Quality Control Manager

Job Title

Quality Control Manager

Requisition

JR000014280 Quality Control Manager (Open)

Location

CC-Port Allen - USA502

Additional Locations

Baton Rouge, LA, Port Allen, LA

Job Description

We are seeking a leader with a passion for quality and innovation in the pharmaceutical industry. Join our team at the Port Allen manufacturing facility as a Quality Control (QC) Manager to lead the charge in ensuring the highest standards of quality and compliance.

Why Join Us?

• Dynamic Environment: Be at the forefront of quality control in a state-of-the-art facility.

• Leadership Opportunity: Mentor and develop a talented QC team.

• Impactful Work: Play a crucial role in ensuring the safety, purity, and functionality of our products.

Essential Functions:

• Quality Standards: Develop and implement rigorous standards, methods, and procedures for inspecting, testing, and evaluating materials and final products.

• Team Leadership: Manage and mentor the QC team, ensuring daily tasks and business needs are met.

• Method Validation: Lead method qualification, validation efforts, and method transfer activities.

• Data Analysis: Perform analyses, identify trends in inspection results, and recommend corrective actions.

• Equipment Supervision: Oversee QC testing equipment programs and data trending for annual product review reports.

• Project Management: Supervise projects, communicate progress, and ensure timelines are met.

• Regulatory Compliance: Represent the QC department during external audits and regulatory inspections.

• Cross-Functional Collaboration: Work closely with Quality Assurance, Regulatory Affairs, Materials Management, and Manufacturing departments.

• Budget Management: Assist with annual budget proposals and ensure compliance.

• Safe Work Environment: Maintain safe, clean, and orderly work areas.

Minimum Requirements:

• Bachelor's degree in a scientific discipline

• 6+ years of relevant Quality Control experience in a pharmaceutical, biotechnical, or medical device environment with GC, FTIR, and GMP

• 4+ years of QC supervisory experience

• Strong analytical skills and ability to exercise judgment in selecting methods and evaluation criteria

• Independence with efficient time management and organizational skills

• Proficiency in LIMS and technical analytical skills

• Extensive knowledge of laboratory analyzers and inspection equipment

Preferred Qualifications:

• Master's or PhD degree in a related field

• Quality certification (ASQ CQE, CQM, CQA, etc.)

• Lean Manufacturing experience

Competencies:

• Problem-Solving: Ownership mentality with effective problem-solving skills.

• Communication: Strong communication skills across organizational levels.

• Adaptability: Rapid skill acquisition through training and research.

• Leadership: Strong leadership and personnel development abilities.

• Technical Proficiency: Expertise in mathematics, computer literacy, process optimization, and mechanical aptitude.

Organizational Relationship:

Collaborate closely with QA/QC, Manufacturing, and Materials Management teams. Engage in cross-functional interactions to meet project and investigation requirements.

Join Us and Make a Difference!

If you are a motivated leader with a commitment to quality and excellence, we want to hear from you. Apply today to become part of our dedicated team at the Port Allen, LA facility.

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