- Erfahrung
- 1–4 Jahre
- Gehalt
- —
- Stellenangebote
- 1
- Veröffentlicht
- vor 19 Stunden
- Arbeitsmodus
- Im Büro
- Ausbildung
- Degree in Sciences or Engineering
- Wieder aufnehmen
- Bewerbung erforderlich
Stellenbeschreibung
Company Overview
RevBio, Inc. is an innovative medical device firm focused on regenerative bone adhesives that enhance fracture repair and bone fixation outcomes. Its main product, TETRANITE®, is a bioengineered bone adhesive undergoing multiple FDA-approved clinical trials and backed by patents valid through 2042. TETRANITE® is designed for applications in neurosurgery, orthopedics, and dentistry, addressing a market valued over $10 billion. Characteristics include fast mechanical stabilization, wet-field adhesion, controlled biodegradability, and a scaffold for natural bone regeneration. The technology is inspired by the natural adhesive proteins of the sandcastle worm.
Role Overview
The Research Chemist will focus on characterizing TETRANITE® products across various projects, collaborating with scientific colleagues to plan and perform studies. This role includes developing and validating analytical testing methods, executing SOP-driven assays, analyzing experimental data, and presenting findings to cross-functional teams. Coordination with quality control and assurance teams will be crucial to conduct raw material and in-process manufacturing tests, as well as final product performance evaluations. Interaction with external partners and management of their data are also required.
Key Responsibilities
- Conduct analytical laboratory testing and develop relevant test methods utilizing techniques such as Liquid Chromatography.
- Assist in the development and validation of in vitro test methods.
- Create methodologies for analyzing and optimizing therapeutic release kinetics from products.
- Perform tests and report data on both raw materials and finished goods using various analytical instrumentation.
- Design analytical studies conforming to RevBio's Quality Management System requirements to verify product specifications.
- Analyze prior study data to discern trends and build scientific rationale to advance technology understanding.
- Formulate test protocols in compliance with international and domestic test standards.
- Develop, author, and review test methods and standard operating procedures (SOPs).
- Support troubleshooting efforts for test methods and equipment; ensure scheduled calibration of analytical instruments.
- Maintain documentation fulfilling RevBio's Quality Management System, including managing corrective and preventative actions, non-conformities, and lot release records related to testing.
- Apply creative problem-solving, engineering principles, and statistical analysis to develop innovative solutions.
- Perform other relevant duties as assigned.
Required Expertise and Abilities
- Proficient working in cross-disciplinary teams.
- Capable of managing project timelines independently or as part of a team.
- Experienced in chemical, physical, and material characterization testing for product evaluation.
- Self-motivated to push projects towards successful completion.
- Skilled at rallying support from both internal and external resources.
- Strong communicator regarding project progress and outcomes.
- Willing to comply with regulatory standards including FDA 21 CFR Parts 58 and 820, and ISO 13485.
- Flexible and cooperative to handle various responsibilities essential for overall success.
Qualifications
- Degree in Chemistry, Biomedical Engineering, Biochemistry, or related scientific/engineering fields.
- Bachelor’s degree holders with 2 to 4 years’ experience or Master’s degree holders with 1 to 3 years’ experience in medical devices, pharmaceuticals, or biotechnology preferred.
- Preferred experience in drug delivery systems, release kinetics, and pharmacokinetics.
- Strong wet lab background including physical, thermal, and moisture analyses.
- Required expertise with HPLC-UV-MS and highly desirable experience with NMR, FTIR, SEM techniques.
- Preferred knowledge in crystalline phase characterization using XRD or similar methods.
- Meticulous attention to detail.
- Excellent verbal and written communication skills.
- Authorization to work in the United States.
- Demonstrated competence understanding and applying design controls and product development processes.