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Empower Lims Jobs (NOW HIRING)

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Experience with Empower, LIMS, or similar systems * Strong documentation, data integrity (ALCOA+), and troubleshooting skills * Ability to work independently and in a fast-paced manufacturing setting ...

Experience with laboratory software (e.g., Empower, LIMS, CDS systems) * Experience with Maximo * Strong documentation and technical writing abilities * Project management and leadership capability

Experience with laboratory software (e.g., Empower, LIMS, CDS systems) * Experience with Maximo * Strong documentation and technical writing abilities * Project management and leadership capability

Instrument systems (e.g., Empower, LabX) * Strong cross functional communication skills in regulated environments. Preferred Qualifications * Experience supporting LabWare upgrades or major LIMS ...

Proficiency in data analysis tools and laboratory systems (e.g., Empower, LIMS, OpenLab), with a strong attention to data integrity and detail * Excellent organizational, planning, and communication ...

Labvantage,LabWare,SampleManager,StarLIMS,Empower,Lab Management Systems,Caliber LIMS,AR_VR_MR

Preferred Skills • Experience in Labware, Empower LIMS systems • Experience in validating Lab equipments Job Roles/Responsibilities • Act as Validation and Qualification Lead on a large global ...

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Empower Lims information

See salary details

$68.5K

$144K

$190.5K

How much do empower lims jobs pay per year?

As of Jun 10, 2026, the average yearly pay for empower lims in the United States is $144,009.00, according to ZipRecruiter salary data. Most workers in this role earn between $117,500.00 and $169,000.00 per year, depending on experience, location, and employer.

What are the main responsibilities of someone working with Empower LIMS in a laboratory setting?

Professionals working with Empower LIMS are primarily responsible for configuring, maintaining, and troubleshooting the LIMS platform to support efficient laboratory operations. Their daily work often includes managing user access, integrating laboratory instruments, performing data integrity checks, providing user support, and ensuring the system adheres to regulatory requirements. They also play a key role in training laboratory staff on system use and collaborating with IT and quality assurance teams to implement software updates and process improvements. This ensures seamless data flow, reliable sample tracking, and regulatory-compliant record keeping throughout the laboratory environment.

What are the key skills and qualifications needed to thrive in the Empower Lims position, and why are they important?

To thrive in an Empower LIMS (Laboratory Information Management System) specialist role, you need a solid understanding of laboratory workflows, data management, and analytical processes, typically supported by a degree in a scientific or IT field. Familiarity with Empower LIMS software, SQL, and laboratory instrumentation, as well as experience with system validation and compliance standards such as GLP or GMP, are highly valued. Strong problem-solving abilities, attention to detail, and effective communication skills help professionals excel when supporting laboratory teams and managing complex data requirements. These skills are essential for maintaining data integrity, ensuring regulatory compliance, and maximizing laboratory efficiency.

What is an Empower LIMS job?

An Empower LIMS job typically involves working with the Empower chromatography data system (CDS) used in laboratories for managing, processing, and reporting analytical data. Professionals in this role may support method development, validation, troubleshooting, and compliance with regulatory requirements. They often collaborate with scientists, quality control teams, and IT staff to ensure seamless operation and data integrity.

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What cities are hiring for Empower Lims jobs? Cities with the most Empower Lims job openings:
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Infographic showing various Empower Lims job openings in the United States as of June 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $144,009 per year, or $69.2 per hour.

QC Consultant (Empower & LIMS Specialist)

Abzena Inc.

San Diego, CA • On-site

$40 - $60/hr

Contractor

Posted 6 days ago


Job description

With extensive experience in developing biologics and bioconjugates, we offer a seamless service delivered by fully integrated teams, from early discovery to commercial manufacturing.
Forward-thinking and committed, we find the best solution and use the right technologies to design, develop and manufacture your products to ensure we get vital medicines to patients quickly and safely.
We are dedicated to quality excellence. We are driven to get better treatments to market, efficiently and responsibly by reducing timelines and delivering the highest quality products and services.
We are Abzena. More than a CDMO, we are a responsible and dedicated partner that takes care of your products from concept to patient.
We are seeking an experienced QC Contractor or Consultant to support the implementation and transition of laboratory electronic systems within a GMP Quality Control environment. This role will focus on the migration from existing Agilent OpenLab chromatography systems to Waters Empower, as well as the implementation and integration of a Laboratory Information Management System (LIMS).
This role requires strong hands-on technical, operational, and compliance support to ensure a smooth system transition, data integrity, and alignment with GMP regulatory requirements.
Responsibilities
System Implementation & Migration
  • Support migration of analytical methods, data, and workflows from Agilent OpenLab to Waters Empower.

  • Assist in configuration, setup, performing test runs, and verification of Empower system in alignment with GMP requirements.

  • Support LIMS implementation, including workflow mapping, sample management, and data integration with CDS systems.

  • Participate in system validation activities including User Requirements Specifications (URS), Functional Specifications (FS), and Installation/Operational/Performance Qualification (IQ/OQ/PQ).

  • Maintain a cGMP quality level of work for the QC operations to include training, documentation, demonstrated expertise in Agilent HPLC systems using OpenLab CDS, and extensive hands-on experience with Maurice Flex (Compass) for icIEF and CE SDS (required). Write and reviews data, technical reports, deviations, OOS investigations and test results and provide conclusions and proposals for future directions. Extensive hands-on experience with.

  • Initiate quality records as needed and perform technical writing of SOP's and protocols associated with electronic migration process and investigations. Supports audit preparations.

GMP Compliance & Data Integrity
  • Ensure all activities comply with GMP, ALCOA+ principles, and data integrity regulations (FDA, EMA, ICH guidelines).

  • Review and support validation documentation, test scripts, and execution records.

  • Identify and escalate compliance risks during system transition.

Method & Workflow Support
  • Assist in transfer and verification of HPLC and CE (Maurice) /analytical methods into Empower.

  • Support QC analysts in troubleshooting system-related issues during transition.

  • Collaborate with analytical development (AMD) and QC teams to ensure method readiness in new systems.

Training & Change Management
  • Provide training and user support for Empower CDS and LIMS to QC analysts and stakeholders.

  • Develop or support creation of SOPs, work instructions, protocols, and system user guides.

  • Facilitate user adoption and minimize disruption during transition.

Cross-Functional Collaboration
  • Work closely with QC, QA, IT, and external vendors during system implementation.

  • Participate in project meetings, status updates, and risk assessments.

  • Support audit readiness activities related to system implementation.

Qualifications
Required Qualifications and Skills:
  • Bachelor's degree in chemistry, Biochemistry, Pharmaceutical Sciences, or related scientific field.

  • 3-7+ years of experience in GMP Quality Control laboratory environment.

  • Hands-on experience with HPLC/UPLC systems and chromatography data systems.

  • Direct experience with either Empower CDS or LIMS implementation preferred.

  • Strong understanding of GMP regulations and data integrity expectations.

Preferred Skills & Experience:
  • Prior experience transitioning from OpenLab, ChemStation, or similar CDS to Empower.

  • Exposure to LIMS configuration or implementation projects.

  • Experience supporting CSV (Computer System Validation) activities.

  • Strong problem-solving and troubleshooting skills in analytical environments.

  • Ability to work independently in a fast-paced project environment.

$40 - $60 an hour
Abzena is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local Jaws.
This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, and training.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.