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Added 2 mins ago
VV
Senior Optical Engineering Specialist
Veracity Ventures Inc.
Rochester, NY
- $120,000 to $155,000 USD / year
The ideal candidate is an experienced Optical Engineer with a strong background in electro-optical and infrared systems, optical sensor payload design, and engineering development.
Added 2 mins ago
VV
Senior Mechanical Engineering Specialist
Veracity Ventures Inc.
Rochester, NY
- $115,000 to $140,000 USD / year
The engineer will collaborate closely with cross-functional teams across optical, electrical, software, systems engineering, manufacturing, and program management. The role involves…
Added 2 mins ago
VV
Lead Systems Engineering I Systems Integration Test
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- $140,000 to $178,000 USD / year
Lead, Systems Engineering – Systems Integration & Test (SI&T)
Added 4 mins ago
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Virtual Three, CO
Use Model Based Systems Engineering (MBSE) tools like SysML and Cameo
Added 4 mins ago
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Arvada, CO
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Northrop Grumman
Boulder, CO
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AE
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Advanced Energy Industries, Inc
Fort Collins, CO
- $90,000 to $120,000 USD / year
Added 4 mins ago
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Littleton, CO
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Added 5 mins ago
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Littleton, CO
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Added 5 mins ago
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Colorado Springs, CO
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Added 5 mins ago
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Systems Engineer- Collection and Mission Management (Mid)
Added 5 mins ago
Systems Architect, Staff Principal
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Colorado Springs, CO
…thing. Kratos Space Federal is seeking an experienced, motivated Systems Architect, Staff Principal who will help lead Satellite Ground Systems Engineering activities on a critical…
Added 5 mins ago
Network Engineer - Sr. Staff
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Colorado Springs, CO
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Staff Full Stack Engineer (Infrastructure) - FT telework - EADGE-T
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Colorado Springs, CO
EADGE-T is seeking a full stack engineer to join the project team with a focus as an Infrastructure Systems Engineer. In this role, you will:
Added 5 mins ago
Staff Systems Engineer - ExPat
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Use Model Based Systems Engineering (MBSE) tools like SysML and Cameo
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RHEL - Sr. Full Stack Engineer - FT Telework
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Colorado Springs, CO
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Bridge Design Engineer
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Added 5 mins ago
Transmission Line Engineer I, II, III, or Senior
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Westminster, CO
…will possess an extensive and considerable understanding of engineering principles and practices, and the ability to apply that knowledge and experience to all aspects of the projects…
Added 5 mins ago
EG
Databricks Data Engineer
Eliassen Group
Denver, CO
- $150,000 to $154,000 USD / year
Our client seeks a Databricks Data Engineer to design, build, and maintain scalable, reliable, and secure data pipelines, infrastructure, and systems that support consulting services and…
Added 5 mins ago
EG
Cloud Engineer
Eliassen Group
Denver, CO
- $70 to $88 USD / hour
Our client seeks a senior Cloud Engineer to own and stabilize a legacy GCP and Azure footprint while assisting with conversions and decommissioning. The role will support automation efforts…
Added 7 mins ago
G
Senior Mechanical Engineer
GPAC
Ankeny, IA
- $110,000 to $140,000 USD / year
We are seeking an experienced Senior Mechanical Engineer who can perform engineering related duties for the design and planning phases of multiple and/or large, complex design and…
Added 7 mins ago
G
Senior Mechanical Engineer
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Johnston, IA
- $110,000 to $140,000 USD / year
We are seeking an experienced Senior Mechanical Engineer who can perform engineering related duties for the design and planning phases of multiple and/or large, complex design and…

AstraZeneca

Associate Director Principal Engineer

Mt. Vernon, IN, United States
Mt Vernon, IN, United States
Mt Vernon, United States

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Job details

Apply by: May 3, 2027
Education: Bachelor’s degree
Experience: ▪ Minimum of 10 years’ experience in pharmaceutical production, process engineering, project engineering, or project management.
Posting language: English
Posted: Nov 4, 2026

Original job description

The Associate Director Principal Engineer is responsible providing technical support for process manufacturing, including investigation and correction of process-related problems and deviations from standards. Serves as a Subject Matter Expert for multiple processing operations and provides technical leadership within the Process Engineering team. May lead and manage Technology Transfers to and from the site.

