Lab Project Manager

Pharma Medica Research Inc.; Mississauga; On-site; CAD 80,000 - 100,000; Full time

Benefits offered by this job

Competitive compensation plan

Fully paid benefit plan including healthcare

Opportunities for advancement

Job summary

A leading contract research organization in Mississauga is seeking a Lab Project Manager. The ideal candidate has a B.Sc. or relevant diploma and 5 years of supervisory and bioanalytical experience. Responsibilities include managing laboratory operations, ensuring compliance with GLP guidelines, and documenting study procedures. The role offers a comprehensive benefits package, opportunities for career advancement, and a supportive work environment.

Qualifications

• 5 years of Supervisory/Management experience in a laboratory.
• 5 years of Bioanalytical experience.
• Proficient in documentation practices and record keeping.

Responsibilities

• Complete SOP and GLP training tasks.
• Write and maintain updated Standard Operating Procedures (SOPs).
• Ensure laboratory personnel are trained on analytical methods.

Skills

Excellent knowledge of equipment

Strong verbal and written English communication skills

Ability to multitask the management of several ongoing projects

Strong proficiency in computer usage and software applications

Great interpersonal skills

Education

B.Sc. or Community College Diploma in Chemical Technology

Tools

Analytical instrumentation and equipment

Job description

Overview

Pharma Medica Research (PMRI) Inc. is a Contract Research Organization that strives for innovation and original solutions in a highly regulated and competitive industry. If your career goals align with innovation and original thinking you will be the perfect candidate to be part of an inclusive, adaptable, and forward-thinking organization. Our reputation for delivering high quality research is outstanding. At PMRI we are committed to making a difference in healthcare and people’s lives. Come join our team! We are currently looking for a Lab Project Manager to join our team.

Responsibilities

• Complete SOP and GLP training tasks as required, provide suggestions and recommendations as to how to improve the operation of the laboratory and the structure and content of the SOPs, and compliance with GLP requirements.


• Write and maintain updated Standard Operating Procedures (SOPs) as required.


• Prior to receiving study samples, the Lab Project Manager ensures that all laboratory personnel involved in the assigned project are trained on the analytical method.


• Ensure that all supplies for the study are available and ready before the first day of analysis. Prepare BVP / BSAP and setup project in LDMS prior to starting the project.


• Understand and ensure that the laboratory staff under his/her supervision operate according to regulatory agency guidelines, GLP procedures, Laboratory and PMRI SOPs, clinical study protocols, and BVP / BSAP.


• Responsible for tracking all assigned ongoing bioanalytical method development, method validation, non-clinical and clinical trial sample analysis.


• Collaborate with the Lab Operations Manager/Lab Production Manager to allocate proper resources for the completion of all assigned projects, as well as assuring that these time frames are met.


• Responsible for verifying all raw data generated from bioanalytical validations and studies. Communicate deviations to the Principal Bioanalytical Investigator/designate in a timely manner.


• Responsible for all project-specific documentation and sample/data integrity assessments. Address all audit findings for completed validations and studies to ensure the study completion timelines are met.


• Ensure that Laboratory Management is kept up to date regarding project status, analytical or instrumentation issues and provide staff performance feedback.


• Participate in analytical troubleshooting, as required.


• Other duties as required.

Qualifications

• B.Sc. or a Community College Diploma in Chemical Technology or a suitable related scientific area.


• 5 years of Supervisory/Mana


• 5 years of Bioanalytical experience.


• Excellent knowledge of equipment, instrumentation, analytical troubleshooting, GLP and regulatory guidelines.


• Strong verbal and written English communication skills.


• Great interpersonal skills.


• Ability to respectfully lead a team.


• Proficient in documentation practices and record keeping.


• Ability to multitask the management of several ongoing projects.


• Strong proficiency in computer usage and software applications.

We offer

• Competitive compensation plan


• A benefit plan that is fully paid for by PMRI, including healthcare, dentalcare, vision care, LTD, Life Insurance, AD&D, along with a Health Spending and Wellness Spending Accounts and a voluntary RRSP Contribution Plan


• Opportunities for advancement and career progression


• A generous Employee Milestones Awards Program


• Corporate Discounts Program


• Learning Support Programs


• Friendly atmosphere, culture of learning

Please note all applications must be eligible to work within Canada.

PMRI is an Equal Opportunity Employer; promoting accessibility and inclusivity at work and offering accommodation for applicants as required and requested.

We thank all applicants for their interest; however, only those selected to proceed in the interview process will be contacted.