Quality Control Manager, PCT

WuXi Biologics; Cranbury Township (NJ); On-site; USD 73,000 - 128,000; Full time

Job summary

WuXi Biologics is seeking a Quality Control Manager in Cranbury, NJ, responsible for leading the QC Physiochemistry team. This role involves ensuring compliance with regulatory standards, driving continuous improvement, and supervising team members. Candidates should have over 7 years of QC experience in biopharmaceuticals and exceptional analytical and leadership skills. The position offers a salary range of $73,000 - $128,000 based on experience and expertise. A Bachelor's degree is required; a Master's degree is preferred.

Qualifications

• 7+ years of QC experience in the pharmaceutical or biopharmaceutical industry.
• Strong working knowledge of QC operations for biologics.
• Proven capability to balance strategic planning and hands-on execution.

Responsibilities

• Provide leadership and oversight for daily QC Physiochemistry operations.
• Ensure testing activities comply with cGMP, GLP, CFR, and internal SOPs.
• Supervise, mentor, and develop QC staff; conduct performance management activities.

Skills

QC experience

Regulatory knowledge

Leadership

Analytical skills

Communication

Education

Bachelor’s degree

Master’s degree

Tools

HPLC/UPLC

Capillary Electrophoresis

LIMS

Empower

Job description

Position title

Quality Control Manager, PCT

Work location

Cranbury, NJ (onsite 5 days a week). Laboratory and office-based role

Job Summary

The QC Physiochemistry Lead is responsible for the strategic and operational leadership of physiochemical testing in support of clinical and commercial biologics manufacturing. This role oversees method execution, data integrity, investigations, and continuous improvement while managing and developing a high‑performing QC team. The position serves as a key scientific and quality partner to Manufacturing, QA, Regulatory, and Client Program teams.

Responsibilities

• QC Operations & Compliance:
• Provide leadership and oversight for daily QC Physiochemistry operations.
• Ensure all testing activities are conducted in compliance with cGMP, GLP, CFR, and internal SOPs.
• Lead and oversee data review, investigations, deviations, and CAPAs.
• Serve as site Subject Matter Expert (SME) for physiochemical testing and related investigations.
• Review and approve laboratory documentation, including notebooks, worksheets, protocols, and final reports.

• Continuous Improvement & Risk Management:
• Drive continuous improvement of QC processes, efficiency, and right‑first‑time execution.
• Identify and mitigate risks related to method performance, capacity, and compliance.
• Support site readiness for regulatory inspections and client audits.

• People & Resource Management:
• Supervise, mentor, and develop QC staff; conduct performance management activities.
• Ensure appropriate training and qualification of personnel.
• Promote a culture of quality, accountability, and scientific excellence.

• Client & Cross‑Functional Support:
• Serve as QC lead or key contributor in client meetings related to testing, deviations, or investigations.
• Partner with QA and Regulatory teams to support filings and responses.
• Communicate effectively with Manufacturing and Technical teams to ensure timely testing support.

Qualifications

• 7+ years of QC experience in the pharmaceutical or biopharmaceutical industry with a Bachelor’s degree
• 5+ years with a Master’s degree
• Proven experience supporting clinical and/or commercial manufacturing environments
• Strong working knowledge of QC operations for biologics, including method execution, data review, and laboratory compliance.
• In‑depth understanding of global regulatory requirements and guidance, including cGMP, FDA, EMA, ICH, and major pharmacopeias.
• Experience supporting IND, BLA, and post‑approval regulatory filings.
• Demonstrated competency in investigations, root cause analysis, and CAPA.
• Ability to analyze complex data sets and make sound, risk‑based decisions.
• Proven capability to balance strategic planning and hands‑on execution.
• Excellent written and verbal communication skills.
• Strong organizational skills with the ability to manage competing priorities.
• Comfortable working in a fast‑paced, client‑facing environment.
• Flexibility to support some evening or global conference calls.

Technical Expertise

• Strong scientific understanding of protein and biologics analytical methods, including but not limited to:
• HPLC/UPLC
• Capillary Electrophoresis (CE‑SDS, icIEF)
• Identity methods
• Protein Concentration methods
• Proficiency in the use and oversight of advanced analytical instrumentation and laboratory systems such as LIMS, Empower, etc.
• Ability to critically evaluate method performance, trends, and assay suitability

Leadership and Collaboration

• Demonstrated people-management experience in a QC or biomanufacturing environment.
• Ability to coach, develop, and engage scientific staff.
• Strong cross‑functional collaboration skills across QC, QA, Manufacturing, MSAT, Regulatory, and Client teams.
• Ability to communicate clearly with internal stakeholders and external clients.

The anticipated salary range for this position is $73,000 - $128,000.

The job description does not intend to list all the duties and responsibilities assigned to this position. Employee holding this position would be required to perform other job‑related duties/responsibilities based on their expertise and company business needs.