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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.

Benefits

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

Manager – Human Resources

The candidate will support the company’s employees and managers both individually and collectively in such a manner that they are able to personally grow and optimize their contribution to the process of achieving the business objectives set by the organization. The candidate will ensure the safety of every employee’s work experience (physical, environmental and emotional), and report directly to the CEO.

Responsibilities:

  • Recruitment: position description, classification, internal & external postings, interview process and final selection, employment offers, and final contract
  • Training: new employee orientation, safety, wellness & health, skills
  • Communication: history, events, training & internal job opportunities, company news
  • Performance Management: training, facilitation, evaluations, regular reviews
  • Team Building: training, facilitation
  • Career & Competency Management: regular individual reviews and personal development plans
  • Compensation review: industry surveys, position and classification review and updates
  • Payroll Administration including time-keeping (vacation, stat holidays, sickness, personal days, etc.)
  • Company & Personnel Policy: compliance, workplace ethics and values, review and communication
  • Manpower planning: industry trends, company direction
  • Culture and employee attitude surveys
  • Benefits administration, including review, alignment, contract negotiation
  • Social activities
  • Company filings: WSIB, EHT, CRA Submissions

Training

  • Safety Awareness Training as per MOL requirements, Regulator requirements
  • Rights and Responsibilities regarding the Occupational Health and Safety Act and Regulations
  • WHMIS
  • Violence & Harassment in the Workplace
  • AODA

Education & Certification

  • Post-secondary education in Human Resources, Business Administration or a related discipline
  • Appropriate profession related credits and certifications

Knowledge and Relevant Experience

  • Minimum 10 years of progressive HR experience, primarily in a Generalist role
  • Knowledge of employment legislation and payroll management practices
  • Proficiency in MS Office

Skills & Qualifications

  • Excellent facilitation skills
  • Strong people management and leadership skills
  • Excellent organizational skills
  • Excellent judgment, analytical and problem-solving skills in establishing strategies and resolving HR matters
  • Skilled in workplace conflict and resolution strategies
  • Self-motivated, flexible and adaptable
  • Excellent communication skills (written & verbal) coupled with strong interpersonal skills
  • Demonstrated ability to maintain confidentiality and to deal with issues in a sensitive, efficient and business-like manner

Please Send Your Resumé By Email

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Research Analyst

Diteba is a global leader in complex analytical and bioanalytical testing, providing solutions and services to the pharmaceutical, biopharmaceutical and nutraceutical industries. We are currently seeking a Research Analyst to join our team in support of our growing testing capabilities.

Responsibilities:

  • Perform laboratory analysis including DNA extractions and cloning, cell transformation, protein extractions and analysis
  • Operate general analytical instruments such as PCR, UV Spec, and Absorbance Plate Reader
  • Perform testing and document as per SOPs, GMPs/GLPs and regulatory guidelines
  • Report deviation and OOS results and assist in the quality investigations.
  • Follow the Health and Safety Guidelines in all laboratory tests.
  • Support other laboratory test activities as required
  • Must be able to work after hours and weekends to support laboratory activities
  • Works and coordinates well in a team setting
  • Work well under pressure to meet deadlines
  • Other duties as assigned

Qualifications

  • M.Sc. with experience in Molecular Biology or Biochemistry, with at least 2 years’ laboratory working experience
  • The candidate must demonstrate a good understanding of molecular biology approaches including but not limited to knowledge of PCR, designing of plasmids, primers, and probes, DNA cloning, cell transformation as well as basic biochemistry and cell culture techniques
  • Ability to perform routine bench and instrumental analysis
  • Works well independently and in the team
  • Demonstrates good organizational skills to complete daily tasks
  • Ability to learn and perform the new technologies (or instruments and analytical tests), as needed
  • Candidates must have good problem-solving skills and logic for analytical testing
  • Proficient in using various computer software (MS Office Suite,
  • Excellent command of the English language, both written and oral.
  • Excellent interpersonal and oral communication skills to be able to communicate with the other implementation teams.

Please Send Your Resumé By Email

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Scientific Writer & Reviewer

Scientific Writer and Reviewer is responsible for ensuring that all documentation related to the successful release of laboratory work is complete and conforms to all Diteba Standard Operating Procedures (SOPs) and current Good Manufacturing Practices (cGMPs). He /She is responsible for writing and reviewing various technical reports and raw data generated by internal departments with minimum supervision.

Responsibilities

  • Review and prepare protocols, reports, SOPs, change controls, OOS/UR/OOT investigations and deviation investigation reports with minimum supervision. Consult regarding changes to existing production processes and the impact to product quality and stability.
  • Provide technical support to reviewers and participate in departmental meetings and also work as designate in the absence of the QC-Review Manager.
  • Review raw data generated by analytical development laboratory and analytical reports and C of A’s. Ensure test methods, protocols and applicable SOPs have been followed during the testing. Follow up to ensure that all necessary corrections are executed in accordance with cGMP standard.
  • Verify the integrity and traceability of all data generated and reported. Notify direct manager regarding omissions, incomplete testing results or other irregularities.
  • To comply with all Employee Health and Safety requirements and participate in EH&S training programs.
  • Other tasks as assigned

Qualifications

  • Minimum B.Sc. in Chemistry, Biology, Life Sciences or other related field and/or equivalent experience. 3+ years of pharmaceutical industry experience, preferably in an analytical development or QA function.
  • Basic understanding of common analytical technologies (e.g. HPLC, GC, UV spectroscopy, titration) Basic understanding of cGMP, ICH and FDA requirements.
  • Excellent computer proficiency with MS office programs. Ability to meet deadlines and prioritize. Excellent written and oral communication skills. Proficiency with the English language required.

Please Send Your Resumé By Email

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Analytical Chemists (Level II to IV)

Responsibilities:

  • Perform all laboratory analysis for raw materials, in-process and finished products by using general analytical instruments such as HPLC, GC, UV, IR, TLC and Karl Fisher.
  • Support other laboratory test activities as assigned.
  • Develop, transfer and validate analytical methods.
  • Perform and document all test procedures in compliance and follow regulatory guidelines as well as SOPs.
  • Report deviation and OOS results and assist quality investigations.
  • Comply with GMP/GLP requirements as well as health and safety guidance in all laboratory tests.
  • Be able to troubleshoot for analytical methods and also instrument performance.
  • With excellent interpersonal communication skills and ability to work in a team environment.

Qualifications:

  • B.Sc., M. Sc, or Ph.D in chemistry or related science, with at least 2 years’ working experience in pharmaceutical laboratories.
  • The candidates must demonstrate a good understanding of basic chemistry, such as chromatography (eg HPLC, GC, TLC) and spectroscopic technologies (eg UV, IR).
  • Candidates must have good problem solving skills and logics for analytical analysis.
  • Excellent written and oral communication skills
  • Works well independently and in team environment

Please Send Your Resumé By Email

Apply Now