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Scientist
- Contract
- Biological Sciences
- United States
This vacancy has now expired. Please see similar roles below...
Scientist - Contract - Cambridge, MA
Proclinical is working alongside a pharmaceutical company seeking a Scientist to join their growing team.
Primary Responsibilities:
The successful candidate will contribute to the development of novel vaccine programs from preclinical through clinical stages. This role involves designing and executing experiments with a focus on process development and characterization. You will play a key role in supporting the advancement of vaccine processes and ensuring compliance with scientific and regulatory standards.
Skills & Requirements:
- Masters/Bachelors in related fields such as Biochemistry/Biology/Molecular Biology/Chemical Engineering with 1+ years' experience.
- Industry experience with process characterization, process development, scale-up experience, and assay development preferred.
- Experience in DOE and JMP software preferred.
- Similar experience in protein purification and chromatography experience will be considered.
- Independent, detail-oriented, and organized with excellent oral and written communication skills.
- Demonstrated ability to work in a dynamic environment as a team player with a strong work ethic.
- Able to maintain written records in the form of laboratory notebooks.
The Scientist's responsibilities will be:
- Perform design and execution of experiments to support process development of advance novel vaccine programs from preclinical through clinical stages with minimal supervision, maintaining good scientific practice.
- Perform process characterization / process development studies for the MAPS program
- Perform data analysis from process characterization / process development studies
- Support the development of new processes or improve existing processes using scientific expertise, literature review or by seeking inputs from Subject Matter Experts.
- Support Tech transfer of developed processes to support GMP manufacturing.
- Complete archiving of raw and processed data as per our policy
- Operate and maintains designated lab equipment and train others as needed.
- Complete the documentation of experimental results as per GMP/GLP regulations.
- Complete the authoring of technical reports in collaboration with QA / RA / MSAT / ARD teams and assist in submission to regulatory agencies such as FDA.
- Complete additional duties and responsibilities as required.
If you are having difficulty in applying or if you have any questions, please contact Jackie Cerchio at j.cerchio@proclinical.com
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
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