Technician I, Process Development

ADMA BioCenters; Boca Raton (FL); On-site; USD 45,000 - 65,000; Full time

Benefits offered by this job

401(k) plan with employer match

Medical, vision, life and dental insurance

Pet insurance

Company-paid STD and LTD

Three weeks paid time off

Tuition assistance

Free shuttle to Boca Tri-Rail station

Job summary

ADMA BioCenters in Boca Raton seeks a Technician I, Process Development. The role conducts laboratory and pilot-scale experiments to develop new technologies and optimize manufacturing processes.

Applicants should possess a B.S. in relevant scientific fields and up to two years of lab experience. The position includes benefits like a 401(k) plan, medical insurance, and paid time off.

Qualifications

• Up to two years of laboratory experience; preference for regulated environments.
• Capacity to work at small scale and transfer to larger applications.
• Familiarity with basic lab equipment.

Responsibilities

• Conduct lab-scale studies involving plasma proteins.
• Perform testing to generate data for validation and special projects.
• Assist manufacturing operations team with equipment and systems.

Skills

Time-management skills

Organizational skills

Critical-thinking and problem-solving abilities

Strong interpersonal and collaborative skills

Education

B.S. in Microbiology, Chemistry, Biochemistry, Biology, or a related discipline

Tools

pH meter

Spectrophotometer

Scale

Pipettes

Pumps

MS Word

Excel

LIMS

Job description

Technician I, Process Development

ADMA Biologics is a biopharmaceutical company relentlessly committed to creating superior products for immunodeficient patients at risk for infection. We are devoted to this underserved population and employ a hands‑on approach to production and development.

Position Summary

The Technician I, Process Development conducts laboratory and pilot‑scale experiments that support the development of new technologies. The role is partially responsible for optimizing manufacturing processes and implementing regulatory requirements, assisting in process development activities, creating scalable processes with improved product yield and reduced manufacturing system costs, researching new methods and technologies to enhance operations, collecting, analyzing, interpreting data to improve processes.

Responsibilities

• The standard schedule is 8:00 AM to 5:00 PM, but employees may frequently be required to work 12‑hour rotating shifts during operational campaigns and manufacturing model runs.
• Conduct lab‑scale studies involving processing of plasma proteins.
• Conduct laboratory and pilot‑scale experiments to evaluate and develop new technologies.
• Operate centrifuges, filtration apparatus, and chromatography systems.
• Use monitoring instruments such as pH/conductivity meters, spectrophotometer, and scale.
• Perform sample and buffer preparation, including labeling.
• Clean equipment and area.
• Complete documentation and data entry for procedures and tests performed.
• Adhere to Safety and cGMP practices.
• Perform testing to generate data for validation and special projects.
• Fulfill requests from management for assistance in other matters.
• Assist in creating scalable processes.
• Assist the manufacturing operations team in problem solving with regard to equipment and systems.
• Participate in the design and start‑up of new manufacturing facilities and equipment.

Competencies

• Time‑management skills and ability to balance multiple job assignments.
• Strong organizational, critical‑thinking, reasoning, and problem‑solving abilities.
• Strong interpersonal and collaborative skills.

Education & Experience Requirements

• B.S. in Microbiology, Chemistry, Biochemistry, Biology, or a related scientific discipline.
• Up to two years of experience in a laboratory setting; prior experience in a regulated environment (FDA, EPA, etc.) is preferred.
• Capacity to work at small scale and transfer to larger applications.
• Familiarity with basic lab equipment (pH meter, spectrophotometer, scale, pipettes, pumps, etc.).
• Computer skills (MS Word, Excel, LIMS, etc.).
• Excellent organizational skills and ability to interact effectively with internal and external colleagues and managers.

Preferred Experience

• Compliance knowledge: understanding FDA regulations and company policies governing sales, marketing, and documentation. Ability to participate in compliance reviews, report potential issues, and stay updated on relevant regulations.

Benefits

• 401(k) plan with employer match and immediate vesting.
• Medical, vision, life and dental insurance.
• Pet insurance.
• Company‑paid STD and LTD.
• Company paid holidays.
• Three weeks paid time off within the first year.
• Tuition assistance after the first year.
• Free shuttle to the Boca Tri‑Rail station.

EEO Statements

ADMA Biologics uses E‑Verify to confirm the employment eligibility of all newly hired employees. To learn more about E‑Verify, including your rights and responsibilities, please visit www.dhs.gov/E‑Verify.

ADMA Biologics is an Equal Opportunity Employer.