Resultados de la búsqueda: 124 vacantes
...For Quality services in the Manufacturing area.
WHAT MAKES YOU A FIT:
The Technical Part:
Bachelor's Degree with five (5) years of Manufacturing Operations experience within the pharmaceutical or regulated industry.
Bilingual (English & Spanish).
Project...
Description:
Independently lead the execution of manufacturing/quality systems such as non-conformances, process validation, procedures, training, and new product introductions. Apply advanced process, operational, scientific expertise, compliance knowledge, and analytical...
...Título del Puesto: Operadores de Manufactura "Somos un patrono con igualdad de oportunidades en el empleo que mantiene la política de emplear y retener a los mejores candidatos independientemente de la raza, color, edad, religión, sexo, origen nacional, discapacidad física...
...Degree in Engineering
Strong experience within Medical Devices and/or Pharmaceutical industries. Exposure to engineering and manufacturing environment.
Performs Validation & CSV Activities, Characterization, Process Qualifications, and Equipment Qualification (new...
...framework for measuring and improving our performance. Compliance Specialist 2018 2 Job Description GIDEP).
Act as a point of contact... ...experience
~3-10 years of compliance experience within a manufacturing environment
~ Ability to understand commercial, quality and...
...for process, utility, and clean room systems.
Knowledge, Skills, and Abilities
Background in programming, installation of manufacturing process controls, automation, and field instrumentation technologies.
Working knowledge of pharmaceutical/biotechnology...
...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...
...product MPs. Approve process validation protocols and reports for manufacturing processes. Request Quality on incident triage team. Approve... ...that operations for licensed pharmaceutical products are manufactured, tested, and stored, according to current Good Manufacturing...
...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...
...project management.
Job Description
Review and approve product MPs.
Approve process validation protocols and reports for manufacturing processes.
Represent Quality on incident triage team.
Approve Environmental Characterization reports.
Release of...
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...
...travel/lodging/transportation expenses (employees only)
General Description:
With minimal supervision, support the execution of manufacturing/quality systems such as non-conformances, process validation, procedures, training, and new product introductions. Apply process...
...The Validation Specialist I should have experience in validation life cycle and will also c ontribute intermediate to advanced level... ...levels.
Responsible for providing technical support such as manufacturing support, regulatory documentation and continued process...
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...
...under the highest ethics standards for the following position:
~Specialist QA
Description:
Perform one or more of the following... ...MPs.
~Approve process validation protocols and reports for manufacturing processes.
~Request Quality on incident triage team.
~Approve...
...EXPERIENCE REQUIRED
:
• You will perform review, approval and tracking of cGMP processes, procedures, testing (methods) in manufacturing, documents and records, batch record review, MES, EBR, SAP, Trackwise; including but not limited to Deviation’s, CAPAs, and validations...
...fields.
Log on now to our website qrcgroup.com / to learn more about our services and solutions!
Job Description
Specialist QA with experience in:
Aseptic Technics
Change Control
New Product Introduction
Qualifications
Doctorate degree...
$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... ...systems crucial for pharmaceutical product development and manufacturing. This position involves maintaining the integrity of data and...
...Employees
• Respect for Diversity
• Nimble
• Fight for What’s Right
STILL INTERESTED? Please continue !
A Patient Care Specialist 2 (PCS2) contributes to AHF by embodying
our commitment to excellence in patient care and operational
efficiency. Through...
...Qualified 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...
