USA - Quality Lab Associate III
USA - Quality Lab Associate III
Posted on :
06-12-2024
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1 Vacancy
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Job Description
68 week assignment
Lab Investigations
Location Marion NC
Onsite
Position Summary
The deviation owner leads the investigation of deviations that occur in operations and is responsible for authoring the investigation summary report. Partners with Quality Operations Engineering Maintenance and Supply Chain to ensure appropriate and timely determination of scope product impact root cause and corrective and preventive actions. Interacts will all levels of staff and provides status updates as well as present the strategy for closure of deviations. Manage several investigations at a time.
Job Responsibilities
Determine scope product impact root cause and corrective actions for deviations from manufacturing procedures. Determine appropriate preventive actions to avoid reoccurrence of the deviation.
Conduct personnel interviews to determine root cause of the deviation.
Foster collaborative relationships focused on high quality investigations meaningful corrective actions and the reduction of deviation generation rate.
Set up and run meetings with cross functional teams.
Close deviations in a timely manner to meet business and compliance needs.
Work with minimal supervision to drive deviations to closure.
Work with Subject Matter Experts and Quality Approvers to determine the breadth and scope of the investigation to identify the appropriate root cause implement corrective and preventive actions complete trending analysis and recommend product disposition.
Present and defend investigations during regulatory inspections as required.
Sustain a clean and safe work area using 6S principles
Learn understand and apply rigorous quality standards Standard Operating Procedures (SOPs) and Current Good Manufacturing Practices (cGMP)
Knowledge Skill and Abilities
Strong communication and project management skills. Must have a thorough understanding of pharmaceutical manufacturing process and equipment preferably parenteral solutions and current Good Manufacturing Practices (cGMPs). Must have good analysis troubleshooting and investigation skills. Must be able to put complex thoughts and issues into writing in such a manner than an educated but uninformed reader can understand and make decisions based on the written investigation report. Must be able to interact with and influence others at various levels in multiple departments.
Understand verbal and written safety and quality instructions and read and comprehend written work instructions including words and drawings.
Must have basic English written and oral communication skills adequate to communicate with other team members.
Required Education and Experience
Bachelors degree in science or engineering; advanced degree in the life sciences physical sciences or engineering with 23 years of experience in root cause evaluation interpreting regulations and quality systems. Minimum of 58 years of experience in Manufacturing Operations and or Quality or related field in the medical products industry.
Lab Investigations
Location Marion NC
Onsite
Position Summary
The deviation owner leads the investigation of deviations that occur in operations and is responsible for authoring the investigation summary report. Partners with Quality Operations Engineering Maintenance and Supply Chain to ensure appropriate and timely determination of scope product impact root cause and corrective and preventive actions. Interacts will all levels of staff and provides status updates as well as present the strategy for closure of deviations. Manage several investigations at a time.
Job Responsibilities
Determine scope product impact root cause and corrective actions for deviations from manufacturing procedures. Determine appropriate preventive actions to avoid reoccurrence of the deviation.
Conduct personnel interviews to determine root cause of the deviation.
Foster collaborative relationships focused on high quality investigations meaningful corrective actions and the reduction of deviation generation rate.
Set up and run meetings with cross functional teams.
Close deviations in a timely manner to meet business and compliance needs.
Work with minimal supervision to drive deviations to closure.
Work with Subject Matter Experts and Quality Approvers to determine the breadth and scope of the investigation to identify the appropriate root cause implement corrective and preventive actions complete trending analysis and recommend product disposition.
Present and defend investigations during regulatory inspections as required.
Sustain a clean and safe work area using 6S principles
Learn understand and apply rigorous quality standards Standard Operating Procedures (SOPs) and Current Good Manufacturing Practices (cGMP)
Knowledge Skill and Abilities
Strong communication and project management skills. Must have a thorough understanding of pharmaceutical manufacturing process and equipment preferably parenteral solutions and current Good Manufacturing Practices (cGMPs). Must have good analysis troubleshooting and investigation skills. Must be able to put complex thoughts and issues into writing in such a manner than an educated but uninformed reader can understand and make decisions based on the written investigation report. Must be able to interact with and influence others at various levels in multiple departments.
Understand verbal and written safety and quality instructions and read and comprehend written work instructions including words and drawings.
Must have basic English written and oral communication skills adequate to communicate with other team members.
Required Education and Experience
Bachelors degree in science or engineering; advanced degree in the life sciences physical sciences or engineering with 23 years of experience in root cause evaluation interpreting regulations and quality systems. Minimum of 58 years of experience in Manufacturing Operations and or Quality or related field in the medical products industry.
Employment Type
Full Time
Key Skills
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