Resultados de la búsqueda: 56 vacantes
...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...
...~ Perform oversight of the process and procedures/GMP tasks.
~ Manage Change Controls and deviations for review and approvals as QA contact.
~ Work with operations to resolve basic compliance discrepancies.
~ Knowledge in Validations and Laboratory area and equipment...
...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...
...standards for the following position:
Specialist QA
Shift: Mon/Tue then Fri/Sat/Sun on alternate... ....
~Approve NC investigations and CAPA records.
~Approve change controls.
~Provide... ...with Manufacturing Process Audit and Batch Record Review experience.
~Knowledge or to be...
QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world...
...Approve Environmental Characterization reports.
- Release of sanitary utility systems.
- Approve planned incidents.
- Represent QA on NPI team.
- Lead investigations.
- Own site quality program procedures.
- Designee for QA manager on local CCRB....
...in support of Quality Assurance program, acts as the technical specialist. Review and approve product MPs.
Functions:
Approve process... ...utility systems.
Approve planned incidents.
Represent QA on NPI team.
Lead investigations.
Own site quality program...
...your middle name, keep reading! We’re looking for a passionate QA who likes to finish what they started and is confident in their... ...In support of Quality Assurance program acts as the technical specialist.
Review and approve product MP’s.
Approve process validation...
...fields.
Log on now to our website qrcgroup.com / to learn more about our services and solutions!
Job Description
Sr Specialist QA with exposure to regulated industries and experience in:
Change Control
Non Conformance Review
Preventive...
Expertise required:
Aseptic Techniques, Change Control and New Product Introduction.
Requirements
Education and years of experience requirements;
Doctorate degree or Master's degree and 3 years of directly related experience
or Bachelor's degree and ...
Expertise required for this project opportunity;
Experience in change control
Non conformance review
Preventive maintenance review
Minor deviations
Work orders and job plans
Requirements
Years of experience and education required;
Doctorate degree...
...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...
Delivery Specialist-PR
Category: Retail Stores
Location: 627 Yauco Plaza II
Yauco Puerto Rico 00698-4448
Rent A Center... ...menos 18 años de edad
~Licencia de conducir válida y un buen record choferil--Estarás conduciendo vehículos de la compañía
~Puede...
...Experience in leading multiple, contending priorities in a fast-paced environment with minimal direction.
Experience managing quality records (deviations (major and minor), CAPAs, CAPA-EV, Change Controls) using TrackWise System
Experience navigating and executing...
...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...
...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...
Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management...
Mentor Technical Group (MTG) provides a comprehensive portfolio of technical support and solutions for the FDA-regulated industry. As a world leader in life science engineering and technical solutions, MTG has the knowledge and experience to ensure compliance with pharmaceutical...
Description
Position at Pilgrim's
Job Summary:
Analytical position focused on developing controls and analysis that will lead the complex to stability and process improvements in key indicators that influence the results. The analyst will be an integral part of...
For EHS services in the Manufacturing area.
WHAT MAKES YOU A FIT:
The Technical Part:
~ Bachelor’s Degree and at least five (5) years of exposure in Environmental Health & Safety activities within the Pharmaceutical or Medical Devices industry.
~30hrs. OSHA Certification...
