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Mid level
LIMS Master Data Specialist III in Rensselaer, NY Build your future at Curia, where our work has the power to save lives Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of …
Skills: LIMS Configuration, Data Governance, LabVantage, GMP Compliance, FDA 21 CFR Part 11
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Senior Specialist LIMS in Rensselaer, NY Build your future at Curia, where our work has the power to save lives Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experienc…
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Town of East Greenbush, New York, United States · On-site
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Bernalillo County, New Mexico, United States · On-site
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Town of East Greenbush, New York, United States · On-site
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Town of East Greenbush, New York, United States · On-site
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Training Program Manager in Rensselaer, NY Build your future at Curia, where our work has the power to save lives Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experie…
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City of Rensselaer, New York, United States · On-site
$24/hr–$28/hr
Mid level
Quality Control Lab Technician III in Rensselaer, NY Build your future at Curia, where our work has the power to save lives Curia is a global contract development and manufacturing organization (CDMO) with over 30 years …
Responsible for creating and revising master data elements within the LabVantage LIMS platform, including test methods and specifications. The role involves ensuring data integrity, collaborating with SMEs to map workflows, and supporting regulatory audits.
Requirements
Requires an Associate's or Bachelor's degree in Life Sciences, Engineering, or a STEM field with 2-5 years of experience in a GMP-regulated laboratory. Proficiency with LIMS platforms like LabVantage, LabWare, or STARLIMS is highly preferred.
Full job description
LIMS Master Data Specialist III in Rensselaer, NY
Build your future at Curia, where our work has the power to save lives
Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to advance our customers’ therapies from curiosity to cure and ultimately to improve patients’ lives.
We proudly offer
Generous benefit options (eligible first day of employment)
Paid training, vacation and holidays (vacation accrual begins on first day of employment)
Career advancement opportunities
Education reimbursement
401K program with matching contributions
Learning platform
And more!
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Essential job duties
Data Configuration: Create and revise master data elements in the LabVantage LIMS platform, including test methods, specifications, analytical procedures, sampling plans, product parameters, and instrument mapping.
Data Governance & Quality: Enforce data integrity standards, version control, and data accuracy across all laboratory processes. Ensure compliance with global corporate policies and regulatory standards (e.g., FDA 21 CFR Part 11, cGMP, ISO 17025).
Cross-Functional Collaboration: Partner with lab subject matter experts (SMEs) to gather business requirements and map existing workflows to system capabilities. Partner with IT System Admin to develop, test and implement new functionality.
System Support & Troubleshooting: Serve as the first line of support for end-user issues, troubleshoot master data anomalies, and assist with data migration during system upgrades. Support routine troubleshooting of data-related issues and escalate technical problems to System Admin or vendor as needed.
Documentation: Own and update Master Data Standard Operating Procedures (SOPs), data maps, and validation documentation associated with LIMS.
Build and maintain test definitions, sampling plans, specifications, and stability protocols in LIMS, in collaboration with QC SMEs.
Work closely with IT, QA, and QC leadership to test system settings, user roles, and permissions.
Support internal and external regulatory audits and inspections by providing LIMS documentation and system access as required.
Execute validation test scripts associated with LIMS
Work with QC leadership to support ongoing LIMS improvements and upgrades
Education, experience, certification and licensures Required
Associate’s or Bachelor’s degree in Life Sciences, Engineering, or a related STEM field.
Minimum of 2–5 years of experience in a GMP-regulated pharmaceutical or life sciences laboratory environment.
Understanding of analytical testing and techniques
Preferred
Experience with LIMS as an end user and/or participation in an LIMS implementation.
Knowledge, skills and abilities
Technical Skills:
Experience with major LIMS platforms such as LabVantage (preferred), LabWare, or STARLIMS.
Soft Skills: Exceptional analytical thinking, strong attention to detail, and excellent verbal/written communication skills to bridge technical and scientific teams.
Supervisory responsibilities
This position does not have supervisory responsibilities.
Physical requirements
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Work environment
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
The above statements are intended to describe the general nature and level of work performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all job duties performed by the personnel as classified. Management reserves the right to revise or amend duties at any time.
