Please note that relocation to Mississauga, ON is expected in mid-2026.

Reporting directly to the Director/BUMA, Dept. of Chemistry, the OOS investigator will work within BPT and working closely with QA Dept, the OOS Investigator is responsible for leading and executing Out of Specification (OOS), Out of Trend (OOT), and atypical result investigations within the Analytical Quality Control laboratory. This role ensures that laboratory investigations are conducted in a scientifically sound, timely, and compliant manner in accordance with GMP/GLP and internal quality systems. The OOS Investigator evaluates analytical data, identifies root causes, determines product impact, and supports the implementation of effective corrective and preventive actions (CAPAs) to maintain data integrity and product quality.

A suitable candidate must be energetic, well-organized, self-disciplined and flexible. Efficient communication is a mandatory requirement to interact within the Team and with Management, in a fast-paced environment, sometimes under pressure, while remaining proactive, resourceful, and efficient. A high level of professionalism and confidentiality is crucial to this role. Additional roles and duties may be assigned as needed.

The OOS investigator must:

Strong knowledge of OOS/OOT investigations
Demonstrated experience conducting laboratory and full‑scale OOS investigations in compliance with GMP/ISO requirements.
Thorough understanding of analytical techniques
Hands‑on experience with methods such as HPLC, GC, UV‑Vis, FTIR, titrations, wet chemistry and Microbiology skills relevant to QC testing.
Expertise in root cause analysis (RCA)
Proven ability to apply tools such as Fishbone, 5‑Whys, fault tree analysis, and trend analysis.
Solid understanding of GMP, GLP, and data integrity principles
Including ALCOA+ expectations, documentation practices, and audit readiness.
Experience reviewing laboratory data and raw records
Ability to critically evaluate chromatograms, calculations, system suitability, logbooks, and analyst practices.
Strong deviation and CAPA management skills
Experience authoring clear, defensible investigation reports, defining CAPAs, and assessing effectiveness.
Knowledge of method validation and verification principles
Ability to assess method performance, variability, and suitability during investigations.
Cross‑functional collaboration skills
Ability to work effectively with QC & QA teams, as well as communicating with other Departments.
Excellent technical writing skills
Capable of producing clear, concise, and inspection‑ready investigation reports, as well as writing eloquent professional emails to the Clients delivering the OOS results/reports.
Ability to distinguish laboratory error vs. process‑related issues
Strong scientific judgment to determine testing assignable cause versus true product failure.
Experience supporting audits and inspections
Confidently defending OOS investigations during internal, customer, or regulatory audits.
Strong organizational and time‑management skills
Ability to manage multiple investigations simultaneously while meeting timelines.
Proficiency with LIMS and electronic documentation systems
Comfortable navigating laboratory systems and electronic quality records.
Conduct timely, scientifically sound OOS Investigations.
Ensure full compliance with Phase I vs Phase II Investigation principles according to Internal SOPs as well against the FDA guidance for Investigations.
Manage and schedule Retesting and Re measurement in a controlled manner
Deliver and keep high-quality, Inspection ready OOS documentation.
Drive effective CAPAs and prevent recurrence.
Collaborate effectively with Clients, within the Team and with Management.
Identify and Trend OOS / OOT signals proactively.
Maintain Inspection Readiness and Regulatory Awareness.
Ensure that work is performed in compliance with good manufacturing practices (GMP), standard operating procedures (SOPs);
Participate in typing and reviewing of Methods/Workbook templates/SOPs in electronic format in eLIMS;
Participation in meetings and routine Lab Support Operations, contribution to Lab Audit preparations in assistance with tasks assigned by QA and QC Management.
Work productively and cooperatively with other departments and supervisors to attain company objectives.
Follow SOPs on investigations and CAPAs.
Ensure all lab personnel are working safely and in adherence to company health and safety policy and procedures.

Qualifications

B.Sc. or higher degree in Chemistry, Biochemistry, or diploma in related field;
A solid background and understanding of Analytical Chemistry, variety of Wet Chemistry and Instrumentation techniques and GMP/GDP/GLP requirements is mandatory.
Computer proficiency- Microsoft Office, eLIMS, etc..
Any certificate or course related to Investigations or QA/QC related courses are an asset.
At least 5 years working in the QC Lab - with different analytical instrumentation.
2-5 years of experience in leading investigations.
Ability to perform preliminary data review as part of investigation.
Experience working in contract Laboratory considered an asset.

Experience working with pharmaceutical products, NHPs, and variety of formulations viz solid dosage, liquid dosage forms along with creams, lotions, ointments and other challenging matrixes is an asset
Work competently without direct supervision while applying technical laboratory skills.
Strong computer, organizational skills.
Clear verbal and written communication skills.
Skilled in data/report generation, retrieval and interpretation of routine analysis.
Perform other related duties as assigned.

Specific Desired Experience

2-5+ years working with applied chemistry techniques.
Experience working with pharmaceutical clients and products.
Experience working in a contract laboratory considered an asset.

Technical Skills:

Good computer skills - proficiency with MS Office.
Working knowledge of Laboratory Information management Systems (LIMS).

WORKING CONDITIONS

This position is working in a laboratory environment where standing is required for greater than 50% of the time to work at the bench for analyses. Light lifting requirements of no more than 20 lbs. Hazardous materials are handled using established safety procedures and appropriate PPE. Since there are no direct reports for this Team Leader role, there are no significant managerial responsibilities and the position remains eligible for overtime pay.

Additional Information

Please note that relocation to Mississauga, ON is expected in mid-2026.

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.

This posting is for a current vacancy and the successful candidate will start as soon as possible.

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.

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