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Pharma Software Jobs in New York (NOW HIRING)

At Aniesis Pharma, we're dedicated to improving lives through cutting-edge pharmaceutical solutions ... Remote Software Engineer Opportunity About the Role: We are seeking a talented and motivated Remote ...

Data Architect - Remote

Parsippany, NJ · On-site +1

$64 - $82.50/hr

NAVA Software solutions is looking for a Data Architect Details: Data Architect Data Warehouse ODI and OIC Location: 100% Remote Duration: 6-12 months Mandatory: * Strong understanding of Pharma data ...

Software Engineer

Manhattan, NY · On-site

$200 - $298/hr

Our customers are pharma, payers, and health systems who actually want to do something meaningful ... Staff‑level software engineer with deep systems chops--self‑reasoning about memory, parallelism ...

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Showing results 1-20

Pharma Software information

See New York salary details

$86.4K

$190.4K

$225.4K

How much do pharma software jobs pay per year?

As of Aug 24, 2026, the average yearly pay for pharma software in New York is $190,380.00, according to ZipRecruiter salary data. Most workers in this role earn between $154,800.00 and $224,300.00 per year, depending on experience, location, and employer.

What is a Pharma Software?

A Pharma Software job involves developing, implementing, and maintaining software solutions tailored for the pharmaceutical industry. Professionals in this role work on applications that support drug development, regulatory compliance, clinical trials, and supply chain management. They collaborate with healthcare professionals, regulatory bodies, and IT teams to ensure software meets industry standards and enhances efficiency. Skills in programming, data management, and knowledge of pharma regulations like FDA and GxP are often required.

What types of projects or software systems do Pharma Software professionals typically work on?

Pharma Software professionals commonly work on systems that support drug development, clinical trials, laboratory data management, and regulatory compliance, such as LIMS (Laboratory Information Management Systems), electronic data capture tools, and manufacturing execution systems. Daily tasks often include collaborating with scientists, regulatory teams, and other IT specialists to design, validate, and maintain software that must meet stringent industry regulations. This role offers unique opportunities to work at the intersection of technology and life sciences, providing valuable insights into both software engineering and pharmaceutical workflows. As you gain experience, there are career paths toward leading project teams, specializing in systems validation, or advancing into IT management within the pharmaceutical sector.

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

To succeed in Pharma Software roles, you need strong skills in software development or engineering, a solid understanding of pharmaceutical industry regulations (such as FDA or GxP), and often a degree in computer science or a related field. Familiarity with programming languages like Python or Java, experience with validated systems, and knowledge of tools such as LIMS, ERP, or electronic lab notebooks are commonly required. Strong analytical thinking, teamwork, and effective communication set outstanding candidates apart. These abilities ensure the delivery of compliant, secure, and efficient software solutions essential for pharmaceutical operations.

What are popular job titles related to Pharma Software jobs in New York?

For Pharma Software jobs in New York, the most frequently searched job titles are:

What job categories do people searching Pharma Software jobs in New York look for?

The top searched job categories for Pharma Software jobs in New York are:

Infographic showing various Pharma Software job openings in New York as of August 2026, with employment types broken down into 100% Contract. Highlights an 50% In-person, and 50% Remote job distribution, with an average salary of $190,380 per year, or $91.5 per hour.

Design Software Quality Consultant (Medical Devices)

Stark Pharma Solutions Inc

Piscataway, NJ • Remote

Contractor

Re-posted 24 days ago


Job description

Hi,

My name is Karthik Mutyala, from Stark Pharma Solutions Inc, we are hiring talents for our client. I am working on Design Software Quality position right now. Please send me your updated resume if you have relevant experience and interested in this position. The detailed job description is as follows

Role: Design Software Quality Consultant (Medical Devices)

Location: REMOTE
Duration: Long Term
 

Position Overview

We are seeking an experienced Design Software Quality Consultant to support post-acquisition integration activities for a medical device product portfolio. This role will focus on ensuring software design quality, regulatory compliance, and successful integration of acquired products into the client's quality management system.

The ideal candidate will have deep expertise in Software Design Quality, Model-Based Systems Engineering (MBSE), and medical device software compliance, with experience supporting new product development in regulated environments.

Key Responsibilities

  • Review and assess Design History Files (DHFs) and product development documentation for acquired medical device products.
  • Support software design quality activities during post-acquisition product integration.
  • Ensure compliance with internal quality standards and global regulatory requirements.
  • Lead Model-Based Systems Engineering (MBSE) activities for software-enabled medical devices.
  • Review software engineering deliverables to ensure compliance with design controls and quality requirements.
  • Partner with cross-functional teams including R&D, Software Engineering, Quality, and Regulatory Affairs.
  • Support risk management, usability engineering, and software lifecycle compliance activities.

Required Qualifications

  • 10+ years of Software Quality Engineering experience in the medical device industry.
  • Strong experience with Software Design Quality and Design Controls.
  • Hands-on experience with Model-Based Systems Engineering (MBSE).
  • Experience supporting software quality for new product development or medical device integration/remediation projects.
  • Knowledge of IEC 62304, IEC 60601, ISO 14971, and medical device software regulations.
  • Experience with Software as a Medical Device (SaMD).
  • Strong understanding of software verification, validation, and compliance within regulated environments.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.  

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/

Thank you,

Karthik Mutyala

Recruiting Manager

Stark Pharma Solutions Inc

Email: karthik@starkpharma.com

15 Corporate Place S, Suite 350,

Piscataway, New Jersey 08854

www.starkpharma.com