QA Associate I/II, Operations - Shift B

Lever, Inc.; Bristol Township (Bucks County); On-site; USD 52,000 - 78,000; Full time

Job summary

Abzena is a leading biopharmaceutical CDMO providing end-to-end development and manufacturing services from concept to patient. The Associate I, Quality Operations delivers on-floor QA oversight for GMP manufacturing, ensuring procedures and cGMP standards are followed and supporting real-time issue resolution.

The role collaborates with Manufacturing, QC, and other Quality teams, performing batch record reviews and documentation support to ensure compliant product disposition and continuous

Qualifications

• Bachelor’s degree in science or engineering, or equivalent experience.
• 0-3+ years of relevant GMP-biopharmaceutical experience.

Responsibilities

• Provide on-floor QA oversight during GMP manufacturing.
• Participate in the QA walkthrough program to identify gaps in the GMP facility.
• Escalate quality issues and support real-time troubleshooting.
• Support batch disposition through documentation review.
• Review batch records, logbooks, and GMP documentation for completeness.
• Review incoming material disposition packets and verify documentation.
• Perform QA review of SOPs, forms, and controlled documents.
• Contribute to quality improvement and lean initiatives.
• Assist across Quality functions including document control, training, audits, and systems.
• Communicate effectively with cross-functional teams and uphold quality standards.

Skills

Attention to detail

Communication skills

Independent work

Education

Bachelors in science or engineering

Job description

With extensive experience in developing biologics and bioconjugates, we offer a seamless service delivered by fully integrated teams, from early discovery to commercial manufacturing.

Forward-thinking and committed, we find the best solution and use the right technologies to design, develop and manufacture your products to ensure we get vital medicines to patients quickly and safely.

We are dedicated to quality excellence. We are driven to get better treatments to market, efficiently and responsibly by reducing timelines and delivering the highest quality products and services.

We are Abzena. More than a CDMO, we are a responsible and dedicated partner that takes care of your products from concept to patient.

The Associate I, Quality Operations provides day‑to‑day QA oversight and documentation review to support GMP manufacturing of intermediates and drug substances. The role ensures production activities are executed in compliance with cGMP requirements through on‑floor QA presence, batch record review, and support of batch disposition. The position works closely with Manufacturing, QC, and other Quality functions to identify, escalte, and resolve issues in real time.

Responsibilities

• Provide on‑floor QA support during GMP manufacturing to ensure compliance with procedures and cGMP standards.
• Participate in the QA walkthrough program to identify potential gaps/issues in the GMP facility.
• Escalate quality issues promptly and support real‑time troubleshooting.
• Support batch disposition through compilation of required documentation.
• Review batch records, logbooks, and GMP documentation for completeness and.
• Review incoming material disposition packets and verify documentation completeness.
• Perform QA review of SOPs, forms, protocols, and other controlled documents.
• Contribute to quality improvement, lean initiatives, and process efficiency projects.
• Assist across Quality functions including document control, training, audits, and systems.
• Communicate effectively with cross‑functional teams and uphold company quality standards and policies.

Qualifications

• Bachelor’s degree in science or engineering, or equivalent experience.
• 0-3+ years of relevant experience in a GMP‑regulated biopharmaceutical environment.
• Working knowledge of GMP regulations (US, EU, ROW), GDP, 21 CFR, USP, and applicable standards.
• Strong attention to detail and effective written and verbal communication skills.
• Ability to work independently and cross functionally on common goals.

Physical Requirements

• Ability to stand for 1-2 hours at a time, sit for 2 to 3 hours at a time.
• Frequently lift and or move objects up to 30 pounds.
• Visual abilities including near and far sight, color, peripheral vision, depth and ability to focus.

FLSA: Non-Exempt

Abzena is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws.

This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, and training.