6085 - Senior CQV Engineer / Senior Validation Engineer - Holly Springs

We are seeking a Validation Engineer to join our team. The ideal candidate will have experience in commissioning and qualification in regulated industries. · Develop documentation for CQV activities · Write and execute protocols (field verification) · ...

We exist to be the trusted solution for our clients as they strive to build a better working world and improve the human experience. · The Senior Validation Engineer will perform Commissioning, Qualification, and Validation (CQV) activities with a strong focus on safety. The role ...

The Manager of CQV enables efficient tech transfer and new product introductions at the Holly Springs facility. · Leads the Upstream and Downstream drug substance manufacturing validation engineering team · ...

+The Manufacturing Science and Technology (MSAT) intern will support execution of process validation and material science activities. · ...

The Senior Director QA Ops DSM oversees Quality Product and Validation teams while ensuring released batches meet Good Manufacturing Practices regulations. · Develops strategic plans · Leads quality assurance operations · ...

The Director QA Ops oversees the Quality Product and Validation teams ensuring compliance with Good Manufacturing Practices regulations. · Develops strategic plans for QA team operations sets measurable goals and oversees supervision development performance of personnel. · ...

The Sr. Specialist, Contamination Control supports cGMP manufacturing by owning the Contamination control strategy and work with site teams to prevent, detect, and mitigate microbial contamination across facilities, utilities, processes, and products. · ...

Unirse a un equipo de 17.000 miembros que trabaja en la tecnología que impulsa el mundo. · ...

The QA Specialist partners with operations day teams to ensure quality oversight of drug substance manufacturing processes. · ...

The QA Specialist is responsible for partnering in the Quality oversight of DSM project processes ensuring applicable systems and processes are operated/maintained in a validated state throughout their lifecycle. · ...

Job summary · As a member of the Upstream Process Engineering Team you will support starting up upstream process equipment during your internship time. ...

The Intern (Automation) is a supporting member of the Automation Team within the area of Drug Substance Manufacturing (DSM) by gaining first-hand experience on a groundbreaking greenfield project. · ...

The QA Specialist is responsible for supporting quality assurance activities for project deliverables in accordance with governing processes and procedures within assigned quality areas. · Supports QA for project deliverables in accordance with the governing processes, · Assesses ...

The Intern on the CQV team integrates into ongoing work supporting building out needed processes for execution of testing reviewing documentation partnering with leads to identify drive opportunities for improvement. · Collaborates with manager experienced Engineers on identified ...

The Scientist 2 is responsible for coordinating analytical method transfers into Quality Control laboratories of FUJIFILM Biotechnologies. This role ensures GMP compliant laboratory operations in accordance with regulatory guidelines. · ...

The Scientist is responsible for coordinating the transfer of analytical methods for Technology Transfer (TT) of drug substance (DS) and drug product (DP). · Leads analytical chemistry method tech transfer and execution including method verification, transfer and validation. · ...

The Process Engineering Intern will support the Initial Purification area, · * Currently enrolled in an Engineering or Scientific Undergraduate or Master's degree Program · * Proficient in Microsoft Word, Excel, and PowerPoint ...

RoviSys is seeking an experienced engineering professional to lead the delivery of holistic · MES solutions across industries, · including Production Management, Directed Work, Quality, · Traceability, Maintenance Management, · & Performance.Competitive Base Salary: $80 · ,000–$ ...

The Manufacturing Execution System (MES) Specialist owns the end-to-end design, configuration, testing, and lifecycle support of electronic Master Batch Records (eMBRs) within PAS-X. · This role ensures eMBRs align with manufacturing process requirements, cGMP/regulatory standard ...

The Process Engineer provides engineering guidance to support capital projects, technology transfer, and manufacturing operations. · ...

The Senior Analyst supports the implementation of plate and cell-based analytical methods for Technology Transfer (TT) of drug substance (DS) and drug product (DP) into the Quality Control laboratories. · ...