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Clinical nurse Jobs in Angus, ON

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Clinical nurse • angus on

Last updated: 2 days ago
  • Promoted
Manager, Clinical Product Development Quality Assurance

Manager, Clinical Product Development Quality Assurance

Company is ConfidentialOntario, Canada
CA$110,000.00–CA$150,000.00 yearly
Full-time
Manager, Clinical Product Development Quality Assurance.The primary purpose of the Manager, Clinical Product Development Quality Assurance (DPQA) is to lead the communication, facilitation and exec...Show moreLast updated: 14 days ago
Clinical Research Associate I / II - Oncology - Toronto

Clinical Research Associate I / II - Oncology - Toronto

ICON Strategic SolutionsOntario, Canada
Full-time
As a CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Oversee multiple oncology trials, ensuring high-quality exec...Show moreLast updated: 4 days ago
Clinical Neuropsychology

Clinical Neuropsychology

University of TorontoOntario, Canada
DutiesDuties for the position may vary and include : supervising and training students on various psychological tests, oversee testing, administrative and clerical duties, email contact with student...Show moreLast updated: 18 days ago
  • Promoted
Non-Invasive Cardiologist

Non-Invasive Cardiologist

Atrium HealthGolden Horseshoe, ON, Canada
Full-time
This position is Sign-on Bonus eligible.Registered nurses with less than six months experience will find more than a job at Floyd. Our 8-week Nurse Residency Program offers education and hands-on wo...Show moreLast updated: 2 days ago
Coordinator, Clinical Information (Tissue)

Coordinator, Clinical Information (Tissue)

Ontario HealthOntario Health, Ontario
CA$31.86–CA$39.82 hourly
Full-time
At Ontario Health, we are committed to developing a strong organizational culture that connects and inspires all team members across the province. Our vision is that together, we will be a leader in...Show moreLast updated: 30+ days ago
Nurse Practitioner - Travel

Nurse Practitioner - Travel

RhynoCareOntario, Canada
This is a TRAVEL posting, meaning you are required to re-locate full-time for a period of up to 6 months.Accommodations will be covered by RhynoCare. RhynoCare is presently seeking an enthusias...Show moreLast updated: 30+ days ago
  • Promoted
Clinical Research Associate (CRA) II / Senior CRA

Clinical Research Associate (CRA) II / Senior CRA

i-Pharm ConsultingOntario, Canada
Full-time +1
Job Title : Clinical Research Associate (CRA) II / Senior CRA.Must Have : Minimum 2 Years of On Site Monitoring Experience & 1 Year of Oncology Experience. Our client is a global leader in healthcare da...Show moreLast updated: 11 days ago
Registered Nurse RN - full time days

Registered Nurse RN - full time days

Kindred Hospital OntarioOntario, CA
CA$43.92–CA$64.05 hourly
Pride, Teamwork, Compassion, Integrity, Respect, Fun, Professionalism, and Responsibility.As our most acute level of care, our specialty hospitals offer the same. Provide planning and delivery of di...Show moreLast updated: 30+ days ago
Leadless Clinical Specialist - Abbott Medical - CRM (Ontario)

Leadless Clinical Specialist - Abbott Medical - CRM (Ontario)

AbbottOntario, Ontario, Canada
Full-time
As a global leader in Cardiac Rhythm Technologies, we focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats.Provide procedur...Show moreLast updated: 6 days ago
Clinical Manager

Clinical Manager

The Pod GroupPeel Region, ON, CA
Full-time
Quick Apply
COMPASSIONATE • CLIENT-CENTRED • STRATEGIC • COLLABORATIVE • RESOURCEFUL.A growing, community-based organization that provides residential and outreach support for homeless individuals in Peel Regi...Show moreLast updated: 26 days ago
Clinical Research Associate

Clinical Research Associate

Piper CompaniesOntario, Canada
CA$120,000.00 yearly
Full-time
CRA) to join a global leader in clinical research and healthcare analysis for a.CRA) will monitor and participate in clinical trials across the country for a leading Clinical Research Organization....Show moreLast updated: 2 days ago
Perfusionist Cardiovascular Surgery & Critical Care | Kitchener, ON Hospital

Perfusionist Cardiovascular Surgery & Critical Care | Kitchener, ON Hospital

HealthOPMOntario, Canada
Full-time
Quick Apply
Cardiac Registered Respiratory Therapist Perfusionist.HealthOPM is seeking a skilled.This critical role involves operating heart-lung machines, managing extracorporeal life support systems, and col...Show moreLast updated: 30+ days ago
Clinical Specialist Cathlab.

