Scientist I

Streamline Scientific, LLC; Birmingham (AL); On-site; USD 45,000 - 60,000; Full time

Job summary

Streamline Scientific, LLC is seeking an entry-level position for a role focused on molecular diagnostics. This role involves defining testing formats and optimization protocols while ensuring compliance with regulatory requirements.

The ideal candidate will have a four-year degree in basic sciences and strong expertise in qPCR assay design. Candidates should demonstrate problem-solving skills, and the ability to work collaboratively in a diverse team.

Qualifications

• Strong technical expertise in qPCR assay design and optimization.
• Detail-oriented with excellent written and verbal communication skills.
• Ability to collaborate in developing molecular assays for infectious diseases on qPCR platforms.

Responsibilities

• Define testing format and optimization protocols.
• Ensure studies comply with regulatory/GLP requirements.
• Work with scientists to ensure assay performance.
• Drive continuous process improvement and regulatory compliance.

Skills

qPCR assay design and optimization

Collaboration

Technical writing

Problem-solving

Education

Four-year degree in basic sciences (biology or chemistry)

Job description

Job Details

Level: Entry
Job Location: Molecular Designs- PP - Birmingham, AL 35243
Position Type: Full Time
Education Level: 4 Year Degree
Travel Percentage: Negligible
Job Shift: Day
Job Category: Biotech

Molecular Designs is a team of doctors and scientists working to advance molecular diagnostics.

Our founding physicians entered the molecular diagnostics market focused on the most common pathogens that impact the population making products that are cost-effective, reduce waste, and are easy-to-use.

Responsible for working closely with the research team lead to define testing format and optimization protocols. Report out results and data in a clear and concise manner to management. Support Company goals and objectives, Policies & Procedures, Quality System and FDA Regulations.

Essential Functions

• Responsible for working closely with the research team lead to define testing format and optimization protocols.
• Ensure studies are done in compliance with regulatory/GLP requirements, according to Standard Operating Procedures.
• Work with a small group of scientists and focus on ensuring assay performance is based on customer needs.
• Demonstrates passion for problem solving and outside-the-box thinking.
• Strong technical expertise in qPCR assay design and optimization.
• Experience in clinical product development under Design Control is preferred.
• Strong written and oral communication and presentation skills are desired.
• Must be highly collaborative; enjoys working in a diverse team and contributes to a positive work environment.
• Self-motivated, independent, proactive, organized, diligent, and flexible.

Qualifications

• Ability to perform detailed technical work in a laboratory.
• Detail-oriented with excellent written and verbal communication skills.
• Ability to collaborate with a team developing molecular assays for infectious diseases diagnostics on qPCR platforms.
• Knowledge and expertise in molecular assays for infectious disease and drug resistance.
• Ensure projects meet timelines, identify, and remove roadblocks to team success.
• Manage relationships and alignment with internal and external partners.
• Provide assessment of competitive diagnostic comparator assays and help evaluate appropriate comparator assays.
• Actively participate as a member of cross-functional product development teams.
• Drive continuous process improvement.
• Adopt a culture to drive regulatory compliance across the workflow, particularly in the area of new assay formats.

Education Requirements

Four-year degree required. Preferably with a focus on basic sciences, such as biology or chemistry.

Physical Demands

• Must have good eye-hand coordination for pipetting.
• Must be able to lift 50 lbs.
• Must be comfortable working with human pathogens.