Careers

Join Us.

At Biomeme we make things. We make hardware; we work with biological organisms; we hack smartphones. We’re looking for passionate people who are skilled with their hands and have impeccable attention to detail. You should be a fast learner and not afraid of tackling challenges both big and small. No task is above or below your pay grade.

Biomeme is as interdisciplinary as it gets. We combine rigorous biology and chemistry with best-in-class hardware and software engineering. It’s all wrapped up in sublime user design, with the goal of helping our customers enact real-world change. Guided by data and a belief in the iterative process, we develop elegant solutions to complex problems that demand precision.

Our partners and customers span a wide range of industries across the US, Latin America, Africa and Europe. We’ve got great traction in health: we’re testing for STD’s in Philadelphia, Malaria and Ebola virus in Africa, Avian Influenza in Europe, veterinary targets in the Andes and Lyme disease in the US. Outside of health, we have partners in industrial water monitoring, aquaculture, agriculture, conservation biology and more. High school students are testing for mislabeled sushi. Quantified Selfers are tracking their microbiome. Everyday users are even testing their own DNA for genetic markers.

We also recently began work on a multi-year, multi-million dollar contract with the US Government. It’s a good time to come onboard.

Current Openings

Firmware Engineer

Biomeme Inc is looking for a Firmware Engineer to join our team! To be considered for this position please follow the steps located in the attached link https://goo.gl/forms/Q1pe9LlJFq2rCVD63

 

JOB DESCRIPTION:
Lead firmware design and architecture of a multi processor thermocycler
Develop, debug, test firmware in C for scientific instrument
Implement firmware drivers for new features including FAT file system and Bluetooth coms
Maintain C# and Python development tools
Able to self mange and organize development and timelines

REQUIREMENTS:

MUST:
3+ year firmware experience
BS computer science, electrical engineering, computer engineering or similar
Deep understanding of C and compilers
Experience with bare metal and RTOS firmware
freeRTOS preferred
Familiar with ARM Cortex micro controllers
STM32 preferred
Understanding on common communications buses
SPI
RS232 UART
I2C

PREFERRED:
Experience developing under QMS system , ISO 9001 or similar
C# proficient
Python proficient
BLE experience
IAR experience

Administrative Assistant

 

Biomeme Inc is looking for an Administrative Assistant to join our team! Your responsibilities will include, but will not be limited to:
– Filing: managing our paper filing as well as our various share drives
– Bookkeeping: maintaining standard operating procedures, overseeing business expense reimbursement, managing invoices and bills, payments, etc.
– Shipping & Receiving: receive shipments, manage upcoming shipments, package shipments and coordinate with shipping companies, handle customs and import/export
– Inventory: Manage product inventory available for sale. Manage systems on loan.
– Office maintenance: manage cleaning vendor, tidy up office in between cleanings, maintain stock of office supplies
– Events: coordinate special events such as happy hours and staff birthdays
– Marketing Support: support marketing team with conferences, collateral, business cards, etc.

While you should be methodical and predictable, we are a startup, so you should be OK with a lack of clarity, frequent confusion, and a high level of general craziness.

 

To be considered for this position please follow the steps located in the attached link  https://goo.gl/forms/k4k1nuQQkGAwpxoB2

Medical Device / Quality System Engineer

Biomeme is looking for an experienced medical device engineer to guide us through the process of building an FDA-approved Class II medical device.

Candidates for this role:
Must have experience designing & validating medical products within an FDA-compliant quality system
Must be able to create & lead the process validation practices neccesary for FDA compliance
Must be able to generate the appropriate documents for FDA submission
Must be familiar with electronics/circuit design, firmware/software, and mechanical design
Must be familiar with ISO 13485, ISO 14971, Quality Management Systems, Design History Files, Design Reviews, Design Controls, Management Review Meetings, Risk Analysis/FMEA, Complaint/Adverse Event handling practices, Process Validation, Supplier Management, and all other aspects of an FDA 21 CRF 820.30-compliant QMS for Medical Devices
Should be proficient in SolidWorks or other CAD software
Will expand + work within our existing cloud-based QMS

The following are preferred, but not neccesary:
Design For Manufacturing (DFM) experience for electro-mechanical products and/or disposables or diagnostic kitting
Accredation for internal audits, or otherwise the ability to prepare us for an audit
Experience building/designing FDA-compliant quality systems for medical devices
Experience submitting devices for EUA, 510k, CE IVDD and/or IDE clinical studies

To be considered for this position you must fill out the application that is located in the following link.

https://goo.gl/forms/KM6rGU3bOAcm7AQK2

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