Associate Principal Scientist (Analytical)

The role holder is responsible for providing expert technical support to commercial products manufactured internally at AZ sites and externally at contract facilities.  This job description is relevant for on-market technical leaders whose subject matter expertise supports input for Analytical Sciences.  These leadership roles will not have direct reports. 

General Responsibilities include:

• Maintaining skills in assigned core capabilities for example, but not limited to, documentation practices, quality and regulatory compliance, data integrity, change management, GPM, lean capabilities & product security.

• Management of product knowledge throughout the lifecycle.

• Maintain technical knowledge in area of subject matter expertise including up to date advances in new regulations and technologies to aid in the improvement of pharmaceutical processes and or analytical methods.

• Regulatory file authoring, review, license renewals and response to questions.

• Provision of technical leadership to support product supply strategy projects (sourcing, asset transfers, capacity expansion, etc.) and business continuity plans through delivery of the drug product control strategy, and product quality risk management activities throughout the lifecycle.

• Responsible for the technical support during the transfer of established products within sites and to external manufacturing partners including support for equivalency determination as applicable.

• Support complex technical improvements or change activities assuring product performance and analytical methods robustness, including extractables and leachable assessments, nitrosamines risk assessments and risk assessments of elemental and organic impurities.

• Support for drug product PPQ programs in the support of transfer and change activities.

• Provision of technical problem-solving expertise to aid in the resolution of manufacturing/method/formulation issues & complaints impacting supply or manufacturability.

• Assist in the development of CAPAs to eliminate root cause(s).

Specific Responsibilities include:

• Responsible expert for a commercial product or group of commercial products related to the Analytical subject matter area (including analytical sciences and analytical technologies).

• Responsible for analytical lifecycle activities to ensure testing methods, drug product specifications and drug product control strategies are and remain fit for purpose and aligned with technology advancements.

• Leads the review of analytical methods performance via appropriate dashboards to ensure product and methods robustness across the QC network.

• Supports the definition of analytical standards impacting commercial products specific to regulatory expectations and good business or quality standards (including pharmacopeial standards).

• Provides training in subject matter expertise areas.

• May be the product lead for one or more products coordinating TOSI activities and being the main point of contact for general matters for these products as well as representing TOSI in the Global Supply Teams (GST) and/or Pharmaceutical Teams (PT).

• Executes Technical leadership and influencing in Pharmaceutical Teams and within TOSI.

• Develops and manage a prioritized portfolio of TOSI project activities, with appropriate demand and supply oversight.

• Ensures (in collaboration with TOSI SPOC) effective collaboration between PT&D and the AZ sites/External Supply Management (ESM) managed sites/QC laboratories and Global Partners.

• Maintains a technical support model with outstanding customer service for all AZ manufacturing sites and external manufacturing/testing partners.

• Builds effective networks across the Global Operations organisation and with the R&D functions.

• Leads and assess impact of complex technical improvements or change activities assuring product and methods performance and robustness, including extractables and  leachable assessments, nitrosamines risk assessments and risk assessments of elemental and organic impurities.

• Develop solutions to a diverse range of problems requiring complex judgements based on highly developed levels of conceptual thought, strategic vision and analysis.

• Provides Technical leadership to Issue Management Team (IMT).

• Project resource estimations to support the budgeting process.

The role holder will:

• Create an effective partnership, manage expectations and resolve issues positively and in the best interest of AZ.

• Ensure that all work is carried out in compliance with AstraZeneca and external regulatory policies and standards.

• Continuously improve in competence, scientific excellence and innovation.

• Operate at the highest level of risk management.

• Be an excellent communicator with strong interpersonal skills in order to collaborate effectively with stakeholders.

• Conduct activities and interactions consistent with Company values and in compliance with the Code of Ethics and supporting Policies and Standards relevant to the role. Complete all required training on the AZ Code of Ethics and supporting Policies and Standards on time. Report potential issues of non-compliance.

All these activities will have a significant impact on the overall success of Operations as well as ensuring the commercial viability of current products. The activities of the TOSI organization help to ensure availability of all AstraZeneca products to the commercial organization. The role, therefore, has a significant impact on both financial and reputational aspects of the business.

Education, Qualifications, Skills and Experience

Essential

• Have an good understanding of the overall drug development and commercialization process from development, launch and through life cycle management

• Likely to be educated to BSc, MSc or PhD level in an appropriate discipline, at least 5-10 years of experience relevant to the pharmaceutical industry and have professional credibility within the business and industry.

• In-depth understanding of analytical sciences in the Pharmaceutical Industry, applied to raw materials, intermediates and drug products, including definition of control strategies and specification setting.

• Have a thorough understanding of principles, applications and management of SHE and cGMP.

• Business acumen and capability to understand (E) business cases in subject matter areas.

Desirable

• Experience in or exposure to multiple disciplines in CMC and related functions (eg Development, Manufacturing, Quality Control, Regulatory, Quality Assurance, Global Supply)

• Have in depth understanding of multiple disciplines, such as (besides analytical) formulation, packaging, automation, validation.

Date Posted

08-5月-2026

Closing Date

30-8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.