Job Description Summary

Job Description

We are the makers of possible 

BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities. 

We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you’ll be supported to learn, grow and become your best self. Become a maker of possible with us. 

Assembler II, General

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.

In this position the Essential Functions:

• Responsible for completing required documentation (such as batch records, returns, etc.).
• Possess a basic understanding of production processes within area of assignment and a working knowledge of manufacturing equipment.
• Operate equipment in accordance to applicable manufacturing instructions/ operating procedures including machine set-ups and parameter documentation.
• 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 matters 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 business goals, e.g., improve yield, cycle time, quality, and productivity.
• 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

Qualifications

• High School Diploma/GED or 4 months of work experience in a manufacturing environment preferred.
• Work experience in chemical, pharmaceutical, or industry that complies with GMP is highly preferred. 
• Able to read, write, flue