We're #hiring a new Validation Specialist in Clayton, North Carolina. Apply today or share this post with your network.
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Qualification and validation in Pharmaceutical manufacturing
Validation vs Qualification
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new opportunity
BEPC is looking for Staff Validation Engineer for best Medical Device company at Ciudad Juarez. If you are interested please send your resume asap to alozano@bepcinc.com #MedicalDevice #HiringNow #ValidationEngineers
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Temperature Mapping Got You Stressed? | Let me help | Follow for Temp Mapping & Validation Insights ✨
Redefining the Role of a Validation Specialist More Than Just Compliance. ↳ Validation isn't just ticking boxes or following guidelines. It's about much more. Ensuring Quality and Safety. Our goal? ↳ To make sure products and processes not only meet regulatory standards but are also safe and effective for end-users. Making a Difference. ↳ Every day, our work impacts quality, safety, and usability. We're not just specialists; we're trendsetters, making a difference. 🤔 Think About It. Validation is an art and a science. It's about balancing regulations with practicality and safety. Skills That Matter. ↳ Attention to detail defines precision and excellence in our work. ↳ Critical thinking to fuel our problem-solving and innovation. ↳ Effective communication to drive collaboration & success. These aren't just skills; they're our mantra for success in any endeavor. ♻️ Share If You Believe in Quality! Let's celebrate the importance of thorough validation. Protects → Improves → 🫱🏾🫲🏽 #validationengineer #validation #validationspecialist
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urgent contract roles
🔥 🔥 URGENT 🔥 🔥 Consultant hourly paid roles open in a pharma company-Cork. 12 months' length of the contract. ✅ C&Q Engineer/Process Engineer ✅ Validation Consultant ✅ Validation Consultant & Quality Compliance Contact me at bruna@bakerfinn.com
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🌟 Key Skills for Excelling in Continuous Improvement in the Med Device Industry 🌟 Achieving excellence in the medical device industry requires a strong focus on continuous improvement. Here are the three essential skills professionals need: Regulatory Compliance Expertise 📜 Master the intricacies of ISO 13485 and FDA regulations. Staying compliant with these standards ensures product reliability and safety, minimizing risks and maintaining market approval. Data-Driven Analysis 📊 Develop proficiency in tools like Six Sigma and Lean methodologies. Using data to drive decisions helps identify areas for improvement, optimize processes, and enhance overall efficiency. Effective Communication and Feedback Integration 🧠🗣️ Hone your ability to communicate effectively and integrate customer feedback. This ensures that improvements align with market demands and enhances customer satisfaction and loyalty. At Grove Technical Resources, we connect top talent with leading companies in the medical device industry. Follow us for the latest insights and opportunities! #MedicalDevices #ContinuousImprovement #QualityManagement #RegulatoryCompliance #MedTech #StaffingSolutions #FollowUs #Hiring #QualityEngineer #manufacturingengineer
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#hiring *Director, Engineering (Drug-Device Combo Products)*, Philadelphia, *United States*, fulltime #jobs #jobseekers #careers #Philadelphiajobs #Pennsylvaniajobs #Engineering *Apply*: https://lnkd.in/gMesTF7p Director, Engineering (Drug-Device Combo Products) page is loaded Director, Engineering (Drug-Device Combo Products) Apply locations Philadelphia, PA, USA time type Full time posted on Posted Yesterday job requisition id JR106535 Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. We are PCI. Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI. Summary of Objective: The main responsibilities of the Director, Engineering for drug-device combination products are focused on the planning and execution of projects from estimating to launch: Manage and communicate the site portfolio of drug-device combination product NPI projects, ensuring projects are managed to intended capital and resource cost and scope Provide resources and oversight to project estimating activities to develop a trusted project resource plan Own the resource planning process for the NPI engineering team, coordinated with other functional leaders (quality, validation, facilities, etc.) providing resources to project teams. Provide support to project teams, taking on risk mitigations, issue resolution, and escalations to ensure on-time launches at target quality and unit cost Leading change and continuous improvement activities for the drug-device combination products NPI process Primary Key Performance Indicators (KPI) are On Time Equipment Commissioning and Product Launch; Project Cost Performance; Product Launch Quality and Cost Target Achievement Essential Duties and Responsibilities: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The essential duties and responsibilities include the following but other duties may be assigned. Oversees NPI engineering project management for drug-device combination products.Supervises a staff of engineers and/or engineering technicians.Prioritizes and guides engineering and project management resources in the design of new or improvement/expansion of existing assembly and packaging processes to deliver FDA compliant production capacity on time and within budget according to business plan.Plan and manage capital plan for facility and production equipment related spending to assure production can meet new product development, equipment commissioning, product launch, and contract packaging requirements.Works with global engineering to guide the specification and selection of manufacturing equipment/utility equipment and awards architectural and engineering contracts based on competitive
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Sr. Medical Device Executive Recruiter & Certified Senior Account Manager-15 years of experience networking, career management, and helping medical device companies build world class teams. (443) 921-9021
ARE YOU HIRING? Medical Device experienced VP Product Development in search of their next career opportunity-background sneak peek: BS Biomedical and Environmental Engineering 25+ years of medical device development experience with wide breadth of applications Team builder with proven success in project, program and portfolio management Extensive development, regulatory, quality management and commercialization experience FDA & CE Marked Class I/II products from concept through commercialization 45+ product lines and product line extensions Risk-based QMS, including design controls, from development through post-market compliance IP portfolio management and L&A opportunity assessment 30+ 510(k) submissions and clearances spanning 15+ product codes 9 issued patents Spinal orthopedic implantables with instrumentation and medical air quality applications Titanium, stainless steel, polymer, composite and biologic materials applications Conventional and additive manufacturing utilizing steam, EtO and Gamma sterilization KOL relationship champion from surgeon developers to post launch customer interaction Compliance and comprehensive knowledge FDA 21 CFR Part 820 / ISO 13485 / ISO 14971 Product development project team interdisciplinary leader Development team builder including team member mentoring training and talent development For more information, Call/Text/EM 443.921.9021 cgrimes@mriglobalmeddevice.com #medicaldevice #medicaldevices #hiring #nowhiring #job #jobs #recruiting #recruiter #cherylgrimes NOTE: For 14 years I’ve been helping medical device companies find great talent, great talent find great companies, and with networking for #quality #qa #ra #regulatoryaffairs #clinicalaffairs #r&d #development #manufacturing #operations #marketing #supplychain and more. People like working with me because I am relationship driven, not transaction driven. We should know each other!
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