Physiology Knowledge Jobs in Salinas

Sr. Project Manager with experience of GMP s Validation System Life Cycle Methodology CMMS Maximo in pharmaceutical industry. Knowledge and experience in P&ID s and Electrical Schematics SMARTSHEETS.Preferable: Experience with Change Controls CAPA s and Deviations Management More...

Sr Engineer with experience in the Medical Device or Pharma industries. Knowledge and experience working with Change Controls on Trackwise.Knowledge in: Packaging equipmentDesign of new equipment processEngineering ProjectValidations and CommissioningCAPA and ComplianceRequirementsDoc More...

Performs a variety of duties in the electronic mechanical electromechanical and/or optical areas. Constructs troubleshoots calibrates adjusts tests diagnoses and maintains equipment components devices or systems. Works from schematics engineering drawings and written or verbal instruc More...

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 inciden More...

Quality Professional with Manufacturing Process Audit and Batch Record Review experience. In addition some knowledge or to be familiar with DAI process PASx/MES application MAXIMO SAP and LIMS. Available for nonstandard shift which includes nights and weekends.RequirementsDoctorate de More...

Sr Engineer with knowledge and experience working with Change Controls on Trackwise (Preferable) Packaging equipment Design of new equipment process Engineering Project Validations and Commissioning CAPA and Compliance. Experience in Medical Device or Pharma.Shift: Administration Shif More...

Help FEMA support those impacted by disasters! We are seeking an enthusiastic and experienced Team Leader to make a positive impact on our team members and customers. Come join our Team!Capitol Bridge Puerto Rico is located on the west side of the Island in Isabela on 699 Industrial A More...

Quality Assurance Coordinator to build and maintain site dedication to quality and excellence. The ideal candidate is an exceptionally organized methodical professional with the experience necessary to take the operation to the next level with respect to accuracy security and safety. More...

The Facilities and Engineering Support Specialist will be a key contributor to maintaining the integrity and compliance of F&E and our AML manufacturing facilities. This role involves providing crucial support in various areas including documentation changes pest control program m More...

Capitol Bridge's Isabela, Puerto Rico site invites talented individuals to join us as Help Desk Operator Intermediate to support an important government project. In this role, you will be a key player in providing essential IT support to our organization. As a mid-level team member, y More...

We are excited to announce upcoming Customer Service Representative opportunities beginning Summer 2024, in support of a critical government project. If you are interested in exploring this opportunity, please click APPLY NOW at the top of the screen.On-site Hours of Operation: Sunday More...

Capitol Bridge, Puerto Rico, is currently seeking a dynamic and experienced individual to join our team as a Senior Help Desk Operator at our Isabela site to support an important government project. As a leading organization, Capitol Bridge provides top-tier services while prioritizin More...

Capitol Bridge Puerto Rico is currently looking to hire Customer Service Manager for our Isabela, PR site at 699 Industrial Avenue, Isabela, PR 00662. The position requires on-site presence, with responsibilities including guiding, coaching, developing, and mentoring a team of operati More...

Sr Validation Scientist to provides and/or directs the technical validation engineering support of process and/or equipment upgrades, replacements, and modifications in the laboratory, manufacturing or manufacturing support environment.Experience executing cleaning validation in bio-p More...

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 inciden More...

Quality Engineer to serve as primary QA personnel, supporting the day to day manufacturing operations in AVPR.Responsibilities:Investigations QE and ME service engineer to address all the opportunities found in the assigned manufacturing line. QA management representative in the manuf More...

PSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all applicable regulatory requirements. Our goal is to skyrocket our clients success, and you More...

Manufacturing Engineerwith experience in medical devices industry.Project managementExercise knowledge of technical skills and understanding of the business objectives.Review of verification validation activities.CAPA and GMP Process.FDA regulations.RequirementsBS Engineering with 2 y More...

Education and/or ExperienceBachelor s degree in a scientific discipline.5+ years of quality assurance experience in a pharmaceutical or biotech environment.Extensive knowledge and understanding of cGMP regulations, Quality Systems and validation documentation.Technical writingProfic More...

Lead new and existing products change implementation review, from process evaluation through FDA approval and products launch. Execute all related activities to new products introduction andproduct changes and Change Control procedures. Assures that the Company complies with allintern More...

We are seeking Clinical Professionals (RN, LPNs, ADNs, social workers, etc.) to work as Patient Care Coordinators with Chronic Care Patients in a Call Center environmentBi-lingual in Spanish and English.Will service patients by working on their care plan and phone summary provided by More...

Manufacturing Engineerwith experience in medical devices industry.Project managementExercise knowledge of technical skills and understanding of the business objectives.Review of verification validation activities.CAPA and GMP Process.FDA regulations.RequirementsBS Engineering with 2 y More...

Lead new and existing products change implementation review, from process evaluation through FDA approval and products launch. Execute all related activities to new products introduction andproduct changes and Change Control procedures. Assures that the Company complies with allintern More...

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 inciden More...

Project Engineer with experience in process validations, equipment qualification, engineering projects, preferably in medical device industry. Verify manufacturing process documentation and quality documentation or regulations to make changes or modify the product labels as needed. C More...

Sr. Engineer with experience in medical device or pharmaceutical industry. Knowledge in:Packaging equipmentDesign of new equipment processEngineering ProjectCAPA and ComplianceValidations and CommissioningRequirementsDoctorate degree or Master s degree and 3 years of Engineering exp More...

Provides overall quality assurance leadership in the management and qualification of suppliers. Establishes and maintains quality assurance programs, procedures, and controls, ensuring that performance metrics of both the supplier quality systems and suppliers are continually measured More...

Quality Assurance professional with validations and commissioning & qualifications (manufacturing process, equipment and Critical Utilities) experience, technical writing, Quality Systems (Deviations, Change Control), Maintenance (PM, Work Orders, Job Plans review and approval) an More...

Validation Specialist to perform activities related to qualification of laboratory and manufacturing equipment in the Medical Devices industry.RequirementsBachelor Degree3-5 years of experienceKnowledge and experience in a GMP regulated environmentBilingual: English and Spanish; writt More...

We are seeking Clinical Professionals (RN, LPNs, ADNs, social workers, etc.) to work as Patient Care Coordinators with Chronic Care Patients in a Call Center environmentBi-lingual in Spanish and English.Will service patients by working on their care plan and phone summary provided by More...

Project Manager experience in regulated industries, with Sci Tech - Project Management.Oversee, manage and coordinate all operational aspects of ongoing department projects impacting multiple departments. Serve as liaison between project team and department.Change Control Owner (Docum More...

Process Development Sr. Associate Scientist:Identify raw material and container components (glass/polymer) defects.Knowledge regarding primary container components defects andclassifications.Perform experiments, records, organize data and analyze results under minimalsupervision.Under More...