Help us change lives

At Exact Sciences, we’re helping change how the world prevents, detects and guides treatment for cancer. We give patients and clinicians the clarity needed to make confident decisions when they matter most. Join our team to find a purpose-driven career, an inclusive culture, and robust benefits to support your life while you’re working to help others.

Position Overview

The Production Associate I is an entry level position and is the starting point to acquire skills and training required for the Exact Sciences Production Operations team. This role will participate in a variety of Production functions which include bulk reagent production and dispensing, label application, and kitting of finished goods. The position will work within defined protocols and procedures with frequent supervision.

Essential Duties

include but are not limited to the following:

Perform simple buffer preparation and manual dispensing, support Automated Fill / Cap / Label processes, and kitting of finished goods; May participate in complex manufactures and label printing as technical skills and business needs dictate. Assist in improvement efforts, through the Change Request / Change Order process, or via other means.Assist in generating Nonconforming Material Reports, Change Orders, Out of Specifications, Investigations, and Corrective Actions, including any deliverables associated with these items. Support inventory management via KANBAN system for raw materials, intermediates, disposables and spare parts related to the Production areas.Assist in other Production support activities, such as cleaning of Production laboratory spaces. Assist with continuous improvement projects and support other area needs dependent on demand.Strong communication skills and ability to coordinate work with other teams.Ability to follow written procedures with direction.Ability to perform daily work assignments accurately, timely, and in a safe manner.Ability to cooperate with coworkers within an organized team environment or work alone with supervision.Ability to manage time effectively to complete work in expected time frames.Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork.Support and comply with the company’s Quality Management System policies and procedures.Regular and reliable attendance.Ability to work designated schedule.Ability to work 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% of a typical working day. Ability to work standing for approximately 80% of a typical working day.Ability to work on a mobile device, tablet, or in front of a computer screen and/or perform typing for approximately 50% of a typical working day.Ability to grasp with both hands; pinch with thumb and forefinger; turn with hand/arm; reach above shoulder height.Ability to comply with any applicable personal protective equipment requirements.Ability to utilize lab equipment and moving machinery for extended periods of time (includes pipetting, traying robots etc.).Ability to use and wear safety protective gear/equipment (e.g. safety glasses, lab coat, gloves, beard nets, hair nets, booties, hearing protection, etc.) and follow safety guidelines while in the lab etc., for extended periods of time.Ability to work at a laboratory bench or fume hood for extended periods of time.Working in a lab environment will require working with skin irritants, lung irritants, electrical equipment, sharp instruments, toxic materials, and hazardous waste. Ability to perform fine manipulation and simple grasping using hands for extended periods of time. Ability and means to travel between Madison locations.

Minimum Qualifications

Associates degree in life sciences or related field; or High School Degree/General Education Diploma and 2 years of relevant experience in lieu of Associates degree.  1+ years of experience in a general laboratory setting through prior job experience, education, or a combination of both. Demonstrated strong documentation skills and attention to detail necessary in a GMP environment. Proficient in using basic software applications including Microsoft Office.Authorization to work in the United States without sponsorship.Demonstrated ability to perform the Essential Duties of the position with or without accommodation.

Preferred Qualifications

Bachelor’s degree in life sciences or related field.Experience in a GMP environment.Experience following standard operating procedures.Strong documentation practices, cGMP experience.#LI-KB1

Salary Range:

$35,000.00 - $56,000.00

 

The annual base salary shown is for this position located in US - WI - Madison on a full-time basis. In addition, this position is bonus eligible, and is eligible to receive company stock upon hire as well as annually.

Exact Sciences is proud to offer an employee experience that includes paid time off (including days for vacation, holidays, volunteering, and personal time), paid leave for parents and caregivers, a retirement savings plan, wellness support, and health benefits including medical, prescription drug, dental, and vision coverage. Learn more about our benefits.

Our success relies on the experiences and perspectives of a diverse team, and Exact Sciences fosters a culture where all employees can develop personally and professionally with a sense of respect and belonging. If you require an accommodation, please contact us here.

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We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to age, color, creed, disability, gender identity, national origin, protected veteran status, race, religion, sex, sexual orientation, and any other status protected by applicable local, state, or federal law. Any applicant or employee may request to view applicable portions of the company’s affirmative action program.

To view the Right to Work, E-Verify Employer, and Pay Transparency notices and Federal, Federal Contractor, and State employment law posters, visit our compliance hub. The documents summarize important details of the law and provide key points that you have a right to know.