Production Associate I Role
3 days ago
At Exact Sciences, we are committed to changing the way the world prevents, detects, and guides cancer treatment. Our goal is to provide patients and clinicians with the clarity needed to make confident decisions during critical moments. Join us in finding a purpose-driven career, an inclusive culture, and comprehensive benefits that support your life while helping others.
Job Overview:
- The Production Associate I role is an entry-level position designed to develop skills and training for our Exact Sciences Production Operations team.
- This position participates in various production functions, including bulk reagent production, dispensing, label application, and kitting of finished goods.
- The position works within defined protocols and procedures with frequent supervision.
Key Responsibilities:
- 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 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.
Required Skills and Qualifications:
- Associate 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.
Benefits:
- Paid time off (including days for vacation, holidays, volunteering, and personal time).
- Paid leave for parents and caregivers.
- A retirement savings plan.
- Wellness support.
- Health benefits including medical, prescription drug, dental, and vision coverage.
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