Job Details

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 (https://www.tiktok.com/@abbvie) .

Job Description

Purpose

• This role requires four 10-hour shifts.

Sets up equipment for routine processes. Operates complex equipment and monitors manufacturing processes. Conversant with overall functionality of departmental processes. Communicates all operational events and issues with appropriate individuals. Identifies opportunities for improvement throughout the operations and assists in the implementation of changes both in physical operations and written documents. Operates all certified jobs and maintains operating conditions within the desired range with minimal supervision. Sets up equipment to accommodate minor processing changes. Is knowledgeable on work processes to assist with identifying and implementing work improvements.

Responsibilities

• Prepared to take on leadership responsibilities.

• Has conducted and is comfortable preparing training for others.

• Engagement in process workflows and process improvements.

• Ability to train team members.

• Knowledgeable of jobs in assigned area of responsibility and Good Manufacturing Practice (GMP) policies. Demonstrates compliance to local and industry quality and safety standards.

• Records work performed in regards to GDP guidelines in a regulated environment.

• Operates either manual or controlled process equipment in an aseptic manufacturing environment with mammalian cell culture.

• Wears gowning for Grade C environment.

• Has knowledge of equipment and manufacturing process and can operate with minimal help of the certified and qualified trainer. Comprehends and applies all required technical, regulatory, and safety training.

• Ability to troubleshoot problem situations with minimal assistance.

• Under minimal supervision makes timely decision to accomplish department goals. Recommends improved manufacturing and departmental processes, and takes ownership of tasks.

• Listens actively to acquire information and understand work procedures. Participates in the sharing of information to promote overall efficiency of production. Attends and actively participates in meetings

• Works to resolve conflict in professional and constructive manner with individuals inside and outside operating environment.

Qualifications

• Minimum High School diploma or GED required.

• Minimum 3 years experience in a cGMP environment. Clean room environment experience a plus.

• Must have strong technical knowledge with manufacturing experience in a chemical, biological, pharmaceutical, or similar environment.

• Prior supervisory experience is a plus.

• Must have a comprehensive understanding of plant economics to make decisions aimed at efficiency, quality, safety and reliability.

• General computer knowledge (i.e. Microsoft Office, Email, etc.). Proficient use of manufacturing monitoring systems to track and trend data critical to processes (i.e. PI, SAP, etc.)

Additional Information

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

Salary: $26.1 - $47.1