Quality Specialist, Product Quality

For over 50 years, SCIEX has been developing groundbreaking technologies and solutions in mass spectrometry and capillary electrophoresis. Our products enable our customers to quickly respond to environmental hazards, better understand biomarkers relevant to disease, improve patient care in the clinic, bring relevant drugs to market faster and keep food healthier and safer. At SCIEX, you’ll find a rewarding role that amplifies your impact on the world and helps you realize life’s potential.

SCIEX is one of 10 Life Sciences companies of Danaher. Together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health.

**Purpose of this role**:
This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following:
Perform outgoing product release (Device History Records buy-off) and inspection on instruments according to documented procedures.
Work with process owners to support the resolution of non-conformances detected at outgoing product release & inspection.
Generate charts/ trends of outgoing product release & inspection performance.
Analyze quality data, correctly interpret results and make appropriate recommendations where applicable.
Maintain & comply with the requirements of ISO9001, ISO13485, FDA 21 CFR Part 820 and other applicable regulatory requirements.
Support external and internal audit for product release compliances.
Escalate process and procedural gaps to the process owners/SMEs for continual improvements.
Update procedures where applicable.
Ensure compliance, within area of concern, to all relevant EHS regulatory requirement and SCIEX safety policies, procedures, and guidelines
Other duties/ ad hoc tasks as assigned.

Why you?

**Basic Qualifications**:
We are looking for professionals with these required skills to achieve our goals:
Diploma/ ITE in Engineering or equivalent.

1-2 years of relevant working experience in QA

Ability to read technical drawings and experience in writing procedures to QMS requirements.

**Preferred Qualifications**:
**If you have the following experiences, it would be a plus**:
Experience with working in a manufacturing environment is preferred.

Knowledge of the following QMS standards - ISO9001 QMS, ISO13485 QMS and FDA 21 CFR Part 820 is strongly desirable.

Knowledge in using measuring tools/ equipment like CMM, smartscope & vernier calipers, etc., will be an advantage.

When you join us, you’ll also be joining Danaher’s global organization, where 69,000 people wake up every day determined to help our customers win. As an associate, you’ll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System tools and the stability of a tested organization.

Danaher is committed to a diverse and inclusive culture where everyone feels they belong and all voices are heard. We believe in our associates and the unique perspectives they bring to every challenge, which is why we’ll empower you to push the boundaries of what’s possible.

If you’ve ever wondered what’s within you, there’s no better time to find out.

When you join us, you’ll also be joining Danaher’s global organization, where 80,000 people wake up every day determined to help our customers win. As an associate, you’ll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System tools and the stability of a tested organization.

At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

If you’ve ever wondered what’s within you, there’s no better time to find out.