Job description
Technical Investigation Writer
SRG offers flexible staffing solutions with a national presence. We provide contract, contract-to-hire, direct hire and executive search services. SRG utilizes an innovative approach to identify and qualify talent that is unique to the Staffing industry, featuring a cutting-edge platform that allows us to rapidly and precisely match professionals to client requirements. We have a proprietary database of over one million candidates and maintain continuous contact with our qualified talent.
Job Scope:
Minimum Requirements:
EOE/ADA
SRG offers flexible staffing solutions with a national presence. We provide contract, contract-to-hire, direct hire and executive search services. SRG utilizes an innovative approach to identify and qualify talent that is unique to the Staffing industry, featuring a cutting-edge platform that allows us to rapidly and precisely match professionals to client requirements. We have a proprietary database of over one million candidates and maintain continuous contact with our qualified talent.
- Title: Technical Investigation Writer
- Location: Philadelphia, PA
- Industry: Pharmaceutical
- Hours: M-F 800am - 5:00pm (Remote / Onsite hybrid schedule)
- Salary: Up to $38 based on experience (Paid Weekly - Benefits Available)
- Employment Type: 6 Month Contract (potential for direct hire)
Job Scope:
- Perform thorough investigations of Supply Chain non-conforming events and customer complaints that could include review of cGMP documents and historical review of the quality management system
- Perform investigations using structured root cause analysis tools (fishbone, 5 Why s, etc.) and partner with team members to determine true root cause
- Participate in defining right CAPA after investigation process is complete
- Conduct personnel interviews of those individuals involved with the event or customer complaint
- Write concise and accurate investigation reports with the goal to be successful in the first pass through the quality review
- Write interim reports and extensions for investigations that exceed 30 days
- Adjust work hours across our 24x7 operation, when needed, to get all information required for accurate investigations
- Generate trend analysis reports of historical investigation on an as needed basis.
- Partner with local and global teams on required process and system enhancements.
- Support client communications both written and oral with investigation follow ups
Minimum Requirements:
- Bachelor s Degree preferred, preferably in Science or Business (e.g., Chemistry, Pharmacy, Engineering, Operations)
- Minimum of 2 - 5 years of CAPA, investigations, or manufacturing quality assurance experience
- Minimum of 5 years manufacturing/technical experience in a regulated GMP environment; pharmaceutical industry preferred
EOE/ADA
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