📑 Performance Validation, Inc has provided Commissioning, Qualification and Validation services to the life science industries for 35 years. PV is a 100% employee owned company with teams in Indiana, Michigan, Illinois, Kansas, North Carolina, and Washington providing support throughout the US and overseas.PV is committed to providing growth opportun ...
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📑 Solutions Architect Role Overview: As a Solutions Architect, you will be responsible for designing and implementing comprehensive technical solutions that address complex business challenges. Leveraging your expertise in Azure and other IT tools, you will collaborate closely with internal stakeholders to gather and tra ...
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📑 Description Summary Currently seeking candidates interested in upcoming projects: The Revenue Cycle Solution Lead provides consulting services to clients on Cerner-related projects. You will provide subject matter expertise during client engagements to deliver solutions to achieve defined benefits. You ...
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📑 THE COMPANY : Juul Labs’ mission is to impact the lives of the world’s one billion adult smokers by eliminating combustible cigarettes. We have the opportunity to address one of the world’s most intractable challenges through a commitment to exceptional quality, research, design, and innovation. Backed by leading techno ...
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📑 Title: Validation EngineerLocation: California (Onsite)Duration: 12 MonthsOn W2 onlyInjectable Filler / IV Bags Filling experience must.Aseptic Processing is must.knowledge of validation lifecycles for computerized systems (CSV), aseptic processing, sterilization validation, and equipment/facility/utility validation.GMP compliance knowledgePositio ...
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📑 The Validation Consultant is a key member of the project team, focusing on the validation of equipment, processes, and systems in large-scale, sterile pharmaceutical manufacturing environments. This role involves the development, implementation, and execution of validation strategies to ensure compliance with industry standards and regulatory requi ...
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📑 Hughes Engineering & Consulting is an exciting, fast-growing company focused on Process Engineering, Project Engineering, Project Management and CQV solutions for the pharmaceutical industry. We offer great benefits, and exciting challenges for both career development as well as personal leadership development.Company Culture Guidelines & Values:We ...
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📑 VTI Life Sciences (VTI)is seeking forward-thinking and ambitious engineers looking to accelerate their career in the pharmaceutical, biotechnology and medical device industries. We offer an opportunity to help support our teams of industry subject matter experts and thought leaders while consulting with some of the biggest companies in the Life Sci ...
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📑 VTI Life Sciences (VTI) is seeking forward-thinking and ambitious engineers looking to accelerate their career in the pharmaceutical, biotechnology and medical device industries. We offer an opportunity to help support our teams of industry subject matter experts and thought leaders while consulting with some of the biggest companies in the Life Sc ...
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📑 Job Purpose:Working in a team environment, the Quality Validation Manager is responsible for managing and providing oversight for projects and team members responsible for execution of validation deliverables for all local manufacturing sites, including, but not limited to equipment, utilities, facilities, cleaning, and computer systems. The manage ...
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📑 Project Description: New Filling LinesContractor Tasks and Responsibilities:Job Description:The client is looking for 6 Process Validation Engineer consultants who have experience doing process validation in an aseptic filling line manufacturing facility.There are 5 filling lines and need to help with the process validation.The Process Validation e ...
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📑 Our client, a global bio-pharmaceutical company, that specializes in core therapeutic and business areas, including gastrointestinal and inflammation, rare diseases, plasma-derived therapies, oncology, neuroscience and vaccines, is actively looking to add a Sr. Validation Engineer to their team. This position will be on-site in Los Angeles.Salary: ...
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📑 Validation Engineering Manager, ADC Manufacturing - Songdo, South KoreaThis is a stellar opportunity responsible for leading ADC Validation Engineering processes and serving as a SME for ADC manufacturing. This is a once-in-a-lifetime Global Expat leadership opportunity within the World’s Largest biologics CMO expanding to 620,000L total mammalian ...
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📑 Join a leading force in the contract manufacturing and pharmaceutical development industry, which operates on a global scale in partnership with leaders in the pharmaceutical and biotechnology field.This organization is at the forefront of innovation, having played a part in countless product development and commercialisation efforts throughout the ...
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📑 Join a leading force in the contract manufacturing and pharmaceutical development industry, which operates on a global scale in partnership with leaders in the pharmaceutical and biotechnology field.This organization is at the forefront of innovation, having played a part in countless product development and commercialisation efforts throughout the ...
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📑 CSV EngineerBoston/Rhode Island Responsibilities:Draft and implement Quality System documentation designed to establish good validation practices within the organization.Author URS, FRS, Risk Assessments, Configuration specification, design specification and CSV test protocols and execute them in compliance with GDP guidelines and internal quality ...
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📑 CQV EngineerBoston/Rhode Island Responsibilities:Draft and implement Quality System documentation designed to establish good validation practices within the organization.Author URS, IQ, OQ and PQ protocols and execute them in compliance with GDP guidelines and internal quality standards.Design validation approaches, supported by appropriate statist ...
