Development Associate, Process Development Laboratory

Job category: Continuous improvement and project management

Job posting ID: 6791

Employment status: Regular full-time

Position's anticipated start date: 2025-02-17

Classification: PTS/MGT/IT B

Salary/Rate of pay: $78,895 - $92,638

Application deadline: 2025-01-17

Application requirements:

• Your up-to-date resume.
• We recommend you save a copy of the job posting for reference throughout the recruitment process.
  
  
  

Do you currently work for Canadian Blood Services? All employees must apply via the internal career page .

Together, we can make all the difference in the lives of others.

Be part of a dynamic, collaborative and caring organization committed to saving and improving lives. Thousands of patients depend on us every day for reliable access to safe blood, plasma, stem cells and organs and tissues.

If you are looking for a rewarding experience with a values and mission-driven team, join Canada’s Lifeline and make a meaningful difference.

We acknowledge that the work of Canadian Blood Services spans many Territories and Treaty areas across the country, and we are grateful for the Traditional Knowledge Keepers and Elders who have guided us in this important work. We recognize the land and waters that have inspired our work and offer gratitude to those Indigenous peoples on whose territory we work, live and play.

About The Role

Canadian Blood Services is looking for a regular full-time Development Associate, Process Development Laboratory to join our dynamic Process Management team in Dartmouth, Nova Scotia.

The Process Management team manages process ownership and enhancements for operations functions.

The Development Associate is responsible for routine operation of the development and testing areas. Responsibilities include participating in the planning and effective operation of the respective functions, generating and analysing testing data, including the creation of documents such as study protocols and final reports. The Development Associate makes recommendations to management on how processes can be implemented with optimal efficiency and manages confidential information linked to Requests for Purchase (RFPs) and Intellectual Property (IP) belonging to partnering vendors.

Formula for success

• Drawing on your expertise in documentation, you will lead and participate in the creation of documents, including study protocols and reports.
• Utilizing your knowledge of process improvement, you will make recommendations to management on the development and implementation of new procedures, equipment, and/or policies with a focus on product quality and optimal efficiency and productivity.
• Collaborating with process owners, you will liaise to identify and recommend process development requirements for projects and improvement initiatives.
• Applying your skills in research design, you will design, plan, and conduct investigations in accordance with established procedures or approved study protocols.
• Leveraging your understanding of manufacturing operations, you will perform manufacturing and distribution functions in accordance with established procedures, study protocols, or for the development of new procedures and products.
• Committing to safety and compliance, you will perform work in accordance with the provisions of the Canadian Blood Services Corporate Health and Safety Policy and Procedures.
  
  
  

Desired Education And Skills

• Post-secondary level education in Biological Sciences, Clinical Laboratory Science or a relevant discipline from a recognized academic institute, university degree preferred.
• Minimum 5 years related experience working in a medical or research laboratory.
• Demonstrated experience with technical writing, critical thinking, and working closely with management to solve operational problems.
• Excellent skills in planning, organization and attention to detail.
• Excellent skills in understanding and analyzing data, including generating valid conclusions.
• Ability to work independently and with a team.
  
  
  

What We Offer You

• 4 weeks' vacation.
• Annual performance award up to 6%.
• Comprehensive group health, dental and vision benefits for you and your family.
• Defined benefit pension plan.
• Employee discounts, wellness program, professional resources.
  
  
  

What You Can Expect

• This is an onsite role with requirements to be onsite Monday to Friday, 37.5 hours per week, 7.5 hours per day.
• Travel may be required for team events and meetings within Canada.
  
  
  

Diversity and inclusion play a vital role in ensuring health equity for patients across Canada. We are committed to reflecting Canada’s population in our organization and fostering an environment where all employees can be their authentic selves, with equal opportunities to succeed and contribute.

If this role resonates with you, we encourage you to apply by providing your up-to-date resume. This could be your first step towards a meaningful and inspiring career. Come to work each day knowing that you save lives.

We thank all applicants for their interest. However, only those considered for an interview or those invited to participate in an assessment will be contacted. Emails are sent directly from our system, to ensure you receive them please add [email protected] and [email protected] to your safe senders list.

Applicants who require accommodation should discuss their needs with us.