Jobs in Canada

25+ jobs

Group jobs by employerEmail me new jobs Save this search

Added 1 min ago
PQ
Director, Technical Product Management
Prime Quadrant
Toronto, ON
- $150,000 to $180,000 CAD / year
- Full-time
…Learning & Enablement, while working closely with Engineering, IT Operations, project delivery, and senior leadership. You should be equally comfortable discussing a user journey with a…
Added 1 min ago
RN
Nike - Lead - Marketmall
Retailors NA Limited Partnership
Calgary, AB
- Full-time
…its business portfolio in Canada, and the role of the Store Director is pivotal in leading the future of Nike Retail Stores within the…
Added 1 min ago
CO
Drop-In Winter Relief Cleaner
Christie Ossington Neighbourhood Centre
Toronto, ON
- Full-time
- Other duties as assigned by the Manager of Shelter Operations or Director of Hostels & Housing
Added 1 min ago
PW
B2B Business Development Specialist
Permanent Windows Solutions Inc.
AB · Edmonton, AB
- Full-time
Work closely with installation and operations teams to ensure smooth project execution.
Added 1 min ago
O
Business Process Director
OpenText
Mississauga, ON
- Full-time
…processes work across Product, Sales, Professional Services, Cloud Operations, Customer Success, Finance and IT. We are seeking a Director, Enterprise Process Design to identify where…
Added 1 min ago
N
Personal Lines Team Lead
Navacord
Elmira, ON
- $75,000 to $80,000 CAD / year
- Full-time
Complete one-on-one meetings with team as per schedule outlined by Director of General Insurance Operations.
Added 1 min ago
MS
Director of Transportation Sales
MacDonald Search Group
Toronto, ON · Greater Toronto Area, Canada
- $150,000 to $180,000 CAD / year
- Full-time
…Canadian transportation and logistics organization, is seeking a Director, National Transportation Sales to spearhead new business development and drive revenue growth across…
Added 1 min ago
S
IT Operations Lead
SJC
Toronto, ON
- $80,000 to $95,000 CAD / year
- Full-time
Our IT team is seeking an IT Operations Lead to manage the people and systems that keep our infrastructure, network, and endpoints secure, reliable, and well maintained. This is a…
Added 1 min ago
EM
Directeur(trice), opérations commerciales corporatives
Emballages Mitchel-Lincoln Packaging
Montreal, QC
- Full-time
Le/La Directeur(trice), opérations commerciales corporatives est responsable de définir, standardiser et améliorer en continu le système d’exploitation commercial de l’organisation. Il…
Added 16 mins ago
R
Nike - Sales Coach/Coach de vente - Laval
Retailors
Laval, QC
- Full-time
…its business portfolio in Canada, and the role of the Store Director is pivotal in leading the future of Nike Retail Stores within the…
Added 16 mins ago
OT
Manager, Member Journey Orchestration & Relations Strategy
Ontario Teachers' Pension Plan
Toronto, ON
- Full-time
…& Relations, Complex Care, Product, Technology and service operations teams to translate experience intent into effective day-to-day service delivery. The Manager also works with…
Added 16 mins ago
M
Relationship Manager
Moneris
Toronto, ON
- Full-time
Reporting Relationship: You will report to the Director, Product Partnerships.
Added 16 mins ago
SR
Directeur de Surccursale
Sunbelt Rentals, Inc.
Levis, QC
- Full-time
Must have a valid driver’s license and acceptable driving record history
Added 16 mins ago
M
Environmental Services Manager , Senior Living (Contract)
Maquise
Windsor, ON
- Full-time
Provide hands-on oversight of facility maintenance operations, including monitoring building systems such as HVAC, plumbing, electrical, life safety, and preventative maintenance programs.
Added 16 mins ago
D
Director
Desjardins
Montreal, QC · Levis, QC · Complexe Desjardins Montréal
- Full-time
Your role involves using your in-depth knowledge of the sector to manage all large-scale sales and operations activities or a major support sub-function offering specialized services to all…
Added 31 mins ago
RG
Cook - Long Term Care Home
River Glen Haven Nursing Home
Sutton, ON
- Part-time
Must have current Food Handler Certification Course (Safe Food Handling Certificate)
Added 32 mins ago
SC
Site Security Lead (Former Police Experience Required)
Securitas Canada
Toronto, ON
- Full-time
Must have attended and completed Police College if you are a former or current officer · Candidates must have a minimum of 5 years' experience as a Municipal, Provincial or RCMP police officer
Added 32 mins ago
Manager, Project Management
Metso
Sudbury, ON · Burlington, ON · Montreal, QC
You will report to the Director, Services Execution.
Added 1 hour ago
OA
Product Launch Specialist, HealthTech Saas
OceanMD, a WELLSTAR Company
Toronto, ON
- Full-time
This is a full-time, hybrid role requiring two to three days per week in our Toronto office
Added 1 hour ago
CW
Workplace Consultant
CTI Working Environments Inc.
Mississauga, ON
- Full-time
Reporting to the Director of Furniture Solutions, we are hiring a Workplace Consultant. You will lead consultative sales engagements for commercial furniture and workplace projects,…
Added 1 hour ago
LH
Receptionist - Physiotherapy Clinic
Lifemark Health Group
Vancouver, BC
- $19 to $21 CAD / hour
- Full-time
Provide administrative support to the Care Coordinator Manager and Clinic Director
Added 1 hour ago
YU
Student Conduct and Resolution Specialist - New Brunswick
Yorkville University
Fredericton, NB
- Full-time
This is a full-time hybrid role based at our New Brunswick campus, requiring three days per week on campus and two days working remotely · Beginning in early 2027, the position will transition to four days per week on campus and one day remote
Added 1 hour ago
CD
Nurse Practitioner & Clinic Lead
CMHA Durham
Oshawa, ON
- Full-time
…running of the clinic holding accountability to the Senior Director Clinical Operations, the Board of Directors and Ontario…
Added 1 hour ago
UO
Director, International Student and Visitor Services
University of Alberta
Edmonton, AB
- Full-time
International Education and Enrolment (IEE) is hiring a Director, International Students and Visitor Services (ISVS) to lead a team with passion and vision in the pursuit of service…
Added 1 hour ago
NG
Account Manager, Saskatchewan
Normet Group
Saskatoon, SK
- Full-time
Participating in Normet strategy workshops, and day-to-day business operations as specified by North American Sales Director

