Associate Process Engineer
Novo Nordisk US Bio Production, Inc. in West Lebanon, NH has an exciting opportunity for an Associate Process Engineer to join our team! This role will be responsible for assisting with design and implementation of manufacturing processes, instrumentation and equipment start-ups from the laboratory through manufacturing scale.
Relationships:
Reports to: Senior Manager, Manufacturing Engineering & Validation
Main Job Tasks:
Assist with coordinating fabrication, procurement, installation, engineering start-up, and validation activities of new equipment and systems, including documentation of IQ/OQ protocols, test executions, and summary reports
Participate in the development and implementation of procedural or automation improvement changes
Participate in design and hazard reviews of plant expansions or process changes.
Support person for process improvement activities; including performing or authoring equipment specifications, user and functional requirements specifications, and necessary FAT and SAT protocols
Performs all job duties and responsibilities in a compliant and ethical manner and in accordance with all applicable healthcare laws, regulations and industry codes.
Incorporates the Novo Nordisk Way and 10 Essentials in all activities and interactions with others.
Physical Requirements:
Travel: 0-10%.
Knowledge, Skills and
Experience:
Requires a Bachelor's degree in Chemical Engineer, Mechanical Engineering, or related discipline
One (1) year of related experience, preferred.
Ability to follow routine work instructions for new and ongoing projects and assignments.
Knowledge of Automation and GMPs requirements preferred.
Excellent communication skills and ability to work in a high-paced team-oriented environment.
. Apply now!Estimated Salary: $20 to $28 per hour based on qualifications.
Relationships:
Reports to: Senior Manager, Manufacturing Engineering & Validation
Main Job Tasks:
Assist with coordinating fabrication, procurement, installation, engineering start-up, and validation activities of new equipment and systems, including documentation of IQ/OQ protocols, test executions, and summary reports
Participate in the development and implementation of procedural or automation improvement changes
Participate in design and hazard reviews of plant expansions or process changes.
Support person for process improvement activities; including performing or authoring equipment specifications, user and functional requirements specifications, and necessary FAT and SAT protocols
Performs all job duties and responsibilities in a compliant and ethical manner and in accordance with all applicable healthcare laws, regulations and industry codes.
Incorporates the Novo Nordisk Way and 10 Essentials in all activities and interactions with others.
Physical Requirements:
Travel: 0-10%.
Knowledge, Skills and
Experience:
Requires a Bachelor's degree in Chemical Engineer, Mechanical Engineering, or related discipline
One (1) year of related experience, preferred.
Ability to follow routine work instructions for new and ongoing projects and assignments.
Knowledge of Automation and GMPs requirements preferred.
Excellent communication skills and ability to work in a high-paced team-oriented environment.
. Apply now!Estimated Salary: $20 to $28 per hour based on qualifications.
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