Principal Scientist - Flow Cytometry
Principal Scientist - Flow Cytometry
Posted on :
15-03-2025
Employer Active
1 Vacancy
Job Alert
You will be updated with latest job alerts via emailValid email field required
Send jobs
Share
Send me jobs like this
Job Alert
You will be updated with latest job alerts via emailValid email field required
Send jobs
Job Description
Enabling critical work and rubbing shoulders with the scientists who are contributing to the impact of our worlds health that is what Principal Scientists at KCAS Bio get to do every day. If that gets you excited too then maybe working at KCAS Bio is for you.
When you work as a Principal Scientist in our Flow Cytometry group at KCAS Bio you get to further our mission by partnering with the Associate Director and Test Facilities Management to assign projects to your team members for completion under your guidance.
You will also be responsible for the management and oversight of all assigned studies within your business unit including the following tasks: planning development implementation validation interpretation and reporting.
Learn more about our work in Flow Cytometry here: Flow Cytometry Services KCAS Bio
In this role we will rely on you to:
- Be responsible for the development and of protocols for preclinical and clinical studies
- Write and/or edit high quality development plans and reports
- Be responsible for the design implementation and of experiments for client specific projects
- Serve as the principal investigator (PI) role for designated studies as described in SOPs
- Establish and maintain communications with existing and potential clients
- Collaborate with business development and marketing teams in the preparation of material for tradeshows and professional conferences
- Provide technical and scientific input to the Sales team for client proposals and discussions
- Coaching mentoring and training junior members and scientists as required
- Be responsible for the maintenance of a positive work environment for both inter and intra business divisions.
- Be responsible for the weekly monthly and quarterly reporting to your line manager for KPI reporting revenue recognition technical issues client interactions project advancements or delays
- Be responsible for the analysis and summary of findings from studies for the purpose of decisions regarding safety and efficacy to support investigational new drug submission and new drug applications or clinical study reports
- Lead multiple projects in development optimization of bioanalytical methods complying to applicable ICH/FDA/EMA guidelines under GLP/GCLP environment
- Ensure that all necessary remedial actions are taken and documented whenever significant deviations from the laboratorys established performance specifications are identified
- Troubleshoot basic testing and/or analytical method related issues
- Together with the Test Facility management be responsible for overseeing the optimal performance of laboratory equipment and as deemed necessary overseeing any nonroutine maintenance including corrective actions and the authorizations of equipment use
- Maintain awareness of scientific developments within your area of expertise both in terms of new methodology and new research activities as well as the identification of potential clients
- Attend appropriate scientific meetings to maintain technical competency and promote awareness of research activities in area of expertise
To qualify specifically for this role you will have:
- University degree (Master or PhD) in biological science related fields
- 5 years of combined work experience in the field of analytical method development including biochemistry and/or ligand binding assays
- SME in bioanalytical techniques and a wider knowledge of other methods (cellbased assays/ flow cytometry)
- SME in GLP GCP and/or GDPR compliance
- Excellent communication skills (written and spoken) in English and French
- Effective communication skills with the ability to transfer knowledge and communicate effectively to internal/external stakeholders
- Excellent social skills ability to work in matrixed teams and collaborate with diverse partners crossfunctionally
- Ability to think critically with excellent problem solving and troubleshooting skills
- High ethical standards good judgement and trustworthiness
- Ability to act in a leadership capacity and mentor others
- Perform all aspects of the job in a way that supports company brand mission vision and values
WHAT WE OFFER YOU
In addition to the usual benefits we offer you the opportunity to develop your professional career through a vigorous training policy. You will evolve within a team with a human face concerned about the wellbeing and inclusion of all its employees.
WHO ARE WE
We are a fastgrowing contract research organization (CRO) based in Lyon. We are pioneering the latest drug development in the human health field.Demand for our expertise is growing and so is our need for great people to work in nimble empowered teams committed to one anothers growth. At KCAS Bio we advance both great science AND great people.
Required Experience:
Staff IC
Employment Type
Full-Time
Key Skills
Report This Job
Disclaimer: Drjobpro.com is only a platform that connects job seekers and employers. Applicants are advised to conduct their own independent research into the credentials of the prospective employer.We always make certain that our clients do not endorse any request for money payments, thus we advise against sharing any personal or bank-related information with any third party. If you suspect fraud or malpractice, please contact us via contact us page.
