Senior Engineer, Process Engineering (2nd/3rdShift)

Member of the Engineering Team engaged in supporting all manufacturing processes and providing technical support to the Manufacturing Team. The Senior Engineer, Process Engineering (shift) is responsible leading the equipment reliability program, championing continuous improvement, running capital projects, and being the site expert on manufacturing process and systems. The role combines the benefit of small site (agile and broad responsibilities) with the structure, knowledge, and resources of a leading global pharmaceutical company. This is a senior level role where the engineer can assess current state issues, develop plans, initiate projects, and drive execution to eliminate process and equipment issues/failures. This position is 5 days a week onsite, aligned with the manufacturing shift operations (day, swing, or night) and may require after hours or weekend support as required.

Typical Accountabilities:

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

Report potential issues of non-compliance.

• Ensures compliance with AZ Corporate Policies and Directives. Site Standard Operating Procedures. Regulatory requirements, and industry best practice (cGMPs, GAMP,ITIL,PMI).
• Maintains a safe work environment and performs work in accordance with site Environment, Health and Safety (SHE)
• policies and procedures.

Manufacturing Process SME

• Expertise in equipment and manufacturing process, capability to support multiple process areas
• Leadership and project management skills; Lead executions of Manufacturing related engineering projects. Works on several different projects and prioritizes these projects with guidance
• Proficiency in all of the following disciplines equipment, process/materials, maintenance, project delivery
• Lead investigations, owns CAPAs, and responsible or product impact assessment, and risk assessments related to manufacturing processes. 
• Lead troubleshooting activities to resolve critical escalations, planned and unplanned activities, and anticipate future engineering developments within maintenance/process area
• Designs studies, executes experiments/protocols and perform data analysis. Develop and optimize processes within own area of process engineering.
• Track, trend, and analyse in-process data using statistical process control (SPC) methods. Monitor and improve process performance.
• Share technical knowledge and expertise with personnel in AstraZeneca to aid  technical developments within the organization.
• Recommend and implement transformation/ continuous improvement initiatives within site with focus on cost saving and improvement of quality and efficiency.

• Employ Good Engineering Practices to streamline project executions
• Collaborates with cross-functional teams to solve problems
• Provide mentorship and coaching to junior engineers, interns, and manufacturing technicians
• Guide execution of processes (e.g., validation, qualification, operation, evaluation and troubleshooting of process deviations) within process engineering area.
• Participate in communications with relevant internal teams (e.g., regulatory) for management of change control.
• Guide and track compliance of own work and work of others with SHE and other applicable standards and regulations. Provide engineering solutions to manufacturing challenges and meet all safety, quality, supply and requirements. 
• Develop contacts across a range of departments and external groups acting as engineering representatives.
• Equipment Management:
• Prepare equipment for qualification activities, including but not limited to: TOP preparation and review, initial testing and qualification readiness
• Manages production equipment. Maintain equipment maintenance strategies, and equipment lifecycle management
• Lead/ guide planning, managing, and monitoring of major manufacturing and maintenance plan projects from concepts to implementation
• Lead equipment specification, design, build, commissioning and qualification to meet technical/safety/ and business

Essential Requirements:

• Entry-level Master’s/ PhD degree in engineering, science, technology, or related field (OR) Bachelor’s degree with 3+ years of relevant experience.
• Experience working with procedures and compliance with GMP & SHE requirements.
• Experience managing process engineering processes (e.g., validation, qualification, operation) across PETs within a highly regulated environment.
• Experience in some of the following areas: new technology investigation, process development, capital project execution, and sales product support.
• Experience working with digital tools and applications related to reporting, documentation, and analysis.
• Breadth of experience is a key requirement to establish credibility with key stakeholders. Preferably the following:
• Industry experience in a GMP environment 
• Experience with spray-drying technology 
• Experience with equipment maintenance 
• Experience with regulatory inspections and handling deviations.
• Experience working within cross-functional teams.
• Has experience in change control, budget and project management, including a track record of driving continuous improvement initiatives
• Project management track record of delivering projects timely, in-full, and on-budget
• Technical role managing project aspects within a specialist area

Preferable Qualifications:

• Large Capital project management and execution experience
• Lean certification
• Experience with automatic process controls
• Root cause investigation training/ 6-simga
• TPM experience
• Data Analysis tools (SQL, JMP, Minitab) , visual management tools (Powerbi, PowerApps)
• Experience with spray-drying technology 
• Experience in the following areas: Process scale up; validation activities for commercial production; feedstock and drying processes; and, setting up new equipment– (URS, PID, DQ, IQ, OQ, PQ)

The annual base pay (or hourly rate of compensation) for this position ranges from $ 101,643.20 - $152,464.80. Our positions offer eligibility for various incentives—an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.

Date Posted

31-Mar-2026

Closing Date

16-Apr-2026

Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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 authorisation and employment eligibility verification requirements.