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ESSENTIALS OF THE JOB:
- Performs processing and testing of donor plasma samples to support automated workflows.
- Possesses experience with immunological assays, such as ELISA, and with liquid handlers.
- Assists with sample submission, sample handling and storage, and data reporting. Provides suggestions to streamline the sample management process.
- Ability to work accurately in a fast-paced environment to meet the requirements of quality and quantity.
- Analyze data and adhere to strict guidelines on documentation when recording, reviewing, and submitting data.
- Ability to work with laboratory information management systems to perform schedule testing, data review, and release results.
- Ensure data integrity requirements are met by completeness, consistency, and accuracy of generated cGMP documents within quality systems.
- Maintains compliance with standard operating procedures, regulatory requirements, and internal company procedures.
- May be responsible for training other analysts or technicians to perform routine high throughput screening assays on automated instrumentation in a quality control laboratory.
- Be able to perform routine maintenance of robotic workstations and integrated analytical instrumentation, such as spectrophotometers and microplate washers per standard operating procedures.
- Ability to adhere to testing timelines while maintaining efficiency and organization. Perform other related duties assigned by management.
- Frequently communicates status updates to management and recommends solutions to problems encountered.
- Provides relevant technical skills, teamwork, effective in problem solving, and maintains active communication skills.
- Be familiar with Biosafety Level 2 (BSL-2) Laboratories and working in a BSL-2 environment. Maintains a clean and safe working environment.
- Be aware of and keep up to date with health and safety issues in all aspects of the work undertaken.
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Education Requirements: Bachelor’s degree in related science discipline or Associate’s Degree or equivalent in biology, medical technology or related field
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Experience Requirements:Â 0-2 years in cGMP environment with preferred knowledge of assay automation (i.e., Hamilton), and experience in testing using immunological methods, such as ELISA. Ability to navigate in a fast-paced demanding environment. Possess strong verbal and written communication skills.
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In addition to competitive compensation, we offer a comprehensive benefits package including:
- 401K plan with employer match and immediate vesting
- Medical, Vision, Life and Dental Insurance
- Pet InsuranceÂ
- Company paid STD and LTD
- Company Paid Holidays
- 3 Weeks’ Paid Time Off (within the first year)
- Tuition Assistance (after the first year)
- Easily accessible to Tri-Rail
- Free shuttle to the Boca Tri-Rail station
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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.Â
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ADMA Biologics is an Equal Opportunity Employer.