Engineering Services Jobs in Carolina Ak
Engineering Services Jobs in Carolina Ak
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Associate Tech Engineering with experience in Packaging Equipment such Thernoformer Cartoner Case Packer Labeler assembled equipment Vision System Serialization Sensors Cobots Mechanical Adjustment Motor replacement VFD PM Train Tool PLC Back Up Pneumatic Electrical / Mechanical Troub 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...
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...
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...
Manufacturing Systems Engineer with:Ability to read and update electrical design packages including User Requirements (URS) Functional Specifications (FS) Design Specifications (DS) wiring diagrams and P&ID.Proficient in PLC Controller and HMI programming skills.Qualifications: Ba More...
Industrial Mechanic with experience in regulated industry working with packaging and filling equipment to perform equipment maintenance troubleshooting set up. RequirementsAD Industrial Mechanic Engineering Instrumentation or relatedAt least 3 years of experience with packaging or fil More...
Engineer to support the execution of manufacturing/quality systems such as deviations process validation process monitoring procedures training and new product introductions. Apply process operational scientific expertise basic compliance knowledge and analytical and troubleshooting s More...
Engineer with background in regulated industries and experience in: Biotechnology Purification Processes Process Troubleshooting Product Impact Assessment Technical WritingRequirementsMasters or Bachelors degree in Engineering & 2 years of Engineering experienceTechnical WritingBi More...
Sr. Validation Scientist with experience in Validation with preference in Process Validation in a regulated environment. To provide technical validation engineering support of process and/or equipment upgrades replacements and modifications in the laboratory manufacturing or manufactu More...
Project Manager with experience in:Change Control Deviations (as owner)Managing/leading New Product Introduction (Product Transfer)Product lifecycle managementProcess Improvements ProjectsRequirementsDoctorate degree or Masters degree and 2 years of Project Management experience or Ba More...
Sr Associate Buyer with experience in:Management of requisitions PO conversion per SAP Report. SAP experienceManage supplier communication and escalation regarding; PO delivery postponement past due/missed orders PO quantity discrepancies closing balances missing documents COA / packi More...
Help Desk Operator Intermediate - Junior Operator
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...
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...
Operations Call Center Help Desk Manager
Capitol Bridge LLC is seeking an experienced Operations Call Center Help Desk Manager to join our Isabela, Puerto Rico leadership team. The Operations Call Center Help Desk Manager must be on-site daily as scheduled and will be supporting projects that provide contact center, leadersh More...
About Capitol Bridge Founded in 2012, Capitol Bridge is based in Arlington, Virginia and is an SBA 8(a) Certified Small Disadvantaged Business with proven expertise providing independent medical reviews, records/data management services, medical coding, administrative staffing, and More...
Job SummaryCapitol Bridge Puerto Rico is seeking an on-site Quality Assurance Analyst for our Isabela site located at 699 Industrial Avenue, Isabela PR 00662. Come join our Team! To prepare you for this endeavor, Capitol Bridge Puerto Rico will offer paid, comprehensive training that More...
Capitol Bridge Puerto Rico is seeking on-site Customer Service Representatives (Level I) for our Isabela site located at 699 Industrial Avenue, Isabela PR 00662.Pay Rate: $13.00 p/hCome join our Team! To prepare you for this endeavor, Capitol Bridge Puerto Rico will offer paid, compre More...
Capitol Bridge Puerto Rico is seeking a full-time Training II Specialist that is responsible for facilitating classroom training (onsite and remotely). This trainer will support the design, development, and distribution of training programs and materials. This role includes partnering 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...
Equipment Qualification Specialist with experience in the pharmaceutical industries to support equipment qualification projects. Experience with utilities and manufacturing equipment qualification processes. Experience in technical presentation, issue organization, and analytic 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...
Quality Assurance Specialist to provides support to complaint product return, investigation, and resolutions and conduct quality-related activities to deliver consistent, high-quality documents, services, products, and processes.Responsibilities:Completes compliant documentation and p More...
Validation Specialist with experience in regulated industry to perform chemist laboratory equipment validations.RequirementsBachelor in Science or EngineeringAt least five years experience with laboratory equipment validationsBilingual (Spanish/English)Technical writing Bachelor in Sc More...
Validation Specialist
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...
Validation Quality Specialist
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...
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...
Care Technician I with experience in customer service, product support, IT, and telecommunications in medical device industry tomonitoring inquiries and complaints from health care professionals, field personnel, patients, and various internal departments.Answer inquiries regarding te More...
To provide support on ongoing construction projects for a medical devices industry. Will coordinate constructions projects and will serve as liaison between project team and department management.RequirementsBachelors Degree in EngineeringExperience coordinating constructions projects 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...
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...
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...
Experience as Specialist QA in Pharmaceutical GMP regulated manufacturing.Responsibilities:Review and approve product MPs.Approve process validation protocols and reports for manufacturing processes. - Request Quality on incident triage team.Approve Environmental Characterization repo 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...
Quality Assurance Specialist to provides support to complaint product return, investigation, and resolutions and conduct quality-related activities to deliver consistent, high-quality documents, services, products, and processes.Responsibilities:Completes compliant documentation and p 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...
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