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You will be updated with latest job alerts via email$ 162947 - 162947
1 Vacancy
What we expect of you
We are all different yet we all use our unique contributions to serve patients. The professional we seek will possess these qualifications.
Basic Qualifications:
Doctorate degree
Or
Masters degree & 2 years of engineering experience in a GMP environment
Or
Bachelors degree & 4 years of engineering experience in a GMP environment
Or
Associate degree & 8 years of engineering experience in a GMP environment
Or
High school diploma / GED and 10 years of engineering experience in a GMP environment
Preferred Qualifications:
Advance degree in Computer Electrical Mechanical Chemical Engineering or Biomedical Engineering
Knowledge and/or experience of pharmaceutical/biotech processes especially in the area of final drug product operations
Knowledge in Data Integrity and Security
Extensive understanding and background in programming design installation validation and lifecycle management of manufacturing process controls automation field instrumentation technologies
Expertise in Machine Vision (Cognex) and Rockwell software platform
Knowledge in Deep Learning
Direct experience with leading and managing Systech Serialization projects including experience with Guardian Advisor Sentri and other Systech ancillary devices.
Ability to interpret and apply GAMPs and GMPs and familiarity with documentation in a highly regulated environment
Comprehensive understanding of validation protocol execution requirements as well as knowledge of validation processes and requirements as applied to new equipment installations
Excellent communication skills together with ability to work in a team environment.
Organizational project management problem-solving as well as validation protocol and technical writing capability
Track record of leading and executing multi-functional projects.
Strong teamwork excellent interpersonal and communication skills.
Direct experience with medical devices/combination products and associated manufacturing processes.
Experience in working with third-party vendors and equipment suppliers.
Ability to work in a highly regulated and ever-changing industry.
Ability to learn and rapidly adapt to new requirements in a fast paced environment.
An Operational Excellence and Lean Transformation approach to work product driving rapid results.
A passion to deliver an excellent work product and develop others with an infective positive attitude!
What you can expect from us
As we work to develop treatments that take care of others we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture well support your journey every step of the way.
The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to relevant skills experience and qualifications.
In addition to the base salary Amgen offers a Total Rewards Plan based on eligibility comprising of health and welfare plans for staff and eligible dependents financial plans with opportunities to save towards retirement or other goals work/life balance and career development opportunities that may include:
.
Salary Range
142955.00 USD - 162947.00 USD
Required Experience:
Senior IC
Full Time