Equipment Process Engineer
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About this opportunity
Career Category
Engineering
Job Description
Live
What you will do
Let’s do this. Let’s change the world.
Amgen Dun Laoghaire (ADL) is looking for an Equipment Process Engineer to join our Drug Product Engineering team to support commercial aseptic Drug product filling on site. Amgen Dun Laoghaire (ADL) is a 37,000 square metre aseptic drug product operations facility, specialising in secondary manufacturing activities – Formulation, Vial/Syringe Filling, Lyophilisation and Packaging.
This position will be responsible for performance drug product equipment on site. The Equipment Process Engineer will report to the Engineering Lead and should have knowledge and proficiency in the use of statistical analysis tools, continuous improvement methodologies, problem solving and applied engineering skills relating to mechanical, electro-mechanical and associated automation systems. The Equipment Process Engineer will also have responsibility for the reliability and life cycle of equipment.
Key Responsibilities:
Support a safe working environment by complying with all pertinent environmental health/safety practice, rules and regulations
Ownership of equipment/systems in a GMP regulated manufacturing setting that support the Drug Product manufacturing processes
Monitoring of day-to-day performance, including trend analysis of all performance aspects of their system and equipment to identify and proactively manage performance trends.
Support system improvements, development of detailed specifications, engineering documents and standard operating procedures
Support technical root cause analysis, incident investigations and after action reviews when troubleshooting issues related to manufacturing equipment/systems
Solving complex problems, project management, equipment lifecycle management and operational excellence initiatives related to their systems / equipment
Develop and manage change control requests per established SOPs and processes
Support new product introductions or new technology introductions by performing engineering assessments, implementation of system changes and supporting engineering runs
Communicating with key stake holders, in a responsive manner to ensure they are kept informed on all engineering activities
Working in a collaborative manner within cross functional work centre team, and contributes to investigations, Non-Conformance and CAPA closure.
Develop a structured maintenance schedule which will align with the manufacturing schedule to minimise downtime. This includes routine PM’s and long term planning for vendor support on site and the procurement of major spare part assemblies in a timely manner to support larger overhauls
Development and maintenance of spare parts lists for their system and appropriate levels of spares are maintained.
Win
What we expect of you
The successful candidate for this role will bring the following education, skills and experience
Basic Qualifications:
Bachelors in Engineering (Mechanical, Manufacturing, Mechatronics, Electrical or Chemical).
Manufacturing experience in a regulated environment.
Experience in the use of statistical analysis tool & continuous improvement methodologies.
Problem solving and applied engineering skills relating to mechanical, electro-mechanical and associated automation systems.
Preferred Qualifications:
Manufacturing experience in biopharmaceutical Formulation/Fill/Finish or Active Pharmaceutical Ingredient (API) facilities.
Technical writing, and communication/presentation skills.
Experience in change control, non-conformance, corrective and preventative actions, and validation practices.
Experience in developing strategies for new product introduction and new technology deployment.
Support the translation of strategic opportunities and emerging technology solutions into tangible pragmatic executable plans.
Support the development of business area strategy and engineering/equipment strategy where appropriate.
Development and presentation of project plans to management.
Day to day vendor management.
Independent, self-motivated, organized, able to multi-task in project environments and skilled in communication and collaboration.
Team player, prepared to work in and embrace a team-based culture that relies on collaboration for effective decision-making.
Travel at various times may be required to support execution of projects.
Thrive
What you can expect of us
In addition to a competitive salary structure, Amgen offers a generous Total Rewards Plan for staff and eligible dependents. Comprehensive employee benefits package, including retirement and savings plan with generous company contributions, group medical, life and disability insurance. Discretionary annual bonus program. Exceptional learning, development and career advancement opportunities, empowering employees to grow and build long-term careers. At Amgen, we are committed to nurturing talent and providing meaningful pathways for professional development.
Amgen is an equal opportunities employer
. Salary Range
55,960.60 EUR - 75,711.40 EUR
Job details
How this role compares
Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.
We currently track 3753 comparable Manufacturing & CMC roles across 173 biopharma companies.
Salary context
921 of 3753 peers report a salary range (USD, annualized)
Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.
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Seniority mix
1670 of 3753 peers have a known seniority level
Therapeutic area mix
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