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📑 Seeking a qualified chamber validation specialist to play a critical supportive role to the Facility Engineer. Must have proficiency with chamber (cold room, refrigerator, freezer, bio safety cabinet, etc.) validation and equipment troubleshooting. Also competent in protocol development and execution with experience with Kaye Validator (or similar) ...
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📑 Client Platform Validation Engineer will work with internal teams and our OEM customer teams during post silicon platform development, own the execution and automation of our validation strategy to ensure coverage plans are executed on time to meet customer development or sustaining milestones.The Person:The ideal candidate is a hardware/software e ...
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📑 Previous Pharmaceutical/Biotech experience is mandatory for this role.MMR Consulting is an engineering and consulting firm specializing in the pharmaceutical and biotechnology industries. Its services include Engineering, Project Management, and other Consulting services. MMR’s Engineering expertise includes Process, Automation, Facilities engineer ...
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📑 VTI Life Sciences (VTI) is seeking forward-thinking and ambitious engineers looking to accelerate their career in the pharmaceutical, biotechnology and medical device industries. We offer an opportunity to help support our teams of industry subject matter experts and thought leaders while consulting with some of the biggest companies in the Life Sc ...
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📑 Senior CQV / Validation Engineer / Specialist - PHARMACEUTICALPrevious Pharmaceutical/Biotech experience is mandatory for this role.MMR Consulting is an engineering and consulting firm specializing in the pharmaceutical, and biotechnology industries in North America and globally. Its services include Engineering, Project Management, Validation and ...
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📑 Senior Validation EngineerAre you a validation expert looking for a new, dynamic environment? I am partnering with a rapidly growing full service CDMO who are specialised within sterile product development, manufacturing and packaging, and am working with the leadership team to help appoint a number of new hires.For this specific hire, we are seeki ...
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📑 *US Citizens or Greencard Holders only***No C2C**Work Schedule: Onsite - M-FSalary: $60-70/hrDuration: 4 monthsPrimary Responsibilities:Support the Quality Engineering group with documentation and validation needs.Draft URS documents, design specifications, testing protocols, and final reports.Perform hands on validation execution for automation im ...
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📑 VTI Life Sciences (VTI)is seeking forward-thinking and ambitious engineers looking to accelerate their career in the pharmaceutical, biotechnology and medical device industries. We offer an opportunity to help support our teams of industry subject matter experts and thought leaders while consulting with some of the biggest companies in the Life Sci ...
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📑 VTI Life Sciences (VTI)is seeking forward-thinking and ambitious engineers looking to accelerate their career in the pharmaceutical, biotechnology and medical device industries. We offer an opportunity to help support our teams of industry subject matter experts and thought leaders while consulting with some of the biggest companies in the Life Sci ...
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📑 Title – Quality EngineerLocation – North Haven, CT (Onsite)MEDICAL DEVICE MANUFACTURING • Contribute to continuous improvements in overall product cost and quality.• Participate in DFM / DFA activities assuring that packaging/production processes and equipment are taken into consideration.• Collaborate with Quality Engineering to provide manufactur ...
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📑 The Automation Consultant is a vital player in the pharmaceutical manufacturing industry, offering expertise in the design, implementation, and validation of automation systems. With proficiency in a range of automation technologies including Rockwell, Siemens, Cyvita, Allen Bradley, DeltaV, Emerson, Veeva, Honeywell, Johnson Controls, SCADA, Maste ...
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📑 VTI Life Sciences (VTI) is seeking forward-thinking and ambitious engineers looking to accelerate their career in the pharmaceutical, biotechnology and medical device industries. We offer an opportunity to help support our teams of industry subject matter experts and thought leaders while consulting with some of the biggest companies in the Life Sc ...
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📑 Location: Charleston, South Carolina, USReporting to: Head of Manufacturing EngineeringSHL Medical is the world-leading solution provider in the design, development, and manufacturing of advanced drug delivery systems with more than 5000 employees worldwide. Our customers include top pharmaceutical and biotech companies from around the globe that r ...
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📑 PharmaLex is now part of Cencora. We are one of the largest providers of Development Consulting & Scientific Affairs; Regulatory Affairs; Quality Management & Compliance; and Pharmacovigilance, Epidemiology and Risk Management worldwide. Through our US, European and Asia-Pacific offices, our trusted consultants provide specialized, regulated servic ...
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📑 Job Title: Validation & Verification Engineer - ADASQualification: BE/BTech/ME/MTech/MS-Electronics And Communication Engg Experience: 7 To 12 Year(s)Skill set: C, Python, or similar programming knowledge, CAN, Ethernet.Domain knowledge1. Knowledge of XCP/ISO26262/ISO14229 2. Automotive domain experience 3. Knowledge of Ethernet/SOMEIP/CAN/LIN 4. Kn ...
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📑 Tata Elxsi brings together the best technology and user-centric design expertise to help customers deliver innovative solutions and great consumer experiences. Our integrated Design and Technology teams help enterprises reimagine their products and services – from strategy, consumer research and insights, to service and experience design, technolog ...
