Quality Systems Engineer

Reposted 23 Days Ago
Be an Early Applicant
Singapore
In-Office
Mid level
Biotech
The Role
The Quality Systems Engineer will administer the QMS, support quality efforts, facilitate management reviews, and ensure compliance with safety and quality standards.
Summary Generated by Built In

When joining PerkinElmer, you select an experienced and trusted leader in scientific solutions, with the support of a global service network and distribution centers, providing the right solution, at the right time, to meet critical customer needs.  With over an 80+ year legacy of advancing science and a mission of innovating for a healthier world, our dedicated team collaborates closely with commercial, government, academic and healthcare customers to deliver our broad portfolio of analytical solutions, and OneSource services.

Job TitleQuality Systems Engineer
Location(s)
Singapore

To support the Global Quality Systems Leader, and Site Quality Leader to execute the QMS and drive key indicators across the business, in order to maintain site certification. The primary focus is to be the site focal for Quality Systems, and additionally provide guidance and support to the business on Quality Systems related issues.

Responsibilities:

  • Demonstrate knowledge and adherence to site safety requirements.

  • Execute goals & strategy based on company’s business objectives.

  • Administer the site QMS. Including (but not limited to); document control, audit management, management of change, training system facilitation, control of records, and NCR & CAPA facilitation.

  • Facilitate the Site Quality Management Review

  • Support the Global QMS as required.

  • Collaborate as required in site processes, procedures and work instructions.

  • Perform other duties deemed necessary for the effective operation of the QMS.

Qualifications:

  • Bachelor Degree Holder

Experience:

  • Minimum 3 years experience as a Quality Engineer or equivalent

Preferred Characteristics:

  • Experience of Quality Management Systems in a manufacturing environment, preferably ISO 9001:2015

  • Experience of working with an electronic Document Management System

  • Demonstrating strong attention to detail and experience in technical writing (policies, procedures, work instructions etc.)

  • Understanding Root Cause Analysis and Quality tools (including CAPA, and MOC)

  • Experience of participation in Quality Management Review, including compiling data, trend analysis, inputs and addressing resulting actions

  • Demonstrable experience in the audit process (internal and external), including being certified as an internal auditor

  • Strong PC skills including Microsoft Office applications

  • Meticulous

  • Good oral and written communication

  • Strong analytical and interpersonal skills

  • Strong bias for action and results oriented. Ability to prioritize and work independently and proactively is critical for success

  • Self-motivated and able to manage multiple and complex tasks in a fast paced and challenging environment

  • Demonstrates diplomacy, confidentiality and professionalism

Top Skills

Document Management System
Iso 9001:2015
MS Office
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The Company
HQ: Shelton, CT
6,342 Employees

What We Do

For 85 years, PerkinElmer has pushed the boundaries of science from food to health to the environment. We’ve always pursued science with a clear purpose – to help our customers achieve theirs. Our expert team brings technology and intangibles, like creativity, empathy, diligence, and a spirit of collaboration, in equal measure, to fulfill our customers’ desire to work better, innovate better, and create better.

PerkinElmer is a leading, global provider of technology and service solutions that help customers measure, quantify, detect, and report in ways that help ensure the quality, safety, and satisfaction of their products.

Learn more at www.newperkinelmer.com.

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