Manufacturing Tech 2 – Night Shift Position Available In Durham, North Carolina

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Company:
Biofire Diagnostics
Salary:
JobFull-timeOnsite

Job Description

Manufacturing Tech 2 –

Night Shift Location:

Durham, NC, United States

Position Type:

Unfixed Term

Job Function:
Manufacturing :

to facebook to twitter to A world leader in the field of in vitro diagnostics for more than 60 years, bioMérieux provides diagnostic solutions which determine the source of disease and contamination to improve patient health and ensure consumer safety. In North America we have more than 6,200 team members across 11 sites or subsidiaries, including Salt Lake City-based BioFire Diagnostics and one subsidiary in Montreal, Canada. Come and join a family-owned globalpany with a long-term vision, and a human-centered culture. Description Benefits at bio

Merieux:

Low-cost medical, dental, and vision benefits starting day one.
11 paid holidays
160 hours of paid time off
Annual bonus
9.5% 401kpany contribution with no vesting period
Tuition reimbursement up to $10,000 per calendar year
Onsite cafeteria with daily food stipend

Position Summary & Responsibilities:

Normal working hours: 7:00pm – 7:30am working a 2-2-3 rotation schedule. The Process Technician position is responsible for the operation of high-speed equipment used in the production and packaging of BacT/ALERT bottles and/or preparing and formulating the liquid reagents that fill the finished BacT/ALERT bottle in a cGMPpliant manner. Production
Operate high speed manufacturing equipment, in some cases highly automated, using

HMI/SCADA

interfaces
Execute production activities per approved Manufacturing Directions while maintainingpliance with all job-related SOPs
Quality
Ensure that all batch paperwork ispleted in an accurate, thorough, and timely manner
Perform and document all processes and procedures in a timely manner, while maintainingpliance with allpany and regulatory agency regulations
Provide assistance with the review and revision of Manufacturing Directions and SOPs necessary for the manufacture and packaging of product.
Assist with manufacturing deviation analysis, CAPA actions and other process equipment related quality concerns
Maintain all work areas in a wellanized, clean and tidy manner at all times inpliance with cGMP requirements
Operate cleaning equipment, utilize SOP and documentation to record data manually or through identified software applications.
Perform self-audit of rooms and processes
Train and certify teammates on production processes and procedures
Safety
Comply with all safety policies and procedures at all times
Appropriately use PPE (Personal Protection Equipment) as required to perform routine and non-routine duties.
Other Duties
Generate reports, charts and KPI’s and interpret the data to identify problems, and proceed with proper decision making
Work with other departments and assist with executing validation protocols associated with manufacturing/packaging equipment and procedures including revalidation as scheduled or required to maintain systems in a validated state
Attention to detail and the ability to accurately interpret technical documentation are critical
Performputer applications including learning and execution of SAP transactions
Communicate with Materials Management, Production Operations, and Quality Control on a daily basis to ensure the timely and efficient production of all of our customer requirements
Other duties as assigned by manager
Assess when manufacturing or quality issues require escalation to senior staff or management to promptly address potential impacts on business continuity.
Executing tasks accurately and efficiently is fundamental to meeting customer expectations and maintaining business continuity. Any disruptions in workflow directly impact production targets, affecting customer satisfaction and, ultimately, thepany’s financial health.

Education, Skills, & Experience:

High School Diploma or GED Required with 2+ years of relevant experience in a regulated production/operations environment, OR Equivalent military experience, OR BioWorks, LEAN or other Continuous Improvement Certificate,
Associate’s Degree with 1+ year of relevant experience in a regulated production/operations environment also accepted
Certification in a Bioworks Program or equivalent is preferred Demonstrated proficiency in the operation of high speed, highly automated, production equipment preferred. Knowledge of and experience in following OSHA regulations (LOTO, electrical safety, etc.) preferred. Knowledge of FDA and/or GMP regulations preferred. Mechanical background preferred. Please be aware that recruitment related scams are on the rise. Fraudulent job postings are being placed on other s, and individuals posing as bioMérieux Talent Acquisition team members are reaching out via email or text message in an attempt to collect your personal and confidential information. In some cases, these scammers are also conducting bogus interviews prior to extending fraudulent offers of employment. Beware of individuals reaching out using general phone numbers and non-bioMerieux email domains (i.e. Hotmail, Gmail, Yahoo, etc.). If you are concerned that an interview experience or offer of employment might be a scam, please make sure you are searching for the posting on our careers site careers.biomerieux/ or contact us at recruitmentbiomerieux. BioMérieux Inc. and its affiliates are Equal Opportunity/Affirmative Action Employers. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status, or genetic information. Please be advised that the receipt of satisfactory responses to reference requests and the provision of satisfactory proof of an applicant’s identity and legal authorization to work in the United States are required of all new hires. Any misrepresentation, falsification, or material omission may result in the failure to receive an offer, the retraction of an offer, or if already hired, dismissal. If you are a qualified individual with a disability, you may request a reasonable amodation in BioMérieux’s or its affiliates’ application process by contacting us via telephone at (385) 770-1132, by email at recruitmentbiomerieux, or by dialing 711 for access to Telmunications Relay Services (TRS). : to facebook to twitter to

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