Development Associate

Canadian Blood Services; Dartmouth; On-site; CAD 60,000 - 80,000; Full time

Job summary

A health organization in Dartmouth, Nova Scotia, is seeking a Development Associate to manage process ownership and enhancements. You will be responsible for creating documentation, making process recommendations, and conducting investigations. The ideal candidate will have over 5 years of experience in a laboratory setting and possess strong technical writing and analytical skills. This full-time position offers competitive benefits, including vacation and a pension plan, while supporting health equity and diversity.

Benefits

4 weeks' vacation

Annual performance award up to 6%

Comprehensive health benefits

Defined benefit pension plan

Employee discounts and wellness program

Qualifications

• Minimum 5 years related experience in a medical or research laboratory.
• Demonstrated experience in technical writing and problem-solving.
• Excellent attention to detail and planning skills.

Responsibilities

• Lead and participate in the creation of study protocols and reports.
• Make recommendations for process improvements.
• Design and conduct research investigations according to protocols.
• Perform manufacturing and distribution functions as required.

Skills

Technical writing

Critical thinking

Organizational skills

Data analysis

Team collaboration

Education

Post-secondary education in Biological Sciences or equivalent

Job description

Canadian Blood Services is looking for a Regular full-time Development Associate 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.

• 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

• Completion of post‑secondary level education in Biological Sciences, Clinical Laboratory Science or a relevant discipline from a recognized academic institute, university degree preferred.
• Minimum 5 (five) 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 role will work onsite at 270 John Savage Ave, Dartmouth, Nova Scotia.
• Shift/hours – Monday to Friday, 37.5 hours a week, 7.5 hours a 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 [e-mail] and [e-mail] to your safe senders list.

Applicants who require accommodation should discuss their needs with us.