Director Of It Jobs in Juncos

Responsible of performing finance partnering activities to support capital site strategy.Responsible for developing implementing and maintaining the financial plans and policies of the capital organization. In charge of establishing fiscal controls preparing financial reports advising management on...

SummaryThe Quality Applications Specialist supports quality systems and product transfer activities by ensuring compliant validation of computerized systems and manufacturing processes. The role focuses on sterilization equipment process validation and quality system compliance in regulated environm...

The Project Coordinator supports the SAP implementation at the Puerto Rico site by acting as the primary link between the D&T ERP/SAP teams and local business users. The role includes coordinating project activities managing communication assisting with requirement gathering and DevOps tasks maintai...

Bachelors Degree in Engineering preferred Mechanical Electrical or Chemical Excellent written and verbal communication skills Technical writing experience Working knowledge and experience with cGMP procedures and engineering practices on pharmaceutical/biotech production processes facilities and equ...

Preferred candidates will have Validation Experience in Parenteral Manufacturing. Specifically experience focused in Aseptic Process Validation Aseptic Techniques Environmental Monitoring Performance Qualifications Environmental Characterizations Airflow Visualization (Smoke Tests). Experience writi...

Sr Associate Tech Engineering with knowledge on: Mechanical equipment adjustment/troubleshooting. PLC Systems troubleshooting-RockwellVision Systems troubleshooting/adjustment-CognexcGMPs Systech vision systemsFDA regulation Basic control systems hardwareRequirementsMasters Degree or Bachelors Degre...

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...

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...

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...

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 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...

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...

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...