Deviation Investigator # 26-24606
Greenville, NCContract$40–50/hrSeen 1w agoSeen in employer's feed 2 days ago
Most applications go out cold — see where you stand first. No sign-up to start.
Watch jobs like this. New roles like this one near Greenville, NC, by email.
Don't just apply. Show up ready.
Olive works from this exact posting.
At a glance
Olive lists jobs from US employers, including remote roles you can work from the United States.
Job overview
The Deviation Investigator will identify and document deviations from SOPs and regulatory guidelines, conduct root‑cause investigations, and collaborate with cross‑functional teams to develop corrective actions. Responsibilities include maintaining detailed records, preparing reports for management and regulators, ensuring compliance with company policies and industry standards, and supporting continuous improvement initiatives through trend analysis and training participation.
Skills & qualifications
Skills
Qualifications
Full job description
$40-$50 per hour
Greenville, NC
Contract
Duration: 12+ months
Job Description:
-
Identify and document deviations from standard operating procedures (SOPs), quality standards, or regulatory guidelines.
-
Conduct thorough investigations to determine the root cause of deviations.
-
Collaborate with cross-functional teams to develop and implement corrective and preventive actions (CAPAs).
Documentation and Reporting:
-
Maintain accurate and detailed records of all deviations, investigations, and CAPAs.
-
Prepare and present deviation reports to management and regulatory authorities as required.
-
Ensure documentation is completed in accordance with Good Documentation Practices (GDP).
Compliance and Quality Assurance:
-
Ensure all deviations are managed in compliance with company policies, industry standards, and regulatory requirements.
-
Participate in internal and external audits and inspections, providing necessary documentation and information related to deviations.
Continuous Improvement:
-
Analyze deviation trends and provide insights for continuous improvement initiatives.
-
Participate in training programs to enhance knowledge and skills related to deviation management and quality assurance.
Qualifications:
-
Regulated Industry, cGMP environment experience, deviation management, or a e.g., Pharmaceuticals, Manufacturing, Engineering, Medical, Law Enforcement, etc.].
-
Strong Attention to details, technical writing, Analytical and problem-solving skills.
-
Knowledge of regulatory requirements and standards.
-
Intermediate to Advanced skills in Microsoft Suite (Word, Excel, PowerPoint)
-
Excellent communication and interpersonal skills.
Preferred Qualifications:
-
Associate or bachelor’s degree in a relevant field such as Life Sciences, Engineering, Medial, or Quality Management with 2+ years of related experience.
-
Preferred Experience: Biologics, Aseptic, Filling Isolators, Six Sigma Certification, Electronic documentation systems.
-
Familiarity with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP).
About US Tech Solutions:
US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit www.ustechsolutions.com .
US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
AI Statement: By applying, you acknowledge that AI-assisted tools may be used during hiring.
#LI-BP1
You've read the whole posting — now see how you match it.