Contract Pharma QA Data Reviewer - cGMP Compliance Expert
Prostaff Solutions LLC
ProStaff Solutions Inc., located in New Brunswick, NJ, is looking for a Contract QA Data Reviewer to perform critical in-depth reviews of scientific data for Quality Control laboratory documents. The candidate will ensure compliance with cGMPs and regulatory guidelines while leveraging their experience of at least six years in a pharmaceutical environment. Excellent communication and understanding of chromatography are key requirements. Eligible employees will benefit from medical benefits, a 401(k) plan, direct deposit, and weekly pay. #J-18808-Ljbffr Prostaff Solutions LLC
- Job Title Contract QA Data Reviewer - ProStaff Solutions Inc., New Brunswick, NJ Job Summary Performs... ...guidances. Ensures that all documents are in compliance with cGMPs and the site operating... ...supervision within the framework of cGMP/GLP for analytical laboratories. Good...Contract workDataWeekly payFull time
- Amneal Pharmaceuticals is searching for a Peer Reviewer III to ensure laboratory data accuracy and compliance with industry standards. Key responsibilities include... ...candidate will possess comprehensive knowledge of cGMP practices and demonstrate an ability to enhance efficiency...Data
- Amneal Pharmaceuticals LLC is seeking a Peer Reviewer III responsible for reviewing and approving laboratory data to ensure accuracy and compliance with cGMP requirements. The role involves auditing laboratory activities and preparing for audits while continuously improving...Data
- ...and providing regulatory compliance/Affairs guidance, and... ...dossier (Module 2 and 3) review process for... ...CoA's, Analytical raw data) to support regulatory... ...with all departments, contract manufacturing organizations... ...Participating in other QA supporting activities as...Contract workDataLocal areaWorldwide
$40 - $50 per hour
Planet Pharma Group is seeking a Contract Senior Manager, Standards and Systems, Clinical Data Management to enhance data management processes. The successful candidate will manage the development of the Global Library and configure the Rave Safety Gateway module. Proficiency...Contract workData$85k - $105k
...continuous improvement and enhancement of compliance posture. Essential Functions... ...investigation of laboratory results. Review laboratory analysis data for completeness, specification compliance... ...for analysis; understand and apply cGMP requirements applicable to quality...DataTemporary workLocal areaFlexible hours$31 - $35 per hour
...seeking a detail-oriented Quality Assurance Data Reviewer to support Quality Assurance and Quality Systems activities within a cGMP pharmaceutical manufacturing environment.... ...audits and inspections, and ensuring compliance with FDA regulations, ICH guidelines, and...DataHourly payFor contractors- Amneal Pharmaceuticals LLC is seeking a QA Auditing Reviewer to audit production records and manage batch dispositions in Piscataway Township... ...records, determining batch dispositions, and ensuring compliance with GMP standards. The role requires at least 2 years of experience...Data
- This QA Auditing Reviewer role is responsible for thoroughly auditing production records, determining batch disposition (Release, Hold, Reject)... ...properly controlled and stored. It also logs and loads batch data into required databases, regularly audits QA in‑process data,...DataLocal area
$38 - $41.8 per hour
...position interfaces with experts in Process... ...authority questions. Review and adjudicate... ...Facilitate and manage the data verification... ...creation and system compliance for regulatory... ...Experience in bio tech/pharma e2e product... ...posting is for a contract assignment with ASK...Contract workDataHourly payTemporary workWork at officeLocal area- ...product testing and in agroscience Contract Research Organization... ...processes are in a state of compliance with regard to internal, regulatory... .... Maintain the Management Review process. Maintain the laboratory... ...skills and strengths. Your data: As part of any recruitment...Contract workDataFull timeFor subcontractorMonday to Friday
- Quality Assurance (QA) Associate job at Strides. East Brunswick... ...following: With Supervision, review documents/records and provide... ...applicable products, coordinate with Contract Testing Laboratories for... ...investigations related to Strides Pharma Inc. (Strides) frontend...Contract workWork at officeLocal area
- ...is seeking a Quality Assurance Specialist. This role involves inspecting, sampling, and testing incoming materials, ensuring compliance with cGMP regulations, and providing quality assurance oversight. The ideal candidate will have a Bachelor’s degree in science or...Work at office
- ...1 CFR Part 111 and cGMP standards. The QC Manager... ..., safety, and data integrity.... ...finished products. Ensure compliance with product specifications... ...release criteria. Review and approve... ...culture. Partner with QA, Manufacturing, R&D... ...in a CDMO or contract manufacturing environment...Contract workData
