QRC Group, LLC

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 المزيد...

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 المزيد...

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 المزيد...

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 المزيد...

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 المزيد...

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 المزيد...

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 المزيد...

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 المزيد...

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 المزيد...

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 المزيد...

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 المزيد...

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 المزيد...