Process Engineer II

Responsibilities

• Provide technical evaluations and support for Engineering Change Orders and Supplier Changes including updates to specifications, drawings and procedures and required operator training.
• Design and develop equipment and processes for use in the manufacturing of products. This may include in-house design, or the use of products or components as purchased from vendors. Design, build and qualify fixtures, machines, or equipment to facilitate manufacturing capability of products.
• Support integration of new products into the manufacturing operation. Provide input to Development and Operations on materials, processing, the manufacture, and cost aspects of new products.
• Assist in the validation of new and revised manufacturing processes and equipment, ensuring compliance with all applicable company standards, procedures, and all other applicable specifications.
• Design and execute engineering studies to test hypothesis related to project outcomes.
• Applies scientific and technical knowledge to projects and responsible for timely project execution.
• Lead process engineering activities in support of the product line, including: Process Validation, Cleaning Validation, Equipment Qualification, investigations to address root cause
• Bachelor's Degree in engineering or scientific discipline.
• Demonstrated technical knowledge and ability to solve related issues and provide effective solutions that support overall engineering/operational objectives.
• Ability to balance priorities and/or resources to ensure immediate demands are achieved without sacrificing long-term operational strategies.
• Ability to write policies, procedures, and communications to regulators and management.
• Ability to conduct effective training as necessary for the operation of facilities/equipment.
• Uses standard office program m(Microsoft) for daily communications and project work.
• Preferred:
• 3 years' experience of Process Engineering in Pharmaceutical or Medical Device industry is Highly Desirable .
• Prior operations experience in a GMP regulated environment Desirable .
• Experience with equipment/parts specification , qualification ( PQ ) Desirable .
• Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
• We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
• This job is eligible to participate in our short-term incentive programs.
• AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
• US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
• US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
• https://www.abbvie.com/join-us/reasonable-accommodations.html

Benefits

Additional Information

The primary job function of this position is to provide technical support to cross-functional teams working with little or no supervision, apply project management knowledge, engineering and product/process knowledge, and ingenuity to complete medium size projects from concept through project closure within or across disciplines.

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