Manufacturing Process Investigator - Military veterans preferred

Nephron Pharmaceuticals


Description:

Job Purpose: A Manufacturing Process Investigator is a professional who conducts thorough investigations into issues that arise within a manufacturing environment, focusing on deviations, non-conformances, and other quality concerns. They aim to identify the root cause of these issues, implement corrective actions, and prevent recurrence, ultimately ensuring the quality and compliance of manufacturing processes.

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Essential Duties and Responsibilities:

Ø Use available resources to manage and track workload to meet required timelines.

Ø Prepare thorough investigation reports, ensuring accuracy, completeness, and compliance with regulatory expectations.

Ø Conduct root cause analysis (RCA) for deviations, product complaints, and quality-related incidents.

Ø Work closely with production and quality teams to implement corrective and preventive measures based on investigation findings.

Ø Develop and maintain technical documentation to support manufacturing and quality processes.

Ø Develop CAPA plans with input from operators, Subject Matter Experts (SMEs), and management to ensure effective and sustainable solutions.

Ø Track and monitor CAPA action items to ensure timely completion and assess their effectiveness.

Ø Escalate unresolved CAPA items to management and recommend further actions as needed.

Ø Draft, review, and update Standard Operating Procedures (SOPs) to ensure alignment with regulatory requirements (e.g., FDA, GMP) and industry best practices.

Ø Collaborate with key stakeholders to ensure procedural updates align with internal standards, project timelines, and regulatory requirements.

Ø Provide training on new or updated SOPs, CAPAs, and procedural changes to relevant personnel.

Ø Ensure compliance with cGMPs, safety guidelines, and internal quality policies throughout the facility.

Supplemental Functions:

Ø Performs all other duties as assigned or apparent.

Ø Identify and document areas for improvement in manufacturing and quality systems to enhance efficiency and compliance.

Ø Support continuous improvement projects utilizing methodologies such as Lean and Six Sigma.

Ø Analyze manufacturing data and trends to drive process enhancements and prevent reoccurring quality issues.

Job Specifications and Qualifications:

Knowledge:

Ø Excellent technical writing skills with the ability to clearly document procedures and investigations.

Ø Strong analytical and problem-solving abilities.

Ø Proficiency in root cause analysis tools (e.g., Fishbone diagrams, 5 Whys).

Ø Proficient in Microsoft Office Suite and quality management software.

Ø Strong interpersonal and communication skills with the ability to collaborate effectively across departments.

Education / Experience:

Ø Bachelor's degree in Engineering, Life Sciences, Pharmacy, or a related field preferred.

Ø Certifications in Lean, Six Sigma, or similar continuous improvement methodologies are a plus.

Ø 3+ years of experience in a Quality Assurance, Technical Writing, or Investigation role, preferably in a BFS or pharmaceutical manufacturing environment.

Ø Strong background in SOP writing, CAPA management, investigation writing, and procedural updates.

Ø Working knowledge of regulatory requirements (e.g., FDA, EU GMP) and industry best practices is a plus.

Preferred Licensing and Certifications:

Ø Good Manufacturing Practices Certified Professional

Ø Certified Quality Auditor

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Working Conditions / Physical Requirements:

Ø This position requires bending, typing, lifting (up to 40 1bs.), standing, sitting and walking throughout the facility.

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