Consultant 1
Montrose, CA · On-site
Collaborate with cross-functional teams (Quality, IT, Engineering, Operations, Automation ... Attractive salary and comprehensive benefits package for full-time and part-time employees ...
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Consultant 1
Montrose, CA · On-site
Collaborate with cross-functional teams (Quality, IT, Engineering, Operations, Automation ... Attractive salary and comprehensive benefits package for full-time and part-time employees ...
Application Administrator
Washington, DC · On-site +1
$69K - $158K/yr
As a full stack developer, you can resolve a problem with a complete end-to-end solution in a fast ... Full-time and part-time employees working at least 20 hours a week on a regular basis are eligible ...
Application Administrator
Washington, DC · On-site +1
$69K - $158K/yr
As a full stack developer, you can resolve a problem with a complete end-to-end solution in a fast ... Full-time and part-time employees working at least 20 hours a week on a regular basis are eligible ...
This is a part-time engagement of up to 16 hours per week, with the majority of work performed ... Track infrastructure assessment findings, coordinate remediation with cloud engineering resources ...
New
This is a part-time engagement of up to 16 hours per week, with the majority of work performed ... Track infrastructure assessment findings, coordinate remediation with cloud engineering resources ...
New
Registered Nurse, William Marion Stevenson House
Milford, DE · On-site
$35.39 - $56.63/hr
This position is a part-time benefit eligible position. About The Stevenson House: The William ... Programming is individualized and prescriptive to meet the needs of the youth. Staff is trained to ...
Quick apply
Registered Nurse, William Marion Stevenson House
Milford, DE · On-site
$35.39 - $56.63/hr
This position is a part-time benefit eligible position. About The Stevenson House: The William ... Programming is individualized and prescriptive to meet the needs of the youth. Staff is trained to ...
Our scientists, engineers, sales executives, and visionaries are united by an unwavering commitment ... Advanced knowledge of Google Docs, Word, Excel, basic statistics and familiarity with LIMS systems
Our scientists, engineers, sales executives, and visionaries are united by an unwavering commitment ... Advanced knowledge of Google Docs, Word, Excel, basic statistics and familiarity with LIMS systems
Part Time Labware Lims Developer information
What is a part time Labware LIMS developer?
Part Time Labware LIMS Developers are professionals who specialize in configuring, customizing, and maintaining LabWare Laboratory Information Management Systems (LIMS) on a part-time basis. They work with laboratories to streamline processes, manage data, and integrate instruments with the LIMS platform. Their responsibilities often include coding, troubleshooting, and supporting end-users to ensure the LIMS meets the lab’s needs while working fewer hours than a full-time developer. This role may suit those seeking flexible schedules or balancing other commitments.
What are the key skills and qualifications needed to thrive as a part time Labware LIMS developer?
To thrive as a Part Time Labware LIMS Developer, you need a solid background in computer science or information technology, experience with LIMS platforms (especially LabWare), and knowledge of laboratory workflows. Proficiency in programming languages like JavaScript or Python, SQL databases, and familiarity with LabWare scripting and configuration tools are typically required. Strong problem-solving skills, attention to detail, and effective communication help you collaborate with laboratory staff and translate requirements into technical solutions. These skills are crucial for ensuring the LIMS meets user needs, maintains data integrity, and supports laboratory efficiency.
What are common challenges faced by part time Labware LIMS developers in balancing project deadlines with limited work hours?
Part Time Labware LIMS Developers often face the challenge of managing complex system configurations and troubleshooting within a limited number of weekly work hours. This can require strong time management skills and clear communication with full-time team members to ensure project milestones are met. Close collaboration with laboratory staff and IT teams is essential to prioritize tasks and address critical issues efficiently. Leveraging documentation and version control tools can also help part-time developers stay aligned with ongoing project developments.
What is the difference between Part Time Labware Lims Developer vs Part Time Laboratory Technician?
| Aspect | Part Time Labware Lims Developer | Part Time Laboratory Technician |
|---|---|---|
| Primary Role | Develops and maintains Laboratory Information Management Systems (LIMS) | Performs routine lab tests and sample processing |
| Required Skills | Programming, database management, system configuration | Laboratory procedures, sample handling, data recording |
| Work Environment | Office or lab setting focused on software development | Laboratory setting with hands-on testing |
| Certifications | IT or software development certifications often preferred | Lab technician certifications or training |
While both roles support laboratory operations, the Part Time Labware Lims Developer focuses on software development and system integration, whereas the Part Time Laboratory Technician handles sample testing and data collection. They differ in skills, responsibilities, and work environment but collaborate to ensure lab efficiency.
