Job Description

Pinnaql is a trusted consulting partner to regulated life sciences companies, providing deep technical, validation, and quality expertise across every stage of the product lifecycle. We partner with pharmaceutical, biotech, and medical device organizations to navigate complexity, accelerate project timelines, and maintain a strong state of compliance and audit readiness.

We are seeking experienced Investigation and CAPA Specialists for a 3 month contract in Greenville, SC. The Investigation and CAPA Specialists will provide on-site support for deviation investigations, root cause analysis, and CAPA development within a regulated aseptic manufacturing environment.

The selected resources will support end-to-end investigations from a manufacturing and process perspective, including process review, data collection, personnel interviews, and development of investigation reports and recommended corrective and preventive actions for Quality approval.

This role requires strong investigation execution skills, technical writing capabilities, and the ability to work cross-functionally with Manufacturing, Engineering, Training, and Quality teams.

Key Responsibilities

• Lead and support manufacturing-driven investigations from initiation through completion, in alignment with site procedures and cGMP expectations.
• Perform detailed reviews of manufacturing processes, batch records, and supporting data to support root cause determination.
• Conduct interviews with manufacturing, operations, and support personnel.
• Author clear, concise investigation documentation, including root cause analysis and recommended CAPAs, for Quality review and approval.
• Support development, tracking, and closure of CAPAs, including effectiveness checks as applicable.
• Support ongoing and new investigations while maintaining on-site presence in manufacturing areas as required.
• Interface effectively with Manufacturing, Engineering, Training, and Quality functions.
• Ensure investigation documentation is accurate, complete, and inspection-ready.

Preferred Experience

• Knowledge of gowning practices and aseptic monitoring controls.

Required Qualifications

• Bachelor’s degree in Engineering, Science, or a related technical discipline (or equivalent industry experience).
• Minimum of 5 years of experience supporting investigations in pharmaceutical or biotechnology manufacturing.
• Demonstrated experience leading manufacturing or process investigations and authoring investigation reports.
• Strong technical writing skills and ability to clearly document complex investigations.
• Understanding of aseptic manufacturing processes and cGMP requirements.
• Experience gathering data, conducting interviews, and supporting root cause analysis.
• Ability to manage multiple active investigations concurrently.

At Pinnaql, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.

Excited to build something meaningful together? We look forward to hearing from you.

Pinnaql is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.

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