Clinical Specialist Cathlab.

MedtronicOntario, Canada
CA$29.56–CA$32.88 hourly
Support the clinical development and education, manage inventory and equipment, and customer education programs pertinent to Medtronic defined products and technology. Support the implementation of ...Show moreLast updated: 30+ days ago
Field Clinical Specialist - Critical Care

Field Clinical Specialist - Critical Care

Edwards LifesciencesCanada, Ontario,
CA$80,000.00 yearly
Full-time
For over 50 years, the Critical Care business within Edwards Lifesciences (NYSE : EW) has operated at the intersection of groundbreaking medical innovation and improved patient care.Put simply, we e...Show moreLast updated: 30+ days ago
Nurses Specialized in Wound, Ostomy and Continence

Nurses Specialized in Wound, Ostomy and Continence

Closing the Gap Healthcare GroupHalton, Ontario, CA
CA$35.52–CA$50.85 hourly
Permanent
Title : NSWOC Nurse (Wound Care Nurse).Various Location(s) : Mississauga, Halton, GTA, Central, Dufferin.Closing the Gap Healthcare (CTG) is dedicated to providing Canadians with the highest level of...Show moreLast updated: 30+ days ago
Clinical Provider (Ontario, Canada)

Clinical Provider (Ontario, Canada)

IntellectON, CA
Remote
Quick Apply
Are you passionate about making a difference in mental health? Join Intellect as a Clinical Provider, where you’ll play a vital role in supporting clients on their journeys toward better mental hea...Show moreLast updated: 29 days ago
Orthodontics Clinical Specialist

Orthodontics Clinical Specialist

Straumann GroupHalton
CA$62,000.00–CA$73,000.00 yearly
Equal Opportunity and Affirmative Action Employer (US applicants only).Straumann Group is an equal opportunity employer and will not discriminate against any employee or applicant for employment on...Show moreLast updated: 30+ days ago
EAP Clinical Counsellor (Arabic Speaking)

EAP Clinical Counsellor (Arabic Speaking)

Workplace OptionsON, CA
CA$62,000.00 yearly
Full-time
Quick Apply
Who we are : Founded in 1982, WPO is the largest independent provider of holistic wellbeing solutions.Through our customized programs, and comprehensive global network of credentialed providers and ...Show moreLast updated: 22 days ago
Manager, Clinical Product Development Quality Assurance

Manager, Clinical Product Development Quality Assurance

Company is ConfidentialOntario, Canada
14 days ago
Salary
CA$110,000.00–CA$150,000.00 yearly
Job type
  • Full-time
Job description

Manager, Clinical Product Development Quality Assurance

Pay :

110,000 - $150,000 CAD

Job Description : Purpose and Scope :

The primary purpose of the Manager, Clinical Product Development Quality Assurance (DPQA) is to lead the communication, facilitation and execution of the DPQA strategy to ensure high quality and compliant Clinical Trial Materials (CTM) are being manufactured, packaged, labelled, tested and released for clinical use in both regional and global settings.

This position provides Quality Assurance (QA) oversight of the execution of CTM (Clinical Trial Materials) activities associated with manufacture, testing, packaging, and distribution. With limited management support, Leads and progresses QA activities and processes for the identification and resolution of critical issues through risk management.

Serves as QA lead or representative on assigned project teams to provide direction regarding quality and compliance, to escalate compliance issues to management and to oversee completion of assigned quality related action items.

Essential Job Responsibilities :

  • Manages overall Good Manufacturing Practices (GMP) QA support activities for multiple projects requiring CTM support for the manufacturing, testing, packaging and distribution for regional and global products in the development phase, including at third party manufacturers.
  • Responsible for the timely review and approval of Contract Manufacturing Organizations (CMOs), technical documents (e.g. CTM batch records / GMP CTM Documents)
  • Responsible for the timely review and approval of process related deliverables and changes during CTM phases.
  • Manages supplier quality issue resolution by providing product specific knowledge / understanding.
  • With limited management support, leads or supports the development and implementation of quality strategies associated with CTM.
  • Responsible for the timely review and approval of process related deliverables and changes during CTM phases.
  • Manages the development of new CTM Quality Agreements and facilitates periodic review of established CTM Quality Agreements with limited management support.
  • Leads routine supplier audits. Participates in audits related to CTM new product introductions and new Supply Chain initiatives. Supports the CMO during regulatory authority inspections specific to product / project when necessary.
  • Promotes product transition to CMC Product QA Commercial Readiness group through close communication and collaboration toward the product launch in each region.
  • Promotes cohesive coordination and communication across functional areas in support of on-time delivery of CTM.
  • Supports both regional and global new product introduction initiatives and responsible for building strong relationships across multi-functional disciplines.
  • Serves as global QA representative on assigned project teams to provide direction regarding quality and compliance, to communicate compliance issues to management and to oversee completion of quality related action items.
  • Evaluates development and / or implementation of local and global process improvement within Quality Assurance.
  • With minimal management support, provides GMP and process improvement guidance to key stakeholders for processes governed by regulatory compliance requirements throughout the product development lifecycle.
  • Supports the establishment of standards in support of quality systems and interfaces across multiple departments and levels of management. Authors / revises departmental Quality System Documents as necessary.
  • Participates in the periodic review of Quality System documentation and contributes to management review activities.
  • Participates in Quality meetings (Regional and Global) and communicates with appropriate QA personnel or key stakeholders regarding project specific information. Provides direction with management guidance for developing best practices and process improvements for project success.
  • Leads or participates in assigned QA Working Teams which impact DPQA activity.
  • Consistently promotes high standards through example and leads the team in a manner so each team member understands the standards and behaviors expected relative to quality and compliance.
  • Performs other duties as assigned or special projects as needed.
  • Qualifications :

Required :

  • BA / BS in a science or engineering related field, with a minimum of 6 years of pharmaceutical industry experience (in biologic, cell therapy or parenteral manufacturing) in either CMC, GMP, GCP, Process Validation, QC and / or QA.
  • In-depth knowledge of GMPs relating to product development, manufacturing of Investigational Medicinal Product and other relevant regulations including licensing of GMP sites for commercial products, as required, with a broad knowledge of quality principles and industry trends
  • Strong written and oral communication and interpersonal skills, facilitation, and influencing skills with an ability to effectively work across the groups and with external stakeholders
  • Able to communicate verbally and in writing in English
  • GMP auditing experience required. Ability to represent to external stakeholders during vendor audits and during interactions with regulatory agencies
  • Must be a self-starter, proactive and have the ability to manage workload to achieve the desired outputs on a daily basis
  • Has applied industry knowledge and interpretation to anticipate global impact and contribute ideas for strategies and tactics to ensure adequate long-term planning for the Quality Assurance function
  • Has developed / executed quality strategies with management guidance
  • Can make decisions for the department in his / her area of quality expertise with management oversight
  • Willingness to travel
  • Preferred :

  • Applied knowledge of global industry standards and regulatory requirements (US, EU and Japan)
  • Direct experience in CTM manufacturing and supply.
  • Applied knowledge in Biologics, Parenteral, Combination Products and / or Advanced Therapeutic Medicinal Products or new modalities
  • Experience in a pharmaceutical manufacturing preferred
  • Benefits :

  • Medical, Dental and Vision Insurance
  • Generous Paid Time Off options, including Vacation, Sick time, plus national holidays including Heritage Days, and Summer and Winter Breaks
  • RRSP match
  • Company paid life insurance
  • Annual Corporate Bonus and Quarterly Sales Incentive for eligible positions
  • Long Term Incentive Plan for eligible positions
  • Referral bonus program