Other Qualifications
Must pass a background check
Must pass a drug screen
May be required to pass Occupational Health Screening
Pay Range: $100,000-$125,000
Education, experience, location and tenure may be considered along with internal equity when job offers are extended.
We do not accept unsolicited assistance from any headhunters or recruitment firms for any of our job openings. All resumes or profiles submitted by search firms to any employee at Curia, in any form without a valid, signed search agreement by an authorized signatory in place for the specific position, approved by Talent Acquisition, will be deemed the sole property of Curia. No fee will be paid in the event the candidate is hired by Curia because of the unsolicited referral.
All interested applicants must apply online. Please be aware of scammers. Curia will only send offer letters and requests for sensitive personal information from a curiaglobal.com email address. Curia is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Curia is an E-Verify employer.
Curia is a Contract Development and Manufacturing Organization with over 30 years of experience, an integrated network of 25 global sites and 3,500 employees partnering with customers to make treatments broadly accessible to patients. Our biologics and small molecule offering spans discovery through commercialization, with integrated regulatory and analytical capabilities. Our scientific and process experts and state-of-the-art facilities deliver best-in-class experience across drug substance and drug product manufacturing. From curiosity to cure, we deliver every step to accelerate and sustain life-changing therapeutics.
To learn more visit us at curiaglobal.com
**************************************************
⚠️NOTICE: Please Be Aware of False Employment Opportunities
**************************************************
Please be aware there has been reported fraudulent activity within our industry regarding false offers being made to applicants and requests for personal information from individuals or organizations posing as company representatives.
Any applicant who applies to Curia must submit their application through Curia’s career page at https://careers.curiaglobal.com.
Applicants will only receive communication, including offer letters, from a curiaglobal.com email address. Please be aware that recent scams used email addresses that are similar to Curia addresses or use other public domain addresses such as gmail.com, yahoo.com and aol.com. Please confirm the sender’s email address prior to sharing your information.
Offices: 26 Corporate Circle, Albany, NY 12203, US · Plot # 9, Alexandria Knowledge Park, Turkapally, Shameerpet, Genome Valley, RR District, Hyderabad, 500 078, IN · 99 South Bedford Street, Burlington, Massachusetts 01803, US · 291 US Highway 22 East, Lebanon, NJ 08833, US · 201 Jones Road, 3rd Floor East, Waltham, MA 02451, US
Contract ResearchDiscovery BiologyEarly DevelopmentPre-FormulationContract ManufacturingFormulationAseptic Fill FinishSyringe and Vial FillingClinical/Commercial APIsLyophilization
Curia is a Contract Development and Manufacturing Organization with over 30 years of experience, an integrated network of 25 global sites and 3,500 employees partnering with customers to make treatments broadly accessible to patients. Our biologics and small molecule offering spans discovery through commercialization, with integrated regulatory and analytical capabilities. Our scientific and process experts and state-of-the-art facilities deliver best-in-class experience across drug substance and drug product manufacturing. From curiosity to cure, we deliver every step to accelerate and sustain life-changing therapeutics.
To learn more visit us at curiaglobal.com
**************************************************
⚠️NOTICE: Please Be Aware of False Employment Opportunities
**************************************************
Please be aware there has been reported fraudulent activity within our industry regarding false offers being made to applicants and requests for personal information from individuals or organizations posing as company representatives.
Any applicant who applies to Curia must submit their application through Curia’s career page at https://careers.curiaglobal.com.
Applicants will only receive communication, including offer letters, from a curiaglobal.com email address. Please be aware that recent scams used email addresses that are similar to Curia addresses or use other public domain addresses such as gmail.com, yahoo.com and aol.com. Please confirm the sender’s email address prior to sharing your information.
Offices: 26 Corporate Circle, Albany, NY 12203, US · Plot # 9, Alexandria Knowledge Park, Turkapally, Shameerpet, Genome Valley, RR District, Hyderabad, 500 078, IN · 99 South Bedford Street, Burlington, Massachusetts 01803, US · 291 US Highway 22 East, Lebanon, NJ 08833, US · 201 Jones Road, 3rd Floor East, Waltham, MA 02451, US
Contract ResearchDiscovery BiologyEarly DevelopmentPre-FormulationContract ManufacturingFormulationAseptic Fill FinishSyringe and Vial FillingClinical/Commercial APIsLyophilization