Quality Manager

Quality Manager Apply Now Applied To save a job sign in or get started

Job ID:

10215301 Posted today Back Boerne, TX, US Scientific Bachelors Degree Full Time, Direct Hire $90-115K Manager (Manager/Supervisor) On-site Biotechnology/Pharmaceuticals First Shift (Day) Boerne, TX, US $90-115K Manager (Manager/Supervisor) Full Time, Direct Hire Biotechnology/Pharmaceuticals On-site Scientific Bachelors Degree First Shift (Day) Apply Now Applied Job details

Quality Manager Salary Range:

$90,000 - $115,000

Location:

Greater San Antonio Area Industry:

Pharmaceutical Manufacturing Work Schedule:

Days /10 x 4; Monday-Thursday;

Off Friday Benefits:

Full benefits Position Overview We are seeking a seasoned Quality Manager to lead internal quality assurance functions. This role is pivotal in ensuring the integrity of our manufacturing and packaging processes. You will have overall responsibility for batch releases and the execution of critical quality systems, including CAPAs, deviations, and regulatory compliance.

Key Responsibilities Quality Oversight:

Serve as the Subject Matter Expert (SME) for all quality matters related to manufacturing, packaging, warehousing, and supporting operations.

Documentation & Release:

Review and approve GMP Master documents and oversee the final release of all manufactured batches.

Audit Management:

Lead the Internal Audit and Supplier Audit Programs; facilitate and host customer audits and support regulatory inspections (FDA and other health authorities).

Investigations & Compliance:

Manage change controls, deviations, non-conformances, and customer complaint investigations. Ensure effective CAPAs and conduct effectiveness checks.

Reporting:

Coordinate and approve Annual Product Reviews (APRs) and share reports with business partners as required.

Training & Development:

Conduct introductory GMP training for new hires and collaborate with senior leadership on continuous improvement projects for existing Quality Systems.

Qualifications Education:

Bachelor's Degree in a scientific or technical field.

Experience:

Minimum of 5 years of related experience in a GMP-regulated environment (Pharmaceutical industry experience is highly preferred).

Equivalent:

An equivalent combination of education and professional experience will be considered. Technical Skills & Core Competencies Deep understanding of FDA regulatory requirements and GMP standards . Proven track record in managing Quality Management Systems (QMS) . Strong communication skills for interacting with external customers and regulatory bodies. Analytical mindset with a focus on continuous process improvement. For immediate consideration, please forward your updated resume. 10215301 Share this job Copied url To save a job sign in or get started To apply for this job email your details to I want more jobs like this in my inbox.

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