Job Description

Deviation Investigation Support - Operations

6-Month Contract

100% Onsite in Concord, NC

ASAP Start

Position Description

We are seeking a detail-oriented and technically proficient Deviation Investigator to join our team. This role is responsible for investigating and writing technical deviation reports, ensuring thorough documentation and analysis of non-conformances. The ideal candidate will possess a strong analytical mindset, excellent writing skills, and the ability to assess complex issues with precision.

Key Objectives

• Conduct thorough investigations into deviations, identifying root causes and contributing factors.
• Write clear, concise, and technically accurate deviation reports.
• Collaborate with cross-functional teams to gather necessary information and ensure timely resolution of deviations.
• Apply critical thinking and technical knowledge to assess issues and recommend corrective and preventive actions (CAPAs).
• Maintain compliance with internal procedures and regulatory requirements.

Requirements

• Proven ability to write technical documentation or reports.
• Strong attention to detail and analytical skills.
• Ability to assess and interpret technical issues effectively.
• Excellent written and verbal communication skills.
• Proficiency in Microsoft Office Suite or similar tools.

Preferred Attributes

• Background in a technical field such as engineering, life sciences, or quality assurance.
• Experience in pharmaceutical or biotech industries.
• Familiarity with manufacturing environments and processes.
• Understanding of deviation management systems and CAPA processes.
• Ability to work independently and manage multiple priorities.

Other Information

• This position offers a dynamic work environment with opportunities to contribute to continuous improvement initiatives.
• Training and support will be provided to ensure success in the role.
• Candidates without direct pharma or manufacturing experience are encouraged to apply if they meet the core requirements.

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