Quality Manager II

Immediate need for a talented Quality Manager II. This is a 06+months contract opportunity with long-term potential and is located in Toronto, ON(Onsite). Please review the job description below and contact me ASAP if you are interested. 

Job ID: 24-45410

Pay Range: $50 - $55/hour.  Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location).

Key Requirements and Technology Experience: 

• Key Skills; Audit, GMP documentation, Delta V, Computer System Validation
• Manager Intakes: Quality Operations Manager Experience with computerized systems validation, validation of Delta V, Data Historian OSI PI, and Manufacturing Execution System MES is an asset.
• Bachelor’s Degree in the field of Science or Engineering, with 5+ years of experience in a GMP regulated environment.
• Minimum 5 years experience in review and auditing of GMP documentation.
• Strong Quality Mindset                       
• The ability to effectively communicate, both verbally and in written format, through multiple layers of the organization and the ability to think strategically are key to the individual’s success.
• Excellent interpersonal and influencing skills and must be able to work in a cross-functional team-based environment.
• Strong technical background and knowledge in both FDA/EU quality compliance requirements and validation requirements.
• Ability to work in a diverse environment and draw upon experience in determining the actions needed to achieve results and remediate issues.
• Ability to work in a fast paced environment and make balanced quality decisions.
• It would be preferred if the candidate has experience with Document Management Systems (such as QualiPSO etc.) applications and trained in Change Management, Nugenesis, Kneat Paperless Validation system etc.
• Demonstrated ability to meet/exceed timelines/deliverables.
• Experience with computerized systems validation, validation of Delta V, Data Historian OSI PI, and Manufacturing Execution System MES is an asset.
• Bachelor’s Degree in the field of Science or Engineering, with 5+ years of experience in a GMP regulated environment.
• Minimum 5 years experience in review and auditing of GMP documentation.

Our client is a leading Healthcare Industry, and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration.

Pyramid Consulting, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

By applying to our jobs you agree to receive calls, AI-generated calls, text messages, or emails from Pyramid Consulting, Inc. and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy 

.  #Mor2 J2W:CB3