Lilly

Advisor, Analytical Chemistry

Toronto, ON, M5X 1B1, Canada

Full-time

Apply on careers.lilly.com About employer

Applications open in a new tab.

Job details

Job type: Full-time
Posting language: English
Posted: Nov 6, 2026

Original job description

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work - but it’s work worth doing. If you’re driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.

Organization Overview:

At Lilly, we serve an extraordinary purpose - we make a difference for people around the globe by discovering, developing, and delivering medicines that help them live longer, healthier, more active lives. The Radiopharmaceuticals (RLT) Chemistry, Manufacturing & Controls (CM&C) group is at the forefront of advancing therapeutic radiopharmaceuticals from clinical development through commercial launch.

Position Overview:

The Advisor, Analytical Chemist is a critical technical role within the RLT CM&C Technical Operations function. Reporting to the Senior Director, Technical Operations, this position leads the technical transfer, development, optimization, and validation of analytical methods to support phase 1b to phase 3 radiopharmaceutical programs. The Advisor serves as the primary analytical chemistry subject matter expert (SME), driving scientifically sound, phase-appropriate method strategies that meet GMP, ICH, USP, and regulatory expectations.

This role operates at the intersection of analytical science, regulatory compliance, and cross-functional program delivery - collaborating closely with QC, CMC Regulatory, manufacturing, and external CDMO partners to ensure analytical readiness for late-phase development milestones and regulatory submissions.

Key Responsibilities:

Analytical Method Development & Optimization

Lead the design, development, and optimization of analytical methods for radiopharmaceutical API and drug products, including small molecules, peptides, and radiolabeled compounds.
Develop and optimize chromatographic methods (HPLC, UPLC, TLC, GC) and spectroscopic methods (gamma spectroscopy, mass spectrometry, UV/Vis, NMR) as appropriate for late-phase programs.
Apply phase-appropriate development strategies aligned with ICH Q14, ICH Q2(R2), and applicable USP/EP compendial requirements for late clinical phase through commercial programs.
Identify and implement analytical technology improvements and method modernization initiatives to support continuous improvement and commercial readiness.
Troubleshoot complex analytical method performance issues and implement robust, validated solutions.

Analytical Method Validation & Transfer

Author method validation protocols and reports in full compliance with ICH Q2(R2), USP <1225>, and applicable regulatory guidance for late-phase and commercial programs.
Lead analytical method qualification and validation activities at internal sites and external CDMOs/partners.
Perform or oversee technology transfer of validated methods to QC release and stability testing laboratories.
Prepare and review method transfer protocols, comparability studies, and qualification/validation reports.
Ensure validation data packages are complete, defensible, and ready for regulatory submission.

Regulatory & Documentation

Author analytical sections of CMC regulatory submissions (INDs, CTAs, NDA/BLA, MAA), including method descriptions, validation summaries, and specification justifications.
Develop and justify release and stability specifications for starting materials, intermediates, and drug products in collaboration with CMC Regulatory and QA.
Prepare responses to regulatory agency inquiries related to analytical methods and specifications.
Author and review standard test methods, SOPs, change controls, and technical reports in accordance with GMP and Good Documentation Practices.
Support internal and external GMP audits, providing technical analytical expertise as required.

