Associate Principal Process Engineer

Posted 3 Days Ago
Be an Early Applicant
Wuxi, Jiangsu, CHN
In-Office
Senior level
Biotech • Pharmaceutical
The Role
Lead technical process engineering for oral solid dosage manufacturing: apply modelling/digital twins, resolve complex manufacturing issues, support scale-up/transfers, drive equipment/process standardisation, execute physical characterisation studies, and contribute to regulatory CMC activities and product supply strategy.
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

04-8月-2026

Closing Date

29-11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

  • Understanding of overall drug development and commercialization process
  • Process/Chemical Engineering BSc/MSc with 5+ years post-degree OR PhD with 3+ years post-degree
  • Knowledge of unit processes and equipment for OSD manufacturing (mixing, drying, compression, roller compaction, continuous direct compression, coating) and physical characterisation (mechanical testing, PSD, imaging)
  • Experience in process scale-up, manufacturing engineering and digital twins/modelling
  • Experience in data analysis/data science languages and the use of digital tools
  • Experience with CMC elements for commercial manufacturing (process establishment, optimisation, validation, control, stability, packaging) and understanding of SHE and cGMP
  • Experience in Pharmaceutical Operations and/or R&D with project leadership in a matrix organisation
  • Good communication and relationship skills
  • Experience in or exposure to multiple CMC disciplines (Product Development, Operations, Global Supply, Marketing)
  • Training/experience in Lean and Six Sigma, problem solving tools
  • Experience in physical testing techniques of raw materials, intermediate and final drug products
  • Experience in or exposure to coding and programming languages

AstraZeneca Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about AstraZeneca and has not been reviewed or approved by AstraZeneca.

  • Fair & Transparent Compensation Pay is considered competitive across many roles when total rewards are factored in. Senior scientific and leadership bands are described with high ranges that reinforce competitiveness at upper levels.
  • Strong & Reliable Incentives Bonuses, equity eligibility in many salaried roles, and solid sales on‑target earnings with upside are emphasized as meaningful parts of compensation. These elements boost overall value even where base pay is not the very highest.
  • Retirement Support A 401(k) program with a strong company match and immediate vesting is repeatedly cited as a standout. Generous retirement support is viewed as enhancing the total package relative to peers.

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The Company
HQ: Gaithersburg, MD
70,000 Employees
Year Founded: 1999

What We Do

We're transforming the future of healthcare by unlocking the power of what science can do for people, society and the planet.

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