- The Onsite Senior ETL QA will lead quality assurance efforts for data platforms and Power BI solutions... ..., reliability, and compliance across MDM, ETL, and... ...validation where applicable. Review and approve test plans,... ..., or local government contract. #J-18808-Ljbffr Ethereum...Contract workDataPermanent employmentLocal area
- ...Manager – Legal Tech & Pharma Tech V Group is a 25... ...V Group specializes in Contract Lifecycle Management (CLM... ...departments streamline compliance and operations. In... ...Regulatory Tech, Clinical Trial Data Management, and... ...and quarterly business reviews (QBRs). Reporting &...Contract workDataFull time
- ...The Data Reviewer, Office of Data Reliability (ODR) is accountable for critical review of pre-submission applications ready for regulatory... ...data. Area Of Responsibility Ensures compliance with cGMP/cGLP and good documentation procedure during the review...DataImmediate start
$31 - $35 per hour
...environment. The company is committed to quality, compliance, and continuous improvement while... ...: The Quality Assurance Specialist – Data Review & Compliance will support Quality Assurance... ...and Quality Systems activities within a cGMP-regulated pharmaceutical manufacturing...DataHourly payPermanent employmentTemporary workFor contractorsImmediate startMonday to Friday- ...of project execution Review project schedules with... ...Assurance and Quality Control (QA/QC) programs... ...and HR services include contract and direct hire staffing... ...Independent Contractor Compliance, and Managed Services.... ...messages. Message and data rates may apply. Carriers...Contract workDataFor contractorsWork experience placementFor subcontractorWork at office
- Amneal Pharmaceuticals is seeking a Senior Peer Reviewer located in Piscataway, NJ. This role involves reviewing and approving laboratory data to ensure accuracy and compliance with cGMP requirements. The Senior Peer Reviewer will complete audit tasks within specified...Data
- Description Peer Reviewer III is responsible for reviewing and approving data that is generated by the laboratory to ensure accuracy and compliance with procedures and cGMP requirements. Complete audit tasks within specified time frame without compromising quality of audit...Data
- Senior Peer Reviewer job at Amneal Pharmaceuticals Title: Senior Peer Reviewer, Company:... ...responsible for reviewing and approving data that is generated by the laboratory to ensure accuracy and compliance with procedures and cGMP requirements. Complete audit tasks withing...Data
- QA Laboratory Technician L1 page is loaded## QA Laboratory... ...range provided is in compliance with state specific laws. Factors... ...to GMP regulations.* Reviews raw material test data and, if all specifications... ...Test samples from external contract manufacturers* Prepare chemical...Contract workDataLocal areaImmediate startWorldwideFlexible hoursShift work
- ...the state providing detailed inspection reviews, QC/QA overviews of on-site testing of materials... ...to obtaining field measurements and data collection necessary to submit daily work... ...approval Read, understand and interpret contract plans, project documents and schedules to...Contract workDataFor contractorsLocal area
$72k - $145k
...Document Control systems to ensure compliance with FDA regulations and... ...represents Document Control in QA Initiatives and Cross Functional... ...role is responsible for the review, routing, distribution and filing... ...in a timely manner. Attend cGMP training programs as required....Temporary workWork at officeRelocation packageShift work$31.38 - $39.86 per hour
...is a leading provider of GxP compliance and workforce solutions for the... ...Supply/Global Quality. In this contract role, you will ensure seamless... ...and performing shipping data management using tools and systems... ...teams (labs, project managers, QA) and contributing to continuous...Contract workDataHourly payMonday to Friday- ...Title: Lead Business Analyst cum Data Analyst - Risk and Governance... ...), NY, NJ. Mode: Contract Key Responsibilities... ...-to-consumption risk. Review and validate control effectiveness... ..., risk documentation, and compliance guardrails. Standardize...Contract workData3 days per week
- ...staff, and casual staff. The HCMS II reviews documentation for compliance with federal and state regulations,... ...policy, and bargaining unit contracts, and troubleshoots client salary, payroll... ...inquiries. Calculates, reviews, completes data input, and implements daily,...Contract workDataFull timePart timeCasual work
- Quality Assurance Technician - QA - service Contract Quality Assurance Technician Location: Swedesboro, NJ Objective: Inspects and tests materials... ...incoming, in-process, and final. Compiles and evaluates data to determine and maintain quality and reliability of...Contract workDataWork at office
$55 - $57 per hour
...overcome obstacles and ensure compliance with regulatory standards.... ...trial protocols. Prepare and review study tools such as study binders... ...Board (IRB), and finance/contract departments prior to study activation... ...study sponsors and input data into clinical trials database...Contract workDataTemporary workWork at office
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