DiaSorin
Associate Scientist I, ATG
DiaSorin, Austin, Texas, us, 78716
Select how often (in days) to receive an alert:Associate Scientist I, ATG
Published on: Sep 27, 2024Country: United StatesLocation: Austin, TexasCompany: Luminex CorporationJob Category: Research & DevelopmentEmployment type: Regular Part TimeWhy Join Diasorin?
Impactful Work: When you join Diasorin, you become part of a team that's dedicated to improving lives. Your contributions will directly impact patient care, making a meaningful difference in the world.Global Reach & Innovation: Our work transcends borders. Joining Diasorin means collaborating with colleagues from all over the world, expanding your horizons, and contributing to global healthcare solutions at the forefront of the diagnostic industry.Diverse and Inclusive Culture: We believe in the strength of diversity, and our inclusive culture reflects this commitment. We value your unique perspective and offer a supportive, collaborative environment where everyone can thrive.Join Our Team: If you're passionate about innovation, diversity, and making a positive impact on healthcare, Diasorin is the place for you. We're looking for passionate and talented individuals who are ready to embrace new challenges and drive healthcare solutions forward.Are you ready to be part of a dynamic team that's shaping the future of diagnostics? Join Diasorin and become a catalyst for change in the world of healthcare. Apply today and be a part of our exciting journey toward a healthier, more connected world. Together, we can make an impact!Job ScopeThe
Associate Scientist I (ATG)
will participate in the Company's day-to-day production of critical research reagents and other research activities which include: design, execution and interpretation of scientific experiments and design and development of assays based on Luminex's technology platform and chemistries. The position will carry out scientific reagent production/purification and other experiments independently with supervision from senior members of the team.Day-to-day “hands on” work in the laboratory including generating, recording, and analyzing experimental data and maintaining laboratory records. This involves working in Biosafety Level II laboratory with biological samples, preparation of reagents, lab maintenance, nucleic acid synthesis and purification.Occasionally, assemble and present data to departmental, project, and cross-site teamsContribute to writing protocols and reports relating to feasibilityAssist in intellectual property developmentTroubleshoot technical difficulties, as requiredComply with the company quality policies and operating proceduresParticipate in the maintenance of general laboratory organizationOther duties as assigned.Education, Experience and QualificationsAssociate's Degree Community College 2-year diploma (technical) in biochemistry, biology, molecular biology, or a related scientific field required1+ Years Expertise in a variety of molecular and biochemical laboratory procedures preferred1+ Years Knowledge of routine laboratory methods such as PCR, data analyses, specimen handling and processing, and experimental documentation preferred1+ Years Working knowledge or experience with ISO 13485:2016 standards and FDA regulations preferred1+ Years Prior medical device industry experience preferredExcellent oral and written communication skills. (High proficiency)Ability to handle the pressure of meeting tight deadlines (High proficiency)Excellent interpersonal skills with proven ability to work both in a team-oriented environment and independently (High proficiency)Knowledge of Design Control requirements as defined by the FDA Quality System guidelines (High proficiency)Mathematics and statistics aptitude. (Medium proficiency)Data analysis and technical writing aptitude. (Medium proficiency)Proficient in Microsoft Word, Excel, and PowerPoint programs. (Medium proficiency)Highly organized with proven time management and prioritization skills (Medium proficiency)Ability to work independently and with minimal supervision (Medium proficiency)Travel Requirements10% DomesticWhat we offerReceive a competitive salary and benefits package as you grow your career at Diasorin. Join our team and discover how your work can impact the lives of people all over the world.Diasorin is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status, and will not be discriminated against on the basis of disability.
In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and Canada and to complete the required employment eligibility verification document form upon hire.#J-18808-Ljbffr
Published on: Sep 27, 2024Country: United StatesLocation: Austin, TexasCompany: Luminex CorporationJob Category: Research & DevelopmentEmployment type: Regular Part TimeWhy Join Diasorin?
Impactful Work: When you join Diasorin, you become part of a team that's dedicated to improving lives. Your contributions will directly impact patient care, making a meaningful difference in the world.Global Reach & Innovation: Our work transcends borders. Joining Diasorin means collaborating with colleagues from all over the world, expanding your horizons, and contributing to global healthcare solutions at the forefront of the diagnostic industry.Diverse and Inclusive Culture: We believe in the strength of diversity, and our inclusive culture reflects this commitment. We value your unique perspective and offer a supportive, collaborative environment where everyone can thrive.Join Our Team: If you're passionate about innovation, diversity, and making a positive impact on healthcare, Diasorin is the place for you. We're looking for passionate and talented individuals who are ready to embrace new challenges and drive healthcare solutions forward.Are you ready to be part of a dynamic team that's shaping the future of diagnostics? Join Diasorin and become a catalyst for change in the world of healthcare. Apply today and be a part of our exciting journey toward a healthier, more connected world. Together, we can make an impact!Job ScopeThe
Associate Scientist I (ATG)
will participate in the Company's day-to-day production of critical research reagents and other research activities which include: design, execution and interpretation of scientific experiments and design and development of assays based on Luminex's technology platform and chemistries. The position will carry out scientific reagent production/purification and other experiments independently with supervision from senior members of the team.Day-to-day “hands on” work in the laboratory including generating, recording, and analyzing experimental data and maintaining laboratory records. This involves working in Biosafety Level II laboratory with biological samples, preparation of reagents, lab maintenance, nucleic acid synthesis and purification.Occasionally, assemble and present data to departmental, project, and cross-site teamsContribute to writing protocols and reports relating to feasibilityAssist in intellectual property developmentTroubleshoot technical difficulties, as requiredComply with the company quality policies and operating proceduresParticipate in the maintenance of general laboratory organizationOther duties as assigned.Education, Experience and QualificationsAssociate's Degree Community College 2-year diploma (technical) in biochemistry, biology, molecular biology, or a related scientific field required1+ Years Expertise in a variety of molecular and biochemical laboratory procedures preferred1+ Years Knowledge of routine laboratory methods such as PCR, data analyses, specimen handling and processing, and experimental documentation preferred1+ Years Working knowledge or experience with ISO 13485:2016 standards and FDA regulations preferred1+ Years Prior medical device industry experience preferredExcellent oral and written communication skills. (High proficiency)Ability to handle the pressure of meeting tight deadlines (High proficiency)Excellent interpersonal skills with proven ability to work both in a team-oriented environment and independently (High proficiency)Knowledge of Design Control requirements as defined by the FDA Quality System guidelines (High proficiency)Mathematics and statistics aptitude. (Medium proficiency)Data analysis and technical writing aptitude. (Medium proficiency)Proficient in Microsoft Word, Excel, and PowerPoint programs. (Medium proficiency)Highly organized with proven time management and prioritization skills (Medium proficiency)Ability to work independently and with minimal supervision (Medium proficiency)Travel Requirements10% DomesticWhat we offerReceive a competitive salary and benefits package as you grow your career at Diasorin. Join our team and discover how your work can impact the lives of people all over the world.Diasorin is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status, and will not be discriminated against on the basis of disability.
In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and Canada and to complete the required employment eligibility verification document form upon hire.#J-18808-Ljbffr