Deviation Investigation Associate

Medasource; Concord (NC); On-site; Full time

Job summary

A leading company is seeking a Deviation Investigator to join their operations team. The role focuses on investigating deviations, writing technical reports, and ensuring compliance with internal procedures. This position offers an opportunity to contribute significantly to quality assurance and improvement initiatives in a dynamic environment.

Benefits

Medical insurance

Vision insurance

Qualifications

• Proven ability to write technical documentation or reports.
• Strong attention to detail and analytical skills.

Responsibilities

• Conduct thorough investigations into deviations.
• Write clear and concise deviation reports.
• Collaborate with cross-functional teams.

Skills

Attention to detail

Analytical skills

Written communication

Tools

Microsoft Office Suite

Job description

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This range is provided by Medasource. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$35.00/hr - $40.00/hr

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Position: Deviation Investigation Support - Operations

Location: Onsite - Concord, NC

Duration: 6-month contract - possibility for extension or conversion

Schedule: Monday-Friday - 8am-5pm

Start: ASAP

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.

Seniority level

• Seniority level

  Associate

Employment type

• Employment type

  Contract

Job function

• Job function

  Consulting and Writing/Editing

• Industries

  Hospitals and Health Care and Pharmaceutical Manufacturing

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Inferred from the description for this job

Medical insurance

Vision insurance

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