GMP Quality & Compliance

Ensure all analytical activities are conducted in compliance with cGMP, cGLP, applicable FDA, EMA, Health Canada, ICH, USP, PDA, and Lilly quality standards.
Review and approve experimental data from internal labs and external CDMOs/vendors; interpret results and document conclusions accurately.
Lead or support investigations of out-of-specification (OOS) results, analytical deviations, and aberrant data using robust root cause analysis methodology.

Cross-Functional Collaboration & External Partnerships

Serve as the analytical chemistry SME for late-phase RLT programs, providing technical direction to cross-functional CMC teams.
Build and maintain productive working relationships with internal, external CDMOs, analytical service providers, and regulatory partners.
Collaborate with QC, CMC Regulatory, Manufacturing Sciences, and Supply Chain to ensure seamless analytical readiness for clinical and commercial supply.
Represent analytical capabilities in project team meetings, technical reviews, and governance forums.

Basic Requirements:

Earned Bachelor's degree in chemistry, analytical chemistry, or organic chemistry
10+ years of relevant experience in analytical development, analytical validation, and/or analytical testing in a GMP setting.
Demonstrated expertise in the development and full ICH Q2(R2)-compliant validation of chromatographic (HPLC, UPLC, GC, TLC) and spectroscopic (MS, UV/Vis, gamma) analytical methods.
Functional knowledge of GMP regulations and applicable FDA, EMA, ICH, USP, and PDA guidelines relevant to analytical testing.
Proven ability to operate effectively in a cross-functional environment with strong project management and organizational skills.
Proficiency in analytical data systems and laboratory informatics (e.g., Empower, Chromeleon, MassLynx).
Strong oral and written communication skills, with demonstrated ability to present technical data to diverse audiences including senior leadership and regulatory agencies.
Must be a Canadian citizen to be selected for this position.

Additional Preferences:

Master's degree in chemistry field with 5+ years of relevant experience, OR PhD in chemistry field with 2+ years of relevant experience
Experience working hands-on within the biotech or pharmaceutical industry
Experience with radiopharmaceutical analytical testing, including HPLC with radiometric detection, TLC (radiometric), and gamma spectroscopy for PET (F-18) and/or theranostic radioisotopes (Lu-177, Ac-225).
Hands-on experience authoring CMC regulatory submissions and method validation packages for late-phase (Phase 3) or commercial programs.
Experience with CDMO/external partner analytical qualification and method transfer in a GMP context.
Familiarity with regulatory expectations for late-phase radiopharmaceutical analytical control strategies (ICH Q14, Q8/Q9/Q10 pharmaceutical quality system principles).

Other Information:

Standard PPE and radiological safety protocols apply in RLT manufacturing and laboratory areas.
Estimated travel: 5-15% domestically and internationally (CDMOs, partner sites, conferences). A valid passport and eligibility to travel within North America and Europe are required.
Monday through Friday, standard business hours; periodic off-hours responsiveness may be required in support of GMP manufacturing or regulatory timelines.

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.

Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is

$ - $

Full-time equivalent employees may also be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a pension plan; vacation benefits; eligibility for healthcare benefits; flexible benefits (if applicable) life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities). Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.

#WeAreLilly

Apply on careers.lilly.com About employer

More about this job

Responsibilities

The Advisor leads the technical transfer, development, and validation of analytical methods for radiopharmaceutical programs to ensure regulatory compliance and commercial readiness. They serve as the primary subject matter expert, collaborating with cross-functional teams and external partners to support late-phase development milestones.

Requirements

Candidates must hold a Bachelor's degree in chemistry or a related field and possess over 10 years of relevant experience in a GMP setting. Expertise in ICH Q2(R2)-compliant analytical method validation and proficiency in chromatographic and spectroscopic techniques are essential.

Skills

Analytical chemistry
Method development
Method validation
GMP compliance
Radiopharmaceuticals
Chromatography
Spectroscopy
Regulatory submissions
Technical transfer
Quality control
Root cause analysis
Project management
Laboratory informatics
CMC regulatory
Data analysis

Benefits

Pension plan
Vacation benefits
Healthcare benefits
Flexible benefits
Life insurance
Death benefits
Employee assistance program
Fitness benefits
Employee clubs and activities

Visa sponsorship

Not detected in the job text

Keywords

Analytical Chemistry
Radiopharmaceuticals
GMP
ICH Q2(R2)
HPLC
UPLC
Mass Spectrometry
Gamma Spectroscopy
CMC
Regulatory Affairs
CDMO
Method Validation
Technical Operations
Quality Assurance
Empower
Chromeleon
MassLynx
Theranostics
PET
Small Molecules
Peptides
ICH Q14
USP
FDA
EMA
Analytical Development
Stability Testing
Root Cause Analysis
Laboratory Informatics
Compliance

Report this job

Work requirements

Jobs in Canada