Compounding QA/QC Lead - Pharma Compliance & Audits

VIDRINE PHARMACEUTICAL GROUP LLC; Lake Charles (LA); On-site; USD 75,000 - 85,000; Full time

Job summary

VIDRINE PHARMACEUTICAL GROUP LLC in Lake Charles, LA seeks a Compounding Pharmaceutical QA/QC professional to oversee QA across the compounding process, ensuring safety, efficacy, and regulatory compliance. The role collaborates with pharmacists, production teams, and regulators to uphold high quality standards and patient safety.

The candidate will implement QA procedures, conduct audits, review batch records, and drive continuous quality improvements in a sterile/compounding environment.

Qualifications

• Bachelor’s degree in Pharmacy, Pharmaceutical Sciences, Chemistry, or a related field.
• Minimum of 3 years in pharmaceutical compounding QA or related field.
• Knowledge of USP <795>, <797>, <800> and FDA regulations for compounding.
• Understanding GMP and quality management systems; audits and documentation.
• Certifications in QA or sterile compounding are a plus.

Responsibilities

• Develop, implement, and maintain QA procedures for compounding operations.
• Conduct audits of processes, equipment, and facilities for compliance.
• Review batch records, formulas, and QC results prior to release.
• Investigate deviations and coordinate corrective actions (CAPA).
• Train staff on QA policies, regulatory requirements, and best practices.

Skills

Analytical skills

Problem-solving

Communication skills

Attention to detail

Education

Bachelor’s degree in Pharmacy or related field

Master’s or PharmD preferred

Tools

eQMS

LIMS

Job description

VIDRINE PHARMACEUTICAL GROUP LLC in Lake Charles, LA seeks a Compounding Pharmaceutical QA/QC professional to oversee QA across the compounding process, ensuring safety, efficacy, and regulatory compliance. The role collaborates with pharmacists, production teams, and regulators to uphold high quality standards and patient safety.

The candidate will implement QA procedures, conduct audits, review batch records, and drive continuous quality improvements in a sterile/compounding environment.