Role Overview
Lunella Biotech is hiring a mid-level Biomedical Scientist. This is a full-time role in CA. Part of Lunella Biotech's Qa hiring, posted 2 weeks ago. Full responsibilities, required qualifications, and the apply link are listed in the description below.
Salary Context
Salary is not disclosed in this posting. Market median for Mid-level Qa roles is $67k-$99k (based on 144 comparable listings). Many employers share specifics during the interview process or after an initial screen.
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Job Description
Company Description
Chronological ageing is a biological process that results in accumulated cellular damage, ultimately driving the onset of metabolic disfunction. We aim to develop new therapeutic approaches to these ageing-associated diseases, by targeting metabolism in cancer stem cells (CSCs) and senescent fibroblasts. More specifically, we will screen a series of chemical libraries containing FDA-approved drugs, natural products, and novel chemical entities, to identify compounds that can effectively age-associated metabolic features. Through this screening and validation approach, we will identify compounds that preferentially kill CSCs and senescent fibroblasts, using established cell lines.
This position will involve the screening and discovery of drugs that target the metabolic phenotype of senescent cells and cancer stem cells, across multiple cancer types.
Job Description
The purpose of this role is to support Lunella Biotech’s mission in the discovery of anti-ageing and anti-cancer therapeutics. In more detail, you will work as part of a team of scientists, and will be responsible for the co-planning and execution of many experimental aspects of the project. This position will involve the identification and phenotypic validation of drugs that target senescent cells and cancer stem cells. The project will require the use of immunohistochemistry, immunocytochemistry and flow cytometry applied to relevant samples.
Responsibilities
- To perform experiments in the laboratory to test hypotheses regarding ageing and cancer
- To plan and execute the experiments related to the phenotypic validation of identified drugs targeting CSCs and senescent cells.
- To apply complex research techniques for the phenotypic validation of drug hits using immunohistochemistry, immunofluorescence and flow cytometry of relevant samples.
- Take overall responsibility for several experimental components of the project.
- To maintain accurate records of data and analysis performed of specific experiments for a given project, conducts literature searches, and maintains an up-to-date knowledge of all current experimental methods through professional reading.
- To demonstrate a willingness to adapt and develop new skills.
- To write up draft reports for manuscript publication and patent evaluation
- To present data as required, during lab meetings and conferences
- To collaborate with members within and outside of the laboratory
- To comply with Health and Safety regulations
- To promote equality and diversity and sustain an inclusive and supportive work environment
- This role detail is a guide to the work you will initially be required to undertake. It may be changed from time to time to meet changing circumstances
Qualifications
Education
- Completed Master’s or PhD in related biological/pharmaceutical sciences
- Publication record in peer-reviewed journals
Background & Experience
Essential criteria
- Experience in flow cytometry/FACS analysis
- Considerable experience of cell culture techniques
- Experience in fluorescent microscopy
- Experience in drug screening
- Experience and a track record in working with and developing a variety of techniques
- Experience in recording, analyzing and interpreting data
Desirable criteria
- Experience in assays measuring metabolic parameters of cellular models
- Experience in the co-culture of multiple cell types
- Experience in proteomics
- Experience in the generation of stable cell lines using transfection methods
Skills & Competencies
- Proven ability to maintain high experimental reproducibility and reliability to ensure consistent and valid results
- Ability to work independently within an agreed framework
- Excellent communication skills on paper and verbally, including good IT skills
- Ability to work as part of a team
- Proven ability to follow directions
- Ability and willingness to learn new analytical methods and skills
- Good organizational skills
Additional information
As an equal opportunity employer, Lunella Biotech Inc. is committed to achieving a skilled and diversified workforce that reflects the diversity of the Canadian population. We encourage applications from women, visible minorities, people with disabilities and Aboriginal people.
Additional Information
As an equal opportunity employer, Lunella Biotech Inc. is committed to achieving a skilled and diversified workforce that reflects the diversity of the Canadian population. We encourage applications from women, visible minorities, people with disabilities and Aboriginal people.
About Lunella Biotech
Lunella Biotech
lunellabiotech.com
Frequently Asked Questions
How do I apply for the Biomedical Scientist position at Lunella Biotech?
Use the Apply button above to submit your application directly to Lunella Biotech. Most applications take less than 5 minutes if your resume and contact details are ready, and you'll be routed to the employer's official application system to finish.
Where is the Biomedical Scientist position at Lunella Biotech located?
This position is based in CA. Lunella Biotech has not indicated remote or hybrid options for this role, so candidates should plan for on-site work.
What does a Biomedical Scientist at Lunella Biotech earn?
Lunella Biotech has not disclosed a salary range in this posting. Many employers share specifics later in the interview process; you can also ask during a recruiter screen if compensation transparency is important to you.
When was the Biomedical Scientist role at Lunella Biotech posted?
This role was posted on June 14, 2026 (14 days ago). It's still listed as actively hiring; we re-confirm openings against the source system multiple times per day and remove closed roles.
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