More about Part Time Labware Lims Developer jobs
What are the most commonly searched types of Labware Lims Developer jobs?
The most popular types of Labware Lims Developer jobs are:
What states have the most Part Time Labware Lims Developer jobs?
States with the most job openings for Part Time Labware Lims Developer jobs include:
What job categories do people searching Part Time Labware Lims Developer jobs look for?
The top searched job categories for Part Time Labware Lims Developer jobs are:
Full-time, Part-time
Medical, Dental, Vision, Life, Retirement, PTO
Re-posted 27 days ago
Job description
ELIQUENT Life Sciences is the leading global consulting firm providing solutions to life science companies researching, developing, and manufacturing innovative products to serve patients and respond to public health challenges around the world. ELIQUENT is committed to serving clients’ needs with extensive expertise, unwavering integrity, and strategic insight in a manner that supports availability of safe, effective, and high-quality drugs, biologics, and medical devices. For more information, please visit our website at eliquent.com.
We are seeking CSV Consultants at multiple levels (Consultant I, Consultant II, Consultant III) to support validation and compliance activities for computerized systems in a regulated GMP environment. These roles will involve executing validation deliverables, ensuring data integrity, and maintaining inspection readiness across manufacturing, laboratory, and IT systems.
Responsibilities (all levels):
- Author and/or review CSV documentation, including:
- Validation Plans, Protocols (IQ/OQ/PQ/FAT/SAT), and Reports
- User Requirements Specifications (URS), Functional Specifications (FS), and Traceability Matrices
- Risk assessments and Data Integrity assessments
- Execute validation testing and document results in compliance with GMP/GLP standards.
- Support ongoing system lifecycle management: periodic reviews, requalification, and change control.
- Collaborate with cross-functional teams (Quality, IT, Engineering, Operations, Automation).
- Provide support during audits and inspections to ensure systems meet regulatory expectations (FDA, EMA, etc.).
- Ensure compliance with relevant guidelines: GAMP 5, 21 CFR Part 11, EU Annex 11, and company SOPs.
Consultant Levels:
Consultant I (Entry-Level / Junior)
- Experience: 0–3 years CSV or validation experience in GMP environment
- Responsibilities: Execute protocols, perform testing, collect evidence, assist with documentation, learn regulatory requirements under supervision.
Consultant II (Mid-Level)
- Experience: 3–6 years CSV experience, strong working knowledge of FDA/EU regulations, independent execution of validation projects.
- Responsibilities: Lead small projects or system validations, author protocols and reports, manage deviations, interface with clients and auditors, mentor Consultant I.
Consultant III (Senior-Level)
- Experience: 6–10+ years CSV or validation leadership experience, expertise in multiple system types (LIMS, MES, SCADA, ERP, Lab/Automation Equipment).
- Responsibilities: Lead complex CSV programs, oversee multiple system validations, manage validation teams, develop strategies, ensure audit readiness, and advise on compliance.
Qualifications
- Bachelor’s degree in Engineering, Computer Science, Life Sciences, or related field (required)
- Knowledge of GMP, GAMP 5, 21 CFR Part 11, EU Annex 11
- Strong documentation, communication, and organizational skills
- Ability to work independently and within cross-functional teams
- Consulting mindset with adaptability to dynamic project needs
BENEFITS:
What We Offer:
Competitive Compensation: Attractive salary and comprehensive benefits package for full-time and part-time employees, including health, dental, vision, and life insurance, a 401(k) plan with employer match, a generous paid time off policy, and additional perks. Compensation is commensurate with professional experience.
Career Development: Opportunities for professional growth and advancement within a supportive and innovative environment.
Work-Life Balance: Flexible work arrangements and a commitment to maintaining a healthy work-life balance.
Eliquent Life Sciences is proud to be an Equal Opportunity Employer, committed to employee diversity.