Adecco is currently hiring a temporary full-time experienced Quality Control Scientist to work for our client in Toronto, ON. In this role you will play a crucial role in ensuring the highest standards of quality, safety, and regulatory compliance in the development and manufacturing of pharmaceutical and biopharmaceutical products. This position involves the implementation and oversight of quality assurance processes, conducting audits, and supporting regulatory compliance.
If you are a meticulous and results-oriented professional committed to maintaining the highest quality standards in the pharmaceutical or biopharmaceutical industry, apply today!
Location: Toronto, ON
Shift: Monday to Friday | 8:00am – 4:00pm
Job type: Temporary | Full-time
Here's why you should apply:
Paid weekly accurate and on time
Strong health and safety programs
Medical and dental benefits once qualified
Free training programs
New and quicker onboarding process
Responsibilities:
Coordinate with other groups within the company to ensure stability studies are executed efficiently and in a compliant manner.
Support the timely submission of product license applications, license renewals, license amendments, and response to questions, in conjunction with Quality Operations and Regulatory Affairs, through the development and execution of stability studies and data analysis/interpretation.
Ensure training is up to date to perform the designated cGMP activities and requirements for Health and Safety.
Execute changes of stability protocols to ensure change controls are implemented on time.
Provide support to regulatory inspections, audits, and ensure responses and actions are completed by the designated target date.
Support the investigations and closure of quality incidents/deviations, as well as the completion of Corrective and Preventative Actions (CAPAs).
Support the update of site procedures as required
Qualifications:
Must be legally eligible to work, and reside in Canada
Bachelor of Science Degree, with specialization in Biology, Biochemistry, Microbiology, Immunology, Chemistry, or related subject.
1-3 years pharmaceutical experience, preferably with QC experience or knowledge of Stability Studies
Attention to detail
Ability to work independently and in collaboration with others
Proficient organizational skills
Excellent time management.
Desire to work within a team environment.
Strong written, verbal, and interpersonal communication skills.
Proficient in use of MS Office, including Excel, Outlook, PowerPoint, and Word.
Attention to detail,
Technical/Report writing skills are strongly preferred.
Are you interested in this position? Apply now! Our dynamic team of recruiters will reach out if you qualify for this role.
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