Advanced CQV Consultant As an Advanced CQV Consultant you are responsible for the planning, execution, and delivery of commissioning, qualification, and validation (CQV) activities within pharmaceutical, biotechnology, and life science projects. This role independently executes complex CQV
ERP Data Management Lead The ERP Data Management Lead is accountable for ensuring the accuracy, integrity, and sustainability of production-critical master and transactional data across ERP-integrated planning and execution systems. This role provides dedicated ownership of data that underpins site
Validation Area Specialist - Finished Production Facility: Engineering & Technical Location: Clayton, NC, US About the Department You will be joining Fill & Finish Expansions (FFEx), which is responsible for all major expansion activities within aseptic production,
Data And Analytics Manager The Data and Analytics Manager supports the Colleges mission by transforming institutional data into actionable insights that inform strategic planning, enrollment forecasting, institutional effectiveness, and student success initiatives. This position is responsible for managing and
Pharmaceutical Validation Manager This role has responsibility and accountability for: Ensuring that the facilities, equipment, systems, and processes used in the manufacture and testing of Pharmaceuticals have been appropriately validated and maintained in a validated state. Organizing
Job Overview As a Sr. Design Engineer, you will be responsible for the design and engineering of PCX integrated electrical/mechanical assemblies. This role combines electrical power system design with manufacturability and production optimization to deliver safe,
Job Overview The Quality Inspector will be responsible for daily tasks associated primarily with inspecting quality products. This includes primarily the inspection and testing of electrical work, incoming and outgoing inspections, process checks, and adhering to
Job Overview As a Sr. Design Engineer, you will be responsible for the design and engineering of PCX integrated electrical/mechanical assemblies. This role combines electrical power system design with manufacturability and production optimization to deliver safe,
Service Enablement & Continual Service Improvement Manager Location: NC-Clayton, US Contract Type: Regular Full-Time Area: INFORMATION SYSTEMS Would you like to join an international team working to improve the future of healthcare? Do you want to
Administrative Assistant Under the supervision of the Director of Academic Support, the Administrative Assistant provides comprehensive administrative, fiscal, and compliance support to the federally funded TRIO Upward Bound program. Essential Duties and Responsibilities Maintain hard copy
AP Emissions Technologies LLC As a part of the global industrial organization Marmon Holdingswhich is backed by Berkshire Hathawayyoull be doing things that matter, leading at every level, and winning a better way. Were committed to
Technician (Process), Operations The Technician (Process), Operations role is an excellent opportunity for individuals with experience in manufacturing and/or packaging operations who are proficient with hands-on processing and production control activities. This role is responsible for
Sr IT Compliance Analyst Facility: Digital & IT Location: Clayton, NC, US At Novo Nordisk, we are helping to improve the quality of life for millions of people worldwide. For more than 100 years, we have
Sr. Pharmaceutical Automation Engineer Onsite 5 days per week 11810 Clayton, NC Duration: 12 months WebEx and Onsite Interview Summary We are seeking an experienced Senior Pharmaceutical Automation Engineer to support the implementation, commissioning, qualification, startup,
Company Profile The MM (MAYR MELNHOF) Group (MM) is a leading global producer of paperboard and folding boxes with an attractive range of kraft paper and uncoated fine paper for various end uses. MM promotes sustainable
Manufacturing Science And Technology Drug Product Manager You will manage the Manufacturing Science and Technology (MSAT) Drug Product technical delivery for drug product manufacturing of a defined product or product family with a primary focus on
CTE Program Specialist (CIMC) Location: Student Services Pay: Teacher Salary Scale Term of Employment: 12 Months Reports To: Director of Career and Technical Education Job Goal: To lead and support continuous improvement in the CTE program
IT Business Partner at Wilson, MA Job Description: IT Business Partner – Pharmaceutical Manufacturing Role Overview The IT Business Partner – Pharmaceutical Manufacturing serves as the strategic technology partner for Manufacturing, Quality, Engineering, and Supply Chain
Senior Cost Manager Life Sciences Construction Turner & Townsend is a global professional services company with over 22,000 people in more than 60 countries. Working with our clients across real estate, infrastructure, energy and natural resources,
Lab CQV Specialist The QC Laboratory Equipment Qualification & Validation Specialist manages the full lifecycle of quality control laboratory equipment in a GMP-regulated pharmaceutical environment. This role leads the installation, commissioning, qualification, decommissioning, and re-commissioning of analytical