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Jobs at Curia (Now Hiring) — 23 open

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LIMS Master Data Specialist III

Town of East Greenbush, New York, United States · On-site

$100k–$125k/yr

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

Curia logoCuria

Senior Specialist LIMS

Town of East Greenbush, New York, United States · On-site

$117k–$145k/yr

Senior+

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…

Skills: LabVantage LIMS, GxP Compliance, Computer System Validation, Data Integrity, SOP Documentation

Curia logoCuria

Senior Program Manager IV

Town of East Greenbush, New York, United States · On-site

$120k–$149k/yr

Senior+

Senior Program Manager IV in Rensselaer, NY Build your future at Curia, where our work has the power to save lives. The Senior Program Manager IV is responsible for managing the successful technical transfer of client pr…

Skills: Program Management, Technical Transfer, Cross-functional Leadership, Conflict Resolution, Strategic Planning

Curia logoCuria

Continuous Improvement Engineer

Springfield, Missouri, United States · On-site

Senior

Continuous Improvement Engineer in Springfield, MO Build your future at Curia, where our work has the power to save lives. The Continuous Improvement Engineer is a key driver of engineering excellence and operational per…

Skills: Lean Six Sigma, CAPA Coordination, Root Cause Analysis, Statistical Process Control, Process Improvement

Curia logoCuria

Research Scientist III; Chemical Development

Albany, New York, United States · On-site

Senior

Research Scientist III; Chemical Development in Albany, NY Build your future at Curia, where our work has the power to save lives. The Research Scientist III, Chemical Development’s principal responsibility is the synthe…

Skills: Chemical Synthesis, Purification, Process Development, Scale-up, HPLC

Curia logoCuria

Supervisor, Warehouse

Springfield, Missouri, United States · On-site

Senior

Warehouse Supervisor in Springfield, MO 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…

Skills: Warehouse Management, Shipping And Receiving, Hazardous Materials Handling, cGMP Compliance, DOT Regulations

Curia logoCuria

Manager, Production; Operations

Springfield, Missouri, United States · On-site

Senior

Production Operations Manager in Springfield, MO 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 e…

Skills: cGMP, Continuous Improvement, Root Cause Analysis, SOP Development, Operational Excellence

Curia logoCuria

Lab Assistant

Albany, New York, United States · On-site

Entry level

Laboratory Assistant in Albany, NY Build your future at Curia, where our work has the power to save lives. The Laboratory Assistant's role is to perform operations which aid in maximizing the research productivity of the…

Skills: Laboratory Maintenance, Chemical Inventory Management, Glassware Sterilization, SOP Compliance, Chemical Disposal

Curia logoCuria

Data Reviewer III

Town of East Greenbush, New York, United States · On-site

$76k–$94k/yr

Senior

Quality Control Data Reviewer III - Onsite position 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) wi…

Skills: Data Review, cGMP Compliance, HPLC, GC, Data Integrity

Curia logoCuria

Validation Specialist III

Bernalillo County, New Mexico, United States · On-site

Senior

Validation Specialist III in Albuquerque, NM 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 exper…

Skills: Computer System Validation, Equipment Qualification, cGMP Compliance, FDA Regulations, GAMP 5

Curia logoCuria

Senior Program Manager III

Town of East Greenbush, New York, United States · On-site

$96k–$119k/yr

Senior

Senior Program Manager III in Rensselaer, NY Build your future at Curia, where our work has the power to save lives. The Senior Program Manager III is responsible for managing the successful technical transfer of client …

Skills: Program Management, Technical Transfer, Cross-functional Leadership, Conflict Resolution, Strategic Planning

Curia logoCuria

Project Engineer II

Springfield, Missouri, United States · On-site

Mid level

Project Engineer II in Springfield, MO Build your future at Curia, where our work has the power to save lives. The Project Engineer provides technical engineering support and project management expertise to the pharmaceu…

Skills: Project Management, Technical Engineering Support, Budgeting, Vendor Management, Process Design

Curia logoCuria

Mechanical Engineer

Albuquerque, New Mexico, United States · On-site

Mid level

Mechanical Engineer in Albuquerque, NM 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 …

Skills: Project Management, Mechanical Engineering, cGMP Operations, Technical Documentation, Equipment Troubleshooting

Curia logoCuria

Manager, Maintenance

Springfield, Missouri, United States · On-site

Senior+

Manager, Maintenance in Springfield, MO 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…

Skills: Maintenance Leadership, Equipment Reliability, cGMP Compliance, Preventive Maintenance, Predictive Maintenance

Curia logoCuria

Quality Control Analyst III

Camarillo, California, United States · On-site

$85k–$107k/yr

Senior

Quality Control Analyst III in Camarillo, CA Build your future at Curia, where our work has the power to save lives. The Quality Control Analyst III is responsible for supporting the manufacturing department and external…

Skills: HPLC, ELISA, Test Method Validation, Root Cause Analysis, CAPA

Curia logoCuria

Manager, Quality Control

Camarillo, California, United States · On-site

$110k–$146k/yr

Senior

Manager, Quality Control in Camarillo, CA Build your future at Curia, where our work has the power to save lives. The Manager of Quality Control is responsible for overseeing all operations within the Quality Control Lab…

Skills: Personnel Management, Budget Management, Audit Readiness, GLP Compliance, GMP Compliance

Curia logoCuria

Automation Controls Engineer II

Albuquerque, New Mexico, United States · On-site

Mid level

Automation Controls Engineer II in Albuquerque, NM 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: SCADA, PLC Programming, HMI Configuration, Automation Integration, Troubleshooting

Curia logoCuria

Training Program Manager

Town of East Greenbush, New York, United States · On-site

$114k–$143k/yr

Mid level

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…

Skills: Instructional Design, Project Management, Onboarding, Performance Tracking, cGMP

Curia logoCuria

Manufacturing Engineering Technician

Albuquerque, New Mexico, United States · On-site

Mid level

Manufacturing Engineering Technician in Albuquerque, NM 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 yea…

Skills: Aseptic Processing, cGMP Compliance, Equipment Troubleshooting, Cleanroom Manufacturing, Sterilization

Curia logoCuria

Quality Control Lab Technician III

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 …

Skills: Analytical Chemistry, QC Stability Program, cGMP Compliance, Chromatographic Data Analysis, Stability Protocol Writing

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Showing 1–20 of 23

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LIMS Master Data Specialist III

Curia

Town of East Greenbush, New York, United States • On-site

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Mid level

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  • $100k–$125k/yr
  • Full-time
  • associate degree, bachelor degree
  • Generous Benefit Options, Paid Training, Vacation, Holidays, Career Advancement Opportunities, Education Reimbursement
  • Posted 1d ago
  • ~40 hrs/week

Responsibilities

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.

#LI-DR1

Related keywords

LIMSLabVantageLabWareSTARLIMSGMPFDA 21 CFR Part 11ISO 17025Master DataData IntegrityPharmaceuticalLife SciencesCDMOValidationSOPQuality ControlAnalytical Procedures

About Curia

LinkedInVisit site

From curiosity to cure

Industry
Pharmaceutical Manufacturing
Company size
1,001-5,000 employees
Headquarters
Albany, NY
LinkedIn followers
111,157

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
View all jobs at Curia

About Curia

LinkedInVisit site

From curiosity to cure

Industry
Pharmaceutical Manufacturing
Company size
1,001-5,000 employees
Headquarters
Albany, NY
LinkedIn followers
111,157

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
View all jobs at Curia

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