QA Lead Coordinator

QA Lead Coordinator at The Bergaila Companies QA Lead Coordinator at The Bergaila Companies in DEER PARK, Texas Posted in 1 day ago.

Type:

full-time

Job Description:

Join Our Team as a QA Lead Coordinator - Drive Quality and Safety Excellence! Are you passionate about ensuring top-tier quality and safety standards in the manufacturing sector? We are seeking a highly motivated and experienced QA Lead Coordinator to lead our quality assurance programs across multiple sites. This pivotal role offers the chance to influence regulatory compliance, implement industry best practices, and uphold the integrity of our products and processes. If you thrive in a dynamic environment and possess a strong background in GMP standards, ISO certifications, and audit management, this opportunity is for you! What You'll Bring to the Table -

Required Skills:

Extensive experience in chemical manufacturing or related industries. Proven expertise in GMP requirements and ISO standards (ISO 9001, ISO 22000, FSSC 22000, etc.). Strong knowledge of Good Manufacturing Practices (GMP), GFSI, and related regulations. Skilled in leading both internal and external audits with familiarity in audit scope, planning, and reporting. Ability to manage and continuously improve Quality Management Systems (QMS). Bachelor's degree in chemistry or a closely related field. Demonstrated leadership in managing QA programs and cross-functional teams. Excellent analytical, problem-solving, and decision-making skills. Effective communication skills to engage with teams, suppliers, and regulatory bodies. Nice to

Have Skills:

Experience with additional certifications such as EFfCI, RC14001, Kosher, or Halal. Familiarity with risk assessment tools like FMEA and HACCP. Knowledge of validation protocols and revalidation processes. Prior experience managing compliance across multiple sites.

Preferred Education and Experience:

Bachelor's degree in Chemistry, Food Science, or related discipline. Minimum of 5 years of experience in QA leadership roles within manufacturing settings. Track record of managing audits, certifications, and regulatory compliance in a fast-paced environment.

Other Requirements:

Ability to work primarily in Pasadena, TX, with flexibility to support Dayton site as needed. Valid certifications in GMP, ISO, and industry-specific standards are advantageous. Willingness to participate in site audits, training sessions, and continuous improvement initiatives. Commitment to maintaining a safe, compliant, and quality-driven workplace. Ready to make a measurable impact in quality assurance? If you're skilled, driven, and eager to uphold excellence in manufacturing quality and safety, we want to hear from you! Apply now and help shape the future of quality standards at our organization.