Production Associate II

Abbott•Madison, WI

1d•Onsite

About The Position

The Production Associate II is an entry-level role and a starting point for developing the skills and training needed to support Abbott Cancer Diagnostics Production Operations. The associate performs a range of production functions, including bulk reagent production and dispensing, label application, and finished-goods kitting. Work is performed according to defined protocols and procedures, with frequent supervision. Depending on technical skills and business needs, the role may also include complex manufacturing and label printing. The position supports quality-system and continuous-improvement activities, inventory management, and upkeep of production laboratory spaces. It requires accurate and timely work, effective coordination with coworkers and other teams, adherence to safety and quality procedures, and the ability to work as part of a team or independently under supervision. The work takes place in a laboratory environment and involves production and laboratory equipment, protective gear, and exposure to irritants, electrical equipment, sharp instruments, toxic materials, and hazardous waste. The position is based at 650 Forward Dr in Madison, Wisconsin, and requires travel between Madison locations. Travel is listed as 10% of the time. The base pay is $17.00–$34.00 per hour.

Requirements

Associate degree in life sciences or a related field, or a high school diploma/GED and 2 years of relevant experience in lieu of the associate degree.
At least 1 year of experience in a general laboratory setting through prior job experience, education, or a combination of both.
Strong documentation skills and attention to detail appropriate for a GMP environment.
Proficiency with basic software applications, including Microsoft Office.
Legal authorization to work in the country of employment without current or future sponsorship.
Ability to perform the essential duties with or without accommodation.
Strong communication skills and ability to coordinate work with other teams.
Ability to follow written procedures with direction and complete work accurately, on time, and safely.
Ability to cooperate with coworkers in an organized team environment or work alone with supervision.
Ability to manage time effectively and complete work within expected time frames.
Ability to work the designated schedule and overtime as needed.
Ability to lift up to 40 pounds for approximately 25% of a typical working day.
Ability to work seated for approximately 20% and standing for approximately 80% of a typical working day.
Ability to use a mobile device, tablet, or computer and/or type for approximately 50% of a typical working day.
Ability to grasp with both hands, pinch with thumb and forefinger, turn with hand/arm, and reach above shoulder height.
Ability to use laboratory equipment and moving machinery for extended periods, including pipetting and traying robots.
Ability to wear required safety gear and work at a laboratory bench or fume hood for extended periods.
Ability to perform fine manipulation and simple grasping with the hands for extended periods.
Ability and means to travel between Madison locations.

Nice To Haves

Bachelor's degree in life sciences or a related field.
Experience in a GMP environment.
Experience following standard operating procedures.
Strong documentation practices and cGMP experience.

Responsibilities

Prepare simple buffers and perform manual dispensing.
Support automated Fill / Cap / Label processes and kit finished goods.
As skills and business needs dictate, participate in complex manufacturing and label printing.
Assist with improvement efforts through the Change Request / Change Order process or other means.
Assist with Nonconforming Material Reports, Change Orders, Out of Specifications, Investigations, Corrective Actions, and related deliverables.
Support inventory management using the KANBAN system for raw materials, intermediates, disposables, and spare parts related to Production areas.
Assist with Production support activities, including cleaning Production laboratory spaces.
Participate in continuous-improvement projects and support other area needs as demand requires.
Coordinate work and communicate with other teams.
Follow written procedures, complete assignments accurately and on time, and work safely.
Support and comply with the company's Quality Management System policies and procedures.
Maintain regular, reliable attendance and work the designated schedule, including overtime as needed.
Use laboratory equipment and moving machinery, and comply with applicable personal protective equipment and safety requirements.