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Freelance Labware Lims Developer Jobs in New York

Technical Product Manager

Rahway, NJ · On-site

$169K - $195K/yr

Bachelor's degree in Life Sciences, Biomedical Engineering, Chemical Engineering, Computer Science ... LIMS (e.g., Labware), ELN (e.g., Benchling), Apache Kafka, Spark, Databricks, or similar.

IT Business Partner - DPI

Hauppauge, NY · On-site

$92K - $135K/yr

Manufacturing, Packaging, WH, QC, QA, Engineering, Finance, HR etc. and IT Business Partners and ... Knowledge and experience in handling QC systems, LIMS, QA/R&D/RA applications Experience with ...

IT Business Partner - DPI

Hauppauge, NY · On-site

$92K - $135K/yr

Manufacturing, Packaging, WH, QC, QA, Engineering, Finance, HR etc. and IT Business Partners and ... LIMS Vendor * Dimensions IT Manufacturing, Packaging and WH Systems support including IT ...

Manufacturing, Packaging, WH, QC, QA, Engineering, Finance, HR etc. and IT Business Partners and ... LIMS Vendor Dimensions IT Manufacturing, Packaging and WH Systems support including IT ...

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 GMP QC ...

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 ...

Technical Product Manager

Rahway, NJ · On-site

$117 - $184.20/hr

Bachelor's degree in Life Sciences, Biomedical Engineering, Chemical Engineering, Computer Science ... Experience with tools like LIMS (e.g., Labware), ELN (e.g., Benchling), Apache Kafka, Spark ...

Freelance Labware Lims Developer information

What is a freelance Labware LIMS developer?

A Freelance Labware LIMS Developer is an independent professional who specializes in designing, customizing, and maintaining LabWare Laboratory Information Management Systems (LIMS) for laboratories. They work on a contract basis to help labs implement, configure, and optimize LabWare LIMS software to manage samples, workflows, and data efficiently. Their responsibilities often include system integration, scripting, troubleshooting, and user training to ensure that the LIMS meets the specific needs of the organization.

What skills and qualifications are needed to thrive as a freelance Labware LIMS developer?

To thrive as a Freelance Labware LIMS Developer, you need strong programming skills (particularly in Java and SQL), a solid understanding of laboratory workflow processes, and experience with Labware LIMS configuration or implementation. Familiarity with tools such as Labware LIMS, REST/SOAP APIs, and relevant certifications like Labware Certified Professional are highly beneficial. Excellent problem-solving abilities, effective communication, and the ability to work independently are standout soft skills for this role. These competencies ensure the development of robust, user-friendly LIMS solutions that meet client requirements and industry standards.

What are common challenges freelance Labware LIMS developers face when working with multiple clients?

Freelance Labware LIMS developers often encounter challenges such as adapting quickly to diverse client environments, each with unique workflows and data management needs. Balancing multiple projects requires strong organizational skills to manage timelines, requirements, and communication across different stakeholders. Additionally, freelancers must stay current with Labware updates and integration requirements, as clients may use varying versions or have custom configurations. Building strong client relationships and clear documentation practices also help ensure smooth handovers and ongoing support.

What is the difference between Freelance Labware Lims Developer vs Laboratory Information Systems (LIS) Specialist?

AspectFreelance Labware Lims DeveloperLaboratory Information Systems (LIS) Specialist
CredentialsIT or software development background, certifications in Labware LIMSHealthcare or laboratory IT certifications, LIS-specific training
Work EnvironmentFreelance projects, client sites, remote workLaboratories, healthcare facilities, IT departments
Industry UsagePharmaceutical, biotech, research labsClinical labs, hospitals, diagnostic centers
Search & Comparison IntentDeveloping or customizing LIMS softwareManaging and supporting LIS systems

While both roles involve laboratory information systems, Freelance Labware Lims Developers focus on customizing and developing LIMS software, often working independently. LIS Specialists typically manage, support, and optimize existing LIS systems within healthcare or clinical environments. The roles overlap in technical skills but differ in scope and work setting.

What are the most commonly searched types of Labware Lims Developer jobs in New York?

The most popular types of Labware Lims Developer jobs in New York are:

What are popular job titles related to Freelance Labware Lims Developer jobs in New York?

For Freelance Labware Lims Developer jobs in New York, the most frequently searched job titles are:

What job categories do people searching Freelance Labware Lims Developer jobs in New York look for?

The top searched job categories for Freelance Labware Lims Developer jobs in New York are:

What cities in New York are hiring for Freelance Labware Lims Developer jobs?

Cities in New York with the most Freelance Labware Lims Developer job openings:

Infographic showing various Freelance Labware Lims Developer job openings in New York as of August 2026, with employment types broken down into 80% Full Time, 6% Part Time, and 14% Contract. Highlights an 83% Physical, 4% Hybrid, and 13% Remote job distribution.

Senior Associate, Informatics PM/BA

Pfizer, Inc.

