Posted on Monday, March 15, 2021 By Hayden Selvadurai
Enara Bio is expanding its CMC expertise within the organisation, to deliver a pipeline of Cell and Gene Therapy products, including autologous ex vivo gene modified TCR-T therapeutics, to patients with cancer. We are now looking for an enthusiastic lab-based scientist to join the cell process development team, on projects spanning from research to GMP manufacturing.
The main focus of the role is to assess methods and technologies to establish robust manufacturing processes for our cell products. In addition, close collaboration with the research function and other members of the process and analytical development teams, as well as with external partners is expected.
Posted on Monday, March 15, 2021 By Hayden Selvadurai
Enara Bio is expanding its CMC expertise within the organisation, to deliver a pipeline of Cell and Gene Therapy products, including autologous ex vivo gene modified TCR-T therapeutics, to patients with cancer. We are now looking for an enthusiastic lab-based scientist to join the analytical development team, on projects spanning from research to GMP manufacturing.
The main focus of the role is to assess methods and technologies to establish robust analytical assays for GMP release and to characterise our cell products. In addition, close collaboration with the research function and other members of the process and analytical development teams, as well as with external partners is expected.
Posted on Monday, February 8, 2021 By Nouritsa Biberian
Molecule 2 Medicine Limited (M2M) is a private biotechnology and pharmaceutical consulting company based in the UK, that helps a select portfolio of clients achieve the efficient discovery, development and global commercialisation of new human therapeutics.
Posted on Friday, February 5, 2021 By Hayden Selvadurai
Enara Bio is expanding its CMC footprint within the organisation, to deliver a pipeline of Cell and Gene Therapy products, including autologous ex vivo gene modified TCR-T therapeutics, to patients with cancer. We are now looking for a dynamic experienced Project Manager, to support the team on all aspects of CMC development in collaboration with our Research and Development teams as well as external collaborators/3rd party vendors.
The role will report to the VP, Cell Therapy Operations and will be central to ongoing activities to establish and develop robust manufacturing capabilities, build high functioning cross-functional project teams, and advance overall product development milestones.
Posted on Wednesday, January 27, 2021 By Hayden Selvadurai
Enara Bio is expanding its CMC expertise within the organisation, to deliver a pipeline of Cell and Gene Therapy products, including autologous ex vivo gene modified TCR-T therapeutics, to patients with cancer. We are now looking for a dynamic person with extensive scientific and cell process development experience to build the bridge between research and GMP manufacturing.
The role is multifaceted in working closely with the internal research teams on cross-functional projects, such as the development of next gen products, leading cell process development, and the assessment of novel methods and technologies. Further, the role will act as SME on projects with our external partners to establish robust cell processes.
Posted on Monday, January 18, 2021 By Hayden Selvadurai
We are looking for an innovative and enthusiastic Target Validation expert to advance our efforts in validating the expression of novel immunotherapy targets across a range of primary samples and model systems. You will have expertise in molecular and in situ transcript and antigen validation methods (e.g. RT-PCR, ISH, IHC) and an ability to understand and interpret the output of NGS and bioinformatic analyses. This is an opportunity for you to help shape a critical research function within a rapidly growing organisation and contribute to the selection of new cancer treatments for clinical development.
You will work within multiple cross-functional project teams, responsible for key activities to achieve project deliverables and offering insight and expertise to support decision making. Communication and interpersonal skills will be key as you manage external relationships (e.g. with CROs) and provide your expertise to both academic and industrial research partnerships. You will also contribute towards validation work to support the progression of novel therapeutics from research into development, generating supportive data for potential inclusion in regulatory submissions (e.g. IND/CTAs).