Quality control supervisor Offres d'emploi - North York, ON
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Quality control supervisor • north york on
Dernière mise à jour : il y a 12 heures
Our client is a Health Canada licensed distributor of medical grade liquid nitrogen providing on-demand and regular and continuous services to hundreds of clients across Ontario.Their on-site Quali...Voir plusDernière mise à jour : il y a 3 jours
Are you a financial professional with previous experience in the banking / finance industry? Do you have previous experience handling KYC and AML activities? Are you looking for an opportunity to fur...Voir plusDernière mise à jour : il y a plus de 30 jours
Reporting to the QC Manager, the QC Specialist will accurately complete physical product inspections to ensure that quality standards and business operating standards are met and aligned with legis...Voir plusDernière mise à jour : il y a plus de 30 jours
Work in a packaging company inspecting printed packages.Please text 4164004066 if interested.Voir plusDernière mise à jour : il y a 12 heures
Part-Time Quality Control Position (4 Hours)Location : Woodbridge (Martin Grove & Hwy 7 area)Are you a mom looking for part-time work while the kids are at school? We have the perfect opportunit...Voir plusDernière mise à jour : il y a 12 heures
Experience : 3 years to less than 5 years.Co-ordinate activities with other work units or departments.Ensure smooth operation of computer equipment and machinery.
Requisition or order materials, equi...Voir plusDernière mise à jour : il y a 24 jours
College, CEGEP or other non-university certificate or diploma from a program of 1 year to 2 years.Retail / wholesale establishment / distribution centre.
Develop specific plans to prioritize.Organize ta...Voir plusDernière mise à jour : il y a plus de 30 jours
Webuild is an international construction company of civil engineering pioneers who have been at the forefront of the construction business for 120 years.
We are a global player with Italian roots sp...Voir plusDernière mise à jour : il y a 8 jours
Heures de travail : 32 to 35 hours per week.College, CEGEP or other non-university certificate or diploma from a program of 1 year to 2 years.
Co-ordinate activities with other work units or departme...Voir plusDernière mise à jour : il y a 9 jours
By joining the Bio-Techne team you will have an impact on future cutting-edge research.Bio-Techne, and all of its brands, provides tools for researchers in Life Sciences and Clinical Diagnostics.Th...Voir plusDernière mise à jour : il y a plus de 30 jours
Our client, a global consulting firm, is looking for a Quality Control Analyst to join their team.This is a fully remote position starting off as a 6-month contract.
Perform In-Line QC function to e...Voir plusDernière mise à jour : il y a plus de 30 jours
Education : Secondary (high) school graduation certificate.Experience : 1 year to less than 2 years.Supervise, co-ordinate and schedule activities of production workers who operate processing machine...Voir plusDernière mise à jour : il y a plus de 30 jours
Education : No degree, certificate or diploma.Experience : 3 years to less than 5 years.Develop specific plans to prioritize.
Organize tasks to accomplish the work.Co-ordinate activities with other wo...Voir plusDernière mise à jour : il y a plus de 30 jours
Recruitment & Search Firm specializing in identifying, & sourcing top performers for our clientele.Our clients include industry leading organizations who partner with us to be an extension ...Voir plusDernière mise à jour : il y a 2 jours
Come Build Your Career at Aecon!.As a Canadian leader in infrastructure development, Aecon is and building what matters for future generations to thrive! We lead some of the most impactful infrastr...Voir plusDernière mise à jour : il y a plus de 30 jours
Clean and safe work environment.Conduct inspection in the production areas.Report inspection results to supervisor.May train, or assist others in performing assigned work.To maintain written entrie...Voir plusDernière mise à jour : il y a plus de 30 jours
Oversee operational logistics of the organization.Plan and organize operational logistics of the organization.Co-ordinate activities with other work units or departments.
Co-ordinate, assign and rev...Voir plusDernière mise à jour : il y a plus de 30 jours
Job Title : Quality Inspector Department : Quality Assurance Reports To : QA Manager, works alongside the QA Engineer Location : Process Products International Ltd, Markham OntarioJob Summary : The Quali...Voir plusDernière mise à jour : il y a 12 heures
Our ability to deliver uncompromising quality, precision products, on time and at a fair price truly sets us apart from our competition.
Our customers around the world know this.Now, it is time for ...Voir plusDernière mise à jour : il y a plus de 30 jours
In this position, the successful candidate will play a central role in managing all aspects related to quality, encompassing both Quality Assurance and Quality Engineering.This role includes suppor...Voir plusDernière mise à jour : il y a plus de 30 jours
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Description de posteMaintain customer information and fill log databases in MS Access. Maintain filing system for all applicable quality records, including but not limited to testing records, distribution records, and maintenance records. Ensure that quality related records are maintained for required duration. Investigate or participate in the investigation of every complaint on quality or non-conformance that is received and implement corrective action if necessary. Notify the QC manager of the investigation per internal procedures. Conduct product testing as per internal Standard Operating Procedures (SOPs). Review and approve pertinent testing and production documents as per internal SOPs. Review and approve supplier Certificate of Analysis as per Internal SOPs. Release approved product for sale per internal SOPs. Monitor the maintenance of adequate segregation of products in the warehouse. Review sanitation documents per internal SOPs. Ensure all equipment used for QC testing is calibrated per internal SOPs. Review and approve all day-to-day packaging / labelling and distribution related documents. Ensure QC tags are securely stored, and that label sign out logs are completed accurately. Notify the QC manager of any returns, and implement any restocking if approved by the QC manager. Work with warehouse supervisor and technicians to ensure inventory related to licensed activities are maintained and equipment are calibrated per internal SOPs. Monitor other quality control related activities as per internal SOP requirements. Provide regulatory advice to customer accounts when required. Relevant industry experiences – at least two years preferred A diploma from a recognized post-secondary institution in regulatory affairs and quality control for health products is an asset A degree from a recognized post-secondary institution with acceptable specialization in sciences required
Our client is a Health Canada licensed distributor of medical grade liquid nitrogen providing on-demand and regular and continuous services to hundreds of clients across Ontario. Their on-site Quality Control and other experienced personnel present a personal level of experience, to provide the highest quality of product and cost-effective service.
The Quality Control Associate oversees the Q.A. department in quality related distribution activities, testing, and packaging / labelling of medical gas products to ensure full compliance with regulatory and safety requirements. This is an ideal opportunity for those with a few years of experience in Quality Assurance and regulatory affairs to advance their career in this multi-faceted role.
Major Responsibilities
- Maintain Drug Establishment License and Medical Device Establishment License by ensuring annual reviews are submitted on time, and coordinate with accounts personnel to issue payments.
- Host Health Canada audits, including Good Manufacturing Practices (GMP), Pharmacovigilance (GVP) and Medical Device audits, and provide corrective action reports for company management review.
- Provide scientific and / or regulatory advice to company management.
- Review QC related contract changes and amendments.
- Write, revise and maintain all Standard Operating Procedures (SOPs) on Medical Gas and Medical Device distribution related activities.
- Review and approve changes to labels, Certificate of Analysis, and other packaging / labelling documents to ensure compliance with regulations.
- Review and approve the investigation of customer complaints and non-conformance reports, manage reporting to the relevant regulatory authorities if necessary.
- Provide GMP and SOP training for technicians and QC designates.
- Perform GVP literature searches and maintain reports.
- Conduct internal audits to ensure regulations, safety requirements and internal SOP requirements are met. Provide audit report and suggest corrective actions for company management review.
- Maintain job descriptions and the organizational chart.
Other Responsibilities
Qualifications
Hourly rate dependent on experience : $25 / hour - $28 / hour
Pension matching
Extended health benefits
Casual Dress
This position requires in-person attendance at the office.