...Responsible for the review and approval of workorders, risk assessments, validation protocols and reports. Perform Manufacturing Investigations, including RCA and CAPA development and implementation. Own site quality program procedures. Responsible for the development...
Command Investigations LLC is a dynamic and forward-thinking investigative company that has been at the forefront of the industry since its establishment in September of 2012. With a relentless commitment to excellence, we have consistently delivered top-tier investigative...
...Characterization reports.
Release of sanitary utility systems.
Approve planned incidents.
Represent QA on NPI team.
Lead investigations.
Lead site audits.
Own site quality program procedures.
Designee for QA manager on local CCRB.
Review Risk...
...to factory and production conditions.
Inspects performance of machinery, equipment, and tools to verify their efficiency, and investigates and initiates corrective action of problems and deficiencies to ensure product quality.
Develops manufacturing processes that...
...established goal.
Responsible for managing NC/CAPA closure within established goal.
Review equipment/system Root Cause Analysis investigations and support trend evaluations.
Qualifications:
Bachelor Degree
Five (5) years of Previous experience in Manufacturing...
...Characterization reports.
Release of sanitary utility systems.
Approve planned incidents.
Represent QA on NPI team.
Lead investigations.
Lead site audits.
Own site quality program procedures.
Approve NC investigations and CAPA records.
Approve change...
...For CAPA Investigation services in the Quality area
WHAT MAKES YOU A FIT:
The Technical Part:
Bachelor’s Degree in Life Sciences or Engineering and previous exposure in Investigation activities within the Pharmaceutical or Medical Devices industry.
Excellent...
...at . Follow @abbvie on Twitter , Facebook , Instagram , YouTube and LinkedIn .
Job Description
The Senior Investigator Writer Leader is responsible for the writing and/or approval of quality events ( quality investigations, laboratory investigations...
...Conformance and CAPA
1. Ensure that all Non-conformances are triaged within the established goal.
2. Responsible for authoring investigation reports.
3. Responsible for execution of corrective actions.
4. Responsible for managing NC/CAPA closure within established...
...role is to support Bristol Myers Squibb (BMS) as the Senior Specialist, Environmental, Occupational Health & Safety for the Manatí facility... ...and SharePoint for documentation of procedures, forms, SOPs, investigations, reporting, inspections, action items, communications, and...
...industry in Puerto Rico & USA
Responsibilities:
Supporting the product complaint system; leading and managing product complaint investigations, performing data analysis and trending of complaint information to proactively detect signals and take appropriate actions in a...
...complaint system through; leading and managing product complaint investigations, performing data analysis and trending of complaint... ...depending on the nature and complexity of the complaint, the specialist may be responsible of conducting and documenting the investigation...
...Specialist Quality Complaints with experience in manufacturing/packaging deviations, Root Cause Analysis, complaint investigations, project management and compliance.
Requirements
Doctorate degree or Master's degree and 3 years of directly related experience to...
...more about our services and solutions!
Job Description
Specialist Quality Complaints with experience in manufacturing/packaging deviations, Root Cause Analysis, complaint investigations, project management and compliance.
Qualifications
Doctorate...
...Environmental Characterization reports. Release of sanitary utility systems. Approve planned incidents. Represent QA on NPI team. Lead investigations. Lead site audits. Own site quality program procedures. Designee for QA manager on local CCRB. Review Risk Assessments. Support...
...Engineering
Experience operating in a regulated environment, preferably medical devices.
Technical Writing Knowledge.
Investigation and Root Cause Skills (Problem Solving Knowledge).
Process Validation and Computer software validation knowledge.
Quality...
...Ensure documentation is thorough, accurate and entered on a timely basis into the quality system.
Ensures complete and thorough investigation of all product failures and deviations associated with validation sampling and testing.
WHO WE ARE:
We are a Service...
...potentially impact product quality are assessed according to procedures
• Certify that deviations from established procedures are investigated and documented per procedures
• Ensures that production records and testing results are complete, accurate, and documented...
...monitoring quarterly reports.
Ensure that all Non-conformances are triaged within the established goal. Responsible for authoring investigation reports. Responsible for execution of corrective actions.
Responsible for managing NC/CAPA closure within established goal....
...Characterization reports.
Release of sanitary utility systems.
Approve planned incidents.
Represent QA on NPI team.
Lead investigations.
Lead site audits.
Own site quality program procedures.
Designee for QA manager on local CCRB.
Review Risk...
...The Validation Specialist I should have experience in validation life cycle and will also c ontribute intermediate to advanced level... ...improvement and meet site goals.
# Responsible for monitoring and investigating environmental incidents such as spills and malfunctions to...
...requirements into the production plan.
Inspects performance of machinery, equipment, and tools to verify their efficiency, and investigates.
Initiates corrective action of problems and deficiencies to ensure product quality.
Complies with company programs,...
...product complaint system; leading and managing product complaint investigations, performing data analysis and trending of complaint... ...depending on the nature and complexity of the complaint, the specialist may be responsible of conducting and documenting the investigation...
...quarterly reports.
~ Ensure that all Non-conformances are triaged within the established goal.
~ Responsible for authoring investigation reports.
~ Responsible for execution of corrective actions.
~ Responsible for managing NC/CAPA closure within established goal...
Minimum Requirements
Mid-level individual contributor on a project or work team, 3-5 years of experience required.
Bachelor Degree in Engineering
Experience within Medical Devices and/or Pharmaceutical industries.
Experience in equipment IQ, OQ and PQ, Validation...
...Pri General Purpose of the Position
The Onboarding Specialist is responsible for scheduling meetings with new clients to welcome them and establish the communication channel. Onboarding Specialist will be responsible for overseeing active tickets and their completion...
...Schedule: Monday to Friday, 8am-5pm. Open to working overtime and holidays as needed.
Position Summary :Responsible for investigating and resolving Regulation E (Electronic Fund Transfers), Business EFT claims, and Merchant Disputes with potential fraudulent/suspicious...
$30 - $37 por hora
...is a contract role for one year
As a Junior Validation Specialist at our pharmaceutical facility, you will be integral in ensuring... ...methods to ensure process control.
Participate in investigations and troubleshooting of process deviations; identify root causes...
...English.
Experience in:
Federal and Commonwealth rules and regulations.
MS Office.
EHS Assessments programs and incident investigations.
Permits and Reports.
The Personality Part:
~ If you have a commitment to serving customers with high-quality...
...candidates must have the following expertise;
Experience in manufacturing/packaging deviations, Root Cause Analysis, complaint investigations, project management and compliance.
Requirements
Qualified candidates must comply with years of experience and...