Microbiologist I.US-PBF.427

3 days left

Integra LifeSciences
Plainsboro, New Jersey, US
Jun 26, 2021
Jul 30, 2021
Employment Type
Full time
Salary Type
Integra LifeSciencesis a global leader in regenerative technologies and neurosurgical solutions dedicated to limiting uncertainty for clinicians, so they can focus on providing the best patient care.Founded in 1989, Integra develops, manufactures, sells and supplies best-in-class products to regenerate tissue, remove brain tumors, prevent infection and much more. And over the last three decades, weve evolved into one of the worlds leading global medical technology companies with more than 4,000 dedicated employees who deliver innovative medical technology solutions.But thats just the beginning.Integra is growing at an unprecedented rate. Were at a moment in time where the experience youll gain is more robust than the experience you bring. And were out to invest in your future because its the best way to maximize ours.At Integra, we firmly believe our people are our greatest asset and the foundation of our success. Our comprehensive Global Total Rewards program provides competitive compensation and benefits designed to keep our people healthy, motivated and engaged. Investing in our people through these programs is possible because of Integras ongoing commitment to our values and our shared success.Integras health as a company begins with the well-being of our people. Benefit programs vary by country, whether provided through company-sponsored insurance and programs, through statutory government programs, or a combination of both.Regardless of geographic location, our commitment is to offer the following, whenever possible:Benefit plans that meet all local statutory requirementsA range of programs that reflect typical local market practicesAn opportunity for employees to tailor benefits to their specific needsBenefits that balance employees short-term and long-term needsClick HERE for more information regarding our benefits and total rewards program

The Microbiologist I will provide to the QC Microbiology Laboratory as pertaining to the respective responsibilities. Performs functions such a executing laboratory testing for in-process and finished good products, water, stability studies, and validation studies as well as performs environmental monitoring. This position is responsible for operating in compliance with all applicable procedures and policies.ESSENTIAL DUTIES AND RESPONSIBILITIESTo perform this job successfully, anindividual must be able to perform each essential duty satisfactory.Ensure compliance with all company polices and procedures and appropriate regulations, including FDA and ISO 9001, ISO 13485, CMDR and the Medical Device Directive.Perform and document in-house microbiological testing on all in-process and finished products to comply wih acceptance requirements.Perform LAL, water analysis, growth promotion, gram staining, identification of microorganisms and other microbiological testing.Perform and document environmental monitoring in compliance with Standard Operating Procedures.Report any equipment and testing deviations to the Supervisor.Submit samples for shipment to third party labs when necessary.Maintain GMP/GLP laboratory notebooks and documentation relevant to the duties and responsibilities assigned.Assist with proper execution of laboratory Alert/Action (AA) and Out-of-Specification (OOS) investigations.Interact and coordinateactivities with otherdepartments and external vendors to support and meet the facility goals and objectives, especially related to environmental monitoring.Assist management in updating Standard Operating Procedures (SOPs).Perform data entry and assist with trend reporting as needed.Train team members in Microbiology department.Provide gowning training andqualification to operators, cleaning and other essential staff.Handle and dispose of biohazard material in compliance with OSHA and Standard Operating Procedures.Perform other relatedduties as required.

Bachelor's degree, in Microbiology or Biology preferred0-3 years of relevant GMP/GLP laboratoryexperience in regulated industry preferredCapable of effective written and verbal communicationMust be able to work independently with minimal supervisionKnowledge of MS Office Suite

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