Lab Technician 1

Filtrous; Saint Petersburg (FL); On-site; USD 27,552 - 30,307; Part time

Job summary

Filtrous in St. Petersburg, FL is looking for a part-time Lab Technician 1 to manage quality control processes for laboratory supplies. You will manufacture solutions, conduct quality checks, and collaborate on product listings ensuring accuracy and compliance. This role is perfect for someone interested in hands-on quality control and supporting scientific research.

Join a supportive team, where your meticulous work directly impacts scientific advancement and customer trust.

Qualifications

• Strong attention to detail and ability to identify and document deviations accurately.
• Familiarity with quality control procedures, testing equipment, and safety standards.
• Knowledge of safe handling of biohazardous specimens and chemical reagents.

Responsibilities

• Manufacture solutions and PCR panels following standard operating procedures.
• Perform visual and functional inspections on incoming raw materials and finished goods.
• Accurately record inspection and testing results following quality control protocols.

Skills

Attention to detail

Record-keeping

Quality control procedures

Basic computer skills

Education

B.S. degree in Biology, Biochemistry, Microbiology, Molecular Biology, Biotechnology, Chemistry or a related scientific field

Job description

Lab Technician 1

Where Precision Meets Purpose in Every Batch

Why This Role Matters

Every product that leaves Filtrous carries our reputation with it. A contaminated reagent can ruin a clinical test. A mislabeled vial can delay critical research. As our Lab Technician, you are the last line of defense between our products and the labs that depend on them. You’ll manufacture solutions and PCR panels, perform quality control testing, and ensure every lot meets specification before it ships. Your attention to detail directly protects the scientists and patients who rely on what we make.

What You’ll Do

• Manufacture with Precision: Prepare mobile phase bag solutions and PCR panels following standard operating procedures. Ensure every batch meets quality specifications through rigorous QC testing before approval or rejection.
• Inspect and Test at Every Stage: Perform visual and functional inspections on incoming raw materials, in-process products, and finished goods. Use standard testing equipment and document all results, observations, and deviations.
• Keep Our Website Accurate: Collaborate with marketing and product teams to review the website weekly, flagging and resolving issues related to product content, listings, and structure.
• Manage Sample Inventory: Organize and maintain both physical and digital sample inventories on an ongoing basis, ensuring all items are accessible, documented, and updated regularly.
• Document Everything: Accurately record inspection and testing results following quality control protocols. Maintain organized records and assist in generating reports on QC activities, findings, and corrective actions.
• Uphold Compliance and Safety: Adhere to ISO 9001:2015 standards and company policies. Ensure proper handling and disposal of materials, and participate in audits and continuous improvement efforts.

Problems You Will Solve

• Defective products slip through: A single contaminated reagent or mislabeled vial that escapes inspection can ruin a customer’s clinical test or research, and without a vigilant final check those mistakes reach the lab before anyone notices.
• Batches drift out of spec: Solutions and PCR panels are made by hand, so any lapse in following the exact preparation and testing steps lets a lot fall short of specification and arrive at customers unreliable.
• Website information goes stale: Product listings, descriptions, and page layout quietly fall out of date between reviews, leaving customers to act on wrong or confusing information that costs sales and trust.
• Samples become hard to find: Physical and digital samples accumulate without steady upkeep, so items go missing or untracked and the company is caught short when a colleague or auditor needs to locate one.
• Records fail under scrutiny: If test results, deviations, and corrective actions are not captured cleanly as work happens, gaps surface as findings during an ISO audit and put the company’s quality certification at risk.

How Success is Measured

• Maintain 100% SOP adherence on all manufacturing and QC processes
• Zero product escapes: catch all deviations before products ship to customers
• Complete weekly website product reviews with all issues flagged and resolved
• Maintain organized, audit-ready sample inventory with up-to-date documentation
• Pass all internal and external quality audits with zero findings in areas of responsibility

Why You’ll Love It Here

At Filtrous, you’re not just another technician on a factory floor. You’re a critical member of a small, tight-knit team where your work has a direct and visible impact. You’ll develop hands‑on skills across manufacturing, quality control, and even digital product management. You’ll work alongside scientists, operations staff, and leadership in an environment that values initiative and rewards attention to detail. As Filtrous grows, you’ll have opportunities to take on more responsibility, specialize in areas that interest you, and advance your career in quality and manufacturing.

Who You Are

• B.S. degree in Biology, Biochemistry, Microbiology, Molecular Biology, Biotechnology, Chemistry, or a related scientific field
• Strong attention to detail and ability to identify and document deviations accurately
• Familiarity with quality control procedures, testing equipment, and safety standards
• Excellent organizational and record‑keeping skills
• Ability to work independently and collaboratively within a team
• Proficient in basic computer skills, including Microsoft Office and data entry
• Knowledge of safe handling of biohazardous specimens and chemical reagents
• Ability to stand for extended periods, perform repetitive tasks, and lift up to 40 pounds
• Bonus points if you have:
• Basic understanding of ISO 9001:2015 standards
• Previous experience in a QC, manufacturing, or laboratory environment
• Familiarity with PCR‑based assays or molecular biology techniques

About Filtrous

Founded in 2017, Filtrous delivers speed, quality, and value to agile labs. We’re a lab supplies distributor serving laboratories across a wide range of scientific and industrial sectors. Our secret? We combine uncompromising product quality with customer service that actually picks up the phone.

Position Details

• Compensation $20 – $22 per hour
• Job Type Part‑time (20 hours per week)
• Benefits N/A
• Location St. Petersburg, FL (in‑person)
• Schedule Monday to Friday, 20 hours per week
• Travel Some travel may be required

Ready to Join Us?

If you take pride in precision work, want to build hands‑on skills in quality and manufacturing, and are excited about supporting the labs that advance science, we’d love to hear from you.

Filtrous is an equal opportunity employer. We value diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other protected characteristic.