Design Quality Assurance Engineer II Jobs

Apply technical skills including sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues.

Utilize standard statistical analysis and problem-solving techniques to determine product acceptance and evaluate process capabilities.

3+ years of relevant work experience

Demonstrated interpersonal skills with ability to work within a team environment

Experience in the medical device industry

Training experience to FDA regulations or ISO standards

Strong analytical, time management and organizational skills.

Lead / Manage special projects that require collaboration with cross-functional teams and Teva Global Affiliates.

Good working knowledge of SAP, LIMS, Track wise, Excel and Word.

Interpersonal skills: Educates internal and external customers on facts by taking into account differences in level of understanding, needs, and expectations.

Excellent verbal and written communication skills.

Perform release of Teva affiliates and 3rd party products to market.

Technical proficiency gained through education and/or business experience.

Reviews, evaluates, and derives requirements for testability.

Designs, develops, executes, and maintains testing strategies and plans to ensure stability and efficiency, enabling a seamless customer experience.

Proactively provides improvement opportunities to the team to enhance the customer experience.

Drives the testing automation capabilities.

Broader work or accountabilities may be assigned as needed.

Bachelor's degree in computer science or any combination of equivalent education and experience.

Examine, analyze and assess requirements to prepare test plans and test cases.

Minimum 3-5 years of experience as a quality assurance analyst in an innovative environment within a large organization.

Skills sought: Integrity, respect, committed, responsible, customers and results oriented.

Knowledge of the insurance sector, an asset.

An extensive flex pension and benefits package, with access to virtual healthcare

Working knowledge of and experience of Good Manufacturing Practices, Quality Management Systems (ISO Standards)

Adhere to all requirements of the Quality Management System.

Skilled interpersonally; strong negotiation and conflict management skills

Comply with the Health & Safety policies of the company and inform Management of unsafe working conditions.

Understanding and working knowledge of Medical Device Quality Systems (ISO 13485) and Regulatory Requirement.

Demonstrated experience in resolving complex problems

Experience with Project Management an asset

4-8 years’ experience with downhole tools, design and applications

Solid understanding of design process as well as knowledge of tool assembly and functions

Experience in Research& Development (R&D) processes an asset

Knowledge of Packers Plus technologies and procedures an asset

Minimum 2-year Diploma or Degree in Engineering (Mechanical, Chemical, Petroleum or other related field) or equivalent experience

Apply technical skills including sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues.

Utilize standard statistical analysis and problem-solving techniques to determine product acceptance and evaluate process capabilities.

3+ years of relevant work experience

Demonstrated interpersonal skills with ability to work within a team environment

Experience in the medical device industry

Training experience to FDA regulations or ISO standards

Serve in a backup capacity to QA Manager and other QA Specialists for their respective responsibilities.

3 years of relevant experience in pharmaceutical industry (QA, QC, Production or equivalent)

Extensive knowledge of Canadian GMPs especially for importer and distributor

Excellent analytical and problem-solving abilities

Good communication skills (verbal and written)

Plan and coordinate product release activities.

You will report progress and status through regular communication with appropriate managers and other team members.

You are a mentor for peers, assisting with and growing their knowledge.

5+ years of applicable work experience.

In-depth knowledge of software development practices, including both agile and waterfall methodologies.

Experience working within a continuous delivery or continuous deployment model.

Experience with bug prevention and containment strategies.

Purchase material and track inventory of all safety and janitorial supplies with working knowledge of EAM

Bachelor's degreewith 2+ years in food industry or anAssociate'sdegree with 5+ years of experience in food industry

Critical thinking /problem solving. Thorough knowledge of CAPA process

Good communication skills with peers and productionpersonal

Computer skills including Word, Excel, Outlook and Microsoft AX

Excellent oral and written communication skills.

Prepare, Update Design Quality Management Plan ( DQMP).

Coordinate with designer’s quality managers and ensure that the constructability review and design interface are being done.

Excellent problem solving and analytical skills.

Experience overseeing the quality of the design of a project within the field of rail and transit, transportation and infrastructure.

A six-kilometre tunnel and associated tunnelling works from Exhibition to Don Yard portal (west of the Don River)

One above-ground station to be integrated with the existing GO Transit Exhibition Station

·Provide management with status updates on assigned responsibilities and goals and escalate issues in a timely fashion.

·Lead product risk management activities.

·Coordinate team with respect to project demands and facilitating program management functions.

commensurate with education and experience. This is an ESOP eligible role.

We are seeking an experienced

·Ensuring project requirements are clearly identified and stakeholders are kept informed of project status.

Basic knowledge of Quality Management systems and standards (i.e.: GMP, ISO 13485, ISO 9001).

You will release or quarantine product in accordance to client or Kuehne+Nagel instructions and regulatory requirements.

You will support product complaint/inquiry requests or investigations in accordance to client or Kuehne+Nagel requirements.

Experience with GMP's, GDP's, licencing, Federal and Provincial regulations.

You will assist the flow of Operations including Inbound, Returns, Destruction, Outbound, Retention etc. where Quality support may be required.

Train and oversee level I staff as assigned