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Becton Dickinson

Becton Dickinson

Global medical devices and diagnostics provider

Assembler 2

Full-TimeUpdated on 9/18/2026
No salary listed
Junior
El Paso, TX, USA
In Person

About the job

Requirements
  • One to three years of experience in a high-paced medical manufacturing environment.
  • Knowledge of environmental, health, and safety standards and safety procedures.
  • Strong understanding of manufacturing processes and production flow.
  • Knowledge of Good Manufacturing Practices and quality systems, with familiarity with Good Documentation Practices.
  • Ability to interpret and apply manufacturing documentation, including standard operating procedures, batch records, and product specifications.
  • Ability to perform visual, in-process, and final product inspections and testing activities.
  • Intermediate troubleshooting and problem-solving skills related to equipment, processes, and setup conditions.
  • Basic understanding of equipment maintenance principles.
  • Awareness of escalation processes for quality, safety, or production issues.
  • Basic mathematical skills, including addition, subtraction, multiplication, division, fractions, decimals, and percentages.
  • Basic computer skills, including proficiency in a Windows environment and Microsoft Office applications such as Outlook, Word, and Excel.
  • Ability to work independently and within cross-functional teams.
  • Familiarity with product attributes, manufacturing components, and material identification.
  • Root cause analysis and problem-solving methodology.
  • Understanding of occupational health requirements and safe work practices.
  • Ability to operate multiple manufacturing processes across different areas based on certification level.
  • Ability to ensure material readiness and proper flow within assigned processes.
  • Understanding of non-conforming material handling and disposition processes.
  • Knowledge of Lean principles and 5S, with the ability to apply them in the workplace.
  • Basic understanding of continuous improvement concepts.
  • Ability to work in a cleanroom or controlled manufacturing setting while wearing required protective gear.
  • Ability to wear steel-toe, non-slip shoes on the production floor.
Responsibilities
  • Perform assembly, packaging, and labeling of medical devices and pharmaceutical products in compliance with Good Manufacturing Practices, standard operating procedures, and quality standards.
  • Operate and become certified in multiple manufacturing processes or groups of operations across different areas.
  • Execute production activities using batch records, job aids, standard operating procedures, and product specifications.
  • Interpret manufacturing documentation to ensure accurate and efficient process execution.
  • Perform in-process and final visual inspections to ensure products and packaging meet quality requirements.
  • Complete and review batch records, production logs, and documentation in compliance with Good Manufacturing Practices, Good Documentation Practices, Food and Drug Administration, and International Organization for Standardization 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 required materials are available 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.
  • 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.
  • Follow safety requirements and properly use personal protective equipment, including lab coats, gloves, hair or beard covers, shoe covers, hearing protection, eye protection, and specialized cleanroom garments.
  • Maintain regular attendance and punctuality in accordance with company policies.
  • Maintain positive working relationships with peers and supervisors.
  • Maintain open communication so 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 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 company policies and regulatory requirements.
  • Perform other duties as assigned.
Desired Qualifications
  • Completed high school or equivalent.

About the company

BD is a global medical technology company serving hospitals, labs, and healthcare providers with products across BD Medical, Life Sciences, and Interventional. Its offerings include medication management and delivery devices, safe specimen collection and transport systems, and minimally invasive surgical instruments. Its products help safe medication administration, preserve specimen integrity for diagnostics, and enable less-invasive procedures, saving time and improving outcomes. BD differentiates itself with a broad end-to-end portfolio, global reach, and focus on quality, safety, and service to support care across regions; its goal is to improve patient outcomes, lower costs, and increase efficiency in care environments.

Company Size

10,001+

Company Stage

IPO

Headquarters

Franklin Lakes, New Jersey

Founded

1961

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Simplify's Take

What believers are saying

  • Q3 FY2026 revenue reached $5.0 billion, with adjusted EPS of $3.23.
  • BD completed PREVENT trial enrollment in August 2026, advancing Phasix label expansion.
  • July 2026 EMS semaglutide launch expands BD's GLP-1 delivery platform in Brazil.

What critics are saying

  • July 31, 2026 needle-set recall caused four deaths and 45 serious injuries.
  • BD carried about $1.7 billion legal accruals in May 2026, including ports and hernia claims.
  • FDA-requested ship holds on ChloraPrep and PurPrep signal manufacturing controls and warning-letter risk.

What makes Becton Dickinson unique

  • BD spans needles, drug delivery, interventional devices, and diagnostics at global scale.
  • BD Vystra and EMS semaglutide show durable pen-platform expertise across injectable medicines.
  • BD's Phasix, CIRSE training, and tissue-regeneration pipeline reinforce recurring surgeon and hospital relationships.

