Job Information
Mallinckrodt Pharmaceuticals Quality Control Manager in Baton Rouge, Louisiana
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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Mallinckrodt is a global specialty p harmaceutical business that develops, manufactures, markets and distributes specialty pharmaceutical products. Areas of focus include therapeutic drugs for autoimmune and rare disease specialty areas like neurology, rheumatology, nephrology, ophthalmology and pulmonology; immunotherapy and neonatal respiratory critical care therapies; and analgesics and central nervous system drugs. The company's core strengths include the acquisition and management of highly regulated raw materials; deep regulatory expertise; and specialized chemistry, formulation and manufacturing capabilities. The company's Specialty Brands segment includes branded medicines; its Specialty Generics segment includes specialty generic drugs, active pharmaceutical ingredients and external manufacturing.
To learn more about Mallinckrodt, visit www.mallinckrodt.com.
Mallinckrodt Pharmaceuticals (“the Company”) maintains a continuing policy of non-discrimination in employment. The Company is an equal opportunity employer and complies with all applicable laws prohibiting discrimination based upon age, ancestry, color, religious creed (including religious dress and grooming practices), disability (mental and physical), marital status, medical condition, genetic information, military and veteran status, national origin (including language use restrictions), political activities or affiliation, race, sex (including pregnancy, child birth, breastfeeding and medical conditions related to pregnancy, child birth or breastfeeding), gender, gender identity and gender expression, sexual orientation, as well as any other category protected by law. Furthermore, it is our policy to provide equal opportunity to individuals with disabilities and protected veterans in all phases of the employment process and in compliance with applicable federal, state, and local laws and regulations on every location in which the company has facilities. This policy of non-discrimination shall include, but not be limited to, the following employment decisions and practices: recruiting, hiring; promotions; demotions or transfers; layoffs; recalls; terminations; rates of pay or other forms of compensation; selection for training, including apprenticeship; and recruitment or recruitment advertising.
Mallinckrodt Pharmaceuticals is required to report certain payments or transfers of value (such as expense reimbursement, meals, transportation) made to U.S.-licensed healthcare professionals in compliance with the federal Physician Payment Sunshine Act (i.e. Open Payments) and certain state laws.