Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
Division/Site:
Our Whitby Site specializes in commercial manufacturing for a full range of conventional dosage forms with specialized capabilities, and houses a fully integrated pharmaceutical development services (PDS) facility.
Discover Impactful Work:
Provide direction to the functions within Investigations in accordance with Regulatory and Corporate Quality Standards & Guidelines: Deviation Investigations, Complaint Investigations, and Corrective and Preventive Actions to prevent recurrence. Manage the daily activities of the Investigations staff to create a culture of quality awareness and teamwork, while coordinating investigations and working with the appropriate parties to complete product Deviation Reports (DRs) and Complaint Reports. Responsible for on time creation and issuance of Trend Reports to proactively identify trending issues.
Mentor the team to create a culture of quality awareness, teamwork, compliance, and continuous improvement with a focus on strong cross functional service throughout the site.
Monitor performance of Investigations and associated CAPAs through identification, monitoring, trending, and reporting of key performance indicators.
Drive continuous improvement of Investigations, adoption of standard methodologies, application of consistency across the site, and ensure integrity of system in compliance with Regulatory, Corporate, and Site requirements.
Support Regulatory Inspections, Corporate Audits, and Client Audits specific to the functions within the Investigations team. Talk to auditors during inspections to ensure information is provided in a timely, accurate and complete manner.
Keys to Success:
Bachelor of Science (B.Sc.) in Chemistry, Pharmacy or a science related to pharmaceutical analysis
Minimum 8 years of experience within the pharmaceutical, food or cosmetic industry.
Minimum 5 years previous supervisory and/or leadership experience.
Minimum 5 years industry experience performing activities directly related to Investigations (Deviations, Complaints) and CAPAs.
Equivalent combinations of education, training, and relevant work experience may be considered.
Knowledge, Skills and Abilities:
Excellent interpersonal and leadership skills. Extensive understanding of Good Manufacturing Practices, Standard Operating Procedures and CAPA. Strong problem solving skills (identifying and evaluating root cause, and recommending corrective actions / preventative actions (CAPA). Excellent organizational skills with proven ability to prioritize when timeline conflicts exist. Detail oriented with a high degree of accuracy and thoroughness. Ability to problem solve and troubleshoot. Ability to carry out investigations in a non-threatening manner with production staff and to effectively interact with internal and external suppliers and clients. Proficient Microsoft skills (Word, Excel, PowerPoint). Proficiency with the English language (oral and written).
Excellent Benefits
Benefits & Total Rewards | Thermo Fisher Scientific
Medical, Dental, & Vision benefits-effective Day 1
Paid Time Off & Designated Paid Holidays
Retirement Savings Plan
Tuition Reimbursement
OTHER
Relocation assistance is NOT provided
Must be legally authorized to work in Canada
Must be able to pass a comprehensive background check
Compensation
The estimated annualized pay range for this position in Ontario is $85,500.00–$128,250.00.