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📑 VTI Life Sciences (VTI) is seeking forward-thinking and ambitious engineers looking to accelerate their career in the pharmaceutical, biotechnology and medical device industries. We offer an opportunity to help support our teams of industry subject matter experts and thought leaders while consulting with some of the biggest companies in the Life Sc ...
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📑 VTI Life Sciences (VTI)is seeking forward-thinking and ambitious engineers looking to accelerate their career in the pharmaceutical, biotechnology and medical device industries. We offer an opportunity to help support our teams of industry subject matter experts and thought leaders while consulting with some of the biggest companies in the Life Sci ...
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📑 Role: SDET Engineer with Java Automation exp. Location: Issaquah, WA (Onsite) Duration 12 Months Job Duties/Essential Functions for SDET Engineer Creates defects with detailed information pertaining to the failed test case/scenario with supporting documentation (screenshots ...
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📑 Job title: Battery Storage Systems Engineer Location: United States (Remote) TGRC is excited to be partnering with a multinational battery manufacturer to appoint a remote Battery Storage Systems Engineer. This client designs, develops, produces and services batteries in 19 countries with a team of 4000 people ...
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📑 We are currently searching for a Senior Design Quality Engineer to join an exciting medical device start up in Carlsbad, CA. This rapidly growing company is expected to go public in the next 18 months. The Senior Design Quality Engineer will work developing risk management process and design controls for two key medical device systems in different ...
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📑 A key client of mine is seeking a highly skilled and experienced Data QA Engineer to join their team. In this role, you will be responsible for performing data quality analysis and validation, writing test plans, test cases, and test scripts, and validating solutions built on REST APIs, Snowflake, and data pipelines. The successful candidate will b ...
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📑 Join Our Team as a Validation EngineerAre you ready to make a significant impact in the cloud networking industry? Our client, a premier cloud networking company, is seeking a talented Validation Engineer to join their Electrical Design Validation Testing (EDVT) team. As a Validation Engineer, you will play a crucial role in ensuring the functional ...
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📑 Job Purpose:Responsible for directing, managing, and maintaining the development, validation and control ofsoftware products such as embedded software, applications, and software as a medical device(SAMD).Duties:Lead software verification and validation activities for products under development in accordance with company procedures.Author and appro ...
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📑 CVS ConsultantContractRemoteNo H1B and/or C2C Please!!One of our leading pharmaceutical clients is looking for a Computer System Validation Consultant, who will be responsible for creating a Network Operations Plan, Protocols, Documentation, and Standard Operating Procedures (SOPs)Required Skill & Experience:Pharmaceutical experience.3-7 years expe ...
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📑 1. Equipment was installed last year (This is a Kerber, a part of the Harro Heffelinger brand. Any type of experience around visual inspection equipment is ideal, but not mandatory). Currently doing validation of this equipment. Then moving to FAT, installation and qualification of identical equipment2. Bioreactor installation Attention to detail, ...
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📑 VTI Life Sciences (VTI)seeks forward-thinking and ambitious engineers looking to accelerate their careers in the pharmaceutical, biotechnology, and medical device industries. We offer an opportunity to help support our teams of industry subject matter experts and thought leaders while consulting with some of the biggest companies in the Life Scienc ...
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📑 The ideal candidate possesses experience in Biomanufacturing with an Engineering mind and lives in the Raleigh-Durham, North Carolina area as this role is 100% onsite. You will play a critical supportive role to the Engineering team in creating and refining processes in order to improve manufacturing safety, quality, and productivity.Please note th ...
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📑 Job Responsibilities:Ensures that suppliers deliver quality parts, materials, and services.Qualifies suppliers according to company standards and may administer a Certified Supplier Program in receiving inspection to ensure cost effectiveness.Monitors parts from acquisition through the manufacturing cycle and communicates and resolves supplier rela ...
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📑 VTI Life Sciences (VTI) is seeking forward-thinking and ambitious engineers looking to accelerate their career in the pharmaceutical, biotechnology and medical device industries. We offer an opportunity to help support our teams of industry subject matter experts and thought leaders while consulting with some of the biggest companies in the Life Sc ...
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📑 Senior Director, CMC Development- APILocation: Charlottesville, VA or Bay Area, CARivus Pharmaceuticals is searching for a Senior Director, CMC Development to set and lead a scalable CMC strategy to advance a new class of investigational medicines called controlled metabolic accelerators (CMAs) that have the potential to improve metabolic health fo ...
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📑 Software Quality Assurance Analyst - Rochester, NYLong term contract - $40/hr to $50/hrThe Software Quality Assurance Analyst will conduct verification and validation activities for the Shop Floor Information Systems and other computer systems for use in the manufacturing and release of Medical Device products (Contact Lenses) on a project bases an ...
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📑 Associate Quality EngineerDirect Hire Full-Time RoleSalary Range: $80,000 - $100,000 per yearLocation: Santa Clara, CA - Hybrid RoleDuties and Responsibilities:Provide the Quality Department support for products, ensuring that our actions meet our customers' needs while maintaining compliance with federal law and applicable standards.Investigate an ...
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