QA Data Reviewer - Eurofins Cosmetics & Personal Care, Inc.

Eurofins Humangenetik & Pränatal-Medizin; Old Toronto; On-site; CAD 50,000 - 80,000; Full time

Job summary

Join a forward-thinking company as a QA Data Reviewer, where you'll ensure compliance with quality assurance regulations. This role involves reviewing quality documents, assisting with audits, and supporting the training of new staff, all while working in a dynamic lab and office environment. The ideal candidate will possess a degree in a science-related field and have a strong background in QA processes, particularly in GMP settings. If you're detail-oriented and passionate about quality assurance, this opportunity offers a chance to contribute to a recognized leader in analytical testing services while enjoying excellent benefits and a supportive workplace culture.

Benefits

Health & dental coverage

Life and disability insurance

RRSP with 3% company match

Paid holidays

Paid time off

Qualifications

• 2-5 years of QA experience in a GMP or ISO testing facility.
• Degree in a science-related discipline required.

Responsibilities

• Review quality documents and ensure compliance with GMP.
• Assist with internal and external audits and training.

Skills

GMP requirements knowledge

QA experience

English fluency

Communication skills

Organizational skills

Attention to detail

Ability to multitask

Computer skills (MS Office)

Proactive attitude

Education

Degree or diploma in science-related discipline

Tools

Microsoft Office

Job description

QA Data Reviewer - Eurofins Cosmetics & Personal Care, Inc.

• Full-time

Company Overview:

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing.

This position is responsible for ensuring compliance with applicable regulations for clients requiring quality assurance services.

Responsibilities:

• Review and determine the status of quality documents (including raw laboratory data, validation studies, logbooks, and calibration reports);
• Provide support with maintaining Quality System, including drafting and updating quality procedures;
• Assist with internal and external audits;
• Ensure that all reports and raw data are according to GMP, accurate, and acceptable;
• Interact with department staff to acquire information for report writing and auditing purposes;
• Log and review complaints; compile required GMP documents for the evaluation of complaints;
• Perform and manage the internal auditing program if required;
• Manage the ongoing tracking and maintenance of GMP documents;
• Support the training of new staff;
• Evaluate and summarize instrumentation data in final reports;
• Maintain general record-keeping practices according to local and global SOPs;
• Review training records and generate associated reports if required;
• Initiate and conduct deviations and out-of-specification investigations;
• Initiate and conduct Corrective Action and Preventative Action (CAPA) investigations;
• Initiate and assist in Change Control procedures;
• Adhere to the Standard Operating Procedures;
• Circulate Standard Operating Procedures and follow up on training requirements;
• Ensure that all staff members are following the Standard Operating Procedures;
• Assist with the maintenance of Health Canada and FDA accreditation;
• Attend staff meetings;
• Perform any other duties as delegated by the Quality Assurance Manager or designate.

Key Skills, Experience & Abilities:

• Knowledge of GMP requirements;
• 2-5 years QA experience in a GMP or ISO testing or production facility;
• Must speak and write English fluently;
• Excellent communication skills, both written and verbal;
• Excellent organizational skills;
• High level of accuracy and strong attention to detail;
• Ability to work independently and collaboratively;
• Ability to multitask and remain calm under pressure;
• High level of professionalism and discretion;
• Exceptional computer skills with MS Office;
• Proactive, self-disciplined, and productive;
• Willingness to learn and apply knowledge.

EDUCATION:

• Degree or diploma in a science-related discipline;
• Computer proficiency – Microsoft Office, especially Excel.

WORKING CONDITIONS:

This position will be working in office and lab environments. Moderate activity and some light lifting may be required. Evening or weekend work may occasionally be required.

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

Accommodation: Persons with disabilities who need accommodation in the application process may e-mail a request via the website at www.eurofins.ca.

As a Eurofins employee, you will become part of a company recognized 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 interest in this position. Only those selected for an interview will be contacted.