Specialist Manufacturing Tech at Abbott Laboratories Limited

Lewes, Delaware, United States -

Full Time

Start Date

Immediate

Expiry Date

10 Oct, 26

Salary

40.65

Posted On

12 Jul, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Lab Operations, Manufacturing Operations, Inventory Management, Document Control, Device History Records (DHR), Quality Management Systems (QMS), FDA Regulations, GMP, ISO Standards, Chemical Handling, Fermentation, Tissue Culture, Buffer/Media Solution Preparation, SAP, MS Excel, Communication

Industry

Hospitals and Health Care

Description

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000 colleagues serve people in more than 160 countries. Specialist Manufacturing Tech Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to: Career development with an international company where you can grow the career you dream of. Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year. An excellent retirement savings plan with high employer contribution. Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree. A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune. A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists. The Opportunity The Specialist Mfg. Tech works out of our Abbott Park (Lake Bluff), IL location in the Core Diagnostics Division. Our diagnostic solutions are used in hospitals, laboratories, and clinics around the globe. The crucial information derived from our tests, instruments and informatics systems are often the first step in patient care decision making for hundreds of health conditions from heart attacks to blood disorders to infectious diseases and cancers. This position is responsible for the production of In Vitro Diagnostic products in a controlled manufacturing environment. What You’ll Work On Performs routine lab operations and basic manufacturing operations. May assist in performing more complex operations. Ability to read, comprehend, and follow written procedures with attention to detail. Understand verbal instructions and effectively communicate within a team. Accountable for completing assigned work orders in a manner that achieves overall schedule requirements. Performs basic electronic transactions associated with systems used for inventory management and document control. Accurately maintains inventory records and assists with conducting inventory verification checks as needed. Documents manufacturing activities in an accurate, timely and complete manner. Maintains accurate Device History Records (DHR) and quality documents to ensure all parts are traceable. Responsible for ensuring the quality of all products and raising any quality issues to the supervisor. Understanding of and ability to use computer software packages. Works with colleagues and the supervisor to resolve basic issues that arise during day-day operations. Ability to adapt quickly and manage time effectively when workload changes based on the business needs. Understanding of team goals and performance metrics and individually contributes to meet these goals. Performs assigned activities in a manner that contributes to the achievement of team productivity and financial goals. Positively represent the company during tours by demonstrating techniques and sharing appropriate information in a professional manner. Works safely and in accordance with all applicable policies and procedures. Understanding of the job training requirements and ensures all training is conducted on time. Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS)), and other regulatory requirements. Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors. Required Qualifications High School Diploma/GED 2 years related work experience Preferred Qualifications Bachelor's degree (BA, BS) in a scientific or technical discipline is preferred Experience in GMP, ISO, and FDA controlled environments preferred Laboratory, verbal and written communication skills, basic scientific knowledge, basic mathematics, and basic computer skills Highly desirable experience includes participation in teams, GMP/ISO requirements and basic computer/data management. Solution/Chemical handling, Knowledge of regulations and standards affecting IVDs and Biologics 1 – 2 (+) years’ experience with Fermentation, tissue culture and/or making buffer/media solutions SAP, work order tracking system or similar MS Excel Apply Now Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity. Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews. The base pay for this position is $20.35 – $40.65 per hour. In specific locations, the pay range may vary from the range posted.

How To Apply:

Incase you would like to apply to this job directly from the source, please click here

Responsibilities

Responsible for the production of In Vitro Diagnostic products within a controlled manufacturing environment. This includes performing lab operations, maintaining accurate quality documentation, and ensuring compliance with FDA and company regulations.