CMDO QA Supervisor

Germer International; Madison (WI); On-site; USD 80,000 - 100,000; Full time

Job summary

A leading compliance solutions provider in Madison, Wisconsin, is looking for a CMDO QA Supervisor. The role includes overseeing quality systems to ensure the integrity of data generated throughout the product development process. Key responsibilities involve releasing materials, organizing documentation, and collaborating with regulatory affairs. Candidates should have a Bachelor's degree and at least 5 years of relevant experience in quality assurance, with strong knowledge of FDA compliance and continuous improvement practices.

Qualifications

• 5+ years in material release and product development.
• Experience with validation and quality agreements.
• Knowledge of cGMP and FDA compliance.

Responsibilities

• Release raw materials and products for the CDMO business.
• Organize documentation and procedures for compliance.
• Collaborate on regulatory dossier preparation.
• Track and coordinate customer inquiries related to quality.
• Participate in audits and address findings.

Skills

Material release

Product development

Validation

Test method development

Quality agreements

Change controls

Continuous improvement

Education

Bachelor’s Degree

Job description

The CMDO QA Supervisor is responsible for developing, implementing and maintaining the Quality System to support the integrity and compliance of all data generated from process development, engineering batch production, clinical trials, etc. for registration filings before product process validation and related document review. This position is also responsible for development and implementation of a program and related processes for responding to customer inquiries about quality related technical or regulatory compliance for all Company products and services.

This position is 100% onsite.

Responsibilities include

• Release raw materials, products (process development batches, engineering batches, clinical trial batches) and GLP test activities to support the CDMO business.
• Organize the establishment/maintenance of relevant procedures/documents
• Support specification development for CDMO projects.
• Work in collaboration with customers and the CDMO/Regulatory Affairs departments, assist with the preparation of regulatory dossiers supporting CDMO projects.
• Provide direction and advice on the application of quality requirements to CDMO projects.
• Writes CDMO project related Quality Agreements and verifies the Company is compliant with the approved Quality Agreements (including customer notifications) supporting CDMO projects where necessary.
• Responsible for tracking and coordinating responses to all customer communications/inquiries.
• Responsible for continuous improvement of cGMP Quality Systems to support CDMO projects in compliance with FDA, ICH, USDA, ISPE and other pertinent pharma industry requirements.
• Compiles and communicates metrics associated with CDMO projects to management as required.
• Participates in audits and addresses audit findings where necessary.
• Performs CDMO product release and shipping documentation review/approval.

Job Requirements and Qualifications

• Education: Bachelor’s Degree
• Experience
  • Required: 5+ years Material release, product development and validation, test method development and validation, approval of investigations, quality agreement and change controls.
  • Preferred: 10+ years, all of the above plus biologics, drug substances and DMF’s.