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Associate Medical Device Labeling Jobs in Pennsylvania

Our client, a leading organization in the medical device manufacturing industry, is seeking a 2nd Shift Manufacturing Associate - Assembler - 2:00 pm - 10:20 pm to join their team. As a 2nd Shift ...

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Marketing Associate

West Norriton, PA · On-site

$50K - $55K/yr

The Marketing Associate supports the development and execution of marketing initiatives that build ... and medical device marketing. Essential Duties & Responsibilities: * Trade Show Coordination:

Operator II

New Freedom, PA · On-site

$20 - $24/hr

Join Resonetics and be part of a team that's redefining medical device manufacturing. If you're ... to Label and package finished product. • Prepare, organize, and wrap skids in staging and ...

Operator II

New Freedom, PA

$16 - $21.25/hr

Join Resonetics and be part of a team that's redefining medical device manufacturing. If you're ... Label and package finished product. Prepare, organize, and wrap skids in staging and warehouse ...

Operator II

New Freedom, PA · On-site

$16 - $21.25/hr

Join Resonetics and be part of a team that's redefining medical device manufacturing. If you're ... to Label and package finished product. · Prepare, organize, and wrap skids in staging and ...

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Associate Medical Device Labeling information

What is an associate medical device labeling?

Associate Medical Device Labeling professionals are responsible for creating, reviewing, and maintaining the labeling and packaging materials for medical devices. Their work ensures that all product information, instructions, and regulatory warnings are accurate, clear, and compliant with industry regulations. They collaborate closely with regulatory affairs, quality assurance, and product development teams to make sure that labels meet local and international standards. This role is critical in helping ensure patient safety and regulatory approval of medical devices.

What are the key skills and qualifications needed to thrive as an associate medical device labeling?

To thrive as an Associate Medical Device Labeling Specialist, you need a strong understanding of regulatory requirements, attention to detail, and experience in technical writing, often supported by a degree in life sciences or a related field. Familiarity with labeling software, document management systems, and knowledge of FDA or EU MDR regulations are typically required. Excellent communication, collaboration, and organizational skills set top performers apart in this position. These skills are crucial to ensure label accuracy, regulatory compliance, and patient safety in a highly regulated industry.

What are some common challenges faced by associate medical device labeling, and how can they be addressed?

Associate Medical Device Labeling professionals often encounter challenges such as keeping up with evolving regulatory requirements across different countries, ensuring accuracy and clarity in complex technical information, and coordinating input from multiple departments like regulatory affairs, engineering, and marketing. Addressing these challenges involves staying updated on global labeling standards, developing strong attention to detail, and building effective communication and collaboration skills. Leveraging project management tools and regularly participating in training can also help manage these complexities and ensure timely, compliant labeling deliverables.

What are the most commonly searched types of Medical Device Labeling jobs in Pennsylvania?

The most popular types of Medical Device Labeling jobs in Pennsylvania are:

What cities in Pennsylvania are hiring for Associate Medical Device Labeling jobs?

Cities in Pennsylvania with the most Associate Medical Device Labeling job openings:

General Manufacturing Associat

B. Braun US Device Manufacturing LLC

Allentown, PA • On-site

Other

Medical, Retirement

Posted 5 days ago


Job description

B. Braun Medical, Inc.
Company: B. Braun US Device Manufacturing LLC
Job Posting Location: Allentown, Pennsylvania, United States
Functional Area: Production
Working Model: Onsite
Days of Work: Saturday, Friday, Thursday, Wednesday, Tuesday, Monday, Sunday, Rotating
Shift: 3/4 X 12
Relocation Available: No
Requisition ID: 13579

B. Braun Medical Inc., a leader in infusion therapy and pain management, develops, manufactures, and markets innovative medical products and services to the healthcare industry. Other key product areas include nutrition, pharmacy admixture and compounding, ostomy and wound care, and dialysis. The company is committed to eliminating preventable treatment errors and enhancing patient, clinician and environmental safety. B. Braun Medical is headquartered in Bethlehem, Pa., and is part of the B. Braun Group of Companies in the U.S., which includes B. Braun Interventional Systems, Aesculap® and CAPS®.

