Sr. Scientist, Pharmaceutical Analytical Sciences
About The Position
The Pharmaceutical Analytical Sciences group has an opening for a Scientist based in Rahway, NJ. Join us and experience our culture first-hand - one of strong ethics & integrity, diversified experiences, exceptional science, and a resounding passion for improving human health through innovative drug delivery technologies and predictive analytical tools. As part of our global team, you will have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. In your role as Scientist, you will be part of a GMP analytical team working on cross-functional scientific teams to enable novel small molecule, peptide, and oligonucleotide drug development through laboratory-based analytical characterization and statistical data analysis.
Requirements
- Bachelor of Science degree with, at least, 3 years relevant industry experience or Master of Science degree with, at least, 1-year relevant industry experience.
- Degree in Chemistry, Pharmaceutical Sciences, or other Life Sciences.
- Experience working in a fast-paced analytical laboratory utilizing chromatography instrumentation.
- Excellent written and oral communication skills.
- Interpersonal skills, are necessary to qualify for this role.
- Ability to work in a team environment with cross-functional interactions.
- Adaptability
- Analytical Development
- GMP Compliance
- Good Manufacturing Practices (GMP)
- Laboratory Information Management System (LIMS)
- Pharmaceutical Sciences
- Strategic Thinking
- Troubleshooting
Nice To Haves
- The ideal applicant would have hands-on experience in a GMP environment.
- Advanced chromatographic separation science, spectroscopy analysis, dissolution testing, and other analytical techniques.
- Experience with Empower, Electronic Notebooks and leading laboratory investigations is a plus.
Responsibilities
- Support execution of Good Manufacturing Practices (GMP) activities such as release and stability testing to support development of active pharmaceutical ingredients (APIs), pharmaceutical formulations, and manufacturing processes using both traditional and advanced analytical tools.
- Document the execution, procedure, results, and conclusions of experiments in a detailed and organized manner following SOPs and ALCOA principles.
- Troubleshoot and investigate any challenges associated with the GMP testing through active collaboration with cross-functional project teams and/or Quality stakeholders.
- Validate and implement analytical methods to support release and stability testing of clinical materials.
- Perform data entry, data review, and author analytical reports or data summaries.
- Directly contributes to experimental design, execution, and data interpretation for GMP project support.
- Lead laboratory investigations and deviations including root cause analysis and identification of robust corrective and preventative actions.
- Strong collaboration with Pharmaceutical Analytical Sciences colleagues as well as cross-functional partners such as Global Development Quality, Process Chemistry, and Pharmaceutical Operations.
- Support compliance audit/inspection activities.
Benefits
- medical
- dental
- vision healthcare
- other insurance benefits (for employee and family)
- retirement benefits, including 401(k)
- paid holidays
- vacation
- compassionate and sick days
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What This Job Offers
Job Type
Full-time
Career Level
Senior
