Our F500
Medical Device client has an exciting opportunity for a Systems Test Engineer.
Job Summary:
Develops software systems, applications,
firmware, and/or provides software systems testing and validation in support of
R&D and/or Manufacturing Process Engineering. Responsible for analyzing,
designing, programming, debugging, and modification of local,
network/internet-related computer programs for commercial or end user
applications (i.e. materials management, financial management, HRIS, or desktop
applications products). May interface with users to define system requirements
and/or necessary modifications. Responsible for developing, applying and
maintaining quality standards for software products.
Responsibilities:
1. Designs, develops, debugs, modifies, tests software programs by using
current programming languages, methodologies and technologies.
2. Documents software development and/or
test development by writing documents, reports, memos, change requests. Methods
used are determined by approved procedures and standards.
3. Tracks software development effort by
creating and maintaining records in the approved tracking management tool.
4. Analyzes, evaluates, verifies
requirements, software and systems by using software engineering practices.
5. Investigates, research, selects
software designs, operating systems and/or practices.
6. Continuously improves process and
work methodologies by interfacing with peers/cross-functional groups and
analyzing activities to improve workflow and work processes.
Quality Systems Duties and
Responsibilities:
Build Quality into all aspects of their
work by maintaining compliance to all quality requirements.
·
2
- 4 Years with BS (in Computer science or Electrical Engineering) 1 - 2 Years
with MS
·
Must
have 4-5 years' experience in System Test verification, Python expertise,
Github/Bitbucket exp
Preferred Qualifications
·
Medical
Device industry experience
Other Details:
Schedule: 08:00:AM - 04:30:PM
Work Setup: Onsite in Valencia, CA
Contract Length: 6 Months (2/9/2026 – 08/7/2026)
♦𝐄𝐱𝐜𝐞𝐥𝐥𝐞𝐧𝐜𝐞 𝐭𝐡𝐫𝐨𝐮𝐠𝐡 𝐐𝐮𝐚𝐥𝐢𝐭𝐲♦: 𝐏𝐡𝐚𝐫𝐦𝐚𝐯𝐢𝐬𝐞, 𝐲𝐨𝐮𝐫 𝐬𝐭𝐫𝐚𝐭𝐞𝐠𝐢𝐜 𝐋𝐢𝐟𝐞 𝐒𝐜𝐢𝐞𝐧𝐜𝐞𝐬, 𝐇𝐞𝐚𝐥𝐭𝐡𝐜𝐚𝐫𝐞 𝐚𝐧𝐝 𝐆𝐨𝐯𝐞𝐫𝐧𝐦𝐞𝐧𝐭 𝐬𝐨𝐥𝐮𝐭𝐢𝐨𝐧𝐬 𝐩𝐚𝐫𝐭𝐧𝐞𝐫.
𝗔𝗯𝗼𝘂𝘁 𝘂𝘀 𝗜𝗻𝗳𝗼𝗿𝗺𝗮𝘁𝗶𝗼𝗻:
We provide high-quality, cost-effective people and process solutions for your Quality, Regulatory, Engineering, Clinical, and Healthcare needs. Our company mantra 𝐄𝐗𝐂𝐄𝐋𝐋𝐄𝐍𝐂𝐄 𝐭𝐡𝐫𝐨𝐮𝐠𝐡 𝐐𝐔𝐀𝐋𝐈𝐓𝐘. The safety and quality of the drugs and devices produced for patients are directly related to 2 things, 𝐑𝐎𝐁𝐔𝐒𝐓 𝐏𝐑𝐎𝐂𝐄𝐒𝐒 𝐚𝐧𝐝 𝐐𝐔𝐀𝐋𝐈𝐅𝐈𝐄𝐃 𝐏𝐄𝐎𝐏𝐋𝐄. 𝐖𝐞 𝐝𝐞𝐥𝐢𝐯𝐞𝐫 𝐛𝐨𝐭𝐡.
𝐃𝐢𝐟𝐟𝐞𝐫𝐞𝐧𝐭𝐢𝐚𝐭𝐨𝐫𝐬:
☑𝐇𝐢𝐠𝐡𝐥𝐲 𝐒𝐤𝐢𝐥𝐥𝐞𝐝 𝐓𝐞𝐚𝐦: Our team of experienced consultants with distinct backgrounds in life sciences, including scientists, researchers, and regulatory experts. The quality and expertise of our team significantly impact our client’s success.
☑𝐒𝐩𝐞𝐜𝐢𝐚𝐥𝐢𝐳𝐞𝐝 𝐄𝐱𝐩𝐞𝐫𝐭𝐢𝐬𝐞: We focus on specific niches within the life sciences, healthcare, and government sectors, such as pharmaceuticals, biotechnology, medical devices, regulatory affairs, medical research, and product development. This specialized expertise allows us to offer targeted and in-depth insights to our clients.
☑𝐂𝐮𝐬𝐭𝐨𝐦𝐢𝐳𝐞𝐝 𝐒𝐨𝐥𝐮𝐭𝐢𝐨𝐧𝐬: We offer tailored solutions that align with the specific requirements of each client, rather than one-size-fits-all approaches, demonstrating a commitment to meeting client needs. We do not require a long learning curve, which leads to a faster payback and a greater return on your investment.
𝗣𝗲𝗿𝗳𝗼𝗿𝗺𝗮𝗻𝗰𝗲 𝗛𝗶𝘀𝘁𝗼𝗿𝘆
Over 20 Technical Transfers and 30 product launches.
11 FDA remediations. Warning Letters and or Consent Decrees.
Cost savings and increased efficiency of over 10MM for clients
