Careers

Maxim Biomedical is a cGMP FDA Approved facility located in Rockville MD. Maxim manufactures a variety of HIV diagnostic products. Currently we are in development of products of other disease states. Maxim is a team oriented company. You will have the opportunity to learn and gain exposure to working across different functional areas.

Manufacturing Level 1 Technician

  • Specialty: Medical Device Manufacturing
  • Employee Type: Full Time
  • Work Location: Rockville
  • Education: B.S.


  • Operate automated EIA plate coating and heat sealing equipment
  • Print labels and label components by hand and by using an automated label machine
  • Assemble and inspect kits as schedule following SOPs
  • Clean, calibrate, and maintain laboratory equipment
  • Clean glassware, autoclave equipment and waste as necessary
  • Properly package and dispose of hazardous waste
  • Clean, calibrate, and maintain laboratory equipmentent
  • Maintain accurate production documents, lab records, and log books
  • Follow Good Manufacturing (GMP), Quality System Regulation (QSR), and safety regulations
  • Assist Product Technology with validations
  • Write and revise written procedures (Standard Operating Procedures (SOP), Manufacturing Procedures (MP)) as necessary
  • Support kit assembly and packaging operations, as well as Gel production, when required
  • Other duties as assigned

  • BS/BA degree in the biosciences or related experience
  • Ability to operate basic laboratory equipment
  • Knowledge of basic laboratory techniques
  • Knowledge of sterile filtration and aseptic technique
  • Ability to work both independently and as part of a team
  • Ability to organize and prioritize workload to meet production schedule
  • Good oral, written, and laboratory math skills
  • Working knowledge of QSRs and GMPs

Quality Control (QC) Level 1 Technician

  • Specialty: Quality Control
  • Employee Type: Full Time
  • Work Location: Rockville
  • Education: B.S.


  • Follow Good Manufacturing Practice (GMP)/Good Laboratory Practice (GLP), Quality Systems Regulation (QSR), Environmental Protection Agency (EPA) and safety regulations in an FDA licensed facility
  • Maintain accurate laboratory logbooks and testing documentation, per established procedures
  • Assist in keeping procedures current to QSR guidelines as established by the FDA.
  • Evaluate materials by way of Western Blot, Microbial/Sterility, Infectivity and general chemical analysis testing methods.
  • Evaluate environmental conditions (Surface and Air) per USP and FDA guidelines.
  • Assist in the generation and revision of Standard Operating Procedures (SOP).
  • Assist in the generation and implementation of validation protocols.
  • Conduct stability testing per established protocols, as well as assist in the generation of stability protocols.
  • Conduct complaint investigation testing when requested by Supervisor.
  • Work closely with all areas to ensure quality processes are maintained and supported.
  • Perform incoming inspection and test and subsequent approval of received materials
  • Review batch history records for accuracy and completeness.
  • Assist in QC analyst training and other additional duties as assigned.

  • B.S. in Biological studies or equivalent education or experience.
  • Good clerical, math and computer skills. Knowledge of MS Excel and MSW.
  • Good reading, writing, and speaking skills.
  • Manual dexterity.
  • Knowledge of GMP and GLP.
  • Ability to work independently and as part of a team.
  • Ability to follow written protocols.

R&D Assistant

  • Specialty: R&D
  • Employee Type: Full Time
  • Work Location: Rockville
  • Education: M.S. or higher


  • Maintain accurate laboratory logbooks and testing documentation.
  • Perform routine jobs of bacterial culture, SDS-PAGE, Immunohistochemical Staining (IHS), ELISA, Lateral Flow and/or Molecular Diagnostic assays
  • Assist in inventory control and other additional duties as assigned.

  • 2 or more years of commercial experience
  • Good reading and communicating skills.
  • Good laboratory skills.
  • Cell culture experience preferred.
  • Ability to work independently and as part of a team.

Packaging Assistant

  • Specialty: Kit Assembly/Manufacturing
  • Employee Type: Full Time
  • Work Location: Rockville
  • Education: High School or Higher


  • Maintain accurate documentation and complete batch records.
  • Assist in labeling of manufactured components.
  • Assist in final kit assembly of labeled components.
  • Other duties as assigned.

  • Manual dexterity.
  • Must be able to lift 30-50lbs.
  • Ability to work independently and as part of a team.

Apply now

Please download and send in employment applications with your resume and cover letter to careers@mbidiagnostic.com