Abzena

Sr Quality Systems Associate

Abzena  •  Bristol, PA (Onsite)  •  3 months ago
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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 Sr. Associate, Quality Systems supports and maintains GMP compliance by providing oversight and execution within key Quality Systems, including Deviations, CAPAs, Change Controls, Laboratory Investigations, Risk Management, Equipment Compliance, and Method Qualification. This role leads and supports cross-functional investigations, ensures timely and compliant documentation, and partners with internal teams to drive continuous Quality System improvement. The position works closely with Manufacturing, QC, Analytical Development, and other functions to promote a proactive quality culture and operational excellence.

Responsibilities

  • Provides oversight and ownership of assigned Quality Systems, including Deviations, CAPAs, Change Controls, Laboratory Investigations, and Risk Management.
  • Leads and supports cross-functional investigations to identify root cause, assess impact, and define effective corrective and preventive actions.
  • Develops new Quality Systems and improves existing systems to enhance compliance, efficiency, and program effectiveness.
  • Generates and assesses monthly, quarterly, and annual Quality System metrics to monitor performance against key performance indicators (KPIs), identify trends, and drive continuous improvement.
  • Manages initiation, execution, review, approval, tracking, and trending of assigned Quality System records to ensure compliance and timely closure.
  • Performs QA review and approval of method qualification protocols and reports, method revisions, Certificates of Analysis, and other QC/Analytical Development documentation.
  • Supports GMP equipment onboarding and qualification through QA review and alignment with internal requirements.
  • Conducts QA review and approval of GMP documents and quality records for accuracy, completeness, clarity, and procedural compliance.
  • Collaborates with Manufacturing, QC, Analytical Development, Engineering, and other groups to support a proactive quality culture and continuous improvement.
  • Contributes to site quality initiatives, operational efficiency projects, and activities related to technology transfer and commercialization.
  • Assists other Quality groups as needed, including document control, training, audits, batch disposition, and manufacturing QA support.
  • Communicates effectively with supervisors, colleagues, and teams.
  • Participates as a team member in all aspects of Abzena’s business.
  • Adheres to regulatory and Abzena quality standards, policies, procedures, and mission.
  • Maintain the highest ethical and moral standards

Qualifications

  • Bachelor's degree in science or engineering or equivalent with 5-8 years of relevant experience in the Pharmaceutical, Biologic, Biotechnology, or Medical Device space.
  • Relevant experience as in Quality Assurance, Quality Systems, Quality Compliance, Quality Control, GMP manufacturing and testing.
  • Experienced in leading Root Cause Analysis investigations, developing corrective actions, and performing risk assessments.
  • Experienced in early-phase to commercial quality systems development and maintenance.
  • Adequate knowledge of industry standards and regulation requirements for biologics and small molecules in clinical development and commercial.
  • Adequate knowledge of GMP regulations (e.g. US, EU, and ROW), good documentation practices, cGMP, 21CFR Part 210 and 211, USP and other applicable regulations, standards, and guidance.
FLSA: 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.     
Abzena

About Abzena

Abzena is the leading end-to-end bioconjugate, ADC, and complex biologics CDMO + CRO. From discovery through commercial launch, we support customers with fully integrated programs or individual services designed to de-risk and streamline the development of new treatments for patients in need. With the ability to tailor its strategy and customer experience to each project, Abzena develops and implements innovative solutions that enable biotech and biopharma companies to realize the full potential of their molecule and move medicines forward faster. The company has research, development, and cGMP facilities across locations in San Diego, CA, Bristol, PA, and Cambridge, UK.

Industry
Chemicals & Materials
Company Size
201-500 employees
Headquarters
San Diego, California
Year Founded
2001
Website
abzena.com
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