Associate Principal Process Engineer

Posted Yesterday
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Wuxi, Jiangsu, CHN
In-Office
Senior level
Biotech • Pharmaceutical • Manufacturing
The Role
Provides technical leadership for pharmaceutical process engineering, modelling, simulation, scale-up, equipment integration, manufacturing process transfers, and operational issue resolution. Leads product supply strategy, physical characterization studies, manufacturing improvements, regulatory support, and equipment modernization. Requires expertise in oral solid dose unit operations, CMC, process validation, data analysis, digital twins, cGMP, and pharmaceutical operations or R&D project leadership.
Summary Generated by Built In

Key Accountabilities

The role of the Associate Principal Process Engineer has the following responsibilities:

  • Serve as a key expert in pharmaceutical unit operations with a focus on the mechanistic understanding of process-equipment interface, providing advanced technical leadership and support.
  • Apply process engineering principles to identify, develop and use modelling and simulation tools for predicting process performance, resolving operational issues, and optimising both equipment function and system integration.
  • Provide technical leadership and expertise in resolving complex process-related manufacturing issues, utilising core engineering modelling and simulation to resolve complex manufacturing challenges and enhance process efficiency.
  • Contribute to product supply strategy projects, including sourcing, asset transfers, capacity expansions, and the introduction of new equipment.
  • Lead technical support for the transfer of established product manufacturing processes within internal manufacturing sites and to external partners, employing scale-up modelling, equipment selection, and comprehensive manufacturing engineering support.
  • Propose and execute physical characterisation studies for raw materials, intermediates, and finished products to support investigations and drive improvements in formulation and manufacturing processes.
  • Identify opportunities for manufacturing improvement, lead impact assessments, and support the implementation of technical improvements or major change initiatives with a focus on maintaining product performance, including contributions to regulatory file authoring, license renewals, and responses to regulatory queries, supported by model-based risk assessments.
  • Drive the standardisation and modernisation of manufacturing equipment and processes across Operations, leveraging advanced modelling and simulation to meet regulatory requirements, support good business practices, and ensure manufacturability and quality standards.

Required Skills & Knowledge

  • Demonstrate an understanding of the overall drug development and commercialization process from development, launch, and through life cycle management.
  • Process/chemical Engineering BSc/MSc with 5+ years of relevant pharmaceutical industry experience post degree or PhD level with 3+ years of experience post degree
  • Demonstrate an understanding of a range of unit processes and equipment for OSD manufacturing (e.g. mixing, drying, compression, roller compaction, continuous direct compression, coating) and awareness of physical characterisation of raw material, intermediate and final products (e.g. mechanical testing, PSD, imaging etc).
  • Have experience in process scale up, manufacturing engineering and digital twins/modelling
  • Have experience in data analysis/data science languages and the use of digital tools.
  • Have experience with a range of CMC elements related to commercial product manufacturing process requirements – e.g., process establishment, optimisation and validation, control of drug products, stability, packaging and commercial manufacturing, with good understanding of SHE and cGMP.
  • Experience in Pharmaceutical Operations and/or R&D with a track record of successful project leadership and delivery within a matrix organisation.
  • Evidence of good communication and relationship skills.

Preferred Skills & Knowledge

  • Experience in or exposure to multiple disciplines in CMC and related functions (e.g. Product Development, Operations, Global Supply, Marketing Companies)
  • Have previous experience and training in Lean and Six Sigma, problem solving tools.
  • Have experience in physical testing techniques of raw materials, intermediate and final drug products.
  • Experience in or exposure to coding and programming languages.

Date Posted

20-8月-2026

Closing Date

30-12月-2026

AstraZeneca embraces diversity and equality of opportunity.  We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills.  We believe that the more inclusive we are, the better our work will be.  We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics.  We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.

Skills Required

  • Bachelor’s or master’s degree in process or chemical engineering with 5+ years of relevant pharmaceutical industry experience after degree
  • PhD in a relevant field with 3+ years of post-degree experience
  • Understanding of drug development and commercialization from development through lifecycle management
  • Experience with oral solid dose unit processes and equipment, including mixing, drying, compression, roller compaction, continuous direct compression, and coating
  • Knowledge of physical characterization of raw materials, intermediates, and finished products
  • Experience in process scale-up, manufacturing engineering, and digital twins or modelling
  • Experience with data analysis, data science languages, and digital tools
  • Understanding of CMC activities, including process establishment, optimization, validation, drug product control, stability, packaging, and commercial manufacturing
  • Understanding of SHE and cGMP requirements
  • Pharmaceutical Operations or R&D experience with successful project leadership in a matrix organization
  • Strong communication and relationship-building skills
  • Experience across multiple CMC-related disciplines or functions
  • Lean and Six Sigma training or experience with structured problem-solving tools
  • Experience with physical testing techniques for raw materials, intermediates, and drug products
  • Experience with coding and programming languages
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The Company
90,000 Employees
Year Founded: 1999

What We Do

AstraZeneca is a global, science-led, patient-focused biopharmaceutical company committed to excellence in the research, development, and commercialization of prescription medicines. With approximately 90,000 employees across 85 countries, the company aims to unlock the power of science to deliver innovative medicines that transform patient outcomes and improve healthcare for people, society, and the planet worldwide.

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