Pearl River, NY • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted yesterday


Pfizer rating

8.2

Company rating: 8.2 out of 10

Based on 125 frontline employees who took The Breakroom Quiz

32nd of 86 rated pharmaceutical


Job description

Use Your Power for Purpose
In a world driven by rapid knowledge creation and supported by advanced technology platforms, Pfizer's digital and 'data first' strategy aims to accelerate the development of impactful technology solutions for research, development, and medical functions. By fostering collaboration and information sharing through business technology, we strive to help employees discover the best healthcare solutions for our patients. As part of a team of innovators, you will play a crucial role in maintaining our systems and ensuring the security of our information. We seek dedicated colleagues like you to enhance the quality of patient care through fresh ideas and cutting-edge information technology solutions.
Your expertise in informatics will be instrumental in advancing R&D by developing, supporting, and validating computer systems. You will generate high-quality assay data within a regulated cGLP (current Good Laboratory Practice) laboratory environment to bolster Pfizer's research initiatives and streamline processes. Leveraging your technical and documentation prowess, you will ensure regulatory compliance for the Research Department's software solutions. As an associate, your dedication to the job will drive the completion of project tasks and objectives. Your domain knowledge and commitment will foster a collaborative atmosphere among your colleagues. It is your diligence and focus that will empower Pfizer to reach new milestones and provide aid to patients worldwide.
What You Will Achieve
As a Senior Associate, you will play a key role in translating business needs from laboratory and operations teams into practical info system solutions. You will partner with functional assay leads, operations leads, laboratory SMEs, and informatics partners to define requirements, support solution design, coordinate user testing, and manage project activities across the solution development lifecycle (SDLC). Your work will help ensure that info systems supporting regulated laboratory processes are fit for purpose, properly tested, and supported by appropriate documentation for validated environments.
How You Will Achieve It
  • Partner with functional assay leads, operations leads, laboratory SMEs, and informatics partners to understand business needs and translate them into info system solutions.
  • Elicit, document, and maintain business and end-user requirements for new solutions and enhancements to existing solutions.
  • Support solution design discussions by ensuring proposed system functionality aligns with laboratory workflows, operational needs, compliance expectations, and end-user requirements.
  • Project manage assigned system initiatives through the solution development lifecycle, including requirements gathering, design review, testing, validation readiness, deployment support, and post-implementation follow-up.
  • Develop, review, and execute user acceptance testing activities to confirm system functionality meets approved business and end-user requirements.
  • Guide end users through testing activities, support test execution, document results, capture defects, and coordinate issue resolution with the technical teams.
  • Generate, review, and maintain documentation supporting validated systems, including requirements, test scripts, SOPs, change controls, and related project deliverables.
  • Facilitate regular project meetings with business stakeholders and technical partners to review priorities, status, risks, decisions, and action items.
  • Collaborate with quality, validation, laboratory, and technical teams to ensure system deliverables are aligned with regulated system expectations.
  • Maintain strict compliance with departmental, site, and corporate training, quality, and safety requirements.

Here Is What You Need (Minimum Requirements)
  • MS/MA in a science-related discipline such as computer science / mathematics or biological science with 1+ years of hands-on industry experience. Or BS/BA with 3+ years of hands-on industry experience.
  • Understanding of solution development lifecycle activities in a regulated or quality-driven environment.
  • Strong written and verbal communication skills.
  • Strong organizational skills with ability to manage multiple priorities, timelines, and stakeholders.
  • Proficient in Microsoft Office 365 applications.

Bonus Points If You Have (Preferred Requirements)
  • Experience supporting validated systems in a pharmaceutical, biotech, laboratory, or regulated environment.
  • Familiarity with laboratory informatics systems such as LabWare LIMS and statistical analysis applications such as SAS.
  • Experience creating documentation such as requirements, test scripts, traceability matrices, SOPs, or user guides.
  • Experience working with cross-functional teams across business, quality, and technical organizations.
  • Working knowledge of SQL and basic understanding of computer programming language.
  • Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity. Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use.

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
Occasional evening and weekend work to meet critical deliverables.
Work Location Assignment: Hybrid
The annual base salary for this position ranges from $82,700.00 to $137,900.00. In addition, this position is eligible for participation in Pfizer's Global Performance Plan with a bonus target of 10.0% of the base salary. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life's moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site - U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.
Relocation assistance may be available based on business needs and/or eligibility.
Candidates must be authorized to be employed in the U.S. by any employer.
U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.
Sunshine Act
Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider's name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.
EEO & Employment Eligibility
Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States.
Pfizer endeavors to make www.pfizer.com/careers accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email disabilityrecruitment@pfizer.com. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.
To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers.
Information & Business Tech

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About Pfizer

Sourced by ZipRecruiter

All over the world, Pfizer colleagues work together to positively impact health for everyone, everywhere. Our colleagues have the opportunity to grow and develop a career that offers both individual and company success; be part of an ownership culture that values diversity and where all colleagues are energized and engaged; and the ability to impact the health and lives of millions of people. Pfizer, a global leader in the biopharmaceutical industry, is continuously seeking top talent who are inspired by our purpose to innovate to bring therapies to patients that significantly improve their lives. Our Health and Science System Specialists Team provides leadership across patient care settings in the complex Hospital, Health System, and Key Medical Group environment to bring value to our customers and patients in this dynamic ecosystem.

Industry

Pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

New York, NY, US

Year founded

1849