Chantilly, VA · On-site
$69K - $73K/yr
... LIMS * Perform in-vivo dissolution test related to the biopharmaceutic characteristics of the drug substance and bioequivalence studies using cGMP/cGLP, Empower, Titration, HPLC, dissolution
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Chantilly, VA · On-site
$69K - $73K/yr
... LIMS * Perform in-vivo dissolution test related to the biopharmaceutic characteristics of the drug substance and bioequivalence studies using cGMP/cGLP, Empower, Titration, HPLC, dissolution
$69K - $73K/yr
... LIMS * Perform in-vivo dissolution test related to the biopharmaceutic characteristics of the drug substance and bioequivalence studies using cGMP/cGLP, Empower, Titration, HPLC, dissolution
$69K - $73K/yr
... LIMS * Perform in-vivo dissolution test related to the biopharmaceutic characteristics of the drug substance and bioequivalence studies using cGMP/cGLP, Empower, Titration, HPLC, dissolution
Chantilly, VA · On-site
$69K - $73K/yr
... LIMS * Perform in-vivo dissolution test related to the biopharmaceutic characteristics of the drug substance and bioequivalence studies using cGMP/cGLP, Empower, Titration, HPLC, dissolution
Chantilly, VA · On-site
$69K - $73K/yr
... LIMS * Perform in-vivo dissolution test related to the biopharmaceutic characteristics of the drug substance and bioequivalence studies using cGMP/cGLP, Empower, Titration, HPLC, dissolution
$67.9K - $78.9K
5% of jobs
$78.9K - $89.9K
4% of jobs
$89.9K - $100.9K
4% of jobs
$100.9K - $111.9K
8% of jobs
$115.3K is the 25th percentile. Wages below this are outliers.
$111.9K - $122.9K
9% of jobs
$122.9K - $133.9K
6% of jobs
$133.9K - $144.9K
11% of jobs
The median wage is $146K / yr.
$144.9K - $155.9K
16% of jobs
$164.5K is the 75th percentile. Wages above this are outliers.
$155.9K - $166.9K
14% of jobs
$166.9K - $177.9K
11% of jobs
$177.9K - $188.9K
12% of jobs
$67.9K
$142.8K
$188.9K
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.
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.
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.
For Empower Lims jobs in Virginia, the most frequently searched job titles are:
The top searched job categories for Empower Lims jobs in Virginia are:
Cities in Virginia with the most Empower Lims job openings:
$69K - $73K/yr
Full-time
Re-posted 7 days ago
Granules Pharmaceuticals Inc., (GPI) is a subsidiary of Granules India LTD. Over the past 34 years, we have worked towards strengthening our core and we are currently the 10th fastest growing generic pharma company in the US! With our sites in Chantilly and Manassas, Virginia, we have R&D through manufacturing and packaging of our medicines including pulsatile drug release in tablet and capsule dosage form, orally disintegrating modified release tablets (XR, MR, ER), modified release suspension and controlled substances capabilities in an abuse deterrent technology platform.
We are dedicated to excellence in manufacturing, quality, and commercialization of generic drugs to give customers reliable and affordable options.
Responsibilities:
Submit résumé referencing job code ASY001 to HR, Granules Pharmaceuticals, Inc., 3701 Concorde Parkway, Chantilly, VA 20151
Educational Requirements:
Must have a Bachelor’s degree in Biochemistry, Chemistry, or Biotechnology plus 2 years experience in Quality Control within a Pharmaceutical Manufacturing company.
Skills Requirements:
Skills and knowledge in HPLC, UV-Vis, FTIR, OOS/OOT, Dissolution, Titration, cGMP, LIMS