...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...
$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...
...EQVAL Group, Inc . is a company that provides services to the manufacturing industry ( Medical Devices, Pharmaceuticals, Biotechnologies,... ...service.
We are looking for two Cleaning Validation Specialist with Pharmaceutical (solid dosage) manufacturing experience...
...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...
...completado, Certificaciones en grados técnicos y/o electrónica son un plus• Experiencia previa en posición similar en la Industria de Manufactura• Capacidad para leer e interpretar esquemas, listado de cables y materiales, especificaciones e impresiones• Capacidad para...
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...
...YOU WILL: (The day-to-day on the job)
Review and approve product MPs.
Approve process validation protocols and reports for manufacturing processes.
Request Quality on incident triage team.
Approve Environmental Characterization reports.
Release of sanitary...
...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...
...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...
...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...
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...
...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...
...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...
...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...
...website qrcgroup.com / to learn 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....
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...
...depending on the nature and complexity of the complaint, the specialist may be responsible of conducting and documenting the investigation... ...partners.
Competencies / Skills:
~ Experience in manufacturing/packaging deviations, Root Cause Analysis, complaint investigations...
...depending on the nature and complexity of the complaint, the specialist may be responsible of conducting and documenting the investigation... ...experience
Preferred Qualifications:
Experience in manufacturing/packaging deviations, Root Cause Analysis, complaint...
...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...
...business needs. F lexibility to support 24/7 operations.
Experience in:
Programming, instrumentation and installation of manufacturing process controls.
Automation and field instrumentation technologies.
Rockwell Automation Platform and Allen-Bradley and PLCs...
...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...
...under the highest ethics standards for the following position:
~Specialist Quality Complaints
Primary responsibilities include:... ...~Complaint investigations
~Solid dosage, syringe and device manufacturing and packaging processes.
~Software: Trackwise, Excel, Word...
...practices.
~ Keep abreast of any safety and environmental law or regulation changes that impact the client.
~ Participate in manufacturing meetings to discuss workplace safety and regulatory concerns and opportunities.
~ Actively role model all company and assigned...
The Document Control performs a wide range of duties including the following:
Copy, scan and store documents
Check for accuracy and edit files, like contracts
Review and update technical documents (e.g. manuals and workflows)
Distribute project-related copies...
...Procurement Specialist
JOB SUMMARY : This position is responsible for research and procure all materials required for construction electrical projects and ensure they are provided on time and within allocated budgets.
JOB RESPONSIBILITIES :...
...Specialist QA with experience in:
Aseptic Technics
Change Control
New Product Introduction
Requirements
Doctorate degree or Master's degree and 3 years of directly related experience or Bachelor's degree and 5 years of directly related experience (Education...
...under the highest ethics standards for the following position:
~Specialist Quality Complaints
Primary responsibilities include:... ...Analysis
~Complaint investigations
~ 4+ years of quality and manufacturing experience in biotech or pharmaceutical industry
~Ability to...