CAREERS



Current Job Postings

Job Title: Clinical/Analytical Chemist

Industry: Medical Device and In Vitro Diagnostics

Job Type: Full-time

Description:
Bluejay Diagnostics is a rapidly growing medical device company focusing on rapid near-patient diagnostics. We strive to innovate in ways which completely change the medical decision-making process, ushering in a new era of healthcare. To help us with our mission, we are searching for Clinical/Analytical Chemist. This person will work with a multidisciplinary team to design, develop, optimize, and validate new immunoassays.

Responsibilities:

  • Perform analytical testing of pilot and fully developed devices.
  • Develop SOPs and validation documents.
  • Perform biostatistics and write reports.
  • Work in R&D activities.

Requirements:

  • Bachelor’s degree or higher in biochemistry, chemistry, engineering, or related scientific disciplines.
  • Experienced in CLSI, CLIA, and CAP standards and regulations.
  • Strong experience working in a wetlab environment.
  • Operating understanding of BSL II requirements.
  • Cell culture experience (preferred)
  • Experience in cGMP manufacturing (preferred)
  • Experience in clean room environments (preferred)
  • ISO 9001, ISO 13485, or ISO 17025 experience (preferred)
  • Demonstrate strong organizational, time management, and problem-solving skills.
  • Lead groups and work independently, without instruction.
  • Ability to function in a dynamic environment and balance multiple priorities simultaneously.
  • Ability to commute/relocate to our Acton, MA office (Preferred).
  • Note: This job description is not all-inclusive. Additional duties may be performed, as assigned. It acts as a guideline and is subject review between employee and manager throughout tenure.

Benefits:

  • Paid time off
  • Health insurance
  • Dental Insurance
  • Vision insurance
  • Parental leave

To apply for this position, send your resume at contact@bluejaydx.com

Job Title: Clinical Trial Manager

Industry: Medical Device and In Vitro Diagnostics

Job Type: Full-time

Description:
Bluejay Diagnostics is a rapidly growing medical device company focusing on rapid near-patient diagnostics. We strive to innovate in ways which completely change the medical decision-making process, ushering in a new era of healthcare. To help us with our mission, we are searching for a Clinical Trial Manager.

Responsibilities:

  • Serve as the liaison to our clinical research sites.
  • Manage site set-up, including contracts, CRFs, registrations, and IRB approvals.
  • Serve as a resource for site related issues.
  • Train clinical site personnel on the use of investigational medical devices.
  • Site monitoring, Trial Master File, Essential Documents, audits, data integrity, recruitment, reporting, etc.
  • Understanding of cGCP and ICH guidelines.

Requirements:

  • Bachelor’s degree or higher.
  • Minimum of 3 years of experience as a Clinical Trial Manager.
  • ISO 9001, ISO 13485, or ISO 17025 experience (preferred)
  • Demonstrate strong organizational, time management, and problem-solving skills.
  • Lead groups and work independently, without instruction.
  • Excellent communication skills.
  • Ability to commute/relocate to our Acton, MA office (Preferred).
  • Note: This job description is not all-inclusive. Additional duties may be performed, as assigned. It acts as a guideline and is subject review between employee and manager throughout tenure.

Benefits:

  • Paid time off
  • Health insurance
  • Dental Insurance
  • Vision insurance
  • Parental leave

To apply for this position, send your resume at contact@bluejaydx.com

Job Title: Immunoassay Scientist

Industry: Medical Device and In Vitro Diagnostics

Job Type: Full-time

Description:
Bluejay Diagnostics is a rapidly growing medical device company focusing on rapid near-patient diagnostics. We strive to innovate in ways which completely change the medical decision-making process, ushering in a new era of healthcare. To help us with our mission, we are searching for an Immunoassay Scientist. This person will work with a multidisciplinary team to design, develop, and optimize new immunoassays.

Responsibilities:

  • Support the research and development team.
  • Develop ELISA immunoassays.
  • Protein modifications and conjugations to surfaces and colloids.
  • Quality control and quality assurance.

Requirements:

  • Bachelor’s degree or higher in biochemistry, chemistry, engineering, or related scientific disciplines.
  • Minimum of 3 years of experience in the development of ELISA immunoassays.
  • Strong experience working in a wetlab environment.
  • Operating understanding of BSL II requirements.
  • Cell culture experience (preferred)
  • Experience in cGMP manufacturing (preferred)
  • Experience in clean room environments (preferred)
  • ISO 9001, ISO 13485, or ISO 17025 experience (preferred)
  • Demonstrate strong organizational, time management, and problem-solving skills.
  • Lead groups and work independently, without instruction.
  • Ability to function in a dynamic environment and balance multiple priorities simultaneously.
  • Ability to commute/relocate to our Acton, MA office (Preferred).
  • Note: This job description is not all-inclusive. Additional duties may be performed, as assigned. It acts as a guideline and is subject review between employee and manager throughout tenure.

Benefits:

  • Paid time off
  • Health insurance
  • Dental Insurance
  • Vision insurance
  • Parental leave

To apply for this position, send your resume at contact@bluejaydx.com

Job Title: Medical Director

Industry: Medical Device and In Vitro Diagnostics

Job Type: Full-time

Description: Bluejay Diagnostics is a rapidly growing medical device company focusing on rapid near-patient diagnostics. We strive to innovate in ways which completely change the medical decision-making process, ushering in a new era of healthcare. To help us with our mission, we are searching for a Medical Director. This person will work with a multidisciplinary team to strategically influence R&D, marketing, and regulatory activities.

