Skip to content

Open nowPosted yesterday

(ASSOCIATE) QUALITY MANAGER

Bracco164 open roles

Where
CHN - Shanghai
Get the CV for this job

From $25 per CV, paid once. No subscription.

Your applicationOpen now(ASSOCIATE) QUALITY MANAGERBracco · CHN - Shanghai
  1. YouYes, apply to this one.

  2. CV RocketCV written for this posting.

  3. 25 readersRecruiter, hiring manager, skeptic. Round after round.

  4. CV RocketApplied on Bracco's own form.

The reply lands in your private mailbox

3×more interviews than doing it yourself with ChatGPT.

The clock on this job

Early applications get read.

13.8% of postings close within 7 days. Measured by our own scanner across the market.

Share of postings closed within
  1. 2.2%1 day
  2. 4.7%3 days
  3. 13.8%7 days
  4. 22.3%14 days
  5. 37.8%30 days
  6. 59.0%60 days
This job: posted yesterday

The posting

Bracco is an international Group active in the healthcare sector and a leader in diagnostic imaging. The Group’s main products are contrast agents sold in over 100 countries, both directly and indirectly through branches, joint ventures and license and distribution agreements.

Responsible for the day-to-day operation, maintenance, and improvement of the company’s medical device quality management system (QMS) and quality management of distribution activities, ensuring compliance with Chinese medical device GMP, GSP, ISO 13485, and company QMS requirements. Collaborate with relevant departments on design and development quality support and post-market quality management within assigned responsibilities.

Key Responsibilities

1. Manage the implementation and maintenance of the QMS in accordance with ISO 13485, applicable regulatory requirements, and company procedures. Oversee document and record control, change control, quality training, and corrective and preventive action (CAPA); monitor process performance and quality objectives; and coordinate and follow-up actions to maintain QMS effectiveness and drive improvement.

  • Provide quality support for medical device design and development as needed, helping project teams implement applicable QMS requirements.

3. Plan and conduct internal audits and supplier audits, ensure that audit findings are investigated, audit findings follow up are implemented within timelines, effectiveness verification and closure.

  • Coordinate the assessment and disposition of nonconforming products and quality deviations, ensuring required documentation, approvals, and follow-up actions are completed.

5. Oversee quality operations across the distribution, including qualification review for suppliers, products, and customers; oversee outsourced storage and transportation providers; and ensure effective product preservation, traceability, and control of distribution records.

6. Manage complaint handling and adverse event monitoring processes, including intake, evaluation, investigation follow up, reportability assessment, regulatory reporting, and post-market quality data and trends analysis.

7. Coordinate quality and safety risk review and cross-functional assessments of manufacturing, distribution, and post-market quality risks.

8. Monitor applicable medical device legislation, regulations, standards, and regulatory guidance. Coordinate changes assessment, implementation of necessary procedural updates, training, and compliance actions.

9. Other quality management duties assigned by the line manager.

Qualifications

Education and Experience

1. Bachelor’s degree or higher in medical devices, biomedical engineering, electronic engineering, automation, mechanical engineering, software engineering, medicine, pharmacy, bioengineering, quality management, or a related discipline.

2. At least 5 years of relevant experience in medical device quality management.

3. Experience in active medical devices, software quality management, or MAH management is preferred.

Professional Knowledge and Competencies

1. Strong working knowledge of ISO 13485 and applicable Chinese medical device regulatory requirements, with the ability to translate regulatory and quality system requirements into effective operational controls.

2. Strong cross-functional leadership, communication, and coordination skills, with a structured approach to root cause analysis, risk-based decision-making, and problem-solving.

3. ISO 13485 internal auditor or auditor certification is preferred.

Contract type:

Fixed Term

If you meet the requirements of this opportunity and would like to join an international group working to improve patients' lives, apply now!

At Bracco, we believe in the values of diversity and inclusion. We respect and celebrate the diversity of our people and their experiences, ensuring a fair opportunity for all.

We are #Bracco #JoinUs

From $25, paid onceGet the CV for this job

What happens when you press

One press. We do the rest.

  1. A CV for this posting

    Written against Bracco's own wording, from every piece of relevant proof in your profile.

  2. 25 readers review it

    Recruiter, hiring manager, skeptic and more read every draft, round after round. You get the best round.

    The review screen in CV Rocket: how each CV was read, round by round.
  3. We apply on Bracco's form

    Our application engine gets through the hardest forms there are. Where a question needs you, AI suggests the best answer. Don't want us applying from our IP addresses? Use our Chrome extension: we apply straight from your own browser.

    An application in CV Rocket: every answer filled in on the employer's form.
  4. Every reply, sorted

    Bracco's answer lands in your private mailbox, and we classify it on arrival: interview, question, rejection.

    The CV Rocket inbox: each employer reply classified as an interview, an action or a rejection.
  5. Reply with AI

    AI helps you write the email, checks it and sends it. We show you whether the recruiter read it.

  6. The interview in your calendar

    Full integration with your calendar. The invitation goes straight in.

    An interview invitation in the CV Rocket inbox, added to the candidate's calendar.
Get the CV for this job

From $25 per CV, paid once. No subscription.

Why it works

3×

more interviews than doing it yourself with ChatGPT.

ChatGPT writes a CV and never learns what happened to it. We see every reply. For each CV we know:

  • How it was written, and how the review scored it
  • When we applied, and how long after the posting went up
  • Which posting, which company, which city
  • Who got the interview, and who heard nothing

That is how we know which CVs get called.

Get the CV for this job

From $25 per CV, paid once. No subscription.

The numbers game

More applications. More interviews.

Every application goes out with its own CV, written for that posting and paid once. Send enough of them and the law of large numbers finds you the job.

By hand5–10
With CV Rocket100
applications a day

Nearby

Live postings like this one

Same employer first, then the same role elsewhere.

Before you press

Straight answers

Get the CV for this job

From $25 per CV, paid once. No subscription.

What if my background isn't good enough?

We make the most of the background you have. The CV uses every piece of relevant proof your profile holds, and one of the 25 readers reads your whole profile and flags what the CV left out.

Do you really apply for me?

Yes, on the employer's own form, the hardest ones included. Where a question needs you, you answer it right there and AI suggests the best answer. Don't want us applying from our IP addresses? Use our Chrome extension: we apply straight from your own browser.

Is it a subscription?

No. You pay once per CV, from $25. Every application goes out with its own CV, written for that posting.

One job. One CV.
Paid once.

Pick the posting you want. We write for it, apply for you and catch the reply.

Get the CV for this job

From $25 per CV, paid once. No subscription.