Qc Salary at Static Control Components Inc BETA

Clinical Trial Assistant opening with a Biotech Company! · Develop TMF Plan, conduct ongoing and final QC checks of TMF for sections owned by CPM; providing CRO or Partner with queries/feedback to ensure correctness and completeness of documents and of TMF overall. · Provide support for setting-up studies in Clinical Trial Management System (CTMS), provide information to CTMS team to ensure data fields owned by company are kept up to date. Conduct ongoing and final QC checks of the CTMS, liaise with Partners/CPM to provide feedback and ensure resolution of issues. · Liaise between Partners, CPM, Study Physician, and Legal on local Informed Consent questions and ensure fast resolution. · Check company Data Standard COA Repository and liaise with CPM to identify vendors and obtain licensing agreements. · Request the set-up of study mailboxes for all studies and ensure access management. · Request and review the aggregate financial reports for studies managed by CPM from company Complianc

Clinical Systems Manager - Quality Risk Assessments 1 Year Holly Springs, NC Max PR: $71.60/hr Hybrid role with up to 80% onsite support. Onsite schedule will be as needed. Ideal candidate: Minimum of 12+ years of experience. T Three roles - the team is looking for three different specialties Analytical validation & method Both analytical validation & method experience and writing quality risk assessments (QRA's) for lab sample chain of custody. Strong background in sample, stability, and reserve management. This person is going to assist in implementing the processes in place for the new site. Ideally the candidate will have extensive diversified experience in commissioning of Quality Control (QC) Equipment supporting all QC laboratories, (Chemistry, Bioassay, Raw Material, and Microbiology). The candidate must have at least 15 years of functional experience and capable of leading technical documentation supporting Analytical Method Validation/Verification required to support GMP QC L

Clinical Systems Manager Shift: M-F / 8am-5pm Location: Holly Springs, NC 27540 **HYBRID - 80% onsite** Pay: $65.00-$68.00 /hour Experience Requirements- Clinical Systems Manager Ideally the candidate will have extensive diversified experience in commissioning of Quality Control (QC) Equipment supporting all QC laboratories, (Chemistry, Bioassay, Raw Material, and Microbiology). The candidate must have at least 15 years of functional experience and capable of leading technical documentation supporting Analytical Method Validation/Verification required to support GMP QC Laboratory readiness activities at the North Carolina facility. Ideal candidate: Minimum of 12+ years of experience. Three roles - the team is looking for three different specialties 1) Analytical validation & method 2) Both analytical validation & method experience and writing quality risk assessments (QRA's) for lab sample chain of custody. 3) Strong background in sample, stability, and reserve management. This person

Job Title: QC Support Job Type: Contract - Hybrid Location: Holly Springs NC *CAN ONLY SET UP W2 CONTRACTS - NO C2C* Summary: This senior-level role supports Analytical Method Validation, QC Equipment Commissioning, and GMP QC Laboratory readiness at there North Carolina facility. Ideal candidates bring 12+ years of QC and Analytical Validation experience and expertise in technical documentation, risk assessments, and lab process implementation. Key Responsibilities: Analytical Method Validation: Design, author, and execute protocols/reports for method validations, verifications, transfers, and stability studies. Apply core analytical techniques (e.g., HPLC/UPLC, SEC, ELISA, TOC, peptide mapping). Laboratory Readiness: Create SOPs, O&M procedures, and Equipment Data Integrity Assessments Author Analytical Equipment Qualification Protocols and manage document changes in eQMS Risk & Incident Management: Lead QC Quality Risk Assessments for Sample Chain of Custody and Analytical Testing I

AllSTEM Connections is seeking a Laboratory Systems Manager to work hybrid/onsite in Holly Springs, NC. This is a 12-month contract position. Possible extension/temp-to-hire. Hourly rate is up to $71.50 M-F, 8AM - 5PM. SUMMARY: Three roles - the team is looking for three different specialties: Analytical validation & method Both analytical validation & method experience and writing quality risk assessments (QRA's) for lab sample chain of custody. Strong background in sample, stability, and reserve management. This person is going to assist in implementing the processes in place for the new site. Ideally the candidate will have extensive diversified experience in commissioning of Quality Control (QC) Equipment supporting all QC laboratories, (Chemistry, Bioassay, Raw Material, and Microbiology). The candidate must have at least 10 years of functional experience and capable of leading technical documentation supporting Analytical Method Validation/Verification required to support GMP QC

Job Description Job Description Hybrid role with up to 80% onsite support. Onsite schedule will be as needed. Ideal candidate: Minimum of 12+ years of experience. Three roles - the team is looking for three different specialties 1) Analytical validation & method 2) Both analytical validation & method experience and writing quality risk assessments (QRA's) for lab sample chain of custody. 3) Strong background in sample, stability, and reserve management. This person is going to assist in implementing the processes in place for the new site. Ideally the candidate will have extensive diversified experience in commissioning of Quality Control (QC) Equipment supporting all QC laboratories, (Chemistry, Bioassay, Raw Material, and Microbiology). The candidate must have at least 15 years of functional experience and capable of leading technical documentation supporting Analytical Method Validation/Verification required to support GMP QC Laboratory readiness activities at the North Carolina fac

About The Job Arcadis is the world's leading company delivering sustainable design, engineering, and consultancy solutions for natural and built assets. We are more than 36,000 people, in over 70 countries, dedicated to improving quality of life. Everyone has an important role to play. With the power of many curious minds, together we can solve the world’s most complex challenges and deliver more impact together. Role description: Arcadis is seeking a CQV Engineer who is responsible for executing and managing QC lab analytical equipment activities to meet cGMP requirements. He/She will initiate equipment validation protocol development, including drafting documents, managing review cycles, and protocol approval. Role accountabilities: Become familiar with the user, functional, installation, operation and performance requirements for assigned projects and tasks. Review requirements and source documentation P&IDs, RDs, URSs, SOPs, Specifications), for use in development of equipment comm

Position: Environmental Monitoring Technician (EM Tech) Duration: 6-12 Month contract Location: Durham, NC - ONSITE Schedule: 12 hour day or night shift, 2-2-3 (2 days on, 2 days off, 3 days on, etc.). Contractors will work 36 hours one week, 48 the next, etc. Start: ASAP Summary: The QC Environmental Monitoring Technician will perform routine and investigational environmental monitoring of classified manufacturing, filling, and support areas. Support daily EM laboratory operations. Responsibilities: Support production operations by means of EM sampling of classified manufacturing, filling, and support areas and operations personnel. Support daily EM laboratory operations and process/equipment qualification activities, as necessary. Ensures compliance with current Good Manufacturing Practice (cGMP) and maintain constant inspection-readiness. Ensures that data-integrity is maintained Participate in process streamlining and continuous performance improvement. Responsible for maintaining