General Assembler

Millenniumsoft•El Paso, TX

77d•Onsite

About The Position

At the BD Pharmaceutical Company, what matters most is helping all people live healthy lives. We focus on treating, curing and preventing some of the most devastating and complex diseases of our time. And we pursue the most promising science, wherever it might be found. Our mission drives us. Our patients inspire us. We collaborate with the world for the health of everyone in it. Thriving on a diverse company culture, celebrating the uniqueness of our employees and committed to inclusion. Proud to be an equal opportunity employer. Under direct supervision, trains to perform duties related to the preparation and manufacture of active pharmaceutical ingredients, intermediates, and/or medical devices in accordance with standard operating procedures, as regulated by quality, environmental, and safety agencies (FDA, OSHA, etc.). Performs any combination of tasks involved in the fabrication, manufacture, assembly, testing and packaging of medical devices as well as setting up, operating, performing maintenance on and troubleshooting equipment. May conduct quality inspections on processing line in accordance with quality specifications. Works within clearly defined SOPs and / or scientific methods and adheres to quality guidelines.

Requirements

High school diploma or equivalent.
Zero (0) to one (1) year of manufacturing assembly experience.
Effective communication skills at a level co-workers and Team Lead/Supervisor can understand.
Ability to read, write, interpret and comprehend specifications written in English and perform basic math calculations.
Ability to use basic tools of measurement, such as microscopes.
Must be able to work flexible and/or extended hours and report to work on a regular, punctual basis.
Has good attention to detail
Ability to get along with people and be able to work in a team environment.
Willingness to rotate into different tasks and responsibilities.

Nice To Haves

High School Diploma/GED preferred or 4 months of work experience in a manufacturing environment required.
Experience leading manufacturing machines is preferred.
Work experience in chemical, pharmaceutical, or industry that complies with GMP is highly preferred.
Able to read, write, and understand Basic English preferred.
Operating skills of manufacturing equipment, tools, and hand/pallet jack is preferred.
Basic PC navigation such as the ability to enter data into programs/software applications preferred.
Experience of leading small group of people is preferred.
Problem solving skills is highly preferred.
Ability to communicate and effectively work as part of a team is preferred.
Experience working third shift is highly preferred.

Responsibilities

Possess a basic understanding of production processes within area of assignment and a working knowledge of manufacturing equipment.
Follow GMP, s and standard operating procedures.
Follow process and utility flow diagrams.
Transport materials of varying weight in accordance with established safety guidelines using material handling equipment and additional assistance as required.
Perform area safety inspections to identify safety hazards and report findings in accordance with company protocols.
Demonstrates adherence to safety procedures by monitoring personal and peer behaviors, work environment and housekeeping.
Participate in internal audits and support additional team activities as requested.
Participate on site investigative teams and where applicable, NCR, s and behavioral safety assessments. Correct and/or mitigate findings from assessments.
Available for overtime as needed
Performs all duties with attention to quality, safety, and environmental matter such as wearing appropriate personal protective equipment, identifying, reporting, and appropriately responding to hazards in the work area (spills/accidents/near misses), maintaining proper housekeeping at all times, and properly labeling and storing chemicals.
Carries out duties in compliance with all state and federal regulations and guidelines including FDA, ISO, and OSHA. Complies with all company and site policies and procedures.
Assume responsibility for the environmental effects of work performed and for the identification and recording of environmental problems as they arise.
Follow all applicable aspects of the site Environmental Management System as it pertains to normal job duties.
Complete all regulatory training as assigned ( GPM, s, ISO14001, OSHA , etc.).
Complete Operator Training Program according to established guidelines.
Be available for other projects or assignments as requested by management.
Looking for ways to simplify or improve products, services, systems, and processes to achieve
Makes a positive contribution through demonstration of ability to seek out assistance from co-workers as needed; to suggest ways to improve upon current operations practices and systems; and to learn new skills, procedures and processes