Medical Devices TN Sponsorship Jobs in Pennsylvania
Pennsylvania's medical devices sector spans Philadelphia-area multinationals, Pittsburgh's growing health technology corridor, and established manufacturers across the Lehigh Valley. Companies like Siemens Healthineers, West Pharmaceutical Services, and Teleflex regularly hire internationally. Canadian and Mexican professionals with qualifying degrees can pursue TN visa sponsorship across engineering, regulatory, and scientific roles throughout the state.
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Get Access To All JobsINTRODUCTION
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.
Position Summary
The Chemist I is responsible for supporting analytical testing, method validation, method transfers, and drug stability programs within a regulated laboratory environment. This role performs chemical analysis of raw materials, in-process samples, finished products, and stability samples while ensuring compliance with FDA, GMP, ISO, and applicable regulatory requirements. The Senior Chemist serves as a technical resource for laboratory investigations, data interpretation, and continuous improvement initiatives, contributing to product quality, regulatory compliance, and operational excellence. This position works closely with Quality, R&D, Regulatory, and Manufacturing teams to support business objectives.
IN THIS ROLE, YOU WILL HAVE THE CHANCE TO:
- Perform analytical testing of raw materials, in-process samples, finished products, and stability samples using approved methods and specifications.
- Lead and support drug stability studies, including protocol execution, data review, and report generation.
- Operate, maintain, and troubleshoot analytical instrumentation, including HPLC, GC, and other characterization equipment.
- Lead method transfer, verification, and validation activities, including protocol and final report preparation.
- Investigate Out-of-Specification (OOS) results, deviations, and laboratory non-conformances while supporting corrective and preventive actions.
- Collaborate with cross-functional teams to interpret analytical data and prepare technical reports.
- Provide technical guidance and support to junior scientists and laboratory personnel.
ESSENTIAL REQUIREMENTS
- Bachelor's degree in Chemistry, Pharmaceutical Sciences, or a related scientific discipline required; Master's degree preferred.
- 4+ years of analytical laboratory experience in pharmaceutical, medical device, biotechnology, or other regulated industries.
- Strong experience operating analytical instrumentation, including HPLC and GC.
- Experience with Empower chromatography software and data analysis.
- Experience with analytical method validation, method transfer, and assay and/or impurity testing.
- Working knowledge of FDA, USP, EP, ICH, ISO, and GMP requirements.
- Strong technical writing, problem-solving, and laboratory investigation skills.
PREFERRED EXPERIENCE INCLUDES
- Experience developing, implementing, or maintaining drug stability programs.
- Experience writing stability protocols, reports, and regulatory documentation.
- Experience supporting laboratory compliance and audit readiness activities.
- Applicable industry or professional certifications.
COMPENSATION
- Salary Range: $70,000 - $78,300 Annually
The targeted range for this role takes into account a range of factors that are considered when making compensation and hiring decisions, including skill sets, experience and training, licensure and certifications, and other business and organizational needs. The disclosed range estimate has not been adjusted for any 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.
B. Braun offers an excellent benefits package, which includes healthcare, a 401(k) plan, and tuition reimbursement.
LOCATION
Job Posting Location: Allentown, Pennsylvania, United States
EEO STATEMENT
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.
INTRODUCTION
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.
Position Summary
The Chemist I is responsible for supporting analytical testing, method validation, method transfers, and drug stability programs within a regulated laboratory environment. This role performs chemical analysis of raw materials, in-process samples, finished products, and stability samples while ensuring compliance with FDA, GMP, ISO, and applicable regulatory requirements. The Senior Chemist serves as a technical resource for laboratory investigations, data interpretation, and continuous improvement initiatives, contributing to product quality, regulatory compliance, and operational excellence. This position works closely with Quality, R&D, Regulatory, and Manufacturing teams to support business objectives.
IN THIS ROLE, YOU WILL HAVE THE CHANCE TO:
- Perform analytical testing of raw materials, in-process samples, finished products, and stability samples using approved methods and specifications.
- Lead and support drug stability studies, including protocol execution, data review, and report generation.
- Operate, maintain, and troubleshoot analytical instrumentation, including HPLC, GC, and other characterization equipment.
- Lead method transfer, verification, and validation activities, including protocol and final report preparation.
- Investigate Out-of-Specification (OOS) results, deviations, and laboratory non-conformances while supporting corrective and preventive actions.
- Collaborate with cross-functional teams to interpret analytical data and prepare technical reports.
- Provide technical guidance and support to junior scientists and laboratory personnel.
ESSENTIAL REQUIREMENTS
- Bachelor's degree in Chemistry, Pharmaceutical Sciences, or