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Assembler 2 - 2nd Shift

Becton Dickinson

USA TX - El Paso - Northwestern Dr., USonsite

See all 141 open roles at Becton Dickinson

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About this role



 We are the people who give possibilities purpose

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. 

 Job Description Job Summary:  

Responsible for performing assembly, packaging, and labeling of medical products with a higher level of   proficiency , in compliance with GMP requirements, BD procedures, and quality standards. This role   operates   manufacturing equipment across multiple processes, ensures product quality, and supports manufacturing operations by troubleshooting issues,   assisting   in process execution, and promoting adherence to safety and operational standards.   Additionally, this position provides support to other areas and helps reinforce process awareness among associates.  

Demonstrates initiative, willingness, and a positive attitude to continuously develop skills and knowledge within certified operations. Promotes process awareness among associates and contributes to personal and team development through daily performance.  

Job Responsibilities:  

• Perform assembly, packaging, and labeling of medical devices and pharmaceutical products in compliance with GMP, SOPs, and quality standards.  

• Operate and be certified in multiple manufacturing processes or groups of operations across different areas.  

• Execute production activities using batch records, job aids, SOPs, and product specifications.  

• Interpret manufacturing documentation to ensure   accurate   and efficient process execution.  

• Perform in-process and final visual inspections to ensure product and packaging meet quality requirements.  

• Accurately complete and review batch records, production logs, and documentation in compliance with GMP, GDP, FDA, and ISO standards.  

• Meet daily production targets in alignment with the established day-by-hour production plan.  

• Monitor, capture, and report downtime, scrap, and production performance metrics.  

• Coordinate execution of manufacturing schedules for assigned batches or operations.  

• Ensure availability of required materials before   initiating   operations.  

• Handle, segregate, and dispose of non-conforming materials   in accordance with   established procedures.  

• Maintain cleanliness and organization of work areas, equipment, and operations in alignment with 5S and cleanroom standards.  

• Support manufacturing-related activities including calibration, work orders, and validation processes as   required .  

• Identify , troubleshoot, and communicate production issues, risks, or deviations to the supervisor or designee   in a timely manner .  

• Support and   maintain   a safe work environment, including participation in safety programs such as Employee Safety Observations (ESO).  

• Follow all safety requirements and   properly use   personal protective equipment (PPE), including but not limited to lab coats, gloves, hair/beard covers, shoe covers, hearing protection, eye protection, and specialized cleanroom garments as   required .  

• Maintain regular attendance and punctuality   in accordance with   company policies.  

• Maintain positive working relationships with peers and supervisors.  

• Maintain open communication to ensure operational issues and changes are communicated and resolved   in a timely manner .  

• Provide guidance, training, and knowledge sharing to other associates as needed.  

• Teach and explain operational processes to other associates as   required   to support effective process execution and knowledge transfer.  

• Support continuous improvement initiatives, including 5S, standardization, and process simplification.  

• Participate in Kaizen events and Level 1 Shift Kickoff Meetings as   required .  

• Suggest improvement opportunities related to equipment, processes, quality, or workplace organization.  

• Provide backup support across multiple equipment, operations, or areas as   required .  

• Support production continuity by covering operational activities and assisting in other areas   when   business needs require it.  

• Communicate issues, concerns, and potential risks that may impact product quality or manufacturing processes.  

• Comply with   all company policies and regulatory requirements.  

• Perform other duties as assigned.  

Education and Experience:  

Education:    

• Completed   High School or equivalent preferred.  

Experience:    

• 1   to   3   years of experience in a   high   paced   medical   manufacturing environment.    

Knowledge and Skills:  

Professional   Skills  

• Knowledge of EH&S standards and safety procedures (required).  

• Strong understanding of manufacturing processes and production flow (required).  

• Knowledge of GMP and Quality Systems; familiarity with GDP is   required .  

• Ability to interpret and apply manufacturing documentation (e.g., SOPs, batch records, specifications).  

• Ability to perform inspections and testing activities (visual, in-process, and final product verification).  

• Intermediate troubleshooting and problem-solving skills related to equipment, processes, and set-up conditions.  

• Basic understanding of equipment maintenance principles.  

• Awareness of escalation processes for quality, safety, or production issues.  

• Basic mathematical skills (addition, subtraction, multiplication, division, fractions, decimals, and percentages).  

• Basic computer skills, including   proficiency   in a Windows environment and Microsoft Office (Outlook, Word, Excel).  

• Effective oral and written communication skills; bilingual Spanish/English preferred.  

• Ability to work independently and within cross-functional teams.  

• Fami

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