Responsibilities:

  • Development of Market Requirement Documents.
  • Development of Essential Requirements.
  • Maintain medical licenses (board certifications) and keep current with medical practices.
  • Assist in clinical protocol development and regulatory filings.
  • Serve as medical contact for company.
  • Present and write reports.

Requirements:

  • MD or equivalent.
  • Minimum of 3 years of experience in the medical device industry, point-of-care devices and IVDs preferred.
  • Medical licensure in good standing.
  • Strong knowledge of regulations related to Medical Affairs.
  • Excellent written and verbal communication skills.
  • Experience running clinical trials with knowledge of GCP.
  • Ability to travel both domestically and internationally (~25%).
  • Board certification (preferred).
  • Understanding applicable regulatory requirements including FDA QSR and ISO 13485 (preferred).
  • Experience with product development lifecycle (preferred).
  • Ability to commute/relocate to our Acton, MA office (Preferred).
  • Note: This job description is not all-inclusive. Additional duties may be performed, as assigned. It acts as a guideline and is subject review between employee and manager throughout tenure.

Benefits:

  • Paid time off
  • Health insurance
  • Dental Insurance
  • Vision insurance
  • Parental leave

To apply for this position, send your resume at contact@bluejaydx.com

Job Title: Nanofabrication Engineer

Industry: Medical Device and In Vitro Diagnostics

Job Type: Full-time

Description:
Bluejay Diagnostics is a rapidly growing medical device company focusing on rapid near-patient diagnostics. We strive to innovate in ways which completely change the medical decision-making process, ushering in a new era of healthcare. To help us with our mission, we are searching for a Nanofabrication Engineer. This person will work with a multidisciplinary team to design, optimize, test, and scale manufacturing.

Responsibilities:

  • Support the research and development team.
  • Manufacture nanoparticles.
  • Functionalize and bioconjugate nanoparticles.
  • Quality control and quality assurance.

Requirements:

  • Bachelor’s degree or higher in engineering or related scientific disciplines.
  • Minimum of 2 years of experience in the fabrication of nanoparticles.
  • Strong experience working in a wetlab environment.
  • Experience with aqueous gold nanoparticle synthesis.
  • Experience with liposomal nanoparticle fabrication.
  • Experience in functionalization of nanoparticles.
  • Experience in bioconjugation.
  • Experience in nanoparticle stabilization.
  • Experience with TEM, DLS, Zeta, UV-Vis, and pH.
  • Experience in cGMP manufacturing (preferred)
  • Experience in clean room environments (preferred)
  • ISO 9001, ISO 13485, or ISO 17025 experience (preferred)
  • Demonstrate strong organizational, time management, and problem-solving skills.
  • Lead groups and work independently, without instruction.
  • Ability to function in a dynamic environment and balance multiple priorities simultaneously.
  • Ability to commute/relocate to our Acton, MA office (Preferred).
  • Note: This job description is not all-inclusive. Additional duties may be performed, as assigned. It acts as a guideline and is subject review between employee and manager throughout tenure.

Benefits:

  • Paid time off
  • Health insurance
  • Dental Insurance
  • Vision insurance
  • Parental leave

To apply for this position, send your resume at contact@bluejaydx.com

Job Title: Senior Process Engineer

Industry: Medical Device and In Vitro Diagnostics

Job Type: Full-time

Description:
Bluejay Diagnostics is a rapidly growing medical device company focusing on rapid near-patient diagnostics. We strive to innovate in ways which completely change the medical decision-making process, ushering in a new era of healthcare. To help us with our mission, we are searching for a Senior Process Engineer to work on our revolutionary Symphony product lines. This person will work with a multidisciplinary team to design, optimize, and scale manufacturing.

Responsibilities:

  • Support the manufacturing operations team.
  • Design and optimize new manufacturing production lines.
  • Drive continuous improvements and operational excellence through self-detecting processes and systems.
  • Executes process changes stemming from process changes/optimizations, CAPAs, and new capacity demands.

Requirements:

  • Bachelor’s degree or higher in engineering or related scientific disciplines.
  • Minimum of 3 years of experience as a process engineer
  • Experience in cGMP manufacturing
  • Experience in medical device manufacturing
  • Experience in clean room environments
  • Demonstrate strong organizational, time management, and problem-solving skills.
  • Lead groups and work independently, without instruction.
  • Understanding applicable regulatory requirements including FDA QSR and ISO 13485.
  • Ability to function in a dynamic environment and balance multiple priorities simultaneously.
  • PMP or similar certification (Preferred).
  • Ability to commute/relocate to our Acton, MA office (Preferred).
  • Travel, including international travel up to 20%
  • Note: This job description is not all-inclusive. Additional duties may be performed, as assigned. It acts as a guideline and is subject review between employee and manager throughout tenure.

Benefits:

  • Paid time off
  • Health insurance
  • Dental Insurance
  • Vision insurance
  • Parental leave

To apply for this position, send your resume at contact@bluejaydx.com