Process Technician - Eurofins CDMO Alphora, Inc.
- Oakville, ON
- On-site
- Posted Oct 1, 2026
- 1 position
$50,000 / year
Opens an external site
- Employment type
- Full-time
- Experience level
- Entry, Junior · 0+ years
- Minimum education
- College diploma
- Apply by
- Mar 28, 2027
- Posting language
- English
- Working hours
- 40 hours per week
- Seniority
- Associate
- Application method
- Direct apply is available
Job summary
Carry out pharmaceutical chemical processing operations according to batch records, SOPs, GMP, and safety requirements, including routine tasks such as filtration, phase separation, refluxing, and distillation under supervision. Complete accurate batch documentation and verification, work with technicians and team leaders, and maintain clean equipment and facilities while safely handling chemicals and process waste.
Job details
Eurofins Scientific is an international network of independent life sciences companies, 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 laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies believes that it is a global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and agroscience contract research services. It is also one of the market leaders in certain testing and laboratory services for genomics, and in the support of clinical studies, as well as in biopharma contract development and manufacturing. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In under 40 years, Eurofins has grown from one laboratory in Nantes, France to over 65,000 employees across a decentralised and entrepreneurial network of over 950 laboratories in over 1,000 independent companies across 57 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. The Eurofins network generated EUR 7.296 billion revenues in FY 2025, and has been one of the fastest growing listed European companies for almost three decades. _____________________________________________________________________________________ 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. Job Description Join Our Team as a Process Technician! Are you ready to be part of a dynamic team driving innovation in chemical processing? At Eurofins CDMO Alphora Inc., we’re looking for detail-oriented and safety-conscious individuals to help us deliver excellence in pharmaceutical manufacturing. What You’ll Do: Execute chemical processing operations with precision, following batch record instructions. Ensure compliance with Environmental, Health & Safety standards, SOPs, GMP, and Good Documentation Practices. Perform accurate batch sheet entries and second-person verifications. Collaborate closely with experienced technicians and team leaders to complete tasks “right the first time.” Handle routine operations such as filtrations, phase separations, refluxing, and distillations under supervision. Maintain cleanliness of equipment and facilities and ensure the safe handling of chemicals and process waste. Why You’ll Love It Here: Hands-on experience in a cutting-edge pharmaceutical environment. Supportive team culture with opportunities to learn from seasoned professionals. Commitment to safety, quality, and continuous improvement. If you’re passionate about precision, safety, and teamwork, we want to hear from you! Apply today and take the next step in your career. Qualifications College Diploma or Degree preferred but not mandatory Proficient written and verbal English communication skills Willingness to learn Capable of following detailed instructions Capable of multi-tasking Capable of sound decision-making Good interpersonal skills Good time management skills Good Documentation Practices (GDP) A working knowledge of cGMP principles preferred but not mandatory Experience in a chemical manufacturing facility being a definite asset Experience handling hazardous chemicals being a definite asset Experience working with API or formulation pharmaceutical processing equipment, or related experience in food, cosmetics or specialty chemicals being a definite asset Experience working with computerized chemical processing equipment being a definite asset Experience with shift work preferred but not mandatory: 8 hour - 24/5 and/or 12 hour - 24/7 (Continental shift schedule) Additional Information Disclaimer: Salary information posted on sites other than the official careers page does not reflect the organization’s compensation and may represent estimated ranges provided by third-party job boards. The organization offers competitive wages and a comprehensive total rewards package, which will be discussed during the interview process. The approximate annual base compensation for this position starts at $50,000 CAD (base salary does not include potential shift premiums or overtime). The actual offer, reflecting the total compensation package plus benefits, will be determined by a number of factors which include but are not limited to the applicant’s experience, knowledge, skills, and abilities. 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 At Eurofins CDMO Alphora, we leverage artificial intelligence (AI) technology to support our recruitment process, including preliminary screening of applications and resumes. All hiring decisions are made by human reviewers. This posting is for a current vacancy and the successful candidate will start as soon as possible. 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. NO AGENCIES, CALLS OR EMAILS PLEASE
What you’ll do
Carry out pharmaceutical chemical processing operations according to batch records, SOPs, GMP, and safety requirements, including routine tasks such as filtration, phase separation, refluxing, and distillation under supervision. Complete accurate batch documentation and verification, work with technicians and team leaders, and maintain clean equipment and facilities while safely handling chemicals and process waste.
Requirements
A college diploma or degree is preferred but not mandatory; candidates should communicate effectively in English, follow detailed instructions, learn readily, multitask, make sound decisions, and demonstrate good interpersonal and time-management skills. Knowledge of GDP is expected, while cGMP knowledge, chemical manufacturing or hazardous-chemical experience, pharmaceutical or related processing equipment experience, computerized processing equipment experience, and shift-work experience are preferred or considered assets.
Benefits
• Health And Dental Coverage • Life Insurance • Disability Insurance • RRSP With 3% Company Match • Paid Holidays • Paid Time Off
Listed skills
- Time management · Preferred
- Decision Making · Preferred
Other relevant skills
Identified from the job description. Confirm important requirements above.
- Chemical Processing
- Batch Record Execution
- Good Manufacturing Practices
- Good Documentation Practices
- Environmental Health And Safety Compliance
- Batch Documentation
- Second-Person Verification
- Filtration
- Phase Separation
- Refluxing
- Distillation
- Chemical Handling
- Equipment And Facility Cleaning
- Following Detailed Instructions
- Decision-Making
- Time Management
Job areas
- Manufacturing
- Science & Research
- Engineering
- Security & Safety
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