Scientist

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.