Pharmaceutical project manager Job in Blainville for Neopharm Labs |

Pharmaceutical project manager

April 21 2021
Industries Pharmaceutical, Biotechnology
Categories Health, Medical, Pharma, Biotech, Pharma, Biotech, Sciences, R&D, Pharmacy, Project management, Project Management, Business Analysis
Blainville, QC • Remote


Do you aspire to make significant contributions to the life sciences industry and the global community that improves the lives of patients? Do you want to join a company that is a trusted partner of the largest life science organizations? If you answered yes to either, we would like to hear from you! We have a job opening for a project manager.

The successful candidate will work under the direct supervision of the Director, R&D and Scientific Affairs and will be the KEY resource person for the movement of all projects flowing through the department. As such, the successful incumbent will be the resource person for the 3 team supervisors (development, validation and microbiology teams) who will plan the workload and assure timely deployment of projects according to priority. The candidate will also be responsible for monitoring and reporting on progress of projects with clients, up to the first analysis carried out in Quality Control.


Neopharm Labs has supported leading organizations in the pharmaceutical and life sciences industry for more than 30 years. Our success is the result of our integrity, quality, problem-solving ability and superior customer experience. We offer a full range of chemistry, microbiology and stability tests in the vision of Good Manufacturing Practices. We can process large volumes to meet all the testing needs of our customers. Driven by excellence and our desire to acquire new technologies, we are continually looking for sustainable ways to improve our services to our customers around the world.

Our corporate culture is rooted in positivity, innovation and collaboration. We are a growing company offering essential services to our long-standing clients. We have a customer-focused approach based on transparency, flexibility and reliability. We are proud to play a vital role in our clients' mission to improve the lives of the global community through new medical discoveries.


  • You have a strong sense of organizational skills and understand how to prioritize;
  • You are organized, versatile and a quick learner;
  • You have a strong sense of planning and priorities;
  • You know how to maximize productivity using Microsoft Office tools;
  • You have at least 2 years in a similar position in the life sciences industry;
  • You have experience in method development and/or validation (asset);
  • You have experience in a regulatory environment (GMP);
  • You possess a Bachelor's degree in a relevant field of science and ;
  • You have a certificate in administration or PMP designation (asset);
  • You are fully functional in both French and English;


  • An 18-month contract with potential of permanency;
  • Flexible schedule;
  • Possibility of remote work;
  • Great employee perks;
  • A diverse, warm and friendly work environment;
  • A rapidly changing environment that keeps you up to date with new industry development;
  • Opportunity for personal and professional development;
  • A safe workplace when on site, as we are rated an exemplary employer by the INSPQ in adhering to Covid's prevention guidelines.


  • Plan the work to be done and ensure that deadlines are met in collaboration with supervisors from the development, validation and microbiology teams;
  • Participate in the productivity assessment of the R&D department by maintaining the management tools of the R&D department up to date (KPI calculation);
  • Contribute to the improvement of processes to increase the productivity of the R&D department;
  • Follow up on projects with clients (respect of deadlines) in collaboration with supervisors (technical issues, if necessary);
  • Collaborate with the business development team to enable them to provide clients with bids for new research and development projects (development, research and development analysis, extractables and leachables, validation and transfer);
  • Promote a culture of customer focus to ensure the loyalty of our current customers and increase our credibility to all potential customers;
  • Promote Neopharm Labs' services to existing customers to help grow the business;
  • Take on other related tasks that may be assigned by the immediate supervisor.

Are you interested in this opportunity and want more information? Don't be embarrassed! Send us your CV and we'll get in touch with you.

Neopharm Labs needs people like you to shine!

Apply now!