AbbVie · 18 hours ago
Process Engineer - Clinical Manufacturing Operations (onsite)
Worcester, MA
Full-time
Onsite
Entry, Mid Level
$64K/yr - $122K/yr
2+ years expAbbVie is a company dedicated to discovering and delivering innovative medicines and solutions that address serious health issues. The Process Engineer will apply scientific and engineering knowledge to support Clinical Manufacturing Operations, focusing on the introduction of new products and maintaining a robust product pipeline.
BiotechnologyFinancial ServicesHealth CareMedicalPharmaceuticalVenture Capital
Responsibilities
Responsible for compliance with applicable policies and procedures
Leads equipment and process troubleshooting efforts. Works closely with the maintenance, quality, manufacturing operations, safety, and process development teams to implement equipment and/or process changes, as required
Plans and conducts small- to medium-size assigned projects within engineering specialty requiring conventional types of plans, investigations, and/or equipment. Coordinates and monitors activities/projects. Reviews plans and monitors status of implementation for those assigned to project; makes judgments regarding quality of implementation within discipline; employs contingency plans to recover from schedule slippage and financial overruns when appropriate. Works with the quality team and other stakeholders to develop and implement Corrective/Preventive (CAPA) actions, as required from the investigations
Estimates and coordinates resources needed (materials, budget, time and people) to accomplish assigned individual tasks. Anticipates future directions. Benchmarks internally and externally. Recognizes changes in the environment and present resources as indicators of future problems and opportunities; prepares for such eventualities
Independently executes the design of products/processes/equipment/systems/facilities by applying standard engineering theories, concepts, and techniques within the discipline. Independently investigates, conducts tests or experiments
Creates/modifies designs for intermediate problems. Designs/modifies more complex components/processes; writes detailed design specifications. Predicts patterns/trends. Grasp complexities and sees relationships among data; determines consequences and alternatives; makes recommendations
Implements methods/designs/processes. Recognizes and implements good ideas/innovations/cost reductions; consistently generates/adopts original solutions to problems and reduces them to practices
Mentors others by sharing technical expertise and providing feedback and guidance. Resolves underlying problems. Identifies full range of customer/client needs and proposes solutions to address them; makes alterations in products or services to better meet (recognized or unrecognized) customer needs
Directs the efforts of others such as technicians and outside resources. Performs tasks such as writing Capital Project Proposals, Standard Operating Procedures (SOP’s), safety/quality checklists and job aids, scope documents, etc. Works with the Validation Team to develops and execute validation protocols
Follow the Change Management process. This includes developing and presenting change requests, assures that tasks required for the change are executed and completed per plan, and closing out change requests
Qualification
Required
A Bachelors Degree in Engineering, science or closely related discipline is desired, or equivalent technical experience plus demonstrated competence, with a desired 2+ years of significant engineering and/or operational experience. Additional post-graduate education may contribute towards the desired years of experience
Has demonstrated competency within a discipline
Possesses a working technical knowledge and application of concepts, practices, and procedures. Ability to work on problems of moderate scope where analysis of situations or data requires a review of identifiable factors. Demonstrates judgment within defined procedures and practices to determine appropriate action
Interacts well with diverse groups within engineering and maintains strong working relationships with internal and external collaborators
Listens to and understands others' points of view and articulates tactfully and respectfully one's own perspective orally, in writing, and in presentations
Works well with other engineers in a collaborative, fast-paced goal-driven environment
Possesses interpersonal skills to negotiate and reconcile differences
Preferred
Has a technical background in health care, medical devices, pharmaceutical, biologics, or similar industries
Has experience with the use of single use consumables
Benefits
Paid time off (vacation, holidays, sick)
Medical/dental/vision insurance
401(k)
Company
AbbVie
AbbVie is a biopharmaceutical company focused on immunology, oncology, neuroscience, virology, and aesthetics. It is a sub-organization of AbbVie.
10001+ employees
H1B Sponsorship
AbbVie has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (273)
2024 (190)
2023 (225)
2022 (284)
2021 (186)
2020 (186)
Funding
Current Stage
Public CompanyTotal Funding
$15B2024-02-27Post Ipo Debt· $15B
2023-03-08Post Ipo Equity· $0.25M
2012-12-20IPO
Leadership Team
Robert Michael
Chairman of the Board and Chief Executive Officer
Micah Bregman
Vice President, Global Strategy and Pipeline, Allergan Aesthetics
Recent News
Pharmaceutical Technology
2026-01-13
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