Merck KGaA logo

Digital Products Quality Engineering Lead

Merck KGaASaint Louis, MO

$111,400 - $196,000 / year

Automate your job search with Sonara.

Submit 10x as many applications with less effort than one manual application.1

Reclaim your time by letting our AI handle the grunt work of job searching.

We continuously scan millions of openings to find your top matches.

pay-wall

Overview

Schedule
Full-time
Career level
Director
Remote
On-site
Compensation
$111,400-$196,000/year
Benefits
Health Insurance
Paid Vacation
401k Matching/Retirement Savings

Job Description

Work Your Magic with us! Start your next chapter and join MilliporeSigma.

Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.

Your Role:

Digital Products Quality Engineering Lead is responsible for the strategic guidance and direction of quality assurance and quality control of digital products developed / maintained following Agile framework. You will lead a team of software quality engineers to ensure the digital products meet the quality standards that will enable the end customers to meet their quality and regulatory/validation needs. You will work with cross-functional global teams in various disciplines, promote built-in quality, shift-left practices, continuous verification and enable the software quality engineers to meet the quality objectives of digital products. You are responsible for end-to-end quality assurance and quality control activities for digital products, applying 4 eye principles, managing escalations, solving problems promptly, and fostering a collaborative, high-performance culture.

You are familiar with relevant industry standards and guidance, including GAMP 5 supplier-focused principles and applicable Software related ISO standards, and understand the quality expectations of customers in regulated life-science environments

Can be located in Burlington or St. Louis

Who You Are:

  • You bring 10+ years of combined experience as manager/supervisor level managing; software development / engineering, digital transformation, software quality assurance / control, software quality management, proficiency in life science / pharma regulations/ industry standards / related ISO standards.
  • You have a strong command in software product life cycle, change management, agile ways of product development, DevOps, Lean, Plan-Do-Check-Act, software test automation, risk-based quality management systems, building and developing the team competency/management, cloud-based platforms, implementation experience of CSA-Computer Software Assurance is a plus.
  • You have a proven track record in, shaping digital product's quality engineering, converting challenges into actions to enable faster Go-to-Market Transformation, software operational controls (change, incident, audit support, questionnaire, supplier quality, periodic review, deviations), Continuous Integration and Continuous Delivery software development, communicate with clarity, able to influence software engineering team's quality mindset.
  • You bring hands on experience in, establishing software development processes and its continuous improvement, workflows, template, defining / monitoring key quality indicators, mentoring quality assurance/control team members, design reviews/verification, review of software engineering artifacts (specifications, code/objects, test scripts, executions evidence), product engineering traceability, defect management and corrective/preventive management.
  • You are experienced in ensuring digital product quality meets customer expectations, quality promises, compliance with required/applicable science regulations, industry standards/ benchmark guidance, including GAMP 5 supplier focused principles, related ISO standards, digital product development/lifecycle artifact's inspection readiness, facilitating quality/product audits / inspections, life regulated industry is a plus.
  • Bachelor's or higher degree in Computer Science, Engineering disciplines, Information/ Operational Technology, Digital and Data management or Information Science / Management, Bio-Medical Science, or other Life Science disciplines. Willingness to travel globally based on the need of project and business.

Minimum Qualifications:

Bachelor's or higher degree in Computer Science, Engineering disciplines, Information/ Operational Technology, Digital and Data management or Information Science / Management, Bio-Medical Science, or other Life Science disciplines.

10+ years of combined experience in software development / engineering, digital transformation, software quality assurance / control, software quality management, proficiency in life science / pharma regulations/ industry standards / related ISO standards.

Preferred Qualifications:

Good written and verbal skills.

Excellent computer skills, i.e., Project Planning, Word, Excel, PowerPoint, SharePoint.

Experience with GMPs, GCPs, GLPs, GAMP and Part 11 compliance

Global travel based on the need of project and business.

Pay Range for this position: $111,400-$196,000

The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here.

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Automate your job search with Sonara.

Submit 10x as many applications with less effort than one manual application.

pay-wall

FAQs About Digital Products Quality Engineering Lead Jobs at Merck KGaA

What is the work location for this position at Merck KGaA?
This job at Merck KGaA is located in Saint Louis, MO, according to the details provided by the employer. Some roles may also include multiple work locations depending on the requirement.
What pay range can candidates expect for this role at Merck KGaA?
Candidates can expect a pay range of $111,400 and $196,000 per year.
What employment applies to this position at Merck KGaA?
Merck KGaA lists this role as a Full-time position.
What experience level is required for this role at Merck KGaA?
Merck KGaA is looking for a candidate with "Director" experience level.
What benefits are offered by Merck KGaA for this role?
Merck KGaA offers following benefits: Health Insurance, Paid Vacation, and 401k Matching/Retirement Savings for this position. Actual benefits may vary depending on the employer's policies and employment terms.
What is the process to apply for this position at Merck KGaA?
You can apply for this role at Merck KGaA either through Sonara's automated application system, which helps you submit applications 10X faster with minimal effort, or by applying manually using the direct link on the job page.