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Product Development​/Mechanical Engineer

Job in San Francisco, San Francisco County, California, 94199, USA
Listing for: BioQ Pharma
Full Time position
Listed on 2026-06-27
Job specializations:
  • Engineering
    Manufacturing Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 90000 - 120000 USD Yearly USD 90000.00 120000.00 YEAR
Job Description & How to Apply Below
Position: Product Development / Mechanical Engineer

Product Development / Mechanical Engineer

BioQ Pharma is a privately held specialty pharmaceutical company focused on developing and commercializing ready‑to‑use infusible pharmaceuticals. The Company’s infusion platform addresses pressing unmet needs in drug infusion—cost, medication error, sterility, efficiency, and patient quality of life. BioQ’s objective is to set a new standard of care through proprietary unit‑dose infusion systems that can be deployed quickly and conveniently at the point of care with one touch.

The Company is ISO
13485 certified and partners with leading industry players such as Novartis’ Sandoz, Stada, Cipla, Lee’s Pharm, Lunatus, Galen Limited, POA Pharma, Xantis Pharma, Sophos Biotech, Cooper Pharma, Lenis, Taiba, and West Pharmaceutical Services.

As a Mechanical Engineer you will design and develop ready‑to‑use infusion systems from early concept generation through transfer and production support. The role is primarily mechanical engineering, but knowledge of motors, electronics, and software is also required.

Responsibilities
  • Develop and test product concepts based on user and market requirements.
  • Develop product requirements and specifications.
  • Design new products, subassemblies, or components.
  • Design injection‑molded parts for high‑volume manufacture.
  • Apply design for manufacturability (DFM) and automation principles.
  • Conduct materials research and testing.
  • Generate design output documentation.
  • Document and execute design verification and user validation testing.
  • Develop and document manufacturing processes.
  • Work with suppliers to ensure components meet required quality and specifications.
  • Support transfer and ongoing production at component suppliers and contract manufacturers.
  • Travel domestically and internationally as required.
Qualifications
  • BS or MS in Mechanical Engineering or related field.
  • 5–15 years of experience designing products from concept to manufacturing, including medical device experience.
  • Strong understanding of manufacturing processes such as injection molding, machining, and joining techniques.
  • Solid knowledge of material properties of plastics, metals, and rubbers.
  • Understanding of Design for Manufacturing at high volumes.
  • Experience working with a variety of vendors and contract manufacturers.
  • Proficiency in Solid Works, 2D drafting, prototyping, machining, and common shop tools.
  • Basic understanding of electronics and ability to comprehend software written in

    C.
  • Experience designing and troubleshooting electronics, PCBs, firmware, and embedded systems a plus.
  • Understanding of statistics, DOE, and verification & validation activities.
  • Excellent communication and documentation skills.
  • Prior experience with pharmaceutical container/closure design is a plus.

All information will be kept confidential in accordance with EEO guidelines.

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