Production Tech 1-3rd Shift

Description

Position Summary :

The Production Technician I position is responsible for the operation of high speed equipment used in the production and packaging of VITEK 2 cards in a cGMP compliant manner. The position may perform or assist in the setup, operation, inspection, maintenance, troubleshooting and cleaning of equipment used throughout the VITEK 2 Card Manufacturing and Packaging processes. Additionally, this individual will be responsible for completing production batches and corresponding documentation for the associated tasks, AQL inspections, reworks and material reconciliation that goes along with the batch. Contribute to building a positive work environment.

Primary Duties :

• Execute production activities per approved Manufacturing Directions while maintaining compliance with all job related SOPs.
• Ensure that all batch records are completed in an accurate, thorough, and timely manner.
• Execute validation protocols associated with manufacturing / packaging equipment and procedures including revalidation as required to maintain systems in a validated state.
• Provide assistance with the review and revision of Manufacturing Directions and SOPs necessary for the manufacture and packaging of product.
• Certified in operation of at least one high speed manufacturing equipment efficiently and effectively, in some cases highly automated, using HMI / SCADA interfaces.
• Engage in cage / rack movement, maintain product segregation, retrieve and organize raw materials, and ability to learn fork truck operation
• Follow appropriate departmental cleaning procedures to ensure adequate cleaning of the manufacturing areas
• Setup high speed manufacturing equipment, within defined tolerances, to ensure product runs are started on time and within established guidelines.
• 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.
• Maintain all work areas in a well-organized, clean and tidy manner at all times in compliance with cGMP requirements.
• Perform all work in compliance with company quality procedures and standards
• Performs other duties as assigned

Education and Training :

High School Diploma, GED equivalent

Experience :

No experience required; at least 1 year experience in FDA regulated manufacturing environment and GMP is desired.

Knowledge, Skills and Abilities :

T echnical learning aptitude to quickly understand and acquire new technical knowledge and skills.

Attention to detail and the ability to accurately interpret technical documentation are critical

Ability to perform computer applications including learning and performing SAP transactions

Ability to perform necessary calculations and complex task sequences in order to meet production requirements

Written Communications - including the ability to communicate technical data in written form

Effective verbal communication skills

Effectively navigate social interactions in the workplace

Participate in a way that enhances team performance and cohesion.

Physical Requirements :

Ability to stand for 8-12 hours. Ability to work overtime as required to cover a 24 / 7 operation. Extensive standing, repetitive hand and arm motions, ability to climb steps. Must be able to push a wheeled cage that can weigh up to 600 lbs fully loaded.

Operating within cool temperature and low humidity conditions within the production room. Constant noise is common due to the operation of the air-dry chamber, taping and pouching equipment.

Excellent personal hygiene required. Appropriate gowning requirements necessary for the production areas. Gloves are required to handle the product. Hairnet, clean room gowns and / or lab coats are required. Safety glasses and hearing protection are required personal protective gear.

Occasional environmental odors may be prevalent.

Please be aware that recruitment related scams are on the rise. Fraudulent job postings are being placed on other websites, and individuals posing as bioMerieux 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.com, Gmail.com, Yahoo.com, 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 https : / / careers.biomerieux.com / or contact us at [emailprotected] .

BioMerieux 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 accommodation in BioMerieux's or its affiliates' application process by contacting us via telephone at (385) 770-1132, by email at [emailprotected] , or by dialing 711 for access to Telecommunications Relay Services (TRS).