Job Description SummaryLocation: Morrisville, North Carolina Join Novartis and play a pivotal role in shaping the future of pharmaceutical manufacturing at our growing Morrisville site. As the Validation Lead, you will drive the site’s validation strategy across process, cleaning,
If you’re looking for a special place to build or grow your career, you’ve found it. Whether you’re an experienced professional, a recent college graduate or somewhere in between, IDEX is a place where you can
Job LocationCINCINNATI GENERAL OFFICES Job Description Job Description The Picking Platform Process Engineer will be responsible for optimizing manufacturing processes, improving efficiency, and ensuring product quality for platform picking. As a Picking Platform Process Engineer you will learn
If you’re looking for a special place to build or grow your career, you’ve found it. Whether you’re an experienced professional, a recent college graduate or somewhere in between, IDEX is a place where you can
BandLevel 3 Job Description SummaryStep into a role where your technical expertise directly drives the success of life-changing medicines. As a Process Expert, you will be at the heart of manufacturing operations, ensuring processes run smoothly, compliantly,
Job Description SummaryStep into a role where your technical expertise directly drives the success of life-changing medicines. As a Process Expert, you will be at the heart of manufacturing operations, ensuring processes run smoothly, compliantly, and efficiently.
Position Summary The cleaning validation position will be responsible for developing, maintaining, and approving the cleaning validation requirements ensuring compliance to the applicable business and regulatory standards. Develop and maintains site cleaning and cleaning validation processes from product development
Description Verista’s 500 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific
Position Summary The Multi-Process Press Specialist is responsible for the safe, efficient, and high-quality operation of multi-color lithographic printing presses (up to seven colors) and advanced coating systems. This role requires a high level of technical expertise,
Work ScheduleStandard (Mon-Fri) Environmental ConditionsAdherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Description Discover Impactful Work:
Description Verista’s 500 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific
BandLevel 3 Job Description SummaryJoin a team committed to delivering life-changing therapies to patients worldwide. As a Process Engineer III, you will provide engineering support for manufacturing equipment, facilities, and utilities, driving reliability, compliance, and continuous improvement
Job LocationCINCINNATI GENERAL OFFICES Job Description Role Summary The PrIME Operations BPX serves as the site’s system authority for the PrIME Warehouse Management System (WMS), ensuring reliable system performance, operational continuity, and continuous improvement of warehouse
Job Posting TitleProcess Engineer Job Description SummaryDauch is seeking a Process Engineer to join our world-class team. This is an outstanding opportunity to be part of a leading company in the automotive industry, where you will have
Job Posting TitleProcess Engineer Job Description SummaryDauch is seeking a Process Engineer to join our world-class team. This is an outstanding opportunity to be part of a leading company in the automotive industry, where you will have
Validation Project Lead / Documentation Audit LeadMajor Pharmaceutical Facility Construction Project Location: Durham, NC - FST Life Science office FST Technical Services is seeking an experienced Validation Project Lead / Documentation Audit Lead to support a large pharmaceutical
AVP, Model Validation The AVP, Model Validation is responsible for model validation and ensure they are meeting Model Risk Management policies, standards, procedures as well as regulations. This role requires high level of expertise with minimal technical supervision, requiring
Company Overview: Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal
Position Summary Responsible for creating, optimizing, developing, updating, and sustaining diagnostic assays and reagents in a regulated environment while driving innovative solutions. Design and develop new biomolecules or reagents, collect and manage biological samples to support
Minimum Qualifications: (Education, Experience, Knowledge, and Skills): High School Diploma or equivalent required. Associate’s degree preferred. 2+ years of experience in a manufacturing environment, preferably in the assembly of electrical switchgear and/or power generation equipment. 1+