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Analytical Development Jobs in Quebec (NOW HIRING)

TAME Search Inc.

The ideal business analyst will drive communication between their clients and development teams, going above and beyond to ensure that functional requirements are clearly understood by both ...

Cannara Biotech (Québec) inc

Reporting to the Quality and Research and Development Department, the incumbent will be responsible for conducting chemical analyses on cannabis-based raw materials, extracts, concentrates and ...

Cannara Biotech inc

Reporting to the Quality and Research and Development Department, the incumbent will be responsible for conducting chemical analyses on cannabis-based raw materials, extracts, concentrates and ...

Cannara Biotech (Québec) inc

Reporting to the Quality and Research and Development Department, the incumbent will be responsible for conducting chemical analyses on cannabis-based raw materials, extracts, concentrates and ...

Galderma

Technical Product Lead

Baie-d'urfe, QC · On-site

Strong experience in CMC / product development / manufacturing / analytical development * Proven ability to lead cross-functional, matrix teams * Deep knowledge of QbD, lifecycle management, and ...

Belron Canada

Senior Data Development Lead

Montreal, QC · Hybrid

Strong analytical and technical investigation skills, with a high level of rigor and a strong commitment to solution quality and reliability. * Demonstrated ability to mobilize and align development ...

Urbandale Corporation

CA$50K - CA$70K/yr

Job Summary The Land Development Coordinator plays a key role in supporting the planning ... analysis to guide product design, pricing, and positioning. · Validate site plans, building ...

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Analytical Development information

See Quebec salary details

$30K

$98.4K

$189.5K

How much do analytical development jobs pay per year?

As of Jun 10, 2026, the average yearly pay for analytical development in Quebec is $98,374.00, according to ZipRecruiter salary data. Most workers in this role earn between $64,000.00 and $125,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in Analytical Development, and why are they important?

To thrive in Analytical Development, you need a solid background in chemistry, biochemistry, or a related field, often supported by a relevant degree and experience in analytical methodologies. Familiarity with laboratory instruments such as HPLC, GC, and mass spectrometry, as well as knowledge of regulatory guidelines like ICH and GMP, is essential. Strong problem-solving skills, attention to detail, and effective communication set standout professionals apart in this role. These skills ensure the accurate development, validation, and transfer of analytical methods critical for product quality and regulatory compliance.

What is Analytical Development?

Analytical Development refers to the process of designing, optimizing, and validating methods to analyze the quality, safety, and efficacy of pharmaceutical products. Professionals in this field develop and implement techniques such as chromatography, spectroscopy, and other laboratory methods to test raw materials, intermediates, and finished products. Their work ensures that drug products meet regulatory standards and are safe for patient use. Analytical Development is critical in the pharmaceutical and biotechnology industries, supporting research, quality control, and regulatory submissions.

What are some common challenges faced in an Analytical Development role, and how can job seekers prepare for them?

Professionals in Analytical Development often encounter challenges such as developing robust methods for complex samples, meeting tight project deadlines, and ensuring regulatory compliance. To prepare, job seekers should build strong problem-solving skills, gain familiarity with a range of analytical techniques (such as HPLC, GC, and spectroscopy), and stay current with industry regulations like ICH guidelines. Collaborating effectively with cross-functional teams, such as Quality Control and Research & Development, is also essential for success in this role.

What is the difference between Analytical Development vs Quality Control Analyst?

AspectAnalytical DevelopmentQuality Control Analyst
Primary FocusDeveloping and optimizing analytical methods for new productsPerforming routine testing to ensure product quality
Work EnvironmentLaboratories involved in method development and validationQuality control labs conducting batch testing and release
Required CredentialsBachelor's or higher in Chemistry, Biochemistry, or related fields; experience in method developmentBachelor's in Chemistry, Biology, or related fields; experience in testing procedures

Analytical Development professionals focus on creating and refining analytical methods for new products, while Quality Control Analysts perform routine testing to verify product quality. Both roles require similar educational backgrounds and work in laboratory settings, but their responsibilities differ in scope and purpose.

