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Job type: Contract

Discipline: Biological Sciences

Location: United States

Scientist - Contract - Cambridge, MA

̽��ϼ� 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

̽��ϼ� is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

̽��ϼ� Staffing is an equal opportunity employer.

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