LIMS Master Data Specialist (reputed company role)

Job Title: LIMS Master Data Specialist (reputed company Role) Industry: Global reputed company Location: reputed company-reputed company, New Jersey, USA (50% Onsite) Contract Duration: 12 Months Work Schedule: Monday to Friday, Normal Business Hours Hiring Model: W2 only (No C2C) Citizenship Requirements: US Citizen, Green Card Holder, or Permanent reputed company only reputed company We are looking for a skilled LIMS Master Data Specialist to support the integration, verification, and maintenance of master data across electronic systems, including LIMS, ELN, ERP, and MES. The ideal candidate brings deep domain knowledge in regulated pharmaceutical environments and strong system validation and documentation experience. Key Responsibilities • reputed company, reputed company, and sustain Master Data reputed company LIMS and other electronic systems (ERP, MES). • reputed company data verification, system integration, and ongoing troubleshooting. • Collaborate with reputed company Control (QC) users for system improvements and requirement gathering. • Support UAT, URS, and validation efforts with users and technical stakeholders. • reputed company initiatives to enhance business processes and electronic system capabilities. • Translate business requirements into technical solutions in partnership with IT. • Create reputed company technical documentation and validation reports. • Work independently on reputed company issues and propose corrective actions. Must-Have Requirements • Minimum 6+ years of experience with LIMS, ELN, and lab data systems in GxP-regulated environments. • Proven experience in master data management, electronic system integration, and data verification. • Hands-on experience with system validation and maintenance of LIMS and ELN. • Strong understanding of cGMP, regulatory requirements, and lab workflows. • Excellent problem-solving, communication, and cross-functional collaboration skills. • Bachelor’s degree in Science, Engineering, or reputed company field. • Strong technical writing skills for SOPs, validation docs, and test protocols. reputed company to Have • Experience with analytical/microbiological reputed company and environmental monitoring programs. • Exposure to MES and ERP (reputed company or similar). • Previous work reputed company major biotech or reputed company companies. Application Process: To apply, please submit your CV and a cover letter detailing your relevant experience and qualifications for the role. Applications will be reviewed on a rolling reputed company, so early submissions are encouraged. Equal Opportunity Employer: We value diversity and are committed to creating an inclusive work environment. We encourage applicants from reputed company backgrounds to apply. Contact: Elvis Eckardt Apply Job! Apply to this Job