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About Us

Come work with us

Interested in working at a globally-renowned lab with an industry-leading team of scientists? Check below for current openings. See something you like? We’d love to hear from you.

Diteba is an equal opportunity employer. We thank all applicants for their interest, however only those selected for an interview will be contacted.

Flex Time

We’re a hard-working team that believes in the empowerment of a balanced lifestyle.

Family Friendly

Family comes first, and sometimes family comes to work.


Enjoy full benefits including health and dental.

Geographically Accessible

Located near major highways and public transit, our location makes commuting a breeze.

Training Program

Fresh out of school? Don’t hesitate to apply (Masters and PhD).

Bonus System

We provide great financial incentives including our bonus system.

Job Openings


The Biochemist serves as the source of production doing chemical analysis in the GMO and genetics lab area. They are the primary generators of test results for our customers.

Key Responsibilities & Tasks

  • Perform laboratory analysis including DNA extractions and cloning, cell transformation, protein extractions, and analysis
  • Perform testing and document as per SOPs, GMP/GLPs and regulatory guidelines
  • Report deviation and OOS results and assist with quality investigations
  • Perform routine bench and instrument analysis
  • Support other laboratory tests as assigned

Job Requirments


  • M.Sc. or Ph.D. in Molecular Biology or Biochemistry
  • 2+ years of practical work experience in a laboratory environment
  • Experience in genetic expression and production modification as well as recombinant protein extraction and purification desired


  • Demonstrated understanding of molecular biology approaches including PCR, design of plasmids, primers and probes, DNA cloning, cell transformation as well as basic biochemistry and cell culture techniques
  • Background in health and safety regarding laboratory tests


  • Operate general analytical instruments such as PCR, UV Spec and Absorbance Plate Reader
  • Proficient in MS Office Suite

Chemist III – Method Development

The Method Development Chemist independently takes the lead on all method development and method validation in the chemistry lab.

Key Responsibilities & Tasks

  • Perform chemical analysis in pharmaceutical or biopharmaceutical tests
  • Take lead on method development and method validation
  • Independently perform and document test procedures in compliance with regulatory guidelines as well as SOPs
  • Report deviation and OOS results and conduct quality investigations
  • Conduct scientific summary report writing
  • Coach junior chemists in tests and method development
  • Other duties as assigned

Job Requirements


  • B.Sc., M.Sc., or Ph.D in chemistry or related science
  • 5+ years of practical work experience in pharmaceutical laboratories


  • Strong understanding of GMP/GLP requirements and compendial methods of testing
  • Background in health and safety in regards to laboratory tests


  • Demonstrated Understanding of chromatography (UPLC, HPLC, GC, TLC) and spectroscopic technologies (UV, IR) and Karl Fisher


  • Excellent interpersonal communication
  • Ability to work both in a team environment or independently
  • Problem-solving and logic skills for analytical analysis
  • Excellent written communication skills

LCMS Scientist

Under minimal supervision, the LCMS Scientist works independently performing both method development and validation as well as all routine laboratory analytical testing on pharmaceutical, bioanalytical and other projects.

Key Responsibilities & Tasks

  • Independently perform analytical or bioanalytical method development, method validation, and method transfer
  • Lead junior chemists to perform drug substance, drug product analysis, and method development
  • Provide support for protocol drafting, method writing and method development summary with good GMP practice
  • Perform analytical tests for pharmaceutical and biopharmaceutical materials including raw materials, drug substances, and drug products according to compendial and validated methods
  • Document and report test results as per established SOP’s
  • Provides technical support to other departments and junior chemists for issues related to the stability of drug substance, drug product, and method development as well as the formulation of responses to regulatory agencies requirements

Experience & Educational Requirements:

  • Required: M.Sc. in Chemistry, Life Sciences or Ph.D in organic chemistry
  • Extensive Chemistry or Analytical Chemistry background
  • 5+ years of experience in the pharmaceutical industry, preferably in CRO or bio CRO

Knowledge Requirements:

  • Complete understanding of common analytical technologies such as HPLC, GC, UV spectroscopy, titration, etc
  • Strong understanding of compendial methods including cGMP/GMP requirements, ICH and FDA guidelines as well as USP/EP
  • Proficiency with MS office applications
  • Practical understanding of pharmaceutical instrument validation procedures with knowledge.

Instrumentation Experience:

  • Operational experience on general laboratory instrument for analytical testing including HPLC, GC, UV spectrophotometer, titration, dissolution apparatus, TOC, and physical testing devices
  • Operational knowledge on Waters Millennium or Empower chromatographic software, or similar systems


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