Responsibilities

Provides technical support for formulation areas, including investigation and correction of process related problems and deviations from standards.
Responsible for identifying and executing projects to reduce product cost, improve product quality, improve yield, and reduce material usage.
Collaborates with Production, Engineering, Automation, and Quality to optimize productivity, yield, product quality, and supply reliability.
Assists in designs and execution of process qualifications and validations for approved changes.
Initiates process manufacturing area change proposals as required for projects managed by the Formulation or Process Engineering group.
Authors, updates, reviews, and approves area procedures to ensure correct content and compliance with Good Manufacturing Practices.
Authors, reviews, and approves formulation master batch records.
Serves as a subject matter expert for technical projects affecting formulation during internal audits and regulatory inspections.
Leads technology transfer and implementation of new technologies, equipment, and processes from R&D and other sites, to the Mount Vernon site.
Enhances quality and effectiveness of manufacturing systems related to existing products as the Product Owner. This includes the design, execution, and evaluation of experimental plans to ascertain the required process capabilities, specifications, and robustness.
Executes site PAT strategy to monitor and control existing manufacturing processes.
Responsible for providing pharmaceutical process support to new and existing oral solid dose form (tablet and capsule) products/processes.
Trains and mentors new Process Engineers and interns. ▪ Develops Product/Process knowledge in multiple product streams and technologies.
Leads product scale up activities related to volume increases and/or product demand.
Responsible for Technology Transfer for new solid oral dosage form (tablet and capsule) products being transferred to the site as required.
Designs and executes Process Validation Studies supporting the commercialization of the TT products.
Identifies, recommends, and implements equipment modifications to ensure improved/optimized process performance.
Contributes to Equipment URS development and retrofit. Participates in Equipment FATs, SATs, etc.
Justifies processing parameters and conducts scale-up activities.
Introduces new manufacturing processes, technologies (including Process Analytical Technologies), and systems including the definition of equipment and facilities needed.
Executes the transfer and startup of new products/processes through plant trial runs and or clinical/pivotal stability lots, guaranteeing implementation of a robust and efficient process. Provides technical support for process manufacturing areas, including investigation and correction of manufacturing technical/quality issues that could potentially lead to a disruption in product supply.
Collaborates with Production, Engineering, Automation, and Quality to optimize productivity, yield, product quality, and supply reliability.
Conducts statistical process control and process capability analyses for TT projects and existing products.
Investigates and conducts troubleshooting and root-cause analysis of unexpected trends or results related to product quality and financial aspects due to material and/or process related factors during the execution of TT or routine production.
Identifies best practices in industry related to technology transfers and pharmaceutical manufacturing technologies; implements effective best practices to create a competitive advantage for the site.

Accountabilities

Conduct activities and interactions consistent with Company values and in compliance with the Code of Ethics and supporting Policies and Standards relevant to your role. Complete all required training on the AZ Code of Ethics 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, site policies, work instructions, regulatory requirements, and industry best practice (cGMPs, GAMP, ITIL, PMI).
Maintains a safe work environment and performs work in accordance with site, Safety, Health, and Environment (SHE) policies and procedures.
Immediately report potential unsafe conditions to management.
Supports internal, external, and regulatory inspections including FDA, EMEA, and third party inspections.
Participates in the investigation and resolution of product quality problems.
Executes work in compliance with cGMPs, site policies, work instructions, and SOPs.

Essential Requirements

Bachelor’s degree required, preferably in Science, Chemical Engineering, or other related technical discipline.
Minimum of 10 years’ experience in pharmaceutical production, process engineering, project engineering, or project management. Experience in the OSD pharmaceutical industry required.
Strong understanding of cGMPs; demonstrated leadership, management, and technical capabilities. ▪ Thorough knowledge of product and process development, manufacturing scale-up, continuous process improvement, and troubleshooting tools and analysis.
Excellent verbal, written, and interpersonal communication skills are essential. ▪ Must have demonstrated ability to effectively manage multiple major projects at the same time with minimum supervision.
Must have a proven ability to influence

Desired Requirements

Master’s degree and/or PhD is highly desirable.
Experience with IQ/OQ/PQ and Lean Manufacturing is highly desirable. Six Sigma certification is preferred.
Proven experience with Statistical Process Control, Process Capability Analysis.

Date Posted 04-Nov-2026 Closing Date 10-Nov-2026Our 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.

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