QC Manager

Croda; Alabaster (AL); On-site; USD 110,000 - 170,000; Full time

Benefits offered by this job

Medical, Dental, Vision coverage

PTO

401K Match

Wellness Reimbursement

Parental Leave

Career Development

Life and AD&D Insurance

Short/Long-term Disability

Paid Holidays

Job summary

Croda is seeking a QC Manager - Raw Materials to provide strategic leadership for the Raw Material Release team within Quality Control. You will partner with the Head of Quality Control to oversee testing resources and ensure the timely, compliant release of GMP materials, while mentoring laboratory staff.

You will drive continuous improvement, regulatory compliance, and effective collaboration with Quality, Manufacturing, and Supply Chain to meet site goals and timelines.

Qualifications

• Bachelor's/Master's/PhD in Chemistry, Engineering, or related field.
• Eight+ years of experience in a pharmaceutical or biotechnology analytical laboratory.

Responsibilities

• Provide strategic leadership for QC Raw Material testing activities.
• Lead, mentor, and develop QC Analysts and laboratory personnel.
• Ensure GMP, data integrity, and regulatory compliance across the lab.
• Oversee investigations, CAPAs, and root-cause analysis for OOS/OOT events.
• Collaborate with QA, Manufacturing, Regulatory, and senior leadership.

Skills

Leadership

Project management

Data integrity

Analytical problem solving

Communication

Education

Bachelor's/Master's/PhD in Chemistry or Engineering

Tools

Word

Excel

Outlook

PowerPoint

Job description

QC Manager - Raw Materials

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.
• Generous PTO
• 401K Match
• Wellness Reimbursement
• Parental Leave
• Career Development
• Company paid and voluntary Life and AD&D Insurance
• Short and long term disability
• Paid Holidays

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.