Technical specialist

November 24 2021
Industries Pharmaceutical, Biotechnology
Categories Laboratory, Pharma, Biotech, Sciences, R&D, Quality assurance and control, Validation
Blainville, QC

You want to have a new challenge and at the same time receive a $1000 bonus at the signing of your employment contract? Then don’t hesitate.

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Do you aspire to make meaningful contributions to the Life Science industry and the global community that would improve patients’ lives? Are you interested in expressing your gift of scientific knowledge by joining a company that is a trusted partner of the world’s leading life science organizations? If you have answered yes to any of the above, then we would like to hear from you as we have an opening for a Technical Specialist, chemistry.

The successful candidate must demonstrate a strong ability to coach and mentor colleagues on issues of technical and operational requirements in an analytical lab environment, to ensure an efficient workflow in the QC lab and in documentation procedures. The technical specialist will assist the department supervisors and / or the management team to communicate new procedures / techniques to analysts, while ensuring adequate training is provided for the latter group on an ongoing basis.


Neopharm Labs has been supporting leading organizations in the pharmaceutical and life sciences industry for more than 30 years. Our success is a result of our integrity, quality, problem-solving capabilities and delivery of superior customer experiences. We offer the full range of GMP chemistry, microbiology, and stability testing and can handle large volumes to fulfill all of our clients’ testing needs. Driven by excellence, we enthusiastically acquire new technologies and are continuously looking for sustainable ways to improve our services provided to clients located all around the world.

Our corporate culture is rooted in positivity, innovation and collaboration, and we want your energy to propel us forward. We are a growing business providing must-have services to longstanding clients in partnership, with a strong client-centric approach built on no-nonsense transparency, flexibility and reliability. We are proud to play an integral role in our clients’ mission to better the lives of the global community through new medical discoveries.


  • You have deep knowledge of microbiology and solid analytical judgment.
  • Strong communication ability in both official languages; we work mostly in French, but documentation is in English;
  • You have a flexible schedule in case urgent work orders come up;
  • You have a detail-oriented and thorough approach to your work;
  • You can make important contributions to the advancement of our projects by proposing innovative solutions to solve complex situations (methods, projects, techniques);
  • You easily spot problems in the laboratory processes and provide viable solutions;
  • You have at least a DEC in technical sciences, combined with at least 7 years of relevant experience OR an Undergraduate Degree in Sciences (Health or Pure & Applied), with 3 years experience in a similar position.


  • A competitive base salary and a three-tiered benefit package to choose from;
  • Flexible working hours;
  • A safe workplace environment – We are deemed exemplary employer within our region, in the prevention of Covid infection.
  • A fast-paced environment that keeps you up to date with new industry developments.
  • Continuous opportunities for personal and professional development.
  • We have a longstanding policy of inclusion and diversity at all levels of the company.


  • Train and / or coach Laboratory Analysts:
    1. Orient new and or newly transferred employees to specific laboratory procedures.
    2. Ensure employee training success through close follow-up of objectives.
    3. Act as a coach and knowledge leader for lab analysts by demonstrating industry specific expertise and professionalism.
    4. Monitor the development of analysts as a group and assist supervisors in implementing corrective performance/productivity measures.
  • Production of quality control documents:
    1. Produce quality control reports within prescribed deadlines (for example deviations, investigations of non-standard results, change controls, protocols, analytical reports, methods and procedures);
    2. Update SOPS / procedures in place in accordance pharmacopeia updates.
    3. Implement corrective measures to procedures as required, to assure continuous compliance at all levels of laboratory analyses.
  • Ensure maintenance of pharmacopeia
    1. Apply up-to-date knowledge of pharmacopeia to the lab environment and transfer this knowledge to analysts as required.
    2. Ensure analysts apply new knowledge to their professional practices in the labs.
      1. Recommend and track the number of hours of professional development for lab analysts, and report these to HR as required.
      2. Continuously evaluate analytical techniques applied in the labs.
      3. Assist analysts with more complex analyses and special projects and troubleshoot problems encountered in the work process.
      4. Ensure continuous training is provided to technical staff for all analyses performed and for all related existing regulations.
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