Senior Scientist I, Quality Control

WuXi Biologics; Cranbury Township (NJ); On-site; USD 110,000 - 150,000; Full time

Job summary

WuXi Biologics seeks a Senior Scientist I, QC Physiochemistry Lead, to lead physiochemical testing for clinical and commercial biologics. You will oversee method execution, data integrity, investigations, deviations, and CAPAs while developing a high-performing QC team.

This role partners with Manufacturing, QA, Regulatory, and Client Program teams. You will manage QC staff, ensure training and qualification, and drive continuous improvement in QC processes, supporting regulatory inspections and

Qualifications

• Minimum 3-5 years of hands on expereince with HPLC, CE, ICIEF.
• Minimum 1-2 years of previous management experience with direct reports.
• 3+ years of QC experience in the pharmaceutical or biopharmaceutical industry
• 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.

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 SME for physiochemical testing and related investigations.
• Review and approve laboratory documentation, including notebooks, worksheets, protocols, and final reports.

Skills

Leadership

Communication skills

Time management

Cross-functional collaboration

Problem solving

Tools

HPLC/UPLC

Capillary Electrophoresis (CE‑SDS, icIEF)

Identity methods

Protein Concentration methods

LIMS

Empower

Job description

Position title:

Senior Scientist l, QC 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

• Minimum 3-5 years of hands on expereince with HPLC, CE, ICIEF.
• Minimum 1-2 years of previous management experience with direct reports.
• 3+ years of QC experience in the pharmaceutical or biopharmaceutical industry
• 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 collaboaration skills across QC,QA, Manufacturing, MSAT, Regulatory, and Client teams.
• Abilitiy to communicate clearly with internal stakeholders and external clients.

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.