Jobs in Juncos

Sr Validation Scientist with experience in Parenteral Manufacturing. Specifically experience focused on Aseptic Process Validation Aseptic Techniques Environmental Monitoring Performance Qualifications Environmental Characterizations Airflow Visualization (Smoke Tests). Experience writing protocols...

Sr Validation Scientist with experience in Parenteral Manufacturing. Specifically experience focused on Aseptic Process Validation Aseptic Techniques Environmental Monitoring Performance Qualifications Environmental Characterizations Airflow Visualization (Smoke Tests). Experience writing protocols...

Preventive Maintenance Execution ExperienceKnowledge Reading Drawing (Electrical/Mechanical)Machine Timing Adjustment ExperienceBasic knowledge in PLC/AutomationHydraulic and Pneumatic System KnowledgeVision System basic KnowledgeRequirementsAssociates and 6 months of maintenance work or military ex...

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...

Responsible for providing quality leadership governance and expertise in Quality Assurance processes related to the manufacture. Ensure compliance with regulatory requirements and West procedures. Proactively develop lead and drive the execution of the Quality Assurance strategy. Develop and impleme...

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...

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...

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...

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...

Validation Engineer with experience in automated equipment and vision system validation (protocol generation execution and reporting). Experience in generating manufacturing procedures and preventive maintenance. Strong knowledge generating validation documents: Installation and Operational Qualific...

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...

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

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...

GMP knowledge: Strong background in regulated environments with ability to apply GMP in manufacturing and validation. Validation expertise: Experience in drafting executing and approving validation. Time pressure filling: Hands-on experience with time pressure filling systems. Technical documentati...

Preferred experienceTechnical Report writingDesign of experimentAseptic Manufacturing (Filling)Process ValidationRequirementsDoctorate OR Masters 2 years of Engineering experience ORBachelors in Engineering 4 years of Engineering experiencePreferably Mechanical and Chemical Engineering

Junior Automation Engineer to support the development improvement and maintenance of automated production systems. This role contributes to enhancing product quality operational efficiency and safety while assisting engineering projects equipment upgrades and facility modifications. Duties:Support a...

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...

Specific responsibilities include but are not limited to: Complete Root Cause Analysis Apply Process Expertise capable of understanding process and controls require to assess for potential causal factors Assess process performance by observation of floor operations and review of performance data. S...