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 patient’s lives depend on it. We imagine a world where cancer is a curable disease.

At Replimune, we live by our values:

United: We Collaborate for a Common Goal.

Audacious: We Are Bold and Innovative.

Dedicated: We Give Our Full Commitment.

Candid: We Are Honest With Each Other.

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, an innovative and collaborative culture, a competitive and forward-looking total rewards program, everyone at Replimune has a unique opportunity to contribute to the meaningful work we do which could impact the lives of patients.

Join us, as we reshape the future.

Job Summary:

This role is based within Quality Control department and is a lab-based role that involves various day-to-day lab related activities such as, testing of various samples for release and stability purpose, assay and data review, lab equipment maintenance and troubleshooting, sample and material receipt , inventory management and general documentation.

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

Responsibilities

Perform QC testing of various samples according to Standard Operating Procedures(SOPs). Test methods may include but are not limited to number of cell based and ELISA based assays as well as general property measurement such as appearance, pH, osmolality etc.,
Maintain various cell lines on regular basis by revival and passaging at set intervals.
Review testing data and records of other operators and data verification for reports.
Perform QC sample and material receipt and maintain inventory.
Routine equipment maintenance and troubleshooting as required
Train other analysts within the department within scope of knowledge where applicable .
Write or revise SOPs, protocols, FORMs and update as required.
Participate in QC method transfers, qualification, and stability activities.
Adhere to current Good Manufacturing Practices (cGMP).
General lab tasks such as housekeeping, inventory of supplies, order supplies as required etc.
Write deviations related to QC and assist with investigations and other documentation as required
Assist with internal and regulatory agency audits / inspections.

Qualifications

Education:

Degree in Chemistry/Biochemistry/ other related science. Equivalent experience working in similar set up is also acceptable.

Required Experience:

One year of laboratory-based experience is preferred.
Competent analytical skills and attention for details.
Understanding of GMP requirements
Computer literacy (including MS Word and Excel), good communication and organizational skills.
Ability to work independently and with others in a team

About Replimune
Replimune Group, Inc., headquartered in Woburn, MA, was founded in 2015 with the mission to transform cancer treatment by pioneering the development of a novel portfolio of oncolytic immunotherapies. Replimune’s proprietary RPx platform is based on a potent HSV-1 backbone intended to maximize immunogenic cell death and the induction of a systemic anti-tumor immune response. The RPx platform is designed to have a unique dual local and systemic activity consisting of direct selective virus-mediated killing of the tumor resulting in the release of tumor derived antigens and altering of the tumor microenvironment to ignite a strong and durable systemic response. The RPx product candidates are expected to be synergistic with most established and experimental cancer treatment modalities, leading to the versatility to be developed alone or combined with a variety of other treatment options. For more information, please visit www.replimune.com.