Medial Group in the United States is seeking a Manufacturing Engineer to lead and execute engineering projects within a regulated medical device environment, driving process improvements and supporting manufacturing validations. You will collaborate with Quality, Validation, Operations, Drafting, and
ZEO ScientifiX is seeking a Bioprocess Validation Specialist for its South Florida facility to support process development and validation activities in biologic manufacturing. This on-site role involves writing validation plans, determining acceptance criteria, and performing validation experiments. You will analyze data,
APPLICATION INSTRUCTIONS: CURRENT PENN STATE EMPLOYEE (faculty, staff, technical service, or student), please login to Workday to complete the internal application process. Please do not apply here, apply internally through Workday. CURRENT PENN STATE STUDENT (not employed
Posting number: 291-03 Department: POLICE DEPARTMENT Job classification: VALIDATION RECORDS ASSISTANT Posting type: Open Categories: Public Safety, 911 Telecommunications SummaryThis is a non-exempt position which requires responsible specialized clerical support duties specific to the unit, requiring public
Description Responsible for creating, supporting, and developing new and existing process designs related to manufacturing and fabrication processes. This is successfully accomplished by understanding, accurately specifying, and adhering to customer requirements, utilizing and applying quality tools and
Job SummarySalary: $65,000 to $80,000 Final pay determinations will depend on various factors, including, but not limited to experience level, education, knowledge, skills, and abilities. Our benefits and programs are comprehensive and thoughtfully crafted to ensure
AbbVie is seeking a technical expert to independently investigate, develop, and optimize methods to address critical project needs in barcelona Barceloneta area. The role emphasizes designing and analyzing experiments, mentoring teammates, and contributing to publications. The
Validation Specialist (Cleaning-In-Place) Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering,
Molding Process Engineer Job Description About Company At Ennovi we harness the power of two megatrends - electrification and AI - to help industries innovate at speed, operate smarter, and achieve sustainable growth. By combining these transformative
Molding Process Engineer About Company ENNOVI, a Mobility Electrification Solutions Partner, is a world leader in designing and manufacturing customized interconnect and high-precision system solutions for electric vehicles. We are fully dedicated to the mobility market with
Fresenius Kabi in Melrose Park, IL is seeking a project-focused engineer to lead the design, development and scaling of complex pharmaceutical formulations and processing technologies. You will guide a multidisciplinary team and manage projects from concept
About the job Validation Project Engineer Validation/Project Engineer needs 2-4 years related experience Validation/Project Engineer Bachelors degree in engineering or a related field of specialization. At least 2 years experience as a validation engineer in a similar industry. Experience in
Overview The Senior Business Process Lead – PPM is a Finance-led business process owner responsible for identifying business process capability gaps, standardizing business processes, defining and prioritizing Oracle ERP-enabled capabilities for Project Portfolio Management (PPM). This role leads the
Description We are seeking a Validation Engineer with hands-on experience in biotech/pharmaceutical manufacturing, specifically supporting aseptic filling operations (vials). This role will be responsible for executing and supporting validation activities for equipment, processes, and computerized systems in compliance
Medial Group seeks a Quality Engineer to provide QA support for day-to-day manufacturing operations in a regulated medical device environment. You will be the primary QA representative on the line, partnering with production and engineering to
Vaco is hiring for a Quality Assurance Engineer. Location: Ft Lauderdale, FL Compensation: $116-$129k/annually Position Summary Responsible for developing, maintaining, and improving manufacturing process quality by ensuring production processes are efficient, capable, and compliant with quality standards.
Validation Specialist (Cleaning-In-Place) Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering,
Get AI-powered advice on this job and more exclusive features. Direct message the job poster from BioStem Technologies (OTC: BSEM)Senior Human Resources Business Partner BioStem Technologies Job Type Full-time Description Why BioStem Technologies: BioStem Technologies, Inc.
A leading engineering firm is seeking an experienced engineer in Puerto Rico, specializing in process optimization for the pharmaceutical industry. The role demands a strong background in aseptic processing and regulatory compliance, with at least 4 years
Company Description ZEO ScientifiX is a publicly traded biotechnology company based in South Florida, dedicated to the research, development, and manufacture of new cell-derived biologics. The organization focuses on current and emerging regenerative therapeutics, positioning itself