Total 4 Creative Editor job vacancies in Quality Assurance / Control category in The United States of America

About the company

Pixelogic, a subsidiary of the IMAGICA GROUP, is a global provider of content localization and distribution services for the media and entertainment industry. Built on advanced next generation workflows and operations in Burbank, Culver City, London, Cairo, Cape Town, Seoul and Tokyo,

Pixelogic services the industry’s leading content owners including the major Hollywood studios, broadcasters and digital platforms. Pixelogic services include subtitling and closed captioning, foreign language dubbing, access services, text and metadata translation, audio services, marketing and promotional material design and versioning, digital cinema mastering and key fulfillment, home entertainment mastering, compression and authoring for physical media formats, transcoding and packaging for digital distribution products, archive mastering, and custom software and application development services.

Pixelogic was founded in 2016 as a next-gen media supply chain provider focused on premium localization and distribution services for features and series, including marketing materials such as trailers and TV spots. The company localizes content in over 60 languages and services all worldwide distribution venues and delivery formats. This includes support for digital cinema, physical media (DVD, Blu-ray and Ultra HD Blu-ray) and hundreds of digital media variants. Pixelogic employs nearly 700 full-time employees worldwide.

To support our continued expansion, we are currently looking for “Roll Up Your Sleeves” problem solvers that can work as part of a world-class team. Our work environment is unique. So is the right candidate. This is a fantastic opportunity to join a forward-looking company that offers an exciting, creative and dynamic work environment with tremendous career growth potential.

Responsibilities:

• Responsible for all aspects of subtitle file creation, depending on assignment, whether Conforming, Timing and Spotting, Translating or Proofreading/QC’ing of subtitle files using SST Canvass software and/or Pixelogic proprietary cloud based subtitling software.
• Leverage in-house glossary tool for consistency across products as well as follow client style guide specifications.
• Handle rejections/make corrections in files.
• Meet tight deadlines while maintaining a high standard of quality.
• Manage assignments on a pro-active basis and escalate issues to management.
• Remain current with industry trends and adapt to evolving client requirements.
• Maintain the confidentiality of sensitive content.
• Other miscellaneous tasks as assigned by manager(s).

• Bachelor's or Master's Degree, preferably in Japanese, linguistics and language study majors and/or Entertainment and Media
• Excellent command of English
• Minimum of 2 years of subtitle translation and proofreading experience required
• Knowledge of professional scripting, and subtitling software highly desirable
• Deep sense of urgency and ability to work in a fast-paced environment with high volume.
• Punctuality, dependability, and willingness to adapt to last-minute changes to programming and industry
• Attention to detail and accuracy
• Positive attitude when experiencing obstacles and enthusiastic to get things done
• Ability to follow technical/style guide for multiple client content types
• Must be residing in Tokyo, Japan

(Key Roles)

1 Customer & field return complaints handling & resolution.

Drive for timely identification of root cause and corrective actions plans. Monitor track the effectiveness of corrective action implemented. Internalize and deploy warranty field failure DPPM metrics with alignment to key process improvement including manufacturing, test and development processes

2 Drive subcontractors together with Quality members to build quality into the products through

a) Audits

b) Ensuring system and processes are in placed including but not limited to establishment of critical processes.

c) Deploy effective quality methods and tools across subcon processes

3 Perform evaluations & tests to assess and mitigate risk on Quality issues

4 Participate in new project reviews during development stages and assess product risk

5 Any other Adhoc projects as assigned

(Secondary Roles)

1. Monitor performance of new product quality during development and initial mass production stage

2 Assess new product risk before mass production and readiness of product

3 Review Critical Parts list and Quality plan

4 Conduct periodic team meetings both internal and or subcontractors to align with QA process and address issues with QA tools quality issues & corrective action closure.

5 Set & monitor factories KPIs through quality performance, quality management

6 Conduct system and process audits

7 Work with Subcon to ensure their key suppliers are in compliance of supplied materials

We are looking for a Quality Assurance Specialist who can join immediately to support our quality management system development and implementation, ensuring product development in compliance with ISO 13485 and US Quality System Regulation (QSR). This role will be responsible for daily tasks involving maintaining and our quality processes including but not limited to documentation control, training program, tracking quality performance matrix, and gap analysis.

Responsibilities:

• Quality System Compliance: Ensure adherence to ISO 13485 standards, US QSR and internal SOPs throughout the product development and manufacturing processes.
• Document Control and Change Management: Manage and maintain the document control system to ensure accuracy and accessibility of quality documents. Assist in the development and implementation of quality management policies, procedures, and documentation through change control process.
• Risk Management: Participate in risk assessments and support risk management activities to identify and mitigate potential quality issues.
• Regulatory Compliance: Stay updated on relevant regulatory requirements and standards applicable to medical devices and ensure compliance.
• Quality Audits: Participate in internal and external audits, providing support for corrective and preventive actions (CAPA).
• Supplier Quality: Assist in monitoring supplier and part performance to ensure the quality of components and materials used in the manufacturing process.
• Quality Training: Assist in providing training and guidance to employees on quality assurance practices.
• Non-Conformance Management: Assist in investigating and addressing non-conformance issues, facilitating root cause analysis and corrective actions.
• Continuous Improvement: Contribute to ongoing process improvement initiatives to enhance product quality and efficiency.

Qualifications:

• Diploma or bachelor’s degree with 1-2 years of work experience in a quality assurance role, preferably in the medical device industry.
• Fair theoretical and practical knowledge in ISO 13485 and US QSR.
• Excellent problem-solving and analytical skills.
• Effective communication and interpersonal skills.
• Detail-oriented and able to work independently and in a team.

We are looking for a Quality Assurance Specialist to support our quality management system and ensure product development in compliance with ISO 13485 and US QSR. The ideal candidate should have a background in engineering and 1-2 years of experience in a similar role. This role will be critical in maintaining and improving our quality processes, ensuring the safety and efficacy of our medical instruments.

Responsibilities:

• Quality System Compliance: Ensure adherence to ISO 13485 standards, US QSR and internal SOPs throughout the product development and manufacturing processes.
• Document Control and Change Management: Manage and maintain the document control system to ensure accuracy and accessibility of quality documents. Assist in the development and implementation of quality management policies, procedures, and documentation through change control process.
• Risk Management: Participate in risk assessments and support risk management activities to identify and mitigate potential quality issues.
• Regulatory Compliance: Stay updated on relevant regulatory requirements and standards applicable to medical devices and ensure compliance.
• Quality Audits: Participate in internal and external audits, providing support for corrective and preventive actions (CAPA).
• Test Method Development and Evaluation: Collaborate with cross-functional teams to develop and validate test methods for product quality evaluation.
• Supplier Quality: Assist in monitoring supplier and part performance to ensure the quality of components and materials used in the manufacturing process.
• Quality Training: Assist in providing training and guidance to employees on quality assurance practices.
• Non-Conformance Management: Assist in investigating and addressing non-conformance issues, facilitating root cause analysis and corrective actions.
• Continuous Improvement: Contribute to ongoing process improvement initiatives to enhance product quality and efficiency.

Qualifications:

• Bachelor's degree in Engineering or a related field.
• 1-2 years of experience in a quality assurance role, preferably in the medical device industry.
• Strong knowledge of ISO 13485 and US QSR.
• Excellent problem-solving and analytical skills.
• Effective communication and interpersonal skills.
• Detail-oriented and able to work independently and in a team.