Senior Manager Quality Assurance (mfd)

Stryker; Grenoble; Sur place; EUR 70 000 - 90 000; Plein temps

Résumé du poste

A global leader in medical technology is seeking a Senior Manager to lead quality control at their manufacturing site in Grenoble. The ideal candidate will have 9-10 years of experience in quality processes within regulated industries and a minimum of 4 years in a management role. Responsibilities include establishing quality standards, leading audits, and developing a high-performing team. This position offers a competitive salary, career development opportunities, and a collaborative work environment.

Prestations

Competitive salary and benefits

Career development opportunities

Engaged and inclusive teams

Recognition of performance

Employee Resource Groups (ERGs)

Qualifications

• 9-10 years professional experience as quality process expert in regulated industry.
• 4 years minimum experience as people manager.
• Experience leading audit processes is essential.
• Knowledge of regulatory requirements and standards.

Responsabilités

• Part of the site leadership team responsible for quality activities.
• Lead a team providing technical guidance and direction.
• Develop and implement quality standards and assurance strategies.
• Ensure compliance on every stage of the process.
• Collaborate with business partners at Stryker.

Connaissances

Continuous Integration

Quality Assurance

FDA Regulations

Root cause Analysis

TFS

Food Processing

ICH Q10

Jira

Software Testing

Quality Management

Selenium

Github

Formation

Degree in Engineering Science discipline or equivalent

Business Management or MBA (advantage)

Description du poste

Work Flexibility : Onsite

• Envoyez votre CV en anglais.

Who we want

People developers. Leaders who can coach develop and retain strong talent while providing meaningful growth opportunities for analysts.

Process drivers. Those who spot opportunities to simplify standardize and automate and can successfully implement new processes at scale.

Strong communicators. Individuals who can move seamlessly between the details and the big picture proactively keeping stakeholders informed and ensuring clear concise updates at all levels.

Business partners. People who collaborate cross-functionally build strong relationships and align financial processes with business needs.

What will you do

You will be part of the site leadership team and you will be responsible for all quality related activities at our manufacturing plant in Montbonnot.

You will lead a team of a multiple high performing quality individuals across disciplines that provides technical guidance / direction to the manufacturing and other functional areas.

You will develop and implement quality standards quality assurance strategies and regulations. Furthermore you ensure and execute compliance on every stage of the process.

You will take responsibility for all quality control aspects of the process (operations raw materials production finished product).

In your role you will strongly collaborate with business partners within Stryker to define expected quality standards and the role and responsibilities in the maintenance of these standards.

You will ensure that the organizations conformance and commitment to producing products meets or exceeds customer requirements and the relevant regulatory standards.

You will be responsible for establishing a state of audit readiness and support successful regulatory audits and inspections.

Most importantly! You will have the mission to continue to develop the team to support their career growth and promote a healthy working environement.

What will you need

You have a degree in Engineering Science discipline or equivalent. Business Management or MBA is an advantage.

You have at least 9-10 years of professional as quality process expert ina regulated industry(Medtech Pharma Food Automotive other regulated manufacturing environment).

You have minimum of 4 years experience as people manager.

You have experience leading audit processes.

Ideally you have a profound knowledge of regulatory requirements standards and regulations with experiences of managing inspections / audits by international authorities.

Your excellentEnglish and Frenchlanguage skills enable you to collaborate with stakeholders on a global basis.

What we offer

We grow talent. At Stryker we offer great personal and internal career development for our employees with the possibility to make both vertical and lateral position movement.

Team spirit & engagement. We create engaged and inclusive teams that encourage colleagues to share their diverse perspectives and opinions.

Competitive salary and Benefits. With us you will receive a competitive salary and benefits commensurate with your job.

Recognition of your performance. At our company outstanding individual and cross-functional team performance is rewarded. Ideas projects or other exceptional achievements can be submitted for various awards on a local and global level.

Employee Resource Groups (ERGs). Our ERGs are dedicated to fostering an inclusive diverse and supportive workplace environment. They provide opportunities for development networking and collaboration and are open to all employees. Our ERGs are committed to promoting inclusion and belonging helping every individual thrive and contribute to our shared success.

Are you ready to lead and inspire a high-performing quality team at a global leader in medical technology Stryker is seeking a dynamic and strategic leader for our manufacturing site in Grenoble.

Join us in transforming healthcare through innovation and excellence making a tangible impact on patient outcomes worldwide!

Travel Percentage : 20%

Required Experience :

Senior Manager

Key Skills

Continuous Integration,Quality Assurance,FDA Regulations,Root cause Analysis,TFS,Food Processing,ICH Q10,Jira,Software Testing,Quality Management,Selenium,Github

Employment Type : Full-Time

Experience : years

Vacancy : 1