Deviation Investigator

Proclinical; Clayton (NC); On-site; USD 34,000 - 62,000; Part time

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.

Skills

Associate degree

Pharma experience

GMP knowledge

Written comms

Problem solving

Open office adaptability

Education

Associate degree in technology/engineering

Job description

Deviation Investigator - Contract - Clayton, NC

Help ensure product quality and patient safety by leading deviation investigations that make a real difference in pharmaceutical manufacturing.

Proclinical is seeking a Deviation Investigator to support production and quality assurance activities in North Carolina.

Primary Responsibilities

The successful candidate will focus on investigating deviations, performing quick containment actions, and conducting root cause analyses. You will also ensure compliance with established standards and identify opportunities for process improvement. This position requires adherence to safety and environmental requirements and may involve additional responsibilities as assigned.

Skills & Requirements

• Associate degree in technology, engineering technology, or a related field from an accredited institution (or a high school diploma/equivalent with at least two years of manufacturing experience).
• Preferred experience includes at least one year in a pharmaceutical manufacturing environment, deviation investigation, or quality assurance.
• Knowledge of Good Manufacturing Practices (GMP) and related systems is highly desirable.
• Strong written communication skills and systematic problem-solving abilities.
• Ability to work effectively in an open office environment with potential distractions.

The Deviation Investigator's responsibilities will be:

• 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.