About this opportunity
Work Your Magic with us!
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.
United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.
Your role:
Assist to set up and maintain operation quality document system, guide and monitor document execution, make sure NTLC meets the requirement of GSP and company standard.
Responsible for products inspection and release, be strictly follow with the standards, methods and sampling principles stipulated by GSP, inspect the products purchased and sold return etc. and complete inspection and acceptance record in time.
Responsible for quality operation monitoring, guide and supervise the quality management during processes like purchase, storage, maintenance, sales, rejection, transportation, etc.
Responsible for warehousing quality monitor, including periodic onsite quality check, communications with LSP, quality KPI monitor etc.
Support the investigation, handling and report of quality incident (deviation).
Responsible for non-conforming products confirmation and process supervision.
Product Returns: assessment of product returns and supporting information to verify if products are suitable for return to saleable status or destruction.
Organize and coordinate validation and calibration related activities, to ensure completion in time and compliance with regulatory and company requirements.
Organize and coordinate the training of business operation.
Support the internal and external audits.
Support supplier and distributor qualification and audit.
Responsible for quality management and quality guarantee capability of the carrier authorized for transportation.
Monitor T&T system implementation
Responsible for local quality index data collection and follow-up, report to management team as required.
To recognize a reportable Adverse Event (AE) or Safety Information and ensure the information is forwarded to the Local Patient Safety Person (LPS) in company, Inc. within 24 hours.
Keep well relationship with stakeholders.
Backup for the other quality members.
Who are you:
Bachelor's degree or above in pharmacy, biology, chemistry, medicine, or other related areas
Licensed Pharmacist. is preferred
Good English skill at reading, writing, listening, and speaking
Above 3 years' quality experience in GMP or GDP (GSP) area is preferred
Good communication skills in both scientific and non-scientific information
Professional knowledge in GSP, GMP and GDP
Problem solving ability and skills
Ability to face challenges and self-learning
Teamwork
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!
Job details
How this role compares
Computed from every other active Quality role in our database, not just this employer's listings.
We currently track 757 comparable Quality roles across 94 biopharma companies.
Salary context
145 of 757 peers report a salary range (USD, annualized)
Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.
Where these roles are based
Top locations among the 757 comparable roles
+ 42 more countries
Seniority mix
350 of 757 peers have a known seniority level
Therapeutic area mix
1 of 757 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Similar opportunities
The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.
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How we calculate "similar"
No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.
Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.