QC Raw Materials Specialist I

BioSpace

Boca Raton (FL)

On-site

USD 55,000 - 75,000

Full time

4 days ago
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Benefits offered by this job

401K with employer match
Medical, Vision, Life and Dental
Pet Insurance
STD and LTD
Holidays
Paid Time Off
Tuition Assistance
E-Verify

Job summary

ADMA Biologics is seeking a Specialist I, Raw Materials in Boca Raton, FL. The role involves quality control of raw materials, testing, and data entry in a regulated environment.

The position requires a B.S. or A.S. in a related science or equivalent experience, with 0–3 years in a pharmaceutical setting. A strong focus on cGMP and SOP adherence is essential to support compliant operations and QA/government audits.

Qualifications

  • Education requirements include a B.S. or A.S. in Chemistry, Biochemistry, Biology, or related science, or equivalent experience in a regulated environment (FDA).
  • Experience requirement: 0–3 years in a pharmaceutical company.
  • Compliance and cGMP adherence is expected, with mandatory training and documentation.

Responsibilities

  • Perform quality control raw material processing, sampling and testing per SOPs.
  • Complete testing documentation and data entry for procedures and tests performed in-house and at contract labs.
  • Utilize cGMP practices in documentation and execution of job functions.
  • Perform instrument calibration or qualification according to written procedures.
  • Fulfill management requests and adhere to SOPs and cGMP guidelines.

Skills

Quality control
Data entry
cGMP practices
Documentation

Education

B.S. or A.S. in Chemistry, Biochemistry, Biology or related science
Equivalent working experience in a regulated environment (FDA)

Job description

ADMA Biologics is seeking a Specialist I, Raw Materials in Boca Raton, FL. The role involves quality control of raw materials, testing, and data entry in a regulated environment.

The position requires a B.S. or A.S. in a related science or equivalent experience, with 0–3 years in a pharmaceutical setting. A strong focus on cGMP and SOP adherence is essential to support compliant operations and QA/government audits.

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