Job Title
Quality Control Manager
Requisition
JR000014846 Quality Control Manager (Open)
Location
Raleigh, NC
Additional Locations
Job Description Summary
SUMMARY OF POSITION:
The Quality Control Manager serves as a Quality Control technical resource to the plant. She/he is the primary point of contact for the testing of all raw materials, in-process, finished goods, and stability samples. She/he manages the Quality Control group and compliance activities to achieve key site and corporate objectives. This individual will provide overall QC leadership regarding cGMP compliance concerns and improvements, as well as manage budget line items, overtime, efficiency improvements, and staffing.
Job Description
ESSENTIAL FUNCTIONS:
- Manages the hiring, training, and performance management of all QC personnel.
- Provides subject matter assistance for LIMS, methods, testing, and validation.
- Manages QC testing group to achieve compliant testing in a timely manner.
- Manages Lab investigations and OOSs including remediation of potential compliance concerns.
- Provides overall leadership to QC group regarding cGMP compliance improvement and enhancement.
- Studies and improves various Quality processes providing increased efficiency or process flow using Lean Manufacturing and/ or Six Sigma philosophy of operation.
- Drives Quality consistency through reviewing/revising various analytical methods/SOPs to ensure adequacy with special emphasis on actual utility of methods under normal QC conditions.
- Works with plant Managers/Supervisors and Quality technicians to address any laboratory concerns regarding quality, safety, methods, procedures, or operations.
- Acts as a liaison between the lab and manufacturing/ R&D for investigations and to implement special projects, assist with validations, method transfers, or technology upgrades.
- Works with groups to ensure compliance to EHS and departmental safety requirements and provide proactive leadership toward continuous improvement of safety operations in the laboratory.
- Ensures key turnaround timelines for customer service and compliance requirements are achieved.
- Performs as a subject matter expert during customer and regulatory audits.
- Serves as an Internal Auditor for the site.
- Serves as LIMS Administrator
DEPARTMENT SPECIFIC/NON-ESSENTIAL FUNCTIONS:
- Develops and coaches to build talent.
- Participate in a 5S Workplace System to ensure good housekeeping and organization.
- Prioritizes and plans workload and team assignments to meet all internal and external customer needs for maximum efficiency and accuracy.
- Effectively trains others in a positive manner.
- Other duties as assigned with or without accommodation.
MINIMUM REQUIREMENTS:
Education:
B.S. /B.A. in Physical Science required.
Master’s Degree preferred.
Experience:
10 - 12 years related experience preferred; at least five years of experience in a supervisory role; strong knowledge of current pharmaceutical cGMP requirements
Preferred Skills/Qualifications:
Other Skills/Competencies:
Complete understanding and application of principles, concepts, practices, and standards for testing performed in all QC laboratories
Experience with testing API or Pharma products
Experience leading a group of up to 20 people with 24/7 shift operations
Excellent written and verbal communication and leadership skills
Ability to work in and promote a team environment
Working knowledge of Six Sigma and/or Lean manufacturing tools
Sense of urgency.
Action oriented/drives for results
Excellent communication and interpersonal skills
Team orientation/strong team player
Ability to coach, mentor and teach
Excellent decision making, problem solving and analytical skills
Strong managerial courage
Ability to influence change at all levels of the organization
Detail-oriented with the ability to work under tight deadlines
Excellent conflict management skills
Builds positive relationships with others
Excellent time management and prioritization skills
Excellent technical writing skills
LIMS experience preferred
Knows the difference between managing and leading and when to apply each
Command Skills, Action Oriented, Conflict Management, Customer Focus,
Problem Solving, Priority Setting, Written Communication,
RELATIONSHIP WITH OTHERS/ SCOPE:
- Reports to Manager, Plant Quality (Site Head of Quality)
- Work is performed without appreciable direction
- Develops strategic objectives for group managed
- 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
- Contact with FDA as subject matter expert during site inspections and customers during frequent customer audits
- Regular contacts include Quality Assurance, Materials Management, Logistics, Marketing, R&D, Site Production Leaders and EH&S.
- This position has several direct reports, such as Quality technicians and testing Engineers.
WORKING CONDITIONS:
- 60% normal office and meeting room conditions.
- 40% Laboratory and Plant environment including exposure to raw materials and finished products.
- Must be able wear the required Personal Protective Equipment (PPE) as deemed necessary by EH&S, leadership team, corporate, or safety guidelines.
- Some off shift and weekend work can be expected; travel requirements are minimal
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 required of employees assigned to this position.
Top Skills
What We Do
At Mallinckrodt, we use strategic vision and employee-driven momentum to pursue a powerful mission: Listening for needs and delivering solutions.
As a leader in specialty pharmaceuticals, we develop, manufacture, market and distribute innovative treatments for underserved patient populations within neurology, rheumatology, hepatology, nephrology, pulmonology, ophthalmology, and oncology; immunotherapy and neonatal respiratory critical care therapies; analgesics; cultured skin substitutes and gastrointestinal products. . Our expertise also extends into acute and critical care hospital products, as well as our broad portfolio of generic prescription medicines and active pharmaceutical ingredients.
Together, we’re helping shape the future of the specialty pharmaceuticals industry by leveraging the values our founders instilled over 155 years ago – quality, integrity and service.
To learn more about Mallinckrodt, visit www.mallinckrodt.com.
Equal Opportunity Employer
Mallinckrodt Pharmaceuticals provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, veteran status or genetics. In addition to federal law requirements, Mallinckrodt Pharmaceuticals complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.