Quality Engineer I
Company: B. BRAUN MEDICAL (US) INC
Location: Allentown
Posted on: June 1, 2025
|
|
Job Description:
B. Braun Medical, Inc.Company: B. BRAUN MEDICAL (US) INCJob
Posting Location: Allentown (861 Marcon), Pennsylvania, United
StatesFunctional Area: QualityWorking Model: HybridDays of Work:
Friday, Thursday, Wednesday, Tuesday, MondayShift: 5X8Relocation
Available: NoRequisition ID: 5007B. 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.comPosition Summary: This role supports quality
oversight of supplier-related activities for externally sourced
finished goods for both medical devices and pharmaceuticals. This
role ensures supplier-provided finished goods meet regulatory,
quality and safety standards and supports supplier-related quality
processes across the product lifecycle. Responsibilities: Essential
DutiesEstablishes quality standards for products and processes and
suggest modifications meant to prevent defects in components or
final products.Audits production processes, raw materials or
suppliers/vendors to ensure that established quality standards are
met.Conducts root cause analysis for defects, non conformities or
other quality failures.May be responsible for ensuring compliance
with formal external quality standards, such as ISO 9001.Support
investigations of supplier-related non-conformances, deviations and
complaints. Support root cause analysis and implementation of
corrective and preventive actions ( CAPAs and SCARs) related to
supplier issues. Act as the quality subject matter expert on new
product introductions including review of product lifecycle
documentation such as but not limited to verification and
validation documents, risk analysis documents, labeling, product
test specifications and inspection and release documentation.
Review supplier change notifications as a quality subject matter
expert and ensure changes are appropriately evaluted for risk and
quality impact. Ensure compliance with applicable regulations and
standards (FDA 21CFR Part 820, 210/211, ISO 13485, ISO 14971)Works
closely with cross functional teams, including product design,
product management and production, to identify and mitigate quality
risks.Expertise: Knowledge & Skills Requires full working knowledge
of relevant business practices and procedures in professional
field. Uses standard theories, principles and concepts and
integrates them to propose a course of action.Works under general
supervision. Relies on experience and judgement to plan and
accomplish assigned goals. May periodically assist in orienting,
training, assigning & checking the work of other peers.Judgement is
required in resolving all day-to-day problems.Contacts are with
external contractors/vendors, department supervisors, leads,
subordinates, and peers.Required:Bachelor's degree required.2-4
years related experience required.Applicable industry/professional
certification preferred.Regular and predictable
attendanceOccasional business travel required, Secrecy and
invention agreement and non-compete agreement, Ability to work
non-standard schedule as needed$80,000 -$90,000#LI #ALThe 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.Compensation details: 80000-90000 Yearly
SalaryPI48c8ac3ff707-25660-37700575
Keywords: B. BRAUN MEDICAL (US) INC, Vineland , Quality Engineer I, Engineering , Allentown, New Jersey
Click
here to apply!
|