Job Snapshot
Location:
Kansas City, MO
Base Pay:
$60,000 - $65,000 /Year
Industry:
Pharmaceutical
Consumer Products
Manufacturing
Job Type:
Science
QA - Quality Control
Manufacturing
Experience:
At least 3 year(s)
Contact Information
Description
Quality Compliance Manager
Labtech is a highly specialized recruiting firm that concentrates our efforts primarily on the placement of scientific professionals. We serve clients in the clinical, pharmaceutical, food & beverage and medical industries, to name a few. We have been in business for nearly 15 years and have established a reputation for providing high-caliber candidates in the industries that we serve. Our client base is diverse and strong, and provides our candidates with a wide array of opportunities within multiple scientific disciplines. We are currently seeking candidates for this direct hire position as a Quality Compliance Manager in an manufacturing environment.
Job Summary:
Responsible for managing the quality systems to ensure Regulatory Compliance and associated procedures, compliance training, documentation and internal auditing are conforming to FDA/cGMP and industry-specific requirements.
Job Responsibilities:
- Build a culture of cGMP compliance and quality by implementing operational excellence and quality management programs.
- Develop and maintain a site SOP and documentation system.
- Define and implement site compliance quality training plan and ensure a process for documentation and compliance quality training.
- Responsible for FDA drug submissions and annual registrations for new and modified OTC products.
- Ensure facility plans are in place for receiving inspectors (FDA, Weights & Measures, Kosher) and managing external audits.
- Responsible for roles and responsibilities of all site personnel in conducting FDA visits and external inspections.
- Participate in decisions regarding out-of-specification matters and review results of corrective/preventive action plans to ensure cGMP compliance.
- Ensure establishment of a change control procedure.
- Establish site cross-functional internal audit teams, document adverse findings, develop corrective action plans and follow-up to ensure compliance.
- Collaborate with Marketing and R&D in developing new product plans that ensure new products are of high quality and readily manufacturable with appropriate clinical research and stability studies to ensure safety and effectiveness.
- Maintain awareness of current FDA matters and provide regulatory opinion through the use of external consultants and trade associations.
Requirements
Requirements for Quality Compliance Manager:
- BS in Chemistry, Engineering or technical field
- 3-5 years of Quality Leadership experience in pharmaceutical, cosmetic or consumer products industries
- Familiarity with OTC drug submissions and FDA site visits/inspections
- Familiarity with cGMP (CFR 21 - Parts 210 & 211) and CTFA guidelines.
- Ability to create and deliver cGMP compliance and quality training.
Check out our other openings at www.jobsforscientists.com!
Keywords: Quality Compliance, pharmaceutical, cosmetic, personal care, PCPC, CTFA, FDA, cGMP, Chemistry
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