1

Project Manager Biotech Jobs in Halifax, NS (NOW HIRING)

About Us 3DBioFibR Inc., founded in 2020, is a growing biotechnology company currently located in ... Design and execute laboratory experiments in accordance with approved protocols and project ...

Project Manager Biotech information

What does a project manager in biotech do?

A Project Manager in Biotech is responsible for planning, coordinating, and overseeing projects within biotechnology companies or research organizations. They work closely with scientists, regulatory teams, and other stakeholders to ensure that projects meet deadlines, stay within budget, and comply with industry regulations. Their tasks may include setting project timelines, managing resources, mitigating risks, and communicating progress to leadership. Project Managers play a crucial role in bringing new biotech products or research initiatives from conception to completion.

What are the key skills and qualifications needed to thrive as a project manager in biotech?

To thrive as a Project Manager in Biotech, you need a solid background in life sciences or engineering, experience in project management, and often a relevant degree such as a BSc or MSc, sometimes complemented by a PMP certification. Familiarity with project management software (such as MS Project or Jira), regulatory compliance systems, and budgeting tools is frequently required. Strong leadership, problem-solving, and effective communication skills set standout candidates apart by enabling them to coordinate cross-functional teams and manage complex timelines. These skills are essential to ensure that projects meet regulatory standards, stay on schedule, and achieve scientific and business goals.

How does a project manager in biotech typically collaborate with cross-functional teams to drive project success?

A Project Manager in the biotech sector routinely works with cross-functional teams that include scientists, regulatory experts, manufacturing staff, and quality assurance professionals. They coordinate meetings, align project timelines, and ensure clear communication of goals and milestones. Effective collaboration involves resolving conflicts, facilitating information flow among departments, and adapting plans as scientific or regulatory requirements evolve. This collaborative approach is essential for keeping projects on track, maintaining compliance, and achieving successful outcomes in a highly regulated and fast-paced industry.

What is the difference between Project Manager Biotech vs Clinical Project Manager?

AspectProject Manager BiotechClinical Project Manager
CredentialsBachelor's or Master's in Life Sciences, Project Management CertificationBachelor's or Master's in Life Sciences, Clinical Research Certification
Work EnvironmentBiotech companies, R&D labs, manufacturingClinical trial sites, hospitals, pharmaceutical companies
Industry UsageBiotech product development, research projectsClinical trial management, regulatory compliance
Common Search/ComparisonYesYes

The main difference between a Project Manager Biotech and a Clinical Project Manager lies in their focus areas. The Project Manager Biotech oversees research and development projects within biotech companies, focusing on product development and manufacturing. In contrast, the Clinical Project Manager specializes in managing clinical trials, ensuring regulatory compliance and patient safety. Both roles require strong project management skills and relevant certifications, but they operate in different phases of the biotech and pharmaceutical industry.

Infographic showing various Project Manager Biotech job openings in Halifax, NS as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution.

Research Assistant

Dartmouth, NS • On-site

Full-time

This job post has expired 1 day ago. Applications are no longer accepted.


Job description

Job Title: Research Assistant


3DBioFibR

60 Highfield Park Dr, Dartmouth, NS B3A 4R9


Website: https://www.3dbiofibr.com


About Us


3DBioFibR Inc., founded in 2020, is a growing biotechnology company currently located in the heart of Halifax, Nova Scotia. We produce high-performance biofibers that enable product developers to unlock new solutions.


Collagen fibers produced using our patented dry-spinning technology recapitulate the biomechanical and biochemical properties of natural collagen structures. With a fully automated manufacturing system, we are the first to produce collagen fibers at commercial scales for a variety of tissue engineering applications, including additives for 3D bioprinting and hydrogels, and cellular scaffolds for 2D and 3D cell and tissue culture.


Position Type

Full-time


Anticipated Start Date

October 2026


About the Role

Join 3DBioFibR as a Research Assistant, supporting the research, development, optimization, and validation of biomaterials and manufacturing processes. In this role, you will be working collaboratively with scientists, engineers, and cross-functional teams to execute laboratory experiments, analyze data, maintain accurate documentation, and contribute to the advancement of innovative products from research through manufacturing readiness. This position will report to the Research Lead, assisting other Leads as needed.


This is a full-time, on-site position located in Dartmouth, Nova Scotia.


Responsibilities


Research & Development


  • Design and execute laboratory experiments in accordance with approved protocols and project objectives.


  • Prepare, process, and characterize biomaterials and research samples.


  • Support the development, optimization, and scale-up of manufacturing processes as needed.


  • Perform physical and mechanical testing of materials.


  • Collect, analyze, interpret, and summarize experimental data.


  • Troubleshoot technical challenges and recommend process improvements.


  • Assist with technology transfer activities from research into design and development.


Laboratory Operations


  • Maintain a safe, clean, and organized laboratory environment.


  • Prepare laboratory reagents, buffers, and test solutions.


  • Operate, calibrate, and perform routine maintenance on laboratory equipment.


  • Monitor laboratory inventory and coordinate the procurement of consumables and supplies.


  • Ensure proper handling, storage, and disposal of chemicals and research materials.


Documentation & Quality


  • Maintain complete, accurate, and timely laboratory records in an electronic notebook (ELN).


  • Prepare technical reports, protocols, and experimental summaries.


  • Follow established Standard Operating Procedures (SOPs) and Work Instructions.


  • Assist in the creation and revision of laboratory documentation.


  • Support investigations, corrective actions, and continuous improvement initiatives.


  • Ensure compliance with the company's Quality Management System (QMS).


Qualifications and Skills


Required


  • 1–3 years of laboratory experience in an academic or industrial setting.


  • Experience executing laboratory experiments and documenting results.


Preferred


  • Bachelor's degree in science or engineering.


  • Experience with biomaterials, polymers, tissue engineering, biotechnology, textile engineering, or medical devices.


  • Experience working within a Quality Management System (ISO 9001 and/or ISO 13485).


Experience with one or more of the following is considered an asset:


  • Biomaterial processing and characterization


  • Polymer science


  • Mechanical testing


  • Microscopy and imaging techniques


  • Laboratory instrumentation and calibration


  • Statistical analysis and data interpretation


  • Microsoft Office Suite


  • Electronic Laboratory Notebooks (ELN)