Deviation Specialist Onsite Greenville, NC
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Job Location:
Greenville, NC - USA
Monthly Salary:
Not Disclosed
Posted on:
14 hours ago
Vacancies:
1 Vacancy
Job Summary
Work Schedule
Standard (Mon-Fri)Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards Office Some degree of PPE (Personal Protective Equipment) required (safety glasses gowning gloves lab coat ear plugs etc.)Job Description
As part of the Thermo Fisher Scientific team youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the worlds toughest challenges like protecting the environment making sure our food is safe or helping find cures for cancer.
Location: This role is located onsite (M-F) in Greenville NC.
Job Summary:
A leading pharmaceutical organization is seeking a Deviation Specialist to support its quality and compliance operations within a high-volume sterile manufacturing facility. This role focuses on conducting thorough investigations driving root cause analysis and contributing to continuous improvement initiatives in a regulated environment. This role ensures that all deviations are managed in compliance with company policies and industry regulations and that corrective and preventive actions (CAPAs) are implemented effectively. The ideal candidate will be a skilled technical writer with strong communication and problem-solving abilities and a comfort level in navigating complex production environments.
Key Responsibilities:
Deviation Management:
- 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 into continuous improvement initiatives.
- Participate in training programs to enhance knowledge and skills related to deviation management and quality assurance.
Qualifications:
- Experience in cGMP environment deviation management or equivalent regulated industry.
- Strong Attention to details technical writing Analytical and critical thinking skills.
- Knowledge of regulatory requirements and standards.
- Intermediate to Advanced skills in Microsoft Suite (Word Excel PowerPoint)
- Excellent communication and people skills.
Preferred Qualifications:
- Associate or bachelors degree in a relevant field such as Life Sciences Engineering Medical or Quality Management.
- Preferred Experience: 1-3 years of Biologics Aseptic Filling Isolators Six Sigma Certification Electronic documentation systems.
- Familiarity with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP).
Physical Demands:
While performing the duties of this job the employee is required to walk sit and use hands handle or feel tools or controls reach with hands and arms balance stoop crouch bend talk and hear. Typically located in a comfortable indoor area. There may be regular exposure to mild physical discomfort from factors such as- dust fumes or odors temperature extremes loud noise strong drafts or bright lights.
Work Environment:
This job operates in a professional office environment as well as the Production Laboratory and Warehouse environment in a pharmaceutical facility. This role routinely involves use of standard office equipment such as computers phone photocopiers filing cabinets and fax machines.
Required Experience:
IC
Key Skills
- Experience Working With Students
- Google Docs
- Organizational skills
- Classroom Experience
- Data Collection
- Materials Handling
- Workers' Compensation Law
- OSHA
- Special Operations
- Team Management
- Experience with Children
- Supervising Experience
About Company
Electron microscopes reveal hidden wonders that are smaller than the human eye can see. They fire electrons and create images, magnifying micrometer and nanometer structures by up to ten million times, providing a spectacular level of detail, even allowing researchers to view single a ... View more