Globally, the B. Braun Group of Companies employs more than 64,000 employees in 64 countries. Guided by its Sharing Expertise® philosophy, B. Braun continuously exchanges knowledge with customers, partners and clinicians to address the critical issues of improving care and lowering costs. To learn more about B. Braun Medical, visit www.bbraunusa.com


Position Summary

The General Manufacturing Associate is responsible for assembling, packaging, inspecting, and supporting the production of medical devices in a regulated manufacturing environment. This role ensures products are manufactured in accordance with established quality standards, production schedules, operating procedures, and regulatory requirements. The associate operates production equipment, performs visual and manual inspections, completes required documentation, and supports continuous improvement initiatives to meet safety, quality, delivery, and productivity goals. This position requires attention to detail, manual dexterity, and a commitment to maintaining a clean and compliant work environment.

In This Role, You Will Have the Chance To:

  • Assemble, package, label, and inspect medical devices in accordance with approved procedures, quality standards, and production requirements.

  • Operate manufacturing equipment and production machinery safely and effectively while adhering to established work instructions.

  • Monitor product quality throughout the manufacturing process and identify, segregate, or report non-conforming materials and products.

  • Accurately complete production records, batch documentation, inspection records, and other manufacturing documentation in compliance with Good Documentation Practices (GDP).

  • Perform routine cleaning and housekeeping activities to maintain a safe, organized, and compliant manufacturing environment.

  • Utilize measuring devices, tools, and equipment to verify product specifications and ensure product quality.

  • Support continuous improvement initiatives by identifying opportunities to improve quality, efficiency, safety, and waste reduction.

  • Follow all company policies, safety guidelines, quality procedures, and applicable regulatory requirements.

  • Collaborate effectively with team members, supervisors, quality personnel, and support functions to achieve departmental goals.

  • Cross-train and rotate between workstations as required to support production demands.

Essential Requirements

  • High School Diploma or GED required.

  • Manufacturing, production, assembly, or related experience OR successful completion of PBS requirements and assessment at the appropriate level.

  • Ability to follow written procedures, work instructions, and standard operating procedures.

  • Strong attention to detail and commitment to producing high-quality products.

  • Ability to perform repetitive tasks while maintaining quality and productivity standards.

  • Basic math, reading comprehension, and documentation skills.

  • Basic computer skills and ability to enter or review production information electronically.

  • Ability to work effectively in a team environment and communicate professionally with peers and supervisors.

  • Ability to work a non-standard schedule, overtime, weekends, or shift assignments as business needs require.

  • Regular and predictable on-site attendance.

Preferred Experience Includes

  • Previous experience in medical device, pharmaceutical, manufacturing, or other regulated production environments.

  • Experience with intricate hand assembly and use of fine motor skills.

  • Familiarity with Lean Manufacturing, Continuous Improvement, or 5S principles.

  • Experience using measuring devices, inspection tools, or manufacturing equipment.

  • Demonstrated ability to identify and resolve routine production or quality issues.

Knowledge & Skills

  • Applies basic manufacturing knowledge and follows established procedures and work instructions.

  • Performs routine assignments under direct supervision with guidance provided for new or complex tasks.

  • Demonstrates strong attention to detail and manual dexterity required for product assembly and inspection activities.

  • Exercises limited judgment in resolving routine production issues and escalates concerns appropriately.

  • Maintains a strong focus on safety, quality, productivity, and teamwork.

  • Effectively adapts to changing priorities and production requirements.

  • Interacts primarily with supervisors, peers, quality personnel, and manufacturing support teams.


The targeted range for this role takes into account a range of factors that are considered when making compensation and hiring decisions; included but not limited to: skill sets; experience and training; licensure and certifications; and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. Compensation decisions are dependent on the facts and circumstances of each case. The range provided is a reasonable estimate.

B. Braun offers an excellent benefits package, which includes healthcare, a 401(k) plan, and tuition reimbursement. To learn more about B. Braun and our safety healthcare products or view a listing of our employment opportunities, please visit us on the internet at www.bbraunusa.com.

Through its “Sharing Expertise®” initiative, B. Braun promotes best practices for continuous improvement of healthcare products and services.

We are an equal opportunity employer. We evaluate applications without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, pregnancy, genetic information, disability, status as a protected veteran, or any other protected characteristic. Know Your Rights: Workplace Discrimination is Illegal, click here.


All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or other legally protected status.

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