Job posting has expired
Contract Technical Associate Kit Assembly
![]() | |
![]() United States, Maryland, Germantown | |
![]() 19300 Germantown Road (Show on map) | |
![]() | |
Overview
At QIAGEN, we are driven by a simple but powerful vision: making improvements in life possible. We're dedicated to revolutionizing science and healthcare for the better. From our entrepreneurial roots to our current global presence, we've grown into a force for positive change. With thousands of employees across six continents, collaboration is our greatest strength. We're always striving to identify talented individuals to join our exceptional teams. We have played a pivotal role in shaping modern science and healthcare, and we're just getting started. If you're someone who thrives on new challenges, and wants to make a tangible difference in people's lives, then QIAGEN is the place for you. At QIAGEN, every day is an opportunity to make a real-life impact. Join us, grow with us, and together, let's shape the future of biological discovery. Position Description The Contract Technical Associate in Kit Assembly 1st shift comprehends and performs assigned manual assembly / production tasks according to established Standard Operating Procedures (SOPs). - Adhere to and accurately complete all production-related documentation. - Responsible for set up, trouble shooting and operation of production related equipment within the assembly area. - Responsible for maintaining product quality. - Assist in the setup and preparation (counting/verification) of required production related materials. - Contribute to cross-functional process improvement initiatives. - Contribute to and support department/corporate goals. - Responsible for ensuring on-going compliance to applicable quality and EHS regulations and standards (e.g., ISO, US FDA, MDD, IVDD, EU-PSHA, OSHA, etc.). This position will be hired through a third-party agency and is not directly employed by QIAGEN. Position Requirements - High School diploma or equivalent with 1-3 years of related work experience, or an AA degree with related work experience. - Understanding of FDA and cGMP regulated production practices is preferred. - In-depth knowledge of job tasks; general to minimal supervision required. - Able to use general/automated laboratory/production equipment. - Must be computer savvy - Able to plan use of equipment, materials and personal time efficiently. - Able to complete/review production-related documentation accurately. - Basic mathematical skills are required. - Able to resolve production issues independently. - Work safely and effectively in a team environment. - Strong organization and attention to detail skills. - Able to communicate issues and problems to supervisors. - The work environment is fast-paced and involves the ability to quickly change priorities and multi-task while maintaining a professional demeanor. - Able to read, write and understand the English language. - No travel required. - Must lift up to 50 pounds repetitively. - Must work in a standing position for extended periods of time. Personal Requirements - Dependable - Detail oriented - Strong motivation - Punctual The typical pay rate for this role is $18/hour. This temporary and/or contract position is not eligible for QIAGEN's company benefits. The position includes only those benefits mandated by applicable state and federal law, if any, which are provided by the agency employer. What we offer Our people are the heartbeat of everything we do. Passion drives us as we push boundaries to innovate and evolve.We inspire with our leadership and make an impact with our actions.We cultivate a collaborative, supportive environment where each individual and team can flourish. We champion accountability and encourage entrepreneurial thinking. QIAGEN is committed to creating an inclusive environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, disability or any other status protected by applicable law. QIAGEN complies with applicable laws regarding the confidentiality of employee health information and the reasonable accommodation of individuals with disabilities and/or sincerely held religious beliefs. Candidates who require accommodation should contactrecruting@qiagen.com. This policy is part of QIAGEN's ongoing efforts to support public health efforts and to ensure the safety and-well-being of its employees, customers, business partners, and community. |