To Go Specialist Jobs in Juncos

Expericence in Quality and ComplianceExperience with validation protocols and reports for clean utilities manufacturing processes cleaning processes equipment computerized systems change control records deviationsetc. Experience in biological processes is desired.RequirementsDoctorate OR Masters 2...

QRC Group is a leading provider of consulting engineering validation quality and talent solutions for the pharmaceutical biotechnology and regulated manufacturing industries. Our mission is to connect top-tier talent with essential projects that drive innovation quality and operational excellence fo...

Aseptic Process NPI Change Control FATs Validation and PPQsRequirementsDoctorate OR Masters 2 years of directly related experience ORBachelors 4 years of directly related experience ORAssociates 8 years of directly related experience ORHigh school/GED 10 years of directly related experience.Life...

Lead and execute Computer System Validation (CSV) activities for Quality Information Technology systems in compliance with FDA GxP ISO and global regulatory requirements.Conduct and maintain formal validation documentation including Validation Plans Risk Assessments IQ OQ PQ protocols and reports an...

Change Control Documentation Review Validation PPQRequirementsDoctorate OR Masters 2 years of directly related experience ORBachelors 4 years of directly related experience ORAssociates 8 years of directly related experience ORHigh school/GED 10 years of directly related experience.Bachelor Degr...

Aseptic Process NPI Change Control FATs Validation and PPQsRequirements-Doctorate OR-Masters 2 years of directly related experience OR-Bachelors 4 years of directly related experience OR-Associates 8 years of directly related experience OR-High school/GED 10 years of directly related experience....

NPI Change Control Documentation Review Validation C&Q PPQ FATRequirementsDoctorate OR Masters 2 years of directly related experience ORBachelors 4 years of directly related experience ORAssociates 8 years of directly related experience ORHigh school/GED 10 years of directly related experience.S...

NPI Change ControlFATsValidationPPQsRequirementsDoctorate OR Masters 2 years of directly related experience ORBachelors 4 years of directly related experience ORAssociates 8 years of directly related experience ORHigh school/GED 10 years of directly related experience.Life Science or Engineering

NPIChange ControlDocumentation ReviewValidationPPQFATRequirementsDoctorate OR Masters 2 years of directly related experience OR Bachelors 4 years of directly related experience ORAssociates 8 years of directly related experience ORHigh school/GED 10 years of directly related experience.Bachelor...

Experience with: VeevaTrackwiseCAPAChange ControlRequirementsDoctorate degree OR Masters degree and 3 years of Manufacturing Operations experience ORBachelors degree and 5 years of Manufacturing Operations experience ORAssociates degree and 10 years of Manufacturing Operations experience ORHigh scho...

Experience in deviations DQMS experience in leading multidisciplinary teamsRequirements-Doctorate OR Masters 2 years of Manufacturing Operations experience OR Bachelors 4 years of Manufacturing Operations experience OR-Associates 8 years of Manufacturing Operations experience OR-High school/GED...

Business Strategy & Organizational EffectivenessServe as a strategic HR partner to the Supply Chain function providing input into business and people strategy.Represent the OneHR model and provide strategic guidance aligned to business objectives.Demonstrate fluency in business strategies financial...

Experience with Veeva Trackwise CAPA Change ControlRequirementsDoctorate degree OR Masters degree and 3 years of Manufacturing Operations experience ORBachelors degree and 5 years of Manufacturing Operations experience ORAssociates degree and 10 years of Manufacturing Operations experience ORHigh sc...

Bachelors in Science or Engineering is preferredManufacturing ExperienceHands on experience managing CAPA & Change ControlsDocument revisionsVEEVARequirementsDoctorate OR Masters 2 years of Manufacturing Operations experience OR Bachelors 4 years of Manufacturing Operations experience OR Associate...

Description:Perform one or more of the following duties and responsibilities in support of site Quality Assurance program under minimal supervision. Review and approve product MPs. Approve process validation protocols and reports for manufacturing processes. Request Quality on incident triage team....

Software Application Configuration Specialist to integrate their expertise in the implementation of TULIP System. Background in industries such as Medical Devices & Pharma. Responsibilities: Contribute to practice goals and continuous improvement initiatives technology. Engage in business process a...

The Associate Quality Application Specialist supports the validation administration and compliance of quality-related computerized systems in a regulated environment. This role assists with validation documentation system configuration and cross-functional coordination to ensure compliance with appl...

Applies advanced technical process solutions in packaging technology and process ensuring priorities align with customer needs technology management objectives company goals and government regulations. Implements new packaging technologies for the Site. Leads all the packaging process qualifications...

Specialist Quality Control with experience in the Pharmaceutical Industry Quality Control Laboratory Testing Project Management and Quality processes. Preferable experience as Microbiologist Chemist Biochemistry Molecular Sciences or Chemical Engineering.Skills:Scientific Data AnalysisStrong Technic...

Specialist Quality Control with experience in regulated industry.Skills: Scientific Data AnalysisStrong Technical Writing (English and Spanish) mainly focusesStrong knowledge of Microsoft Excel as a Tool for Data AnalysisGood Communication skillsProject ManagementKnowledge in Computer System and Met...