QC Manager

Croda Singapore; Alabaster (AL); On-site; USD 120,000 - 180,000; Full time

Benefits offered by this job

Medical, Dental, and Vision coverage

Wellness Reimbursement

Life Insurance

AD&D Insurance

Short and long-term disability

Job summary

Croda is seeking a QC Manager for Raw Materials to provide strategic leadership of the Raw Material Release team within Quality Control. You will guide staff, optimize workflows, and ensure GMP compliance while partnering with Quality, Manufacturing, Supply Chain, and senior leadership.

Responsibilities include strategic direction for QC testing, equipment maintenance, investigations, and regulatory readiness.

Qualifications

• Bachelor's, master's, or doctoral degree in Chemistry, Engineering, or a related discipline.
• Eight or more years of experience in a pharmaceutical or biotechnology analytical laboratory.

Responsibilities

• Lead the Raw Material Release team and oversee QC activities for GMP products.
• Manage calibration, maintenance, and qualification of analytical equipment; ensure data integrity.
• Drive investigations for OOS/OOT, deviations, and CAPAs with root-cause analysis and timely corrective actions.
• Support regulatory inspections and customer audits, serving as QC laboratory SME for compliance.

Skills

Analytical testing

Leadership

Data integrity

Regulatory compliance

Project management

Technical writing

Communication

Lab safety

Education

Chemistry/Engineering degree

Tools

MS Office

Job description

Croda is a global specialty chemical company focused on the research and development of novel and highly sustainable raw materials for the Life Sciences and Consumer Care sectors. We are passionate and excited about how we can develop and utilize new technologies to shape and inspire changes within an ever-growing marketplace. As our business looks to deliver its ambitious strategy of growth, we are looking for a QC Manager to join our team.

The Opportunity

The QC Manager - Raw Materials provides strategic leadership and operational oversight for the Raw Material Release team within Quality Control. Working closely with the Head of Quality Control, this role supports departmental strategy, business objectives, and key performance indicators.

This position manages analytical testing resources to support the timely, accurate, and compliant release of raw materials and in-process samples for GMP products. The manager leads, mentors, and develops laboratory personnel while guiding workforce planning, resource allocation, technical problem-solving, regulatory compliance, project tracking, and laboratory workflows.

The role also serves as a key liaison across Quality, Manufacturing, Supply Chain, and other business functions, maintaining clear communication about priorities, project status, and release timelines with cross-functional partners and senior leadership.

What Success Looks Like

Leadership and Team Development

• Establish strategic direction for Quality Control raw material testing activities.
• Build strong partnerships with QA, Manufacturing, MS/TS, Engineering, and Regulatory.
• Drive a culture of accountability, urgency, compliance, operational excellence, transparency, trust, and collaboration.
• Promote data-driven decision-making and continuous improvement.
• Set clear expectations for performance, ownership, and behavior.
• Lead team planning, prioritization, workload balancing, and resource allocation.
• Coach, performance manage, mentor, and develop QC Analysts.
• Establish quality objectives aligned with site business goals and customer requirements.

Laboratory Asset Management

• Ensure laboratory compliance with GMP and Data Integrity requirements.
• Conduct routine laboratory safety audits.
• Review laboratory performance metrics and trends.
• Drive continual improvement in the maintenance and operation of analytical equipment.
• Review and approve quality-impact assessments associated with laboratory equipment qualifications.
• Oversee calibration, preventive maintenance, work-order activities, and equipment readiness when product quality, validated state, or GMP compliance may be impacted.
• Partner with Quality Assurance and Engineering to ensure equipment remains in a qualified state.

QC Investigations Management

• Lead the creation and approval of investigational testing plans for OOS investigations, OOT investigations, analytical deviations, Data Integrity investigations, and QC laboratory CAPAs.
• Ensure investigations identify root cause, product impact, and effective corrective actions.
• Partner with Quality Assurance leadership to improve investigation cycle times, laboratory compliance performance, repeat OOS review, and right-first-time performance in QC laboratory operations.

Regulatory Compliance

• Support regulatory inspections and customer audits of the QC laboratory.
• Serve as the Quality Control subject matter expert for laboratory compliance activities.
• Maintain awareness of current regulations and industry standards for analytical testing.

Capabilities and Expertise

Education and Experience

• Bachelor's, master's, or doctoral degree in Chemistry, Engineering, or a related discipline.
• Eight or more years of experience in a pharmaceutical or biotechnology analytical laboratory.

Knowledge, Skills, and Abilities

• Demonstrated knowledge of analytical equipment, processes, and practices.
• Strong attention to detail, integrity, and reliability.
• Proficiency with Word, Excel, Outlook, and PowerPoint.
• Project management, organization, technical writing, and presentation skills.
• Technical problem-solving proficiency and the ability to troubleshoot time-sensitive challenges.
• Knowledge of and experience with safety and environmental compliance regulations.
• Excellent leadership and team-development skills.
• Excellent verbal and written communication skills.
• Ability to contribute actively to improvements in policies, practices, and procedures.
• Ability to interact and communicate effectively with customers and employees at all levels, including senior management.
• Leadership of QC Analysts and QC Laboratory Administrators

Why Join Croda?

The successful candidate will receive a competitive salary and benefits package including:

• Excellent Medical, Dental, and Vision coverage, available immediately.
• Wellness Reimbursement
• Company paid and voluntary Life and AD&D Insurance
• Short and long term disability

Equal Opportunity Employer

Croda recognizes employees as our strength, and the diversity they bring to our workforce is directly linked to our ongoing success. We are an equal opportunity employer and place a high value on diversity and inclusion. We do not discriminate on the basis of any protected attribute, including age, race, color, religion, national origin, gender, sexual orientation, gender identity, gender expression, marital or veteran status, pregnancy, disability, or any other basis protected under applicable law. In accordance with applicable law, we provide reasonable accommodations for applicants' and employees' religious practices and beliefs, as well as mental health or physical disability needs. Equal Opportunity Employer/Disability/Veterans. This organization participates in E-Verify.