Sandoz Posted June 18, 2026

AS&T (Analytical Science & Technology) Manager

Shanghai (Shanghai), China Full time
Quality Manager

Sandoz is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Job Description Summary

We are looking for a proactive, well-connected colleague to join our team as an AS&T (Analytical Science & Technology) Manager. In this role, you will oversee Analytical Product Stewards, ensuring strong analytical support across product lifecycle activities. Your contribution will directly support the Sandoz purpose by enabling reliable supply and patient access to high-quality medicines.

Job Description

Sandoz continues to go through an exciting and transformative period as a global leader and pioneering provider of sustainable Biosimilar and Generic medicines. As we continue down this new and ambitious path, unique opportunities will present themselves, both professionally and personally. Join us, the future is ours to shape!

We are looking for a proactive, well-connected colleague to join our team as an AS&T (Analytical Science & Technology) Manager. In this role, you will oversee Analytical Product Stewards, ensuring strong analytical support across product lifecycle activities. Your contribution will directly support the Sandoz purpose by enabling reliable supply and patient access to high-quality medicines.

Your responsibilities include, but not limited to:

Acts as Single Point of Contact (SPOC) for all AS&T related activities at the assigned External Suppliers.

Lead and implement global AS&T the requirements/programs in the assigned ESO QA Network and act as project lead in cross functional ESO AS&T project teams.

Lead and own analytical method transfers (AMTs) process within ESO. Support the external suppliers selection process, qualification process and analytical trouble shooting as needed.

Support the regulatory team in submissions, variations and other regulatory activities from an analytical perspective. Support assessments of analytical Change Control records for acceptability. Define studies needed to support the changes.

Support Quality Assurance Manager (QAM) to define and maintain the ESO Stability Program at CMOs and ensure that Stability Programs are state-of-the-art with respect to HA requirements and in line with registration documentation.

Support interpreting stability data, trends and provide scientifically sound conclusions for product shelf-life assessments, storage conditions, packaging and transport categories. Provide corrective actions to address immerging stability issues.

Support QAM in analytical results investigations (e.g. OOS), complaints that require analytical interpretation. Support defining and implementing business processes and SOPs/GOPS necessary to maintain a robust AS&T Quality System within External Supply. Support the QAM in product investigations and assure that they are managed in agreement with Sandoz standards.

Responsible for implementing effective CAPAs at the suppliers/contract labs. Support QAM to ensure Testing Monographs are state-of-the-art with respect to technique and technology and in line with registration documentation.

Responsible SPOC for implementation of compliance alerts for analytical methods / monographs. Provide support for site readiness for Health Authority inspections as required. Participate in audits/technical visits on request as an SME.

Role Requirements:

Education: Advanced university degree (Master’s or equivalent) in Natural Sciences (Chemistry, Pharmacy, Biotechnology, Biology)

Minimum of 8 years’ experience within the pharmaceutical industry in quality control or analytical development that includes method development, method validation, stability testing, method transfers.

Expertise in different analytical techniques required.

Thorough knowledge of cGMP requirements, ICH guidelines, major pharmacopeial requirements, regulatory requirements.

Excellent communicator in both English and Mandarin, with advanced negotiation skills.

Why Sandoz?

Generic and Biosimilar medicines are the backbone of the global medicines industry. Sandoz, a leader in this sector, touched the lives of almost 500 million patients last year and while we are proud of this achievement, we have an ambition to do more!

With investments in new development capabilities, state-of-the-art production sites, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help more patients gain access to low-cost, high-quality medicines, sustainably.

Our momentum and entrepreneurial spirit are powered by an open, collaborative culture driven by our talented and ambitious colleagues, who, in return for applying their skills experience an agile and collegiate environment with impactful, flexible-hybrid careers, where diversity is welcomed and where personal growth is encouraged!

Commitment to Diversity & Inclusion:

We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

#Sandoz

Skills Desired

Continued Learning, Dealing With Ambiguity, Employee Performance Evaluations, Gmp Procedures, People Management, Qa (Quality Assurance), Quality Control (Qc) Testing, Quality Standards, Self-Awareness, Technological Expertise, Technological Intelligence

Job details

Seniority
Manager
Function
Quality
Therapeutic area
Not listed
Location
Shanghai (Shanghai), China
Employment type
Full time

How this role compares

Computed from every other active Quality role in our database, not just this employer's listings.

We currently track 181 comparable Manager Quality roles across 52 biopharma companies.

181Comparable roles tracked
176Currently active
52Companies hiring similar roles
24Countries represented

Salary context

54 of 181 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Quality Control Associate Scientist Overnight Shift · Merck KGaA $27/hr – $46/hr (≈ $56,160–$95,680/yr)
Peer group range $75,920 – $219,500 (median $166,200)

Where these roles are based

Top locations among the 181 comparable roles

United States86
Ireland17
China16
Japan12
India12
Singapore7

+ 18 more countries

Seniority mix

181 of 181 peers have a known seniority level

Manager123
Associate Director37
Associate21

Therapeutic area mix

0 of 181 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

No peers with a known therapeutic area yet.

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.

60%similar
Pfizer Investment Co., Ltd. China Shanghai, China Manager
Same function Same seniority Same country
60%similar
Sanofi-Aventis Pharma Beijing Co Ltd Beijing, China Manager
Same function Same seniority Same country
60%similar
Sanofi-Aventis Pharma Beijing Co Ltd Beijing, China Manager
Same function Same seniority Same country
60%similar
Sanofi-Aventis Pharma Beijing Co Ltd Beijing, China Manager
Same function Same seniority Same country
60%similar
Sanofi-Aventis Pharma Beijing Co Ltd Beijing, China Manager
Same function Same seniority Same country
60%similar
Sanofi-Aventis Pharma Beijing Co Ltd Beijing, China Manager
Same function Same seniority Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

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.

60%
Supply Operation Quality- Senior Manager
Pfizer Investment Co., Ltd. China · Shanghai, China · Manager
Function Therapeutic area Seniority Country
60%
IFB-Quality Assurance Manager-QMS
Sanofi-Aventis Pharma Beijing Co Ltd · Beijing, China · Manager
Function Therapeutic area Seniority Country
60%
M&S-China EM&S Quality Regulatory Manager-Shanghai
Shanghai Rongheng Pharmaceutical Co, Ltd · Shanghai, China · Manager
Function Therapeutic area Seniority Country
60%
R&D Quality Manager
Novartis · Shanghai (Shanghai), China · Manager
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 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.