Analytical Research Chemist
at Thermo Fisher Scientific
Cork, County Cork, Ireland -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 18 Jun, 2024 | Not Specified | 18 Mar, 2024 | 3 year(s) or above | Laboratory Skills,Wet Chemistry,Savings,Characterization,Pharmaceutical Industry,Communication Skills,Method Development,Analytical Techniques,Spectroscopy,Ion Chromatography,Icp,Uv,Validation | No | No |
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Description:
EDUCATION AND QUALIFICATIONS:
- Relevant qualification such as BSc, masters or PhD in relevant scientific discipline with a significant experience (min. 3 years) in industry or academia.
- Experience in analytical method development, characterization and validation would be desirable.
- The candidate should have experience in the following: HPLC, UHPLC, GC, LC/MS, GC/Headspace, GC/MS, UV, IR, KF, ion chromatography, ICP.
KNOWLEDGE, SKILLS, ABILITIES:
- Demonstrated ability to think critically and innovatively combined with a willingness to learn and to overcome challenges.
- The candidate should have good organizational skills and a proven troubleshooting ability, and an ability to respond to technical challenges within agreed timelines. Embrace and participate in PPI (Practical Process Improvement) initiatives to help identify improvements and cost savings to the business.
- Excellent technical writing and communication skills with the ability to work in cross functional teams.
- Knowledge and experience of the pharmaceutical industry with an understanding of the chemistry development process.
- Demonstrated core laboratory skills and expertise in various wet chemistry and analytical techniques such as spectroscopy and chromatography techniques.
Responsibilities:
- Provide technical expertise and analytical support for the introduction of new products to the Cork site, including method development. At times it will be necessary to support the Analytical Development group prior to method validation.
- Lead the troubleshooting of analytical technical challenges during ad hoc investigations and process development. Conduct Impurity Mapping, the Fate of Impurities and PARs investigations in collaboration with the chemistry group by generating, collecting and interpreting analytical data whilst adhering to current regulatory requirements (quality by design, GMP, ICH’s guidelines) for API.
- Contribute to regulatory submissions and patents as required.
- Communicate regularly with the clients, providing updates on projects progress, hosting client visits, addressing technical queries and delivering client project requirements to the defined timelines.
- Develop / Expand scientific, technical knowledge by reading the peer reviewed scientific literature, attending scientific conferences and relevant training.
- Ensure that the site’s technical, quality and safety metrics are maintained.
REQUIREMENT SUMMARY
Min:3.0Max:8.0 year(s)
Pharmaceuticals
IT Software - Other
Clinical Pharmacy
Phd
Proficient
1
Cork, County Cork, Ireland