Burlington, On Product development manager (systems) onsite position Jobs – 5 Openings This Week

Quality Assurance Associate Systems
AtomVie Global Radiopharma Inc. —Hamilton, ON
- From $60,000 a year
- Full-time
- Engineering
- English
- Organizational skills
- Dental care
Quick apply
Field Service Engineer
Evertz Microsystems Limited —Burlington, ON
- $40,000–$48,000 a year
- Full-time
- Customer service
- Computer networking
- Linux
- Employee assistance program
Quick apply
Electrical Engineer Lead
Thermon —Oakville, ON
- Full-time
- AutoCAD
- Microsoft Excel
- Schematics
- Dental care
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Lead Electrical Engineer
Thermon —Oakville, ON
- Full-time
- AutoCAD
- Microsoft Excel
- Schematics
Quick apply

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Quality Assurance Associate Systems

AtomVie Global Radiopharma Inc. -
Hamilton, ON

Quick apply

Job details

Full-time
From $60,000 a year

Qualifications

Engineering
Post-secondary education
English
Organizational skills
Chemistry
Communication skills

Full job description

AtomVie Global Radiopharma Inc. is a global leading GMP manufacturer and distributer of clinical and commercial radiopharmaceuticals. We work with our partners to empower the next generation radiotherapeutics for the detection and treatment of cancer and human diseases.

About the Role

The Quality Assurance Associate Systems helps to ensure GMP compliance for production of new and ongoing radiopharmaceuticals at AtomVie. This position will act as an interface between quality, radiopharmaceutical development, regulatory and production to ensure that all regulated activities listed below are conducted in compliance with relevant regulations and internal procedures

Location: AtomVie Global Radiopharma Inc, Hamilton ON (Onsite).

What You Will Do

Through on-going monitoring and review, ensures that the quality systems are in compliance with regulatory requirements and meet the needs of the AtomVie and its clients
Works collaboratively with stakeholders to ensure the systems are kept current and are effective with current applicable regulations
Manage and Track non-conformances, laboratory investigations, CAPAs, change controls, and complaint system.
Lead job board and change control committee meetings with the internal stake holders.
Prepare quality performance metrics and provides monthly report to Quality Assurance Management
Participates and leads internal audits, including scheduling, conducting and preparing reports.
Participates in on-site audits by regulatory authorities and clients, including preparation and follow-up activities
Co-ordinates the supplier qualification program and participate in vendor audits as needed
Perform compliance review of aseptic process and operator qualification media fills and equipment Qualification/Calibration records.
Performs compliance review of equipment PM and calibration records.
Participates and leads GMP training program for the new employees or as required.
Meet on a regular basis with the Manager QA Systems to provide updates on ongoing activities, track and set priorities, and address issues and problems
Acquire an appropriate understanding of quality processes, developing approaches to achieve compliance that ensure relevant standards are being met.
Support document management system activities
Serve as a primary contact with minimal supervision for QA activities associated with introduction of new QA requirements; these include review of non-conformance, preparation and close-out of CAPAs and change controls, as required.
Assist on project deliverables to ensure that high quality standards are met and are compliant with internal/external requirements and GMP regulations.
Provide guidance and support to QA staff, ensuring the QA system and areas are maintained to AtomVie standards and regulatory requirements, mentoring and coaching these staff members to understand the importance and implications Quality has at AtomVie.
Ensure compliance with Health and Safety for all policies, procedures and regulations applicable to their work.
Other duties as assigned

Experience Necessary

Post-Secondary Education in Engineering, Chemistry, Microbiology or a related field
3 to 5 years of relevant experience
Experience working in a GMP environment is required
Experience preparing/reviewing quality documentation is an asset
Training and experience in quality systems, quality audits, good documentation practices, change controls, CAPAs and review of quality records
Strong understanding of Health Canada and FDA GMP regulations, with specific knowledge of the regulations as they pertain to sterile products
Proficiency in the English language both written and oral, and excellent communication skills; detail-oriented
Ability to work independently and possess excellent organizational skills
Strong client-facing and teamwork skills

Compensation

Annual salary starts at $60,000. Compensation is based on relevant industry experience, academic credentials, and qualifications.

AtomVie Offers

Group Health & Dental Benefits
RRSP Matching
Wellness Benefit
Transportation allowance
Training & Career Development
Opportunity for long-term growth
Collaborative environment with experienced individuals in the field
Join a passionate team making a difference in patients’ lives

AtomVie does not use artificial intelligence or automated decision-making tools in any part of the recruitment, screening, or selection process.

We are committed to fostering a workplace that values diversity, equity, and inclusion. We believe that a diverse and inclusive workforce enhances our ability to innovate, collaborate, and better serve our clients and patients. We thank you for considering a career with AtomVie. Only those candidates selected for an interview will be contacted. Accommodations are available upon request for candidates taking part in all aspects of the recruitment and selection process. We are dedicated to ensuring that every qualified applicant has an equal opportunity to thrive within our organization.

Quick apply

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