Quality Assurance Compliance Specialist
LanceSoft Inc
Job DescriptionLead Quality Assurance resource needed to provide quality support for global computer validation projects in the ERP area, such as SAP, under the guidance of the Global Quality Computer Compliance team.Job duties will include:Reviewing and providing input to validation and test strategiesVerify documentation is in compliance with internal procedures and external regulationsParticipate in review and approval of requirements, test scripts, reports and other SDLC documentation with a focus on quality, and testabilityIn addition, the resource may be pulled to support other programs of the following as needed:Participate in process changes in the organization Participate in audits Participate in change management of additional systems Education/Training/Work Experience: The position requires a Bachelor’s Degree in Engineering or Sciences with a minimum of 5-8 years experience working in life sciences industry with focus in the area of Quality Assurance. Experience working with various GxP Enterprise Computerized Systems (on-premise and Cloud based (SaaS) COTS) used in the life sciences industry. Candidate must be well-versed with Software Development Life Cycle (SDLC) methodologies such as Waterfall and V-model. In-depth knowledge of US FDA regulations, ISO standards, MHRA and EU regulations (including Annex 11), and ICH guidelines and Drug Development Life Cycle process. Extensive experience developing and using risk based approaches for computer systems validation. Experience in managing multiple projects and determined to get job done correctly and on time.Specialized Knowledge and Skills: Knowledge in SAP is a plus. In addition, Microsoft Office experience (Word, Excel, PowerPoint). Experience with Microsoft SharePoint is also recommended. Good organization skills and strong interpersonal skills as well as ability to work with other departments. Additional InformationAll your information will be kept confidential according to EEO guidelines.SummaryType: Full-timeFunction: Quality AssuranceExperience level: Mid-Senior LevelIndustry: Pharmaceuticals
- ...legal and regulatory requirements, the Client Pharma Corporate Quality Manual and Policies, and site procedures and business... ...electronic database system along with GMP, safety, and Ethics & Compliance course requirements. Perform or support any other tasks necessary...SuggestedImmediate start
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$50 per hour
...leading pharmaceutical companies through high-quality manufacturing, operational excellence... ...specifications, and technical data for compliance. *Support drafting, negotiation, and... ...*2-4 years of experience in Quality Assurance within pharmaceutical/biologics manufacturing...SuggestedContract work$86.7k - $170.9k
Position Summary Consultant - Regulatory & Compliance - Enterprise Operations & Risk Our Deloitte Regulatory, Risk & Forensic team... ...verbal communication skillsMeticulous attention to detail and quality of work productAbility to build and sustain professional...SuggestedLocal areaVisa sponsorship- ...Description:The Risk Advisory practice at Withum is experiencing significant growth driven by market demand for assurance services. Our team is seeking a Contract Compliance Senior Consultant with experience performing royalty audits, franchise compliance audits, revenue...SuggestedFull timeContract workWork at officeLocal area
- ...mission centers on delivering only the best quality talent, the first time and every time.... ...to stakeholders in order to maintain compliance without delay to business due to regulatory... ...project and brand specific activities assuring they are correct, complete and on-time including...Work experience placementWork at officeLocal area
- ...Supplements, Annual Reports, Health Authority Meeting Requests and Briefing Packages and other required FDA filings in order to ensure high-quality submissions and expeditious approvals from FDA. Helps to compile high-quality, original NDAs, Amendments, Supplements, and...
$200k - $325k
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...in your penultimate year and ready to grow, learn, and make an impact, this is your opportunity to belong and thrive. Why the Compliance Summer Internship program? As one of the world's largest and most respected full-service banks, Barclays has a huge responsibility...Hourly payPermanent employmentInternshipSummer internshipImmediate startVisa sponsorshipWork visa$90k - $200k
...InvestigationsKroll's North American Investigations, Diligence and Compliance practice is seeking a Senior Manager based in the U.S. This is... ...and project management, and will have responsibility for quality and case completion and follow-up. A key element of the SM's role...Temporary work$122.85k - $163.81k
...the Role:We have a current opening for a Governance, Risk & Compliance (GRC) Specialist, North America and are actively reviewing applications.As... ...issues raised by GRC, internal audit, etc. to ensure the quality and sustainability of risk mitigation;Build effective relationships...Work experience placement$19.5 per hour
...Document Processor / Compliance Analyst Parsippany-Troy Hills, New Jersey, United States Document Processor / Compliance Analyst (Full-Time - NJ) Business Credentialing Services, Inc. (BCS) is a fast-growing technology company in the insurance and risk management...Hourly payFull timeWork at officeRemote workMonday to Friday2 days per week1 day per week$200k - $320k
...practice advising healthcare providers, organizations, investors, and businesses on complex regulatory, transactional, reimbursement, compliance, and enforcement matters. The successful candidate will work closely with experienced healthcare attorneys and have meaningful...Local area- ...Reference26-01781Summary : This Senior Quality Specialist will be responsible for ensuring that... ...products.Partner with the Supply teams in assuring that the stages of the development... ...that these operations are performed in compliance with EH's Global QMS and meet all...Contract work
$22 - $26 per hour
...Quality Control Associate Pay: $22-$26/hour Location: Parsippany, NJ Schedule: Monday-Friday, 8-hour shift Type: Full-Time... ...lbs. Qualifications 1+ year of Quality Control or Quality Assurance experience required, preferably in manufacturing. 2+ years...Full timeMonday to FridayShift work- Company Description About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across...Full timeWork at officeLocal areaRemote work
- ...preparation, submission, and maintenance of regulatory filings to ensure compliance with applicable health authority requirements. This role works closely with cross-functional teams, including Quality, R&D, Manufacturing, Pharmacovigilance, Medical Affairs, Supply Chain,...Full timeWork at officeLocal areaMonday to FridayNight shift
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