Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. We're seekin…
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Full-time
bachelor degree
Posted 78d ago
~40 hrs/week
Responsibilities
The Instrument Scientist will execute analytical tests to ensure dose formulations meet clinical research specifications and maintain laboratory instrumentation. They will also develop chromatographic methods, prepare quality controls, and document results for sponsors.
Requirements
Candidates must hold a Bachelor's degree in Chemistry, Biochemistry, or a related field. A minimum of 3-5 years of hands-on experience with analytical instrumentation and method development is highly preferred.
Full job description
Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
We're seeking an Instrument Scientist to join our Dose Formulation team at our facility in Lincoln, NE, located just south of downtown.
In this lab-based role, you'll execute critical tests to ensure compounds from our in-house pharmacy meet all required specifications for use in clinical research trials.
If you're driven by tight timelines and passionate about advancing human health, this could be the role for you. You'll leverage your expertise in analytical chemistry to ensure every dose is ready for delivery on schedule.
Essential Functions:
Partner with senior scientists to develop chromatographic in support of dose formulation testing
Complete tasks necessary for daily operation in the laboratory: execute analytical tests to ensure the accuracy, homogeneity and precision to support on-site compounding by the Celerion Pharmacy team.
Preparation of standard calibrators, quality controls, mobile phases, and solutions for the purpose of testing dose formulations.
Inventory and re-order parts when used for instrument maintenance and repair
Assist in troubleshooting instrumentation aspects of studies
Take part in instrumentation upkeep by observing the maintenance schedule and performing calibrations and preventative maintenance
Communicate results effectively and in a timely manner to other associates
Initiate, introduce, and implement new guidelines and procedures through the development of working instructions
Optimize instruments to support ruggedness testing, production flexibility, and production
Prepare documentation to share method development results with the sponsor
Write detailed methodologies and provide feedback on Dose Formulation Protocols.
Requirements:
Bachelor's degree in Chemistry, Biochemistry, or related scientific field, advanced degree is a plus
3-5 years of post-academic hands-on experience with analytical instrumentation and/or method development (highly preferred)
Self-directed, self-motivated, and detail-oriented
Strong desire to learn new techniques with openness to cross-training opportunities
Flexibility to work outside normal business hours as needed to meet testing timelines, including occasional long days, evenings and weekends
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Celerion Values: Integrity Trust Teamwork Respect
Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.
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Celerion Can Take You from First-In-Human through Proof-of-Concept.
Industry
Pharmaceutical Manufacturing
Company size
1,001-5,000 employees
Founded
2010
Headquarters
Lincoln, NE
LinkedIn followers
30,132
Celerion, a leader in early clinical research, delivers Applied Translational Medicine. Celerion applies our expertise and experience to translating information gained in research discoveries, to knowledge of drug action and effect in humans to support early drug development decisions and the clinical pharmacology labeling of new medicines.
With over 50 years of experience and 600 global clinic beds (including 24 in-hospital), Celerion conducts and analyzes First-in-Human, clinical proof-of-concept, cardiovascular safety (TQT, robust QT), ADME and NDA-enabling clinical pharmacology studies. Celerion provides expertise on modeling and simulation, study design, medical writing (protocols and reports), clinical data sciences, biostatistics, and PK/PD analysis as well as small and large molecule bioanalytical assays through clinical drug development. Regulatory, drug development and program management complement Celerion’s service offerings.
Our operations are strategically located in:
Lincoln, Nebraska (Corporate Headquarters)
Philadelphia, Pennsylvania
Phoenix, Arizona
Belfast, Northern Ireland,UK
Zurich, Switzerland
Vienna, Austria
Richmond, Virginia
Montreal, Quebec, Canada
For more information, visit: www.celerion.com
Offices: 621 Rose Street, Lincoln, NE 68502, US · 2420 W. Baseline Rd., Tempe, AZ 85283, US · 100 Boulevard Alexis-Nihon, Montreal, Quebec H4M, CA · 22-24 Lisburn Road, Belfast, BT9 6AD, GB · Allmendstrasse 32, Fehraltorf, CH
Applied Translational MedicineGlobal Clinical Research (Phase I and IINDA-enabling clinical pharmacology)Data Management and BiometricsGlobal Bioanalytical Services (discovery through late phase)Drug Development Servicesand Global Clinical DevelopmentHealth CarePharmaceutical
Celerion Can Take You from First-In-Human through Proof-of-Concept.
Industry
Pharmaceutical Manufacturing
Company size
1,001-5,000 employees
Founded
2010
Headquarters
Lincoln, NE
LinkedIn followers
30,132
Celerion, a leader in early clinical research, delivers Applied Translational Medicine. Celerion applies our expertise and experience to translating information gained in research discoveries, to knowledge of drug action and effect in humans to support early drug development decisions and the clinical pharmacology labeling of new medicines.
With over 50 years of experience and 600 global clinic beds (including 24 in-hospital), Celerion conducts and analyzes First-in-Human, clinical proof-of-concept, cardiovascular safety (TQT, robust QT), ADME and NDA-enabling clinical pharmacology studies. Celerion provides expertise on modeling and simulation, study design, medical writing (protocols and reports), clinical data sciences, biostatistics, and PK/PD analysis as well as small and large molecule bioanalytical assays through clinical drug development. Regulatory, drug development and program management complement Celerion’s service offerings.
Our operations are strategically located in:
Lincoln, Nebraska (Corporate Headquarters)
Philadelphia, Pennsylvania
Phoenix, Arizona
Belfast, Northern Ireland,UK
Zurich, Switzerland
Vienna, Austria
Richmond, Virginia
Montreal, Quebec, Canada
For more information, visit: www.celerion.com
Offices: 621 Rose Street, Lincoln, NE 68502, US · 2420 W. Baseline Rd., Tempe, AZ 85283, US · 100 Boulevard Alexis-Nihon, Montreal, Quebec H4M, CA · 22-24 Lisburn Road, Belfast, BT9 6AD, GB · Allmendstrasse 32, Fehraltorf, CH
Applied Translational MedicineGlobal Clinical Research (Phase I and IINDA-enabling clinical pharmacology)Data Management and BiometricsGlobal Bioanalytical Services (discovery through late phase)Drug Development Servicesand Global Clinical DevelopmentHealth CarePharmaceutical