Senior Process Engineer

Allergan; Greenlawn (NY); On-site; USD 80,000 - 120,000; Full time

Job summary

An established industry player is seeking a Senior Process Engineer to drive New Product Introduction in a dynamic biologics manufacturing environment. This role involves leading facility fit assessments, managing projects, and mentoring engineering staff while ensuring compliance with industry standards. The ideal candidate will possess strong project management skills and a solid technical background in engineering and biologics. Join a team dedicated to innovation and excellence, where your contributions will directly impact the development of life-changing therapies and solutions. If you thrive in a collaborative, fast-paced setting and are passionate about making a difference, this opportunity is perfect for you.

Benefits

Paid Time Off

Medical Insurance

Dental Insurance

Vision Insurance

401(k) Plan

Short-term Incentive Programs

Qualifications

• 5+ years of engineering experience in biologics manufacturing.
• Strong project management and technical knowledge required.

Responsibilities

• Lead facility fit activities for New Product Introduction with minimal supervision.
• Mentor engineering staff and manage medium to large projects.

Skills

Project Management

Engineering Knowledge

Problem Solving

Interpersonal Skills

Technical Communication

Education

Bachelor's degree in Engineering or Science

Post-graduate education/degree

Tools

GMP Standards

Bioprocessing Equipment

Job description

Company Description

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

Job Description

Purpose

This Senior Process Engineer is responsible for providing engineering support for New Product Introduction (NPI) within an active Biologics manufacturing facility. This includes support of facility fit assessment through Master Record generation and manufacturing startup. This engineering professional, who, working with little or no supervision, applies scientific knowledge, engineering knowledge, and mathematics to support and execute NPI, manage medium to large projects, equipment optimization, and maintain/track assigned priorities. This individual will leverage their knowledge of other related disciplines beyond their own area of expertise to support NPI. This individual requires strong project management skills as they will be working with other engineering functions, operations and S&T to complete the full scope of NPI.

Responsibilities

• Leads facility fit activities for New Product Introduction (NPI) from clinical phase 1 to commercial projects with little to no supervision. NPI activities also include equipment walkdowns, batch record review, leading technical discussions and working with vendors.
• Effectively assesses and prioritizes mid to long term objectives/tasks and translates them into actionable work streams.
• Responsible for compliance with applicable policies and procedures. Leads early risk assessments and evaluation of potential consequences (defects and failure modes) of design changes to established processes.
• Mentors engineering staff and serves as a technical leader for matters associated with biologics manufacturing and tech transfer.
• Plans and conducts medium to large projects related to bioprocessing equipment and process improvements. Projects may require refining of a given scope and determining overall action plan and timelines. Additionally, it requires generation of validated change plans with validation requirements. Able to execute actions of those plans with minimal oversight and resolve issues as they arise with minimal to no support. Communicate progress to all stakeholders through verbal and written communications.
• Leads troubleshooting activities with little to no oversight to resolve process/equipment anomalies. Describes and communicates required actions to internal and external stakeholders with varying levels of technical acumen. Engages with operational staff on the floor in a GMP cleaning room setting to understand what activities are being performed. Leverages strong process and engineering knowledge to identify issues on the production floor proactively.
• Builds relationships, initiates and cultivates open, honest relationships with colleagues, customers, contractors, and vendors by establishing rapport, developing an understanding of others’ needs, promoting common goals, and following through on commitments.
• Conveys information effectively through verbal, written, and presentations to stakeholders and team members, both internal and external to AbbVie, using appropriate communication protocols. Identifies ways to increase customer satisfaction. Documents agreements and commitments and keeps direct customers informed.
• Facilitates the definition of a project scope with stakeholders. Converts goals to tasks and steps. Within structure, plans own work, manages several, often concurrent, tasks to accomplish assigned tasks to meet or exceed expectations (cost, quality, time). Participates in basic economic analysis and feasibility studies related to project alternatives under guidance. Jointly responsible for achieving the project’s financial targets in support of business objectives.
• Interprets problems and either creates or modifies design solutions. Reviews existing layouts and standards and creates a proposed design. Applies standard engineering principles and methodologies to interpret, draw conclusions and recommend solutions for problems considering a broad range of factors. Improves methods/designs/processes. Recognizes and implements innovations and cost reductions.
• Leads experiments/gathers data to perform detailed analysis and assess relevance to conceptualize complete solutions. Creates or coordinates the design solutions for moderately complex problems; integrates regulatory and operational needs; assesses cost benefit. Explores multiple alternatives. Structures studies and integrates cross-disciplinary and cross-functional issues to arrive at optimal cause of action with minimal support from management.

Qualifications

Qualifications

• Bachelor’s degree in engineering, science, or closely related discipline is desired, or equivalent technical experience plus demonstrated competence, with a desired 5+ years of significant engineering and/or operational experience. A post-graduate education/degree is desired and may contribute towards the desired years of experience.
• Has demonstrated competency within a discipline.
• Possesses a strong technical knowledge and application of concepts, practices, and procedures. Works on problems of complex scope where analysis of situations or data involves multiple competing 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.
• Has a technical background in health care, medical devices, pharmaceutical, biologics, or similar industries.

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:

• The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.

• 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.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.

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