Novartis Posted September 8, 2026

Sr. Spec. DDIT OPS ITOT SM Site Robotics

Changping County (Beijing), China FULL_TIME
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About this opportunity

The Robotics Expert (Super SME) owns the end-to-end robotics technology strategy for shared Work Centres across manufacturing site. The role bridges emerging robotics technologies with site needs, moving solutions from market scan to shop floor, by combining deep technical expertise with close proximity to the vendor and innovation ecosystem.As a robotics expert, will support the development, implementation and continuous improvement of robotics automation solutions.The role is primarily a hands-on technical position, with a strong focus on robot programming, system integration, machine vision, motion control and onsite commissioning. Work with internal teams, equipment suppliers and robotics partners to translate operational needs into practical and reliable robotics solutions.A key focus of this role is to support the site robotics roadmap by implementing industrial robots, collaborative robots, mobile robots and other intelligent automation technologies. Participate in the exploration and implementation of humanoid robotics, identifying suitable use cases, conducting technical evaluations, developing prototypes and supporting deployment in real manufacturing environments.Require strong practical robotics engineering capability, including robot programming, vision-based guidance, sensor integration, end-of-arm tooling, motion optimization and troubleshooting. The role will Independently develop, implement and deploy robotics solutions from concept to operation.

Major accountabilities: • Support the design, development, programming, commissioning and troubleshooting of industrial robots, collaborative robots, mobile robots and humanoid robotics applications. • Develop and optimize robot programs, motion sequences, trajectories and operating logic for manufacturing and material-handling applications. • Integrate machine vision, 2D/3D cameras, sensors, force/torque sensors and other perception technologies into robotic applications. • Support development of robot gripping and end-of-arm tooling solutions for different products, materials and operating scenarios. • Integrate robots with PLCs, production equipment, conveyors, AGV/AMR systems and other automation platforms. • Perform onsite testing, debugging, cycle-time optimization, reliability improvement and technical troubleshooting of robotics systems. • Explore humanoid robotics technologies and support use-case evaluation, proof-of-concept development, testing and implementation in factory environments. • Evaluate new robotics technologies, software platforms, sensors and suppliers through practical testing and technical comparison. • Apply programming and software tools for robot control, data processing, simulation, vision applications and system integration. • Ensure compliance with GMP regulations and security protocols. • Maintain technical documentation including robot programs, system configurations, interface information, test records and troubleshooting documentation.Key performance indicators: • Successful implementation and stable operation of assigned robotics automation solutions.• Timely completion of robotics programming, integration, testing and commissioning activities.• Improvement of robot reliability, cycle time and operational performance.• Effective troubleshooting and resolution of robotics, vision and integration-related technical issues.• Successful completion of robotics proof-of-concept and technology evaluation activities.• Successful identification and implementation of practical humanoid robotics use cases.• Quality and completeness of robot programs, technical documentation and system records.• Positive feedback from manufacturing and technical stakeholders.COMPETENCY PROFILEStrong technical background in industrial robotics, automation, computer vision, and/or physical AI, ideally within regulated (GMP) manufacturing environments. Proven ability to translate emerging technologies into standardized, deployable solutions. Experience defining technical requirements (URSs), standards, and vendor evaluation criteria. Strong stakeholder management skills, with the ability to align across global platforms, sites, engineering, and procurement.EDUCATION & QUALIFICATION REQUIREMENTS• Bachelor's or Master's degree in a relevant technical discipline, such as: - Robotics, Mechatronics, or Automation Engineering - Electrical, Mechanical, or Control Systems Engineering - Computer Science, Artificial Intelligence, or Computer Vision - Industrial / Manufacturing Engineering• 7+ years of experience in industrial robotics, automation, or advanced manufacturing technology, ideally within a regulated environment• Proven track record of evaluating, selecting, and deploying robotics or automation technologies from concept to shop floor• Experience defining technical standards, User Requirement Specifications (URSs), and vendor evaluation criteria• Strong understanding of robotics hardware, integration, and automation architectures.• Knowledge of GMP requirements, data integrity (ALCOA+), and validation principles in regulated manufacturing• Proven experience in managing budgets and project pipelines• Familiarity with GMP regulations and compliance standards• Ability to collaborate with cross-functional teams and key stakeholders• Business fluency in English

Job details

Seniority
Senior
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Changping County (Beijing), China
Employment type
FULL_TIME

How this role compares

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

We currently track 508 comparable Senior Manufacturing & CMC roles across 70 biopharma companies.

508Comparable roles tracked
447Currently active
70Companies hiring similar roles
29Countries represented

Salary context

198 of 508 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 · Sr Manufacturing Technician · Genz. Therap Product LP $2,400/yr – $3,200/yr
Highest disclosed · Associate Director / Director, CMC Product Development · AbbVie $160,500/yr – $305,000/yr
Peer group range $2,800 – $232,750 (median $146,150)

Where these roles are based

Top locations among the 508 comparable roles

United States323
India45
Ireland15
Netherlands15
Singapore11
China's Mainland10

+ 23 more countries

Seniority mix

508 of 508 peers have a known seniority level

Senior319
Principal99
Associate Director90

Therapeutic area mix

0 of 508 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

No peers with a known therapeutic area yet.

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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.

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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.