Company | Meridian Bioscience, Inc. | Department | Operations | # of Openings | 1 |
Meridian Bioscience is a fully integrated life science company that develops, manufactures, markets and distributes a broad range of innovative diagnostic products. We are dedicated to developing and delivering better solutions that give answers with speed, accuracy and simplicity that are redefining the possibilities of life from discovery to diagnosis. We are looking for talented and passionate individuals that help drive our vision. Our innovative culture will allow interested candidates to discover and create, through collaboration, cutting edge solutions to tough problems.
The Production Technician has primary responsibility for production of in-vitro medical diagnostic products in accordance with current manufacturing directions, SOPs, GMPs, and QSR to meet or exceed quality specifications on schedule at or below standard costs. Identify areas, formulate and execute plans for manufacturing process quality and efficiency improvements. Work in collaboration with Manufacturing, Quality Systems, Technical Support, Sales and Marketing to ensure product quality and availability.
Tasks and Responsibilites:
Other Duties:
Minimum Education or Equivalent Experience Required/Preferred
* Bachelor's degree in Molecular Biology, Microbiology, Biochemistry, or similar degree required.
* Experience in a FDA-regulated manufacturing, or laboratory environment is desirable.
* Previous course work in immunology, microbiology cell biology, biochemistry, virology and chemistry is desirable.
Competencies Required or preferred
* Preferred skills include Cell culture, Virus culture, Bacteriology, Protein purification and conjugation, Microscopy, experience with Laboratory equipment including Spectrophotometer pH meter, centrifuges, column chromatography, and performing diagnostic assays.
* Communication skills include: ability to interact with Manufacturing and Quality function; clearly inform supervisory personnel regarding status of projects; and establish and follow target date scheduling and reporting procedures.
* Aseptic technique, general laboratory techniques and metric system knowledge required.
* Excellent documentation skills as required by cGMPs on a timely basis.
* Ability to read, understand and follow all company SOPs and guidelines.
* Must be a self-starter, detail oriented, organized, prioritize and balance workloads and timelines and be able to perform under pressure in a fast-paced environment.
* Ability to maintain regular attendance and punctuality requirements
* Must be able to work hours outside of the normal work day (start early, stay late or weekends) to support department activities.
* Must be able to work independently as well as collaboratively in a team setting with peers and colleagues in a cross functional setting.
* Computer proficient in Microsoft Office programs. Experience in technical writing (GMP documents, protocols, reports, etc) a plus.
*We are proud to be an EEO/AA employer Minority/Female/Disability/Veteran. We maintain a drug-free workplace and perform pre-employment substance abuse testing. (USA Only)*