What are the responsibilities and job description for the Scientist I – Molecular Based Assays, Analytical Sciences position at Dendreon?
Overview
Who We Are:
At Dendreon, we’re transforming the battle against cancer with personalized immunotherapy. Our flagship product, PROVENGE® (sipuleucel-T), was the first FDA-approved immunotherapy for metastatic castrate-resistant prostate cancer, utilizing a patient’s own immune cells to fight the disease.
If you’re driven by the opportunity to make a meaningful impact on cancer patients' lives, we invite you to join our team. With Immunotherapy Manufacturing Facilities in Seal Beach, CA, and Union City, GA, a strong Research & Development group in Seattle, WA, and a highly skilled Commercial team across the nation, Dendreon is at the forefront of cancer treatment innovation.
Core Values
The Scientist I will contribute to cross-functional projects as a hands-on laboratory professional specializing in molecular-based assays. Reporting to the Head of Analytical Development, this role involves experimental design, method development, and technology transfer. The ideal candidate will demonstrate strong problem-solving skills, initiative, and the ability to complete experimental goals within established timelines. Strong communication, collaboration, and a team-oriented mindset are essential.
Responsibilities
Key Responsibilities:
Job Requirements:
Education
Who We Are:
At Dendreon, we’re transforming the battle against cancer with personalized immunotherapy. Our flagship product, PROVENGE® (sipuleucel-T), was the first FDA-approved immunotherapy for metastatic castrate-resistant prostate cancer, utilizing a patient’s own immune cells to fight the disease.
If you’re driven by the opportunity to make a meaningful impact on cancer patients' lives, we invite you to join our team. With Immunotherapy Manufacturing Facilities in Seal Beach, CA, and Union City, GA, a strong Research & Development group in Seattle, WA, and a highly skilled Commercial team across the nation, Dendreon is at the forefront of cancer treatment innovation.
Core Values
- Put Patients First: Every day is an opportunity to improve the lives of those living with cancer.
- Act with Integrity: We commit to transparency, honesty, and always doing what’s right.
- Build Trust: Trust is earned through candid, open communication and a collaborative approach.
- Raise the Bar: We embrace continuous improvement and innovation, always striving to elevate our people.
- Drive Results: We are accountable to each other and deliver success together.
The Scientist I will contribute to cross-functional projects as a hands-on laboratory professional specializing in molecular-based assays. Reporting to the Head of Analytical Development, this role involves experimental design, method development, and technology transfer. The ideal candidate will demonstrate strong problem-solving skills, initiative, and the ability to complete experimental goals within established timelines. Strong communication, collaboration, and a team-oriented mindset are essential.
Responsibilities
Key Responsibilities:
- Design, execute, and analyze experiments related to molecular-based assays such as qPCR and ddPCR.
- Support method development, qualification, and technology transfer from development to GMP environments.
- Prepare and maintain technical documentation including method protocols, development reports, and transfer reports.
- Apply knowledge of cGMP principles in laboratory practices.
- Serve as a technical resource on molecular assays within the team.
- Maintain up-to-date knowledge of scientific literature and best practices.
- Collaborate effectively with cross-functional teams and support timelines and project goals.
- Mentor or support junior team members as needed.
- Other duties as assigned.
Job Requirements:
Education
- BS, MS, or Ph.D. in Molecular Biology, Biochemistry, or a related field.
- A Ph.D. with 2 years of hands-on experience in molecular biology analysis or a BS/MS with 8 years of significant practical experience in molecular biology.
- Working knowledge of cGMP requirements.
- Experience with cell culture techniques, especially iPSC, is a plus.
- Strong analytical and problem-solving skills.
- Excellent written and verbal communication skills.
- Strong organizational skills and ability to prioritize multiple tasks.
- Familiarity with method development, qualification, and technology transfer in a regulated environment.
- Collaborative team player with a proactive approach to projects.
- On-site based role at our Seattle, WA office (NOT Remote)
- This role operates in a standard office setting using standard office equipment.
- Role requires frequent use of video conferencing, standard office software, and digital collaboration tools.
- Must have the ability to lift 10 – 20 lbs.
- Must have the ability to work in an office environment around laboratories, manufacturing areas and equipment with exposure to blood, blood products or OPIM (other potentially infectious materials) while donning required personal protective materials.