Quality Systems Lead - Chemical Manufacturing

The Bergaila Companies"We put the unity in opportunity."

Quality Systems Lead - Chemical Manufacturing
QA/QC

QA/QC

Contract

May 11, 2026

Port Neches,Texas

• Compensation: $49.00/hour
• Location:
  
  Port Neches, TX
• Assignment Duration: 6 months+
• Work Schedule:
  
  Monday-Friday, hybrid, 40 hours +
• Benefits:
  Comprehensive with 401K, holidays and PTO

Join a dynamic team as a Quality Systems Lead in Chemical Manufacturing and play a pivotal role in ensuring the integrity, safety, and compliance of manufacturing processes. This is an exciting opportunity for a seasoned quality professional to lead validation strategies, oversee audits, and drive continuous improvement in a fast-paced, innovative environment. If you're passionate about quality assurance and ensuring product safety at the highest standards, this role offers the perfect platform to showcase your expertise and make a meaningful impact.

• Develop and manage the Validation Master Plan and related protocols to guarantee equipment, systems, and process validation.
• Lead internal and external audit programs, coordinating scope, objectives, and compliance efforts.
• Investigate non-conformities through root cause analysis and implement effective corrective actions.
• Maintain and improve the local Quality Management System, ensuring adherence to industry standards and certifications such as ISO, BRCGS, EXCiPACT, and FSSC
  22000.
• Oversee product safety practices, including risk assessments, cleaning validations, and Critical Control Point (CCP) validations.
• Drive continuous improvement by defining KPIs, updating documentation, and promoting a culture of quality and safety.
• Provide training and support across teams to foster a quality-centric environment.
• Manage budgets, process invoices, and support other QA activities to ensure seamless operations.

• Bachelor's degree in Chemistry or Chemical Engineering.
• 5-7 years of experience in environment compliance and quality assurance within manufacturing.
• Proven track record leading and conducting internal and external audits.
• Strong knowledge of GMP standards and industry certifications (EXCiPACT, FSSC
  22000, BRCGS, ISO 9001, etc.).
• Excellent problem-solving skills, including root cause analysis.
• Ability to develop, implement, and manage validation and quality protocols.
• Effective communication and training skills.
• Proficiency with Document Management Systems and KPI development.

• Experience with ISO 22716, ISO 14001, ISO 45001, RSPO, EFfCI, Kosher, Halal standards.
• Knowledge of product safety management authority and risk analysis.
• Prior experience in the chemical manufacturing industry or related sectors.
• Familiarity with regulatory compliance unrelated to GMP standards.

• Bachelor’s degree in a relevant science or engineering discipline.
• 5-7 years of experience specifically focused on quality systems, audits, and compliance in a manufacturing environment.

• Ability to work a full-time schedule Monday through Friday in a hybrid setting.
• Willingness to support the team with occasional travel or additional responsibilities as needed.
• Commitment to maintaining current quality certifications and seeking ongoing process improvements.