Resume and JobRESUME AND JOB
Eurofins logo

Research Chemist (Drug Product) - Eurofins CDMO Alphora, Inc.

Eurofins

Research Chemist (Drug Product) - Eurofins CDMO Alphora, Inc.

full-timePosted: Jan 16, 2026

Job Description

Description

  • Conduct work in a safe manner and ensure compliance with established safe work practices and procedures.
  • Adhere to the policies and guidelines set out in the Eurofins CDMO | Alphora Employee Handbook.
  • Work harmoniously with all fellow employees.
  • Provide assistance and support for analytical activities including analytical method development, method validation, method transfer, and sample testing in an R&D and GMP environment.
  • Assist in the execution of prototype and GMP stability studies in accordance with ICH or other regulatory guidelines.
  • Provide support for document preparation of material specifications, standard operation procedures, and other necessary documentation for Drug Product Operations.
  • Ensure that all work is performed in compliance with the applicable SOPs, cGMPs and GLPs.
  • Support the Drug Product Operations Team to ensure the timely completion of client projects.
  • Perform other related duties as required.

Qualifications

Desired Minimum Qualifications:

  • Degree in Chemistry, Biochemistry or related field
  • 3+ years' experience in a pharmaceutical laboratory or manufacturing environment
  • 2+ years of method transfer/validation
  • Expertise in GMP, GLP and other Health Canada guidelines

Additional Info

At Eurofins we offer excellent full-time benefits including health & dental coverage, life and disability insurance, RRSP with 3% company match, paid holidays, paid time off.

Accommodation: Persons with disabilities who need accommodation in the application process, or those needing job postings in an alternative format, may e-mail a request via the website at www.eurofins.ca.

As a Eurofins employee, you will become part of a company that has received international recognition as a great place to work. To learn more about Eurofins, please explore our website at www.eurofins.ca

We thank all applicants within commuting distance of GTA, Ontario for showing an interest in this position. Only those selected for an interview will be contacted.

This posting is supported by AI technology to assist in screening candidates and resumes.

NO AGENCIES, CALLS OR EMAILS PLEASE

Company Description

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.

In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

In 2024, Eurofins generated total revenues of EUR 6.515 billion, and has been among the best performing stocks in Europe over the past 20 years.

Eurofins CDMO Alphora Inc. develops and manufactures new therapeutics to improve the lives and health of patients.  Eurofins CDMO Alphora provides contract research & development services to global pharmaceutical and biotech companies, developing their processes and manufacturing their bulk drug substances (Active Pharmaceutical Ingredients -“API’s”) as well as finished dosage products (tablets, capsules, suspensions) for supply to clinical trials and commercial requirements.  Eurofins CDMO Alphora provides a rich and technologically challenging environment with a continuing flow of interesting projects.  Our employees work in close concert with clients throughout the development process to achieve their program objectives.  Eurofins CDMO Alphora Inc. is growing its state-of-the-art organization, with continued investments in modern facilities, equipment, and instrumentation while providing a rich environment for employees to develop their technical skills and careers paths.

Locations

  • Mississauga, ON, Canada

Salary

Estimated Salary Rangemedium confidence

60,000 - 100,000 CAD / yearly

Source: ai estimated

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Analytical method developmentintermediate
  • Method validation and transferintermediate
  • GMP complianceintermediate
  • Stability studies executionintermediate
  • Document preparation (SOPs, specifications)intermediate

Required Qualifications

  • Degree in Chemistry, Biochemistry or related field (experience)
  • 3+ years experience in pharmaceutical laboratory or manufacturing (experience)
  • 2+ years of method transfer/validation (experience)
  • Expertise in GMP, GLP and Health Canada guidelines (experience)

Responsibilities

  • Provide assistance for analytical activities including method development, validation, transfer, sample testing
  • Assist in execution of prototype and GMP stability studies
  • Provide support for document preparation
  • Ensure compliance with SOPs, cGMPs, GLPs
  • Support Drug Product Operations Team for timely project completion

Benefits

  • general: Health & dental coverage
  • general: Life and disability insurance
  • general: RRSP with 3% company match
  • general: Paid holidays
  • general: Paid time off

Target Your Resume for "Research Chemist (Drug Product) - Eurofins CDMO Alphora, Inc." , Eurofins

Get personalized recommendations to optimize your resume specifically for Research Chemist (Drug Product) - Eurofins CDMO Alphora, Inc.. Takes only 15 seconds!

AI-powered keyword optimization
Skills matching & gap analysis
Experience alignment suggestions

Check Your ATS Score for "Research Chemist (Drug Product) - Eurofins CDMO Alphora, Inc." , Eurofins

Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
Format & readability score

Answer 10 quick questions to check your fit for Research Chemist (Drug Product) - Eurofins CDMO Alphora, Inc. @ Eurofins.

