Your career compass awaits
Create a free account to unlock
- ✓ See how you match this role
- ✓ AI resume tailored to this specific job
- ✓ Inside Track Companion — find your insider contact
- ✓ Skills gap analysis and upskill plan
- ✓ Interview prep kit for this role
- ✓ Relocation concierge — salary, tax, cost of living
Free — no credit card required
Process Engineer - Day Shift
✓ This company has sponsored visas before. The posting doesn't say so, but it's still worth applying.
Engineering
💰 Salary Not shared
📊 Market 6,500 GBP–10,000 GBP/mo (78,000 GBP–120,000 GBP/yr)
About the Company
Welcome to Coppell, Texas , one of over 400 sites here at AstraZeneca, providing a collaborative environment where everyone feels comfortable and able to be themselves is at the core of AstraZeneca's priorities, it's meaningful to us that you bring your full self to work every day. THIS IS A 12 HOUR DAY SHIFT ROTATING POSITION WORKING 5am-5pm Day Shift - Process Engineer Shift coverage : 5am to 5pm shift- Ability to work 12-hour rotating shifts (2 days-on, 2 days-off, 3 days on, 2 days-off) working every other weekend per this rotation.
Responsibilities
- ● Ethical conduct and compliance and adhering to AstraZeneca values and behaviors
- ● Become an expert on the process and equipment to successfully lead and implement process improvements
- ● Develops conceptual strategies, processing schemes, feasibility studies, PFD's, and detailed scopes of work
- ● Identify and implement projects to increase safety, reduce product cost, improve product quality, improve yield, and reduce material usage
- ● Work on several different projects and be able to prioritize these projects
- ● Works with contractors and project teams on the buildout and expansion of the facility while demonstrating confidence in voicing concerns and driving the project team to deliver a usable product for the end internal customer
- ● Assists in developing control strategy and instrument process design, including emergency and shutdown procedures, instrument specification sheets, control ranges, alarm points, and automation strategy
- ● Authors, updates, reviews, and approves area procedures and master batch records to ensure accurate content and compliance with Good Manufacturing Practices
- ● Designs studies, implements experiments and performs data analysis
- ● Writes study proposals, progress reports, development reports, and various technical memo's
- ● Evaluates new technologies to improve the commercial production process
- ● Supports scale-up activities from R&D to production
- ● Supports the assurance of a robust manufacturing process for the current registered process as experience is gained post-launch.
- ● Acts as an effective change agent
- ● Acts as a key player for the expansion of projects as needed to increase the scale of manufacture
- ● Investigate deviations from standards of the manufacturing process using effective root cause analysis tools. Recommending and implementing effective corrective and preventative actions
- ● Generate, evaluate, and implement innovative and creative solutions
- ● Assist as subject matter expert for technical projects
- ● Capable of generating a project scope and cost plan to effectively draft a capital request
- ● Develop product and process knowledge in multiple process train areas
Requirements
- ● , commissioning, dry-runs for activities for new systems/equipment.
- ● Minimum requirements:
- ● Bachelor of Science degree in Chemical Engineering or other related
- ● technical discipline with direct chemical processing experience preferably in a pharmaceutical production environment.
- ● years experience preferably in a pharmaceutical production environment or GMP regulated environment.
- ● Ability to read P&ID's, Process Flow Diagrams, and perform mass and
- ● energy balances.
- ● Excellent verbal, written, and interpersonal communication skills are essential.
- ● Displays a high desire to learn while recognizing one's own limitations.
- ● Able to demonstrate technical capabilities using logical thought processes to analyze information and draw conclusions.
- ● High temperature and high-pressure applications
- ● Lean certification or experience with lean concepts
- ● Next Steps - Apply today
- ● To be considered for this great opportunity, please complete the full application on our website at your earliest convenience - it is the only way that our Recruiter and Hiring Manager can know that you feel well qualified for this opportunity. If you know someone who would be a great fit, please share this posting with them.
- ● Date Posted 21-Sep-2026
- ● Closing Date 18-Oct-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.
Confirm Application
Are you applying to ?
We'll track this in your dashboard as Applied.
Saving to your tracker…
Stand out: message someone at AstraZeneca.
A short, personal note to a recruiter can get your application looked at sooner.
⚡ Full Resume Sandbox Canvas