Laboratory Technician

To be considered for this position please complete the following application: Laboratory Technician 

SUMMARY:
This position requires processing samples from individuals suspected of COVID-19. The Laboratory Technician in the Molecular Biology clinical laboratory will be responsible for performing nucleic acid-based assays where high level of proficiency in nucleic acid extraction methods and qPCR is required. High proficiency with independent data analysis required. Preferred experience in a high throughput lab where day to day activities are heavily driven by meeting deadlines.

RESPONSIBILITIES:
Each individual peforming high complexity testing must: 
– Follow the laboratory’s procedures for specimen handling and processing, test analyses, reporting and maintaing records of patient test results
– Maintain records that demonstrate that proficiency testing samples are tested in the same manner as patient specimens 
– Adhere to the laboratory’s quality control policies, document all quality control activities, instrument and procedural calibrations and maintenance performed
– Follow the laboratory’s established policies and procedures whenever test systems are not within the laboratory’s established acceptable levels of performance
– Adhere to safety guidelines, including the appropriate use of Personal Protective Equipment (PPE)
– Be capable of identifying problems that may adversely affect test performance or reporting of test results and either correct the problems or immediately notify the general supervisor, technical supervisor, clinical consultant, or director 
– Document all corrective actions taken when test systems deviate from the laboratory’s established performance specifications; and perform high complexity testing only under the onsite, direct supervision of a general supervisor qualified under Sec. 493.1461
– Train new technicians, as assigned 

As a Production Supervisor, you’ll bring a proven track record of hands-on
experience participating in and organizing day-to-day production workflow in a
manufacturing setting – preferably relating to medical devices, GMP manufacturing,
and/or any regulated industry. You’ve worked in a deadline driven environment
producing a technical product with a sharp eye for quality while meeting business
output goals. The Production Supervisor will be in constant cooperation with upper
management, logistics, quality, and engineering teams to schedule production
efforts and assure that assembly technicians are effectively managed, trained, and
equipped to build product.
As a Production Supervisor, you’ll b
ring a proven track record of hands-on
experience participating in and organizing day-to-day production workflow in a
manufacturing setting – preferably relating to medical devices, GMP manufacturing,
and/or any regulated industry. You’ve worked in a deadline driven environment
producing a technical product with a sharp eye for quality while meeting business
output goals. The Production Supervisor will be in constant cooperation with upper
management, logistics, quality, and engineering teams to schedule production
efforts and assure that assembly technicians are effectively managed, trained, and
equipped to build product.
– Monday – Thursday, 7:00 AM – 5:30 PM 
– Monday – Thursday, 5:00 PM – 3:30 AM
– Friday – Sunday, 7:00 AM – 7:30 PM

Some occasional shift flexibility is required, regular flexibility is preferred. 
The Quality Assurance Analyst is responsible for maintenance and
organization of incoming raw goods and materials for biology
consumable manufacturing as well as quality control testing and
documentation for product in accordance with Biomeme SOPs and
MPIs as well as general regulatory guidelines. This position will report
directly to the Quality Manager and assist in adherence to Biomeme
quality system requirements.
We are expanding rapidly in response to the global pandemic
and are in search of experienced Production Supervisors for
three shifts; Monday-Thursday 7:00 AM-5:30 PM, Monday-
Thursday 5:00 PM-3:30 AM, and Friday-Sunday 7:00 AM-7:30
PM. Some occasional shift flexibility is required, regular
flexibility preferred.
The Quality Assurance Analyst is responsible for maintenance and
organization of incoming raw goods and materials for biology
consumable manufacturing as well as quality control testing and
documentation for product in accordance with Biomeme SOPs and
MPIs as well as general regulatory guidelines. This position will report
directly to the Quality Manager and assist in adherence to Biomeme
quality system requirements.

We are exp

anding rapidly in response to the global pandemic

and are in search of experienced Production Supervisors for
three shifts; Monday-Thursday 7:00 AM-5:30 PM, Monday-
Thursday 5:00 PM-3:30 AM, and Friday-Sunday 7:00 AM-7:30
PM. Some occasional shift flexibility is required, regular

flexibility preferred.

 

REQUIREMENTS:
– Meets education and experience equivalent to guidelines mandated by Centers of Medicare and Medicaid Services (CMS) and with the Pennsylvania State Department of Health (PA DOH) requirements for Technical Personnel 
– A minimum of a Bachelor’s degree in medical technology, clinical laboratory, chemical, physical, or biological science including lab courses involving work with nucleic acid technology 
– 2+ years of relevant work experience with molecular biology skills, including qPCR and DNA/RNA Extraction preferred 
– Must be able to wear appropriate Personal Protective Equipment (PPE)
– Based on work assignment, may be reccomended to have medical testing in accordance with the company’s Occupational Health Program 

Due to ITAR compliance, this position requires candidates to be a U.S. Citizen, Permanent Resident Alien, or Protected Individual per 8 U.S.C. 1324b(a)(3)

Biomeme is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law. 

 

 

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