QRC Group, LLC

Sr. Project Manager with experience of GMP s Validation System Life Cycle Methodology CMMS Maximo in pharmaceutical industry. Knowledge and experience in P&ID s and Electrical Schematics SMARTSHEETS.Preferable: Experience with Change Controls CAPA s and Deviations Management More...

Sr. Project Manager with experience of GMP s Validation System Life Cycle Methodology CMMS Maximo in pharmaceutical industry. Knowledge and experience in P&ID s and Electrical Schematics SMARTSHEETS.Preferable: Experience with Change Controls CAPA s and Deviations Management More...

Industrial Mechanic with experience in regulated industry working with packaging and filling equipment to perform equipment maintenance troubleshooting set up. RequirementsAD Industrial Mechanic Engineering Instrumentation or relatedAt least 3 years of experience with packaging or fil More...

Sr Associate Buyer with experience in:Management of requisitions PO conversion per SAP Report. SAP experienceManage supplier communication and escalation regarding; PO delivery postponement past due/missed orders PO quantity discrepancies closing balances missing documents COA / packi More...

Sr Associate Buyer with experience in:Management of requisitions PO conversion per SAP Report. SAP experienceManage supplier communication and escalation regarding; PO delivery postponement past due/missed orders PO quantity discrepancies closing balances missing documents COA / packi More...

Industrial Mechanic with experience in regulated industry working with packaging and filling equipment to perform equipment maintenance troubleshooting set up. RequirementsAD Industrial Mechanic Engineering Instrumentation or relatedAt least 3 years of experience with packaging or fil More...

Sr Associate Buyer with experience in:Management of requisitions PO conversion per SAP Report. SAP experienceManage supplier communication and escalation regarding; PO delivery postponement past due/missed orders PO quantity discrepancies closing balances missing documents COA / packi More...

Industrial Mechanic with experience in regulated industry working with packaging and filling equipment to perform equipment maintenance troubleshooting set up. RequirementsAD Industrial Mechanic Engineering Instrumentation or relatedAt least 3 years of experience with packaging or fil More...

Engineer to support the execution of manufacturing/quality systems such as deviations process validation process monitoring procedures training and new product introductions. Apply process operational scientific expertise basic compliance knowledge and analytical and troubleshooting s More...

Specialist Technical Writing with MS Office expertise ; previous creating technical documents experience ; regulated environment experience ; SOP WI document version control experience ; excellent communication/writing skills. Duties: Develops writes edits and formats materials such a More...

Specialist QA with knowledge in Warehouse and Incoming QC operations quality oversights and quality records such as deviations CAPAS change controls.RequirementsDoctorate degree or Masters degree and 3 years of directly related experienceBachelors degree and 5 years of directly relate More...

Quality Manager to be responsible for the overall management and effectiveness of the corrective action and preventive action (CAPA) and risk management processes. Duties & Responsibilities: Assures all products conform to existing quality requirements standard operating procedure More...

Process Development Scientist with experience in inspection manufacturing area executing characterization processes and development of documentation (validation and characterization). Lean Six Sigma or any other improvement methodology. RequirementsDoctorate degree or Masters degree a More...

Sr. Engineer with working knowledge and experience with engineering practices and cGMP procedures on pharmaceutical/biotech production process facilities and equipment. Knowledge and experience in: Technical Writing Quality Risk Assessments such as FMEA and/or QRAESChange ControlNonCo More...

Sr. Associate Regulatory Affairs with experience in manufacture quality or distribution in Pharmaceutical or Biotech Industry. Responsibilities: Assist RA CMC Site Regulatory to support regulatory activities (e.g. Facility registrations variations/supplements country specific document More...

Sr. Associate Regulatory Affairs with experience in manufacture quality or distribution in Pharmaceutical or Biotech Industry. Responsibilities: Assist RA CMC Site Regulatory to support regulatory activities (e.g. Facility registrations variations/supplements country specific document More...

Manufacturing Operator with experience in the pharmaceutical industry operating compression machines (Korsh preferable).Availability to work at Newark DelawareRequirementsHigh School diplomaOne year of experience Availability to work 1st 2nd and 3rd shift Availability to work at Newar More...

Experienced Inspection Operator in the pharmaceutical industry specializing in the manufacturing of oral solid dosage (OSD) forms with proficiency in inspecting tablets both manually and automatically. Must have experience performing lot reconciliations and knowledge of vision systems More...