...sanitary utility systems.
Approve planned incidents.
Represent QA on NPI team.
Lead investigations.
Lead site audits.
Own... ...approve EMS/BMS alarms.
Approve NC investigations and CAPA records.
Approve change controls.
Provide lot disposition and...
...procedures, testing (methods) in manufacturing, documents and records, batch record review, MES, EBR, SAP, Trackwise; including but not limited... ...experience with processes involved in manufacturing and distribution, QA, QAL, and Process Development
• Experience with Validation...
...sanitary utility systems.
Approve planned incidents.
Represent QA on NPI team.
Lead investigations.
Lead site audits.
Own... ...approve EMS/BMS alarms.
Approve NC investigations and CAPA records.
Approve change controls.
Provide lot disposition and...
...process
• Perform oversight of the process and procedures/GMP tasks
• Manage Change Controls and deviations for review and approval as QA contact
• Work with operations to resolve basic compliance discrepancies
• Knowledge in Validations and Laboratory area and...
...sanitary utility systems.
Approve planned incidents.
Represent QA on NPI team.
Lead investigations.
Lead site audits.
Own... ...approve EMS/BMS alarms.
Approve NC investigations and CAPA records.
Approve change controls.
Provide lot disposition and...
...fields.
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Job Description
Specialist QA with experience in:
Aseptic Technics
Change Control
New Product Introduction
Qualifications
Doctorate degree...
...under the highest ethics standards for the following position:
~Specialist QA
Description:
Perform one or more of the following duties... ...approve EMS/BMS alarms.
~Approve NC investigations and CAPA records.
~Approve change controls.
~Provide lot disposition and authorize...
...• Perform oversight of the process and procedures/GMP tasks
• Manage Change Controls and deviations for review and approval as QA contact
• Work with operations to resolve basic compliance discrepancies
• Knowledge in Validations and Laboratory area and equipment...
...Functional Role: Procurement Specialist
Contract Role: Subject Matter Expert
Location... ...notification or involvement.
# Complete QA/QC of project deliverables.
# Ensure... ...procurement project closeout and archive records upon project completion.
Competencies...
...testing, issues qualification test reports and approves qualifications plans/reports.
Provides support on activities, documents and records requiring Quality Engineering review and/or approval as deemed necessary.
Alerts the organization to issues in time to resolve...
...The Validation Specialist I should have experience in validation life cycle and will also c ontribute intermediate to advanced level... ...Assists in development of technical training and revision of batch records and SOP's linked to process robustness experiences.
# Foster...
...Sr Quality Documentation Specialist with experience in Technology Transfer of Regulatory Documentation such as, but not limited:
Batch Record
Manufacturing Instructions
SOP
cGMP
Preventive Maintenance
Coordinate meetings with manufacturing area to ensure...
...talented, dedicated individual committed to work under the highest ethics standards for the following position:
~QA Lab Equip. Retirement - Validation Specialist
~QA Lab equipment knowledge
~Data Integrity Assessments (nice to have)
~GMARS (Maximo) - Preventive...
...for businesses.
The Cybersecurity Risk & Incident Response Specialist is responsible for the information security analysis,... ...evaluation of each of the alerts provided by the monitoring tools is recorded in the logs based on the collaboration provided to the Security...
...Perform actions associated with Change Control documents and Corrective/Preventive Actions (CAPA); including ownership of these records.
Provide updates to Supplier Records on behalf of account owners.
Complete Supplier data for metrics and risk management documents...
...Underwriting Support Specialist American International Group, Inc. (AIG) is a leading global insurance organization. AIG member companies... ...Spanish including verbal, written and negotiation.A proven track record of excellent customer service skills.Ability to write reports...
...this role is to support Bristol Myers Squibb (BMS) as the Senior Specialist, Environmental, Occupational Health & Safety for the Manatí... ...existing ones.
Prepare and maintain environmental reports, records, monitoring data and plans as required by regulation or company...
For Computer and System Validation services in the Engineering area.
WHAT MAKES YOU A FIT:
The Technical Part:
Bachelor’s degree in engineering or science. • Training in validation methodologies, technologies and process control computer systems. • Five (5) years...
.... Respond to inspector questions as necessary. Support regulatory inspections by directly interfacing with inspectors to review batch records, process validation, non-conformances, etc.
May present process overviews to inspectors and accompany inspectors on tours of process...
...wherever you are, doing it better than any other company.
As a QA Performance Testing Lead, your role involves ensuring the... ...and experience working in a customer-focused environment.
Track record of working in cross-functional, international teams.
Knowledge...
...highest ethics standards for the following position:
~Permitting Specialist
The Permitting Specialist will play a key role in... ...regulatory agency inquiries or concerns.
~Maintain accurate records of permitting activities and documentation.
Requirements:...
...Procurement Specialist
JOB SUMMARY : This position is responsible for research and procure all materials required... ...decisions in a fast-paced environment.
Maintain records of purchases, pricing, and other important data.
Review and...
...Investigations Specialist with experience in regulated industries. Strong knowledge of complaints and processes deviations. Will be responsible for performing through, detailed and timely investigations and generation of high quality and timely investigation reports...
...Role
Conduct comprehensive testing of mobile games to identify and document crucial defects, taking ownership of the entire QA process to assure quality and user experience.
Coordinate closely with design and development teams, understanding game mechanics...
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...
...the following position:
~Documentation Specialist for GMP Industry
Qualifications:
The... ...Coordinates official documents and Device Master Records changes.
~Serves a liaison between... ...Master Records.
~Assures Device Master Record files actives are properly maintained....
...The residential Solar QA Inspector performs quality assurance inspection services and reporting of residential solar system installations to ensure compliance with product manufacturers’ installation instructions, building/ electrical/ mechanical/ plumbing codes and...
For Equipment Validation services in the Manufacturing area.
WHAT MAKES YOU A FIT:
The Technical Part:
Bachelor’s Degree in Engineering and five years of experience in Validation Life Cycle within the Medical Device Industry.
Bilingual (English and Spanish)...
Delivery Specialist-PR-PR0006
Category: Retail Stores
Location: 1810 Ste 121 El Monte Town Center North Pr 14
Ponce Puerto Rico... ...menos 18 años de edad
~Licencia de conducir válida y un buen record choferil--Estarás conduciendo vehículos de la compañía
~Puede...
...Build and complete validation plans, system test scripts, protocols, and reports, while maintaining appropriate traceability of records
Ensure timely, thorough, and complete execution of all protocols, meeting FDA requirements.
Ensure that all new and existing...