Remote Senior Associate: Pharma - Spokane, WA

A leading consulting firm is looking for a Senior Associate in Information Intelligence & Solutions to manage key client platforms, · This remote position requires a bachelor's degree and at least 2 years' experience in competitive intelligence within the pharmaceutical industry. ...

Job summary · The Sr. · Engineering Manager will lead a team of technical professionals responsible for the design, · installation, qualification, · and ongoing operational improvement of state-of-the-art aaseptic filling equipment for liquid and lyophilized pharmaceutical produc ...

The Senior Process Engineer provides expertise primarily in the areas of pharmaceutical process engineering and technical transfer.This position will manage large scale projects and multi-disciplinary teams. · ...

The QA Compliance lead Associate provides support to the company Deviations,CAPA program through a complete assessment of Root Cause Analysis RCA of deviations and vendor complaints/issues. · Review deviations,investigations and CAPAs to ensure accuracy,consistency and compliance ...

The QA Compliance Associate provides support to the company Deviations, Corrective and Preventive Action (CAPA) program through a complete assessment of Root Cause Analysis (RCA) of Deviations and vendor complaints/issues.Assure product compliance and product safety.Ensure accura ...

The QA Compliance lead Associate provides support to the company Deviations, · CAPAs and vendor complaint program through a complete assessment of Root Cause Analysis (RCA) · of deviations and vendor complaints/issues. Ensure accurate and timely data entry · and oversight of the ...

The Environmental Monitoring Associate is responsible for monitoring biological and airborne particulate levels in clean room environments for the preparation, compounding, and filling of sterile injectable drug products. · ...

The Environmental Monitoring (EM) Associate is responsible for monitoring biological and airborne particulate levels in clean room environments. The EM Associate will be trained on proper aseptic behavior, sanitization processes, and donning of sterile gowns. · Collect environmen ...

The Production Planner handles the planning and scheduling production of SVP filling lines and inspection & packaging. · ...

The Materials Management Technician is responsible for supporting all aspects of operations within Warehouse & Distribution. · Complete cGMP and Non-GMP Receiving · Complete transfer orders, sales orders and reservations on time and in full. · ...

The Environmental Monitoring (EM) Associate is responsible for the monitoring of biological and airborne particulate levels in clean room environments for the purpose of preparation, compounding, and production of sterile injectable drug and drug products. · ...

The QA Auditor is responsible for providing QA inspection/auditing of manufacturing operations to ensure that all products produced meet labeling, dating, and packaging requirements as defined by Standard Operating Procedures (SOP's) and current Good Manufacturing Practices (cGMP ...

The QA Auditor is responsible for providing QA inspection/auditing of manufacturing operations to ensure that all products produced meet labeling, dating, and packaging requirements as defined by Standard Operating Procedures (SOP's) and current Good Manufacturing Practices (cGMP ...

The main function of the Area Specialist is to coordinate personnel to achieve the desired production schedule. · Provide effective day-to-day leadership and oversight for small groups ranging in size from 5 to 25 team members.Schedule team members proficiently to achieve target ...

The Environmental Health & Safety Specialist will participate in the development and maintenance of a comprehensive environmental, health, and safety program for the facility. · EHS inspections · Investigate accidents · Develop and provide safety training and related resources. · ...

The Documentation Reviewer will oversee documentation by working with manufacturing personnel on a daily basis to ensure right first time for all documentation prior to QA release submission. · The specialist will gather, organize, and review all documentation associated with CMO ...

The Documentation Reviewer will oversee documentation by working with manufacturing personnel on a daily basis to ensure right first time for all documentation prior to QA release submission. · ...

The QA Ops Manager supports Quality Assurance activities on weekday nights (B shift). · ...

The Environmental Health & Safety Specialist will participate in developing and maintaining a comprehensive environmental health and safety program for the facility. This includes performing EHS inspections, investigating accidents, developing and providing safety training and re ...

The Compliance Auditor II/III performs internal audits to ensure cGMP compliance. They manage audit programs, coordinate with operational functions and Quality Systems to define processes for auditing and review procedures. · Perform audits to assess compliance with regulations. ...