 2-4 years of experience in the pharmaceutical industry,
- Experience in support of Commercial Protein Drug Product (DP) processing in specific areas such as sterile processing, process characterization, inspection, tech transfer (to commercial DP sites) or validation.
- Be familiar with advanced microscopy (scanning electron microscopy) and spectroscopy (Fourier-transform infrared spectroscopy).
If interested in this posting please feel free to contact Rachel Kent on +353 (0)87 427 8808 or [email protected] for further information.
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Life Science Recruitment | Tel:+353 1 685 4848 | Fax: +353 (0)1 443 05 24 | Email: [email protected] | Copyright © 2021 Life Science Recruitment Ltd
This site uses cookies. More information on cookies can be found in our Privacy Policy | Terms of Use | Registered as a private limited company. No: 445328
Valid XHTML - CSS