Quality Systems Lead - Chemical Manufacturing

The Bergaila Companies

$80K — $110K *
Manufacturing & Automotive
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • 5+ years in chemical manufacturing quality management
  • Strong knowledge of GMP standards
  • Leadership in conducting internal and external audits
  • Expertise in validation protocols and risk assessments
  • Excellent problem-solving and analytical skills
  • Ability to develop and maintain quality management systems
  • Effective communication and team collaboration skills

Responsibilities

  • Spearhead quality systems in a manufacturing setting
  • Manage and conduct internal and external audits
  • Drive continuous improvement initiatives
  • Develop and implement quality management protocols
  • Analyze data for root cause analysis and problem-solving
  • Collaborate with teams to meet certification standards
  • Maintain documentation and manage KPIs for quality metrics

Benefits

  • Opportunity to influence quality standards in the manufacturing industry
  • Engagement in a fast-paced environment committed to safety and compliance
  • Chance to lead and enhance quality initiatives across teams
  • Onsite role fostering workplace relationships and teamwork
  • Support for occasional travel for audits and training activities
Full Job Description
Join a Leading Chemical Manufacturing Company as a QA Lead Coordinator in Port Neches, TX

Are you an experienced quality professional passionate about ensuring product safety, regulatory compliance, and continuous improvement? We are seeking a dynamic QA Lead Coordinator to spearhead quality systems, manage audits, and drive excellence at our Port Neches facility. This pivotal role offers the opportunity to influence quality standards in a fast-paced manufacturing environment committed to top-tier safety and compliance. If you thrive on leadership, process optimization, and maintaining the highest certification standards, this is your chance to make a significant impact.

What You'll Need to Succeed:

  • Proven experience in chemical manufacturing quality management.
  • Strong knowledge of GMP standards and familiarity with certifications such as ISO 9001, BRCGS, FSSC22000, EXCiPACT, Kosher, Halal, and RSPO.
  • Demonstrated leadership in managing and conducting internal and external audits.
  • Expertise in validation protocols, risk assessments (FMEA, HACCP), and validation master plans.
  • Excellent analytical, problem-solving, and root cause analysis skills.
  • Ability to develop, implement, and maintain quality management systems.
  • Effective communication skills to lead committees, deliver training, and collaborate across teams.
  • Proficiency in managing documentation, KPIs, and continuous improvement initiatives.

Nice to Have Skills:

  • Prior experience leading pharmaceutical certification projects (e.g., Pharma/EXCiPACT).
  • Familiarity with FDA regulations, specifically the Foreign Supplier Verification Program.
  • Experience with 5S programs and process mapping.
  • Ability to manage budgets and process invoices efficiently.

Preferred Education and Experience:

  • Bachelor's degree in Quality Assurance, Chemistry, Engineering, or a related field.
  • 5+ years of quality management experience in the chemical manufacturing sector.
  • Certification in quality or food safety management (e.g., Lead Auditor, CQE) is a plus.

Other Requirements:

  • Onsite presence in Port Neches, TX; local candidates strongly encouraged.
  • Ability to support occasional travel or on-site activities as needed.
  • Must be capable of managing multiple projects, audits, and cross-functional teams.
  • A proactive mindset committed to continuous improvement and compliance.

Take the next step in your career by bringing your expertise to a company dedicated to quality and safety excellence. Apply now and help shape the future of our manufacturing operations!

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