Analytical Development jobs near you
Infographic showing various Analytical Development job openings in Quebec as of June 2026, with employment types broken down into 66% Full Time, 30% Part Time, and 4% Contract. Highlights an 83% Physical, 5% Hybrid, and 12% Remote job distribution, with an average salary of $98,374 per year, or $47.3 per hour.

Chemistry Manufacturing & Controls (CMC) Manager

Milestone Pharmaceuticals

Montreal, QC • On-site

Full-time

Posted 25 days ago

Job description

WHY JOIN MILESTONE
At Milestone, we aspire to advance and implement paradigm shifts for cardiac therapy. We are currently focused on developing anti‐arrhythmia treatments for self‐administration outside of the emergency department or hospital setting for patients with acute episodes of paroxysmal supraventricular tachycardia (PSVT) and atrial fibrillation (AFib), as well as other episodic cardiovascular conditions.
In addition to our science and innovation, we are a team guided and driven by our core values. Patient needs and empowerments are continually upheld as central to our mission. Our teamwork is strengthened in an environment in which we support and challenge each other while enjoying and celebrating our achievements. We maintain an entrepreneurial, proactive, and action‐oriented mindset that places high value on grit, courage, and resolve. Decision‐making is based on evaluating information and an idea’s merits; data‐driven proposals are both supported and sought. We act individually and as a team with humility, candor, empathy, and unwavering integrity.
We have been successful in attracting and empowering best‐in‐class talent, and we seek those with passion to join on our journey to develop treatments and to motivate change. We are excited about the possibilities of this team and what we can accomplish together.
YOU WILL BE RESPONSIBLE FOR
  • Manage external manufacturing and analytical activities at contract development and manufacturing organizations (CDMOs) to support commercial supply and clinical programs, ensuring collaboration, communication and scientific expertise.
  • Manage GMP production of drug substance/drug product at CDMOs intended for nasal administration.
  • Manage and support outsourced analytical development, validation and testing activities.
  • Manage stability programs and trending.
  • Provide technical expertise to support the development of new processes and formulations, scale-up, technology transfer and validation.
  • Review batch production records, certificate of analysis, stability reports, validation protocols and reports to ensure technical and cGMP compliance.
  • Review and approve deviations, investigations, CAPAs and change controls as technical subject matter expert and make recommendations to Quality Assurance.
  • Review technical drug substance and drug product documents in a timely matter for regulatory submissions.
EDUCATION AND RESPONSIBILITIES
  • BSc or MSc in Pharmaceutical Sciences, Chemistry, Chemical Engineering, Biochemistry or related field.
  • 5+ years of experience in the biotech or pharmaceutical industry with at least 3+ years in cGMP environment.
  • Hands-on experience with one or more of the following: drug substance/drug product GMP manufacturing, tech transfer, process scale-up and validation, analytical development and validation, formulation development, experience working with CDMOs or contract testing laboratories.
  • Knowledge of GMP, FDA and EU regulations, ICH guidelines, as well as CMC content of regulatory submissions.
  • Proficiency with Word, Excel, PowerPoint, SharePoint, Teams and Acrobat.
KEY ATTRIBUTES
  • Superior interpersonal abilities - including working in a multi-cultural, multi-lingual environment.
  • Exceptional communication skills, with both written and oral presentation abilities.
  • Demonstrated ability to successfully work with and influence contract manufacturing partners while maintaining positive working relationships.
  • Attention to details, strong organization and troubleshooting skills.
  • Able to travel approximately 15% of the time, including international travel when appropriate.

EEOC STATEMENT: Milestone believes in a diverse environment and is committed to equal employment opportunities for all its employees and qualified applicants. We do not discriminate in recruitment, hiring, training, promotion or any other employment practices for race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Milestone will make reasonable accommodations for qualified individuals with known disabilities in accordance with applicable law.

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