Deviation Investigator - Pharma Quality & Process Improvement

Proclinical

Clayton (NC)

On-site

USD 34,000 - 62,000

Part time

7 hours ago

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Job summary

Proclinical is seeking a Deviation Investigator in Clayton, NC to support production and quality assurance activities. You will lead deviation investigations, conduct root cause analyses, and implement quick containment actions to safeguard product quality and patient safety.

The role emphasizes GMP compliance, process improvements, and coordination with QA and manufacturing teams in a contract setting.

Qualifications

Associate degree in technology or related field (or high school diploma with 2+ years manufacturing experience).
At least 1 year in pharmaceutical manufacturing, deviation investigation, or quality assurance.
GMP knowledge and related systems desirable.
Strong written communication and systematic problem solving.
Ability to work in an open office environment with potential distractions.

Responsibilities

Investigate deviations and perform root cause analyses to address issues effectively.
Implement quick containment actions to mitigate potential risks.
Ensure compliance with relevant standards and guidelines.
Identify and recommend process improvement opportunities for routine to moderately complex issues.
Conduct process confirmations and review batch production records (BPRs) as needed.
Follow all safety and environmental protocols.
Perform other duties as assigned.