Scientist I

Molecular Designs, LLC; Birmingham, Northern (AL, KY); Hybrid; USD 42,000 - 65,000; Full time

Job summary

Molecular Designs is seeking an entry-level lab professional to join our Birmingham, AL team. You will work with researchers to define testing formats and optimization protocols for molecular diagnostics, and help report data to management.

This role emphasizes collaboration, attention to detail, and compliance with GLP and regulatory standards, with opportunities to contribute to assay development for infectious diseases.

Qualifications

• Four-year degree required in biology, chemistry, or related field.
• Strong written and verbal communication skills.
• Detail-oriented with ability to document data precisely.
• Ability to collaborate within cross-functional teams on assay development.

Responsibilities

• Collaborate with research team lead to define testing formats.
• Report results clearly to management.
• Support regulatory compliance and quality systems.
• Work with a small team of scientists on assay performance.

Skills

Detail-oriented

Written communication

Verbal communication

Team collaboration

Education

Bachelor's degree (4-year) in biology/chemistry or related field

Tools

qPCR platforms

Job description

Molecular Designs- PP - Birmingham, AL 35243

Overview

Level

Entry

Position Type

Full Time

Job Shift

Day

4 Year Degree

Travel Percentage

Category

Biotech

Description

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 makingproducts 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.

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.

• Must have good eye-hand coordination for pipetting


• Must be able to lift 50 lbs.


• Must be comfortable working with human pathogens