In 2012 the Company began a significant investment in additional hardware and software capabilities across their product lines and began to rollout the next generation of devices to serve their growing customer base which includes pharmaceutical companies, biotechnology companies, fertility clinics, university research centers, and other commercial and academic research establishments worldwide.

Who You Are: Minimum Qualificationa:Bachelors Degree in any engineering discipline 3+ years years of experience in definition, design, development and implementation of production control systems for advanced technology facilities Preferred Qualifications:PLC Programming, Motion Control and HMI experience (AB PLCs and Rockwell Software products)Experience in a commercial medical, biotechnology, Bio-pharmaceutical manufacturing environment is highly preferred.

Master's degree in a quantitative sciences discipline (e.g., Statistics, Mathematics, Computer Science) and a minimum of 6 years of experience in statistics or statistical programming in a pharmaceutical, biotechnology, CRO or related environment.

Independently design complex experiments, analyze and report resultsCollaborate with CST colleagues and with thought leaders to support studies Who you are and what you bring to the team: MS degree in a biological science (e.g. molecular biology, cell biology, biochemistry or biotechnology)At least 5 years of experience or BS with at least 10 years of experience.

As the Scientist, you will be responsible for supporting and executing the development of diagnostic assays in collaboration with top ranking biotechnology and pharmaceutical companies. Experience with In Vitro Diagnostic assay development strongly preferred.

Preferred Qualifications Associates in Electronics, Biotechnology or directly related scientific discipline Medical device and electromechanical device experience Ability to troubleshoot electronics Experience with programming languages Knowledge of electronics manufacturing Abiomed is an Equal Opportunity Employer committed to a diverse workforce.

Bachelor's degree in a science related field and 3-5 years of experience with assay development OR a Master's degree in a science related field with 2-4 years of experience with assay development OR a PhD in a science related field and 1-2 years of experience with assay development.

HTI's customer base consists of fertility clinics, university research centers, animal breeding facilities, pharmaceutical companies, biotechnology companies, and other commercial and academic research establishments.

2-3 years experience in the manufacturing biotechnology or pharmaceutical industry (OPM role) The OPM will be responsible for working between R&D and Operations to implement products into SAP (create BOM's, Part Numbers, etc.

Solid business acumen and knowledge of medical device or biotechnology environment. Device Industry or Clinical background in Mechanical Circulatory Support, Advanced Heart Failure, Cardiac Surgery, Extracorporeal MCS, Cardiac ICU.

This role is responsible for supporting and executing the development of diagnostic assays in collaboration with top biotechnology and pharmaceutical companies. Prepare reagents to execute experiments, conduct automated testing, and scan stained slides for data reporting using Leica Biosystems equipment.

Our client is a growing biotechnology business, with operations across the US, Europe and APAC. In response to the enormous growth the business has seen over recent years due to both organic growth and M&A activities, we are looking to hire an additional HR professional to join the team with a focus on Compensation and Benefits.

An MD or MBBS is required with a minimum of seven years of pharmacovigilance experience within the pharmaceutical or biotechnology industry. Our client is a clinical stage biotechnology company.

Perform routine data entry and analyses data to report results to the project Technical Lead. The Scientist will be responsible for performing required laboratory studies, recording own observations, preparing documents, reporting data, and providing results to support key decisions within the Pharma Partnerships business unit.

Perform routine data entry and analyses data to report results to the project Technical Lead. Work closely with R&D Technical Leads to ensure deliverables are achieved according to the project plan through appropriate scheduling of work and communication on status of assigned tasks.