Specialist QA II Manufacturing Oversight

BioSpace; Boca Raton (FL); Sur place; USD 85 000 - 110 000; Plein temps

Avantages offerts par ce poste

401K plan with employer match

Medical, Vision, Life and Dental

Pet Insurance

STD and LTD

Paid Holidays

Paid Time Off

Tuition Assistance

Shuttle service

Résumé du poste

ADMA Biologics is seeking a Specialist QA II Manufacturing Oversight in Boca Raton, FL. The role focuses on real-time batch record review, documentation assessment, and issue resolution on the manufacturing floor to ensure cGMP compliance and product quality.

The ideal candidate has 3–5 years in pharma/biotech, strong writing and communication skills, and familiarity with LIMS and SAP. The position offers 12-hour rotating shifts and comprehensive benefits.

Qualifications

• Bachelor's degree preferred but can be offset by experience.
• 3-5 years' experience in pharmaceutical/biotech industry.
• Excellent writing and oral communication skills.

Responsabilités

• Perform real-time review of manufacturing batch records.
• Review manufacturing documentation (logs, charts) for compliance.
• Resolve issues on the manufacturing floor in a timely manner.
• Provide 24/7 manufacturing oversight with 12-hour shifts.

Connaissances

Accuracy

Documentation

Communication

Writing skills

Formation

Bachelor's degree preferred

Outils

LIMS

SAP

Description du poste

Job Description ADMA Biologics is a biopharmaceutical company relentlessly committed to creating superior products for immunodeficient patients at risk for infection. It is our devotion to this underserved population that fuels us and our hands on approach to production and development that sets us apart. If you are looking for a dynamic, innovative, growing company in the biopharmaceutical industry that is committed to excellence and integrity, then consider ADMA Biologics. We currently have an exciting opportunity available for a Specialist QA II Manufacturing Oversight in Boca Raton, FL!

Job Description ADMA Biologics is a biopharmaceutical company relentlessly committed to creating superior products for immunodeficient patients at risk for infection. It is our devotion to this underserved population that fuels us and our hands on approach to production and development that sets us apart. If you are looking for a dynamic, innovative, growing company in the biopharmaceutical industry that is committed to excellence and integrity, then consider ADMA Biologics. We currently have an exciting opportunity available for a Specialist QA II Manufacturing Oversight in Boca Raton, FL! Job Title: Specialist QA II Manufacturing Oversight Position Summary The QA Specialist II - Manufacturing Oversight will perform manufacturing oversight activities to ensure compliance with policies and procedures. Oversight activities include, but are not limited to, real-time manufacturing batch record review, review of manufacturing documentation (logs, charts, etc.), and resolution of issues on the manufacturing floor. The QA Specialists team provides 24/7 manufacturing oversight coverage. Specialists are required to work 12-hour shifts (07:00 AM to 07:00 PM or 07:00 PM to 07:00 AM).

Job Title:

Specialist QA II Manufacturing Oversight

Job Description:

Position Summary

The QA Specialist II - Manufacturing Oversight will perform manufacturing oversight activities to ensure compliance with policies and procedures. Oversight activities include, but are not limited to, real-time manufacturing batch record review, review of manufacturing documentation (logs, charts, etc.), and resolution of issues on the manufacturing floor.

The QA Specialists team provides 24/7 manufacturing oversight coverage. Specialists are required to work 12-hour shifts (07:00 AM to 07:00 PM or 07:00 PM to 07:00 AM).

Essential Functions (ES) And Responsibilities

• Possess and understanding of processes such as Quality Systems (e.g., Deviations, Corrective and Preventive Action reports {CAPAs}, Change Controls, and Out of Specifications {OOSs}).
• Perform Quality Assurance review and approval of Deviation Reports.
• Possess an understanding cGMP and regulatory compliance as defined in government regulations such as 21 CFR Parts 11, 210, 211, and 600.
• Perform oversight and inspections of active production areas to resolve problems and to ensure compliance with SOPs and policies.
• Perform general oversight of Buildings 1 and 2 (including cold rooms/freezers) and their associated activities, as required.
• Review and release of Plasma pools to manufacturing.
• Review all manufacturing support documentation (logbooks, log sheets, charts, etc.)
• Review and release of raw materials in LIMS/SAP.
• Perform audits of Nitrogen receipt process.
• Perform notification and disposition of associated Lookback units.
• Assist with quarantining and release of critical systems, equipment, and controlled environments.
• Write, review, and revise QA SOPs.
• Review SOPs and documents from other departments and provide feedback as necessary.
• Work with other departments to assess if Deviations, CAPAs, and Change Controls are required.
• Assist with training of new employees.
• Coordinate and perform any additional activities or projects assigned by QA Management.

Experience With LIMS And SAP Preferred.

Job Responsibilities or Job Requirements

Competencies

Exceptional Organizational And Communication Skills Required

• Must have excellent writing and oral skills

Experience Requirements

• Education Requirements: Bachelor's Degree preferred but can be offset by experience.
• Experience Requirements: 3-5 years' experience in pharmaceutical or biotechnology industry or other related industry.

Preferred Experience

Compliance Requirements (ES)

The minimum compliance expectation for this role entails strict adherence to FDA regulations and company policies governing sales and marketing activities. This includes completion of required compliance training, accurate documentation of sales interactions, and adherence to data privacy regulations. Additionally, the role requires proactive participation in compliance reviews, prompt reporting of any potential issues, and ongoing education to stay updated on relevant FDA regulations.

Job Description Footer:

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 Insurance
• 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

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.