Senior Quality Specialist

Katalyst HealthCares and Life Sciences

$100K — $120K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • BA or BS degree in engineering, life, or natural sciences preferred.
  • 10+ years' experience in Quality Assurance/Quality Control in regulated environments.
  • In-depth knowledge of quality systems like ISO 9000, GMP, and HACCP.
  • Detail-oriented with a strong focus on quality standards.
  • Proven analytical and problem-solving skills.
  • Excellent written and verbal communication abilities.

Responsibilities

  • Lead quality assurance for external manufacturing and supplier activities.
  • Collaborate with Supply teams to ensure compliance with quality requirements.
  • Prepare quality documentation for new product launches and existing product changes.
  • Conduct quality risk assessments for external manufacturing operations.
  • Represent quality during trials and validation at external manufacturers.
  • Schedule and execute audits of external manufacturers to ensure compliance with quality management systems.
  • Ensure timely closure of audit findings and monitor CAPA development.

Benefits

  • Opportunity to work in a strategic, fast-paced environment.
  • Intermittent travel to the Midwest and East Coast.
  • Engagement with cross-functional teams and leadership.
  • Professional development and continuous improvement opportunities.
Full Job Description
Summary :

This Senior Quality Specialist will be responsible for ensuring that NA products manufactured at third party contract sites comply with all the applicable regulations as well as with our corporate quality standards during their whole life cycle. This professional will interface with several areas and will work closely with the Supply teams providing guidance on the quality requirements for the qualification and maintenance of new, existing external manufacturers and suppliers. The role would support continuous improvement efforts at existing manufacturing sites.
Roles & Responsibilities :
  • Provide quality lead for all external manufacturing related activities and suppliers, the resolution of investigations, questions or complaints, and ensuring end-to-end success of projects and products.
  • Partner with the Supply teams in assuring that the stages of the development process comply with all our Quality corporate requirements
  • Analyze and prepare Quality documentation for the launch of new products and for the change of the existing ones, such as technical manuals, technical agreements and good for sale certificates.
  • Perform Quality risk assessments for new and existing external manufacturing operations.
  • Act as Quality representative during trials and validation activities at external manufacturers.
  • Lead the scheduling, execution, reporting and tracking of onsite audits of external manufacturers and suppliers to confirm that these operations are performed in compliance with EH's Global QMS and meet all relevant regulatory requirements.
  • Maintain quality system processes and establish a supplier qualification program (such as Change Control, Supplier Management, Deviations and Investigations, CAPA, and others as needed).
  • Track audit findings for suppliers to completion and ensure timely closure of audit reports and ensure adequate CAPAs are developed by external manufacturers, suppliers and monitor their closures.
  • Analyze errors and deviation from process and procedures, hold key stakeholders accountable, and provide guidance on key actions and steps required to correct deviations.
  • Interfaces with Supply and Procurement leadership for escalation of quality issues.

Required Qualifications :
  • Minimum of a BA or BS degree, preferably in engineering, life, or natural sciences.
  • Experienced in quality systems, such as ISO 9000, GMP, HACCP, and Auditing.
  • 10+ years' experience in Quality Assurance / Quality Control Systems in a regulated environment.
  • Must be quality-focused and detail-oriented.
  • Must possess a high level of strategic mindset, proactive ownership, initiative and adaptability necessary for a fast-paced and founder driven environment.
  • Must possess the competence to perform tasks requiring analytical and problem-solving skills.
  • Must demonstrate outstanding teamwork in interacting with other team members.
  • Excellent written and verbal communication skills, problem-solving, decision-making skills, and computer proficiency.
  • Experienced in Good Manufacturing Practices.
  • Experienced in quality systems, such as ISO 9000, GMP, HACCP, and Auditing.
  • Experience conducting audits including planning and follow-up on CAPAs resulting from the findings.
  • Travel required (approx. 20-30%), intermittent and planned, localized to Midwest and East Coast, and may likely go down over time.

Similar Jobs

More Jobs at Katalyst HealthCares and Life Sciences

More Pharmaceuticals & Biotech Jobs

Find similar Senior Quality Specialist jobs: