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Empower Laboratory Software Jobs (NOW HIRING)

Thorne

Analytical Laboratory Supervisor

Summerville, SC · On-site

At Thorne, we work to deliver high-quality, science-backed solutions to empower individuals to take ... and supporting software. * Maintain the Analytical Laboratory in an inspection-ready state by ...

Actalent

Analytical Scientist

Lexington, MA

$40 - $45/hr

... laboratory software (e.g., Empower, Compass, SoftMax, AccuSEQ, SoloVPE) is highly preferred understanding of veeva vault quality systems Experience Level Entry Level Job Type & Location This is a ...

Eurofins

HPLC Scientist - EMPOWER

Chesterfield, MO · On-site

Experience working with electronic laboratory notebook (ELN) systems and/or GMP documentation practices * Familiarity with Empower or OpenLab software Additional Information * Position is full-time, ...

Kelly Services

Senior Analytical Chemist

Raleigh, NC

$85K - $115K/yr

Experience using Empower, CDS, LIMS, and other laboratory software systems. * Strong knowledge of FDA, ICH, USP, and data integrity requirements. * Demonstrated troubleshooting, root cause ...

New

Kindeva Drug Delivery

Scientist II

Saint Louis, MO · On-site

Proficiency with chromatography data systems and laboratory software platforms, including Empower and Chromeleon, along with a strong understanding of cGMP regulations, FDA and ICH guidance, method ...

Alcami Corporation

Sr. Scientist I - Bioassay

Wilmington, NC · On-site

$83K - $114K/yr

Effectively uses various laboratory software packages (SoftMax, ProCal, Master Control, ELN, etc ... Working knowledge of SoftMax and Empower preferred. Travel Expectations * Up to 5% travel required.

Alcami Corporation

Sr. Scientist I - Bioassay

Wilmington, NC · On-site

$83K - $114K/yr

Effectively uses various laboratory software packages (SoftMax, ProCal, Master Control, ELN, etc ... Working knowledge of SoftMax and Empower preferred. * Up to 5% travel required. The physical ...

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All JobsEmpower Laboratory Software Jobs

Empower Laboratory Software information

What is the difference between Empower Laboratory Software vs Laboratory Technician?

FeatureEmpower Laboratory SoftwareLaboratory Technician
Primary RoleLaboratory data management and analysis softwarePerforming laboratory tests and procedures
Required CredentialsKnowledge of software systems, often with a background in science or ITRelevant scientific or technical certifications, often an associate or bachelor's degree
Work EnvironmentLaboratory or office setting, working with data and softwareLaboratory environment, handling samples and equipment
Industry UsageUsed by labs for data processing and reportingConducts experiments, tests, and sample analysis

Empower Laboratory Software focuses on managing and analyzing laboratory data through specialized software, while a Laboratory Technician performs hands-on testing and sample analysis. Both roles are essential in laboratory operations but serve different functions within the industry.

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Empower Laboratory Software jobs near you
Infographic showing various Empower Laboratory Software job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 8% Part Time, and 4% Contract. Highlights an 88% Physical, 3% Hybrid, and 9% Remote job distribution.

Analytical Development Scientist II

Kindeva Drug Delivery

Bridgeton, MO • On-site

Full-time

Re-posted 10 days ago

Job description

Our Work Matters
At Kindeva, we make products that save lives, ensuring better health and well-being for patients around the world.
The Impact You Will Make
As an Analytical Development Scientist II, you will play a critical role in supporting analytical method transfer, verification, and validation activities for both small molecule and biologic products within a Contract Development and Manufacturing Organization (CDMO) environment. This position contributes to the development and implementation of analytical capabilities while supporting quality control testing, technical investigations, process transfers, and validation activities. You will collaborate closely with the Manufacturing, Quality, Validation, and Technical Operations teams to ensure analytical activities are executed efficiently and in compliance, in support of bringing life-changing therapies to patients around the world.
Responsibilities
Analytical Method Development, Transfer & Validation
  • Execute analytical method transfer, verification, validation, and troubleshooting activities supporting both biologic and small molecule pharmaceutical products.
  • Perform routine and non-routine analytical testing of raw materials, in-process samples, finished products, stability samples, and validation studies.
  • Support technical investigations, specification development, regulatory submissions, and analytical activities associated with cleaning validation and manufacturing support.

Laboratory Operations & Continuous Improvement
  • Support the implementation, qualification, and maintenance of analytical instrumentation and laboratory systems.
  • Identify and implement opportunities to improve analytical methods, laboratory processes, efficiency, compliance, and overall testing capabilities.
  • Maintain technical expertise across a variety of analytical and biochemical techniques while supporting laboratory best practices and data integrity requirements.

Cross-Functional Collaboration & Technical Support
  • Collaborate with Quality Control, Manufacturing, Quality Assurance, Validation, and Technical Operations teams to support routine operations and project activities.
  • Provide technical guidance and training to laboratory personnel as needed.
  • Author and revise analytical methods, protocols, reports, Standard Operating Procedures (SOPs), and other technical documentation while maintaining compliance with current Good Manufacturing Practices (cGMPs) and Good Documentation Practices (GDPs).
  • Support occasional off-shift, weekend, or manufacturing-related activities as business needs require.

Qualifications
  • Bachelor's degree in Chemistry, Biochemistry, or a related scientific field with 5+ years of relevant industry experience; Master's degree with 3+ years of relevant industry experience; or Ph.D. with 2+ years of relevant industry experience. Equivalent combinations of education, training, and experience may be considered.
  • Experience supporting Quality Control or Analytical Development activities within GMP-regulated pharmaceutical, biotechnology, or CDMO environments, including biologics (proteins, peptides, monoclonal antibodies) and small molecule pharmaceutical products.
  • Hands-on experience performing analytical method transfer, method validation, compendial verification, troubleshooting, and analytical testing using techniques such as HPLC, UPLC, LC-MS, GC-MS, FTIR, SDS-PAGE, ELISA, Western Blot, protein concentration assays, Karl Fischer titration, pH analysis, and general wet chemistry methods.
  • Proficiency with chromatography data systems and laboratory software platforms, including Empower and Chromeleon, along with a strong understanding of cGMP regulations, FDA and ICH guidance, method validation principles, data integrity requirements, and laboratory safety standards.
  • Demonstrated ability to troubleshoot analytical issues, critically evaluate data, perform statistical calculations, generate technical reports, protocols, SOPs, and other scientific documentation while providing scientifically sound recommendations and conclusions.
  • Strong verbal and written communication skills with the ability to collaborate effectively across cross-functional teams, manage multiple priorities, and meet deadlines in a fast-paced pharmaceutical manufacturing environment.

Physical Requirements
  • Specific vision requirements include close vision, distance vision, color vision, and the ability to adjust focus.
  • Ability to use computers and laboratory systems for extended periods of time.
  • Ability to follow all cGMP, laboratory, and safety procedures.
  • Must wear required personal protective equipment (PPE) and perform assigned work safely.
  • Ability to use proper lifting techniques and remain aware of workplace hazards.
  • Must occasionally lift and/or move up to 25 pounds.
  • Ability to support occasional weekend, off-shift, or manufacturing support activities as business needs require.

#LI-Onsite
California residents should review our Notice for California Employees and Applicants before applying.
Kindeva does not accept unsolicited assistance from headhunters or recruitment firms for any of our job openings. Any resumes or candidate profiles submitted to Kindeva employees-regardless of format-without a valid, signed agreement and an approved job order from an authorized signatory in Talent Acquisition will be considered the sole property of Kindeva. No fees will be paid in the event that a candidate is hired as a result of an unsolicited resume or referral.
Equal Opportunity Employer:
Kindeva Drug Delivery is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, Protected Veteran status, sexual orientation, or any other characteristic protected by federal, state or local law.
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