Quiz Challenge
10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.

Eurofins logo

Research Chemist (Drug Product) - Eurofins CDMO Alphora, Inc.

Eurofins

Research Chemist (Drug Product) - Eurofins CDMO Alphora, Inc.

full-timePosted: Jan 16, 2026

Job Description

Description

  • Conduct work in a safe manner and ensure compliance with established safe work practices and procedures.
  • Adhere to the policies and guidelines set out in the Eurofins CDMO | Alphora Employee Handbook.
  • Work harmoniously with all fellow employees.
  • Provide assistance and support for analytical activities including analytical method development, method validation, method transfer, and sample testing in an R&D and GMP environment.
  • Assist in the execution of prototype and GMP stability studies in accordance with ICH or other regulatory guidelines.
  • Provide support for document preparation of material specifications, standard operation procedures, and other necessary documentation for Drug Product Operations.
  • Ensure that all work is performed in compliance with the applicable SOPs, cGMPs and GLPs.
  • Support the Drug Product Operations Team to ensure the timely completion of client projects.
  • Perform other related duties as required.

Qualifications

Desired Minimum Qualifications:

  • Degree in Chemistry, Biochemistry or related field
  • 3+ years' experience in a pharmaceutical laboratory or manufacturing environment
  • 2+ years of method transfer/validation
  • Expertise in GMP, GLP and other Health Canada guidelines

Additional Info

At Eurofins we offer excellent full-time benefits including health & dental coverage, life and disability insurance, RRSP with 3% company match, paid holidays, paid time off.

Accommodation: Persons with disabilities who need accommodation in the application process, or those needing job postings in an alternative format, may e-mail a request via the website at www.eurofins.ca.

As a Eurofins employee, you will become part of a company that has received international recognition as a great place to work. To learn more about Eurofins, please explore our website at www.eurofins.ca

We thank all applicants within commuting distance of GTA, Ontario for showing an interest in this position. Only those selected for an interview will be contacted.

This posting is supported by AI technology to assist in screening candidates and resumes.

NO AGENCIES, CALLS OR EMAILS PLEASE

Company Description

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.

In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

In 2024, Eurofins generated total revenues of EUR 6.515 billion, and has been among the best performing stocks in Europe over the past 20 years.

Eurofins CDMO Alphora Inc. develops and manufactures new therapeutics to improve the lives and health of patients.  Eurofins CDMO Alphora provides contract research & development services to global pharmaceutical and biotech companies, developing their processes and manufacturing their bulk drug substances (Active Pharmaceutical Ingredients -“API’s”) as well as finished dosage products (tablets, capsules, suspensions) for supply to clinical trials and commercial requirements.  Eurofins CDMO Alphora provides a rich and technologically challenging environment with a continuing flow of interesting projects.  Our employees work in close concert with clients throughout the development process to achieve their program objectives.  Eurofins CDMO Alphora Inc. is growing its state-of-the-art organization, with continued investments in modern facilities, equipment, and instrumentation while providing a rich environment for employees to develop their technical skills and careers paths.

Locations

  • Mississauga, ON, Canada

Salary

Estimated Salary Rangemedium confidence

60,000 - 100,000 CAD / yearly

Source: ai estimated

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Analytical method developmentintermediate
  • Method validation and transferintermediate
  • GMP complianceintermediate
  • Stability studies executionintermediate
  • Document preparation (SOPs, specifications)intermediate

Required Qualifications

  • Degree in Chemistry, Biochemistry or related field (experience)
  • 3+ years experience in pharmaceutical laboratory or manufacturing (experience)
  • 2+ years of method transfer/validation (experience)
  • Expertise in GMP, GLP and Health Canada guidelines (experience)

Responsibilities

  • Provide assistance for analytical activities including method development, validation, transfer, sample testing
  • Assist in execution of prototype and GMP stability studies
  • Provide support for document preparation
  • Ensure compliance with SOPs, cGMPs, GLPs
  • Support Drug Product Operations Team for timely project completion

Benefits

  • general: Health & dental coverage
  • general: Life and disability insurance
  • general: RRSP with 3% company match
  • general: Paid holidays
  • general: Paid time off

Target Your Resume for "Research Chemist (Drug Product) - Eurofins CDMO Alphora, Inc." , Eurofins

Get personalized recommendations to optimize your resume specifically for Research Chemist (Drug Product) - Eurofins CDMO Alphora, Inc.. Takes only 15 seconds!

AI-powered keyword optimization
Skills matching & gap analysis
Experience alignment suggestions

Check Your ATS Score for "Research Chemist (Drug Product) - Eurofins CDMO Alphora, Inc." , Eurofins

Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
Format & readability score

Answer 10 quick questions to check your fit for Research Chemist (Drug Product) - Eurofins CDMO Alphora, Inc. @ Eurofins.

Quiz Challenge
10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.