Associate , PDT

Replimune’s mission is to revolutionize cancer treatment with therapies designed to activate a powerful and durable full-body anti-tumor response, boldly transforming cancer care because

People are at the center of everything we do, and when it comes to our employees,

Replimune’s mission is to revolutionize cancer treatment with therapies designed to activate a powerful and durable full-body anti-tumor response, boldly transforming cancer care because

People are at the center of everything we do, and when it comes to our employees, we make it personal. With a deep sense of purpose, a strong and evolving culture, a competitive and forward‑looking total rewards program, everyone at Replimune has a unique opportunity to impact on the lives of patients, caregivers and themselves.

The Associate I, PDT is responsible for supporting the day-to-day operation of the PDT laboratories and process activities. The Associate I will perform routine upstream, downstream and drug product formulation process steps to support projects and will provide support for process characterization and formulation development activities.

This position is based in our Framingham location and typically has a 5-day on-site expectation.

• Support upstream tissue culture, downstream virus purification and drug product formulation activities within the PDT laboratory.
• Perform routine laboratory and pilot lab process steps under supervision, including preparation, equipment set-up, sampling, cleaning and documentation.
• Perform general laboratory housekeeping tasks, including maintaining stock levels of laboratory consumables and preparation of reagents while executing good documentation practices.
• Support general laboratory upkeep, including ensuring the laboratory is clean, disposal of waste, sample storage and equipment monitoring.
• When required, operate in accordance with Good Manufacturing Practice (GMP) and company procedures.
• Work in cross-functional teams with Manufacturing, Quality Control, Facilities and Engineering, Analytical Development and Quality Assurance.
• Ensure effective, high‑quality, timely and appropriate documentation in laboratory notebooks.

• Participate with other members of the PDT team in the preparation and purification of viruses, thereby gaining both theoretical and practical knowledge of upstream and downstream processes.
• Support review of batch records, laboratory notebooks and GMP documentation as appropriate.
• Provide support to the facilities group when required.
• Practice and promote safe working habits and adhere to safety procedures and guidelines.

• Bachelor’s degree with 0–2 year of related work experience.

Hands‑on experience in a laboratory setting is desired. Experience in the biotech or pharmaceutical industry is desired. Experience in cell culture, purification, chromatography or formulation would be beneficial. The successful candidate will have the ability to follow protocols and standard operating procedures and the ability to record data in a timely and accurate manner in accordance with procedures. The candidate should be self‑motivated, organized, able to manage time effectively, communicate well, work independently and as part of a small team, and…