Sr Manager - Quality Testing

Mallinckrodt Pharmaceuticals; St. Louis (MO); On-site; USD 100,000 - 130,000; Full time

Job summary

A leading pharmaceutical company seeks a Sr Manager for Quality Testing in St. Louis. This role involves managing product testing and compliance activities, ensuring adherence to cGMP standards, and leading a team to enhance quality processes. The ideal candidate will have extensive experience in quality management and a strong understanding of pharmaceutical regulations. Join a dynamic team committed to quality and excellence in a fast-paced environment.

Qualifications

• Minimum 15 years experience in Quality with 10 years management experience.
• Complete knowledge of pharmaceutical regulations including GXP, GLP, GMP.

Responsibilities

• Manage key product and stability testing groups and compliance activities.
• Provide overall leadership to QC groups regarding cGMP compliance improvement.
• Serve as the Subject Matter Expert during compliance audits.

Skills

Leadership

Communication

Problem Solving

Education

BS in Chemistry

Chemical Engineering

Tools

Six Sigma

Lean Manufacturing

Job description

Job Title

Sr Manager - Quality Testing

Requisition

JR000014963 Sr Manager - Quality Testing (Open)

Location

St. Louis, MO

Additional Locations

Job Description Summary

Manage key product and stability testing groups and compliance activities to achieve site and corporate objectives. Specifically, this position will oversee 24/7 in-process laboratory testing, data release of raw materials, intermediates, stability, and finished product for the St. Louis and Greenville Plants, as well as the microbiological Center of Excellence supporting SpecGx. Additionally, this position will provide overall Quality Control (QC) leadership regarding (current Good Manufacturing Practices) cGMP compliance concerns and improvement for the Generics Business.

Job Description

ESSENTIAL FUNCTIONS:

• Ensure key turnaround timelines for customer service and compliance requirements are achieved
• Manage stability testing to achieve 100% on-time analysis for all stability protocol testing intervals
• Serve as the primary liaison for method transfers into the QC organization
• Accomplishes results through subordinate managers, supervisors, exempt specialist employees and non-exempt employees.
• Provide overall leadership to QC groups regarding cGMP compliance improvement and enhancement
• Serve as the Subject Matter Expert during compliance audits
• Study and improve various Quality processes through increased efficiency or process flow using Lean Manufacturingand/ or Six Sigma philosophy of operation
• Drive Quality consistency through revising or combining various analytical methods to ensure adequacy and quality with special emphasis on actual utility of methods under normal QC conditions
• Work with all Quality managers, supervisors and analysts toaddress any laboratory concerns regarding safety, methods, procedures, or operation
• Act as a liaison between the labs and manufacturing/ R&D in implementing special projects,production campaigns, or assist with validations or method transfers
• Works with various reports and QC groups to ensure compliance to Environmental Health and Safety and departmental safety requirements and provide proactive leadership toward continuous improvement of safety operations in our laboratories
• Ensure compliance with and oversee compendia affairs for SpecGx

MINIMUM REQUIREMENTS:

Education:

BS in Chemistry, Chemical Engineering, related science or equivalent combination of education, experience, and competencies.

Experience:

Minimum of 15 years related experience in Quality with 10 years management experience required. Proven personnel and project management history. Complete knowledge of pharmaceutical regulations including current GXP, GLP, or GMP requirements.

Preferred Skills/Qualifications:

• Excellent communication and leadership skills.
• Ability to work in and promote a team environment.
• Working knowledge of Six Sigma and/or Lean manufacturing tools.
• Complete understanding and application of principles, concepts, practices, and standards within discipline.
• Ability to lead and influence people.
• Understanding of basic statistical principles, expert knowledge of validation principles, techniques, and regulatory expectations.
• Knowledge of US and International pharmaceutical manufacturing regulations.

Other Skills:

• Exercises considerable latitude in determining technical objectives of assignment
• Completed work is reviewed for desired results from a relatively long-term perspective
• Bias toward change, management of change, and achievement of results

COMPETENCIES:

Decision Quality, Developing Direct Reports, Managing Diversity, Learning on the Fly, Managerial Courage, Organizing, Priority Setting, Problem Solving, Building Effective Teams

RELATIONSHIP WITH OTHERS:

Reports to the Sr Director, Quality and Regulatory Affairs. Manages group of exempt direct reports. Develops strategic objectives for groups managed. Contact with FDA as subject matter expert during site inspections. Regular contacts including Logistics, Marketing, R&D, Site Production Leaders, HSE, and DEA.

WORKING CONDITIONS:

• 25% Laboratory exposure to plant products, solvents, reagents, some of which are hazardous or potent compounds
• 75% Office environment which requires sitting for long periods of time and computer use.

DISCLAIMER:

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills require