7 meilleures offres (quality analyst, pickering, on) (à pourvoir)

Quality Analyst
Steris —Whitby, ON
- De 66 000 $ à 84 000 $ par an
- Temps plein
- Baccalauréat
- Assurance Dentaire
- Congés payés
Laboratory Analyst Level 1
Shields Pharma Inc. —Markham, ON
- De 40 000 $ à 50 000 $ par an
- Temps plein
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Assurance Dentaire
- Assurance Vision
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Laboratory Analyst with expertise in LCMS
Shields Pharma Inc. —Markham, ON
- De 60 000 $ à 65 000 $ par an
- Temps plein
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Assurance Dentaire
- Assurance Vision
Postuler rapidement
Production Scheduling Analyst
ProAmpac —Markham, ON
- De 75 000 $ à 90 000 $ par an
- Temps plein
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Junior Payments Quality Assurance Analyst Co-Op
NRT Technology Corp. —Toronto, ON
- Contrat
- Informatique
- Ingénierie
- Anglais
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Senior ERP LN TP Project and Planning Analyst
Armstrong Fluid Technology —Toronto, ON
- De 70 000 $ à 120 000 $ par an
- Temps plein
- Informatique
- Ingénierie
- Systèmes PGI
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il y a 9 jours
AI Tester / AI QA Analyst
MCI Careers —Canada
- Informatique
- Service à la clientèle
- Ingénierie

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Process Analyst
GTT, LLC —Toronto, ON
Strong communication skills high degree of stakeholder interaction including front office and business operations. Knowledge of current and emerging trends.
De 25 $ à 30 $ de l’heure
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Quality Analyst
Steris —Whitby, ON
Instruct other STERIS employees in quality principles, effective corrective actions, and valid statistical techniques.
De 66 000 $ à 84 000 $ par an

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Je souhaite recevoir la dernière alerte emploi pour les postes de ce type : quality analyst (pickering, on)

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Quality Analyst

Steris -
Whitby, ON

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Détails du poste

Temps plein
De 66 000 $ à 84 000 $ par an

Profil recherché

Baccalauréat

Description complète du poste

Position Summary

The Quality Analyst is responsible for assisting in administration of the quality management system at a site to assure adherence to ISO 9001, ISO 13485, FDA 21 CFR Part 820/211, EU GMPs, ISO 17025, ISO 11137 and/or ISO 11135 and other applicable regulatory standards. This role leads complaint/CAPA investigations, supplier quality improvement initiatives, continuous improvement initiatives and countermeasures with the use of statistical techniques and other accepted quality principles. This role executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. The Analyst also supports production and quality operations by coordinating and performing problem-solving investigations, pre-reviews and final acceptance/run release of processing runs that contain non-conformances. Responsible for the activities related to quality and regulatory compliance to ensure all product processing requirements are met in accordance with Customer specifications including calibrations, dosimetry results, generation of test methods, audits, scheduling, validations, record keeping and reporting.

What You'll Do as a Quality Analyst

Coordinate day-to-day tasks and direction for Quality Technicians/Senior Quality Technicians by providing technical support, mentoring and oversight.
Responsible for oversight of all product and/or report pre-reviews and releases conducted by Quality Technicians/Senior Quality Technicians.
Responsible for executing product and/or report releases for all processing runs/lab samples containing a non-conformance, including management of Customer communication and leading the associated non-conformance investigations.
Initiate and/or participate in corrective actions, problem-solving and continuous improvement activities.
Perform internal audits at other AST facilities, including identification of non-compliances and report generation. Responsible for managing remediation of internal audit observations assigned by site Quality Manager.
Manage creation of new quality system policies and procedures and revisions to existing policies/procedures.
Review collected data to perform statistical analysis and recommend process changes to improve quality.
Monitor and report on performance metrics.
Instruct other STERIS employees in quality principles, effective corrective actions, and valid statistical techniques.
Collaborate with other departments and facilities within the company on quality related issues.
Lead quality system programs (i.e. calibration, maintenance, training, CAPA, complaints, non-conformances, supplier quality, management review, operational qualifications,
document control, change control, risk management, etc).
Overall responsibilities include commitment to ensure external and internal requirements are met according to documented policies, procedures, standards and regulations.
Perform other duties as assigned

The Experiences, Skills, and Abilities Required

Bachelor's degree in science or related technical field.
1-5 years of combined Manufacturing/Quality Engineering and/or Quality Systems experience.
1-5 years of experience with medical devices or other regulated industries preferred.
1-5 years of experience working in an ISO certified environment required.
Working knowledge of FDA QSR/ EUGMP regulations strongly preferred.

What STERIS Offers

This is an opportunity to join a company that will invest in you for the long-term. STERIS wouldn’t be where it is today without our incredible people, who take true pride in their work. That’s why we share in our success together by rewarding employees for their hard work. We do this by providing competitive base salary plus bonus (as applicable), comprehensive benefits package that includes medical, dental, vision, paid PTO and holidays, 401K with company match.

#LI-BN1

This posting is for an existing vacancy within our organization.

Pay range for this opportunity is $66,000 - $84,000. This position is eligible for bonus participation, with an annual bonus opportunity of [ENTER PERCENTAGE]% of your fiscal year compensation, subject to the Bonus Plan’s terms and conditions.

STERIS strives to be an Equal Opportunity Employer. STERIS is committed to treating all people in a way that allows them to ‎maintain their dignity and independence. We believe in integration and equal ‎opportunity. Accommodations are available throughout the recruitment process ‎and applicants with a disability may request to be accommodated throughout the ‎recruitment process.‎ We will work with all applicants to accommodate their individual accessibility ‎needs.

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Laboratory Analyst with expertise in LCMS

Production Scheduling Analyst

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Je souhaite recevoir la dernière alerte emploi pour les postes de ce type : quality analyst (pickering, on)

Position Summary

What You'll Do as a Quality Analyst

The Experiences, Skills, and Abilities Required

What STERIS Offers

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