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Benefits

Health Insurance

Dental Insurance

Vision Insurance

401(k) Retirement Plan

Tuition Reimbursement

Growth & Insights and Company News

Headcount

6 month growth

9%

1 year growth

9%

2 year growth

9%
Yahoo Finance
Aug 18th, 2026
Wall Street analysts give Becton, Dickinson a 'moderate buy' rating despite 12% earnings decline forecast

Becton, Dickinson and Company shares have gained 19.6% over the past year, slightly trailing the S&P 500's 20.4% rise. However, in 2026 year-to-date, the stock has outperformed with a 20.2% gain versus the index's 13.7% advance. The medical technology company, valued at $50.5 billion by market cap, manufactures medical supplies, devices, laboratory equipment, and diagnostic products. It has outpaced the iShares U.S. Medical Devices ETF, which declined 9.5% over the past year. BDX's shares rose 3.8% on 6 August after reporting third-quarter results. Adjusted earnings per share of $3.23 exceeded analyst expectations of $3.14, whilst revenue of $5 billion surpassed the $4.9 billion forecast. Among 16 analysts covering the stock, the consensus rating is "Moderate Buy", comprising seven "Strong Buy" ratings and nine "Holds".

PR Newswire
Aug 17th, 2026
BD names Gary Sorsher chief quality officer as Jeff Silvestri retires after 25 years

BD has appointed Gary Sorsher as executive vice president and chief quality officer, effective 8 September. Sorsher brings over 30 years of experience in quality leadership at medical technology companies, most recently serving as chief quality officer at Edwards Lifesciences. The appointment follows the announcement that Jeffrey Silvestri, senior vice president and global head of quality, will retire in October after more than 25 years with BD. Silvestri joined the company in 1998 and has been instrumental in strengthening BD's quality foundation. Tom Polen, BD's chairman, CEO and president, emphasised that quality is central to earning trust with customers and patients. He expressed confidence in Sorsher's ability to advance quality excellence across the organisation.

MedTech Dive
Aug 13th, 2026
BD fully enrolls trial of resorbable mesh for hernia prevention.

BD fully enrolls trial of resorbable mesh for hernia prevention. BD called completing enrollment in the study "a significant milestone in its advanced tissue regeneration strategy and expansion efforts." Published Aug. 13, 2026 Dive brief: * BD said Wednesday it has completed enrollment in a clinical trial of resorbable mesh for preventing incisional hernias after open abdominal surgery. * Investigators enrolled 477 patients across 32 sites in the U.S. and Europe to compare the effect of BD's Phasix mesh and primary suture closure on the rate of incisional hernias. * BD will follow patients through the trial's primary endpoint at 24 months, beyond which it expects to use the data to seek Food and Drug Administration authorization for the indication. Dive insight: Incisional hernia is a serious and relatively common postoperative complication of elective abdominal surgeries where a large incision is made through the abdominal wall. BD's Phasix is a resorbable mesh. CR Bard, which BD bought for $24 billion in 2017, received FDA clearance in 2015 for Phasix in settings including hernia repair. Later, long-term data on the device confirmed the absence of mesh complications such as pain and infection. BD has faced lawsuits over adverse events allegedly linked to Bard meshes made from other materials. By completing enrollment in its PREVENT trial, BD took a step toward expanding the Phasix label to cover the prophylactic use of the device in patients undergoing elective open midline laparotomy surgery. Evaluating Phasix in hernia prevention builds on "decades of innovation in abdominal wall surgery" and will generate evidence that could "help broaden the role of regenerative technologies for patients at risk of post-surgical complications," Rian Seger, worldwide president of surgery at BD, said in a statement. BD called completion of enrollment in the clinical trial "a significant milestone in its advanced tissue regeneration strategy and expansion efforts." Last week, the company reported double-digit growth in sales of its infection prevention and advanced tissue regeneration products in the third quarter of its financial year. Discussing tissue regeneration on BD's third-quarter earnings call, CEO Thomas Polen said the company expects "strong growth going forward." Polen supported the expectations by highlighting clinical trials that the company is running to bring its biomaterial "into new indications to continue to expand our presence in those spaces."

Yahoo Finance
Aug 9th, 2026
BD up 6.8% on Q3 beat, GLP-1 pen partnerships boost biologic delivery outlook

Becton Dickinson reported third-quarter fiscal 2026 sales of $4,983 million, whilst net income fell to $377 million. The medical technology company modestly raised its full-year outlook for low single-digit revenue growth. BD highlighted momentum in biologic drug delivery and GLP-1 partnerships, including a new semaglutide pen collaboration with EMS in Brazil. The company's Vystra Injection Pen platform is gaining traction in chronic disease treatment. FX-neutral revenue grew faster than expected, leading management to nudge guidance higher. However, the sharp drop in year-to-date net income and recent one-off loss raise questions about earnings quality. The company maintained its $4.20 annual dividend. Shares rose 6.8% following the results, though some analysts suggest the stock remains undervalued by approximately 25%.

Yahoo Finance
Aug 7th, 2026
BD reports Q3 fiscal 2026 results with $5B revenue up 5.4% and adjusted EPS of $3.23

BD reported third quarter fiscal 2026 revenue of $5.0 billion, up 5.4% as reported and 4.4% on a foreign exchange-neutral basis. GAAP diluted earnings per share from continuing operations reached $1.64, whilst adjusted diluted EPS came in at $3.23. Year-to-date cash from continuing operations increased 33.3% to $2.1 billion. Free cash flow rose 44.6% to $1.7 billion. The medical technology company updated its full-year guidance, expecting revenue growth towards the high end of its range whilst raising the midpoint of its adjusted diluted EPS guidance. The results represent BD's first full quarter following the 9 February 2026 spin-off of its Biosciences and Diagnostic Solutions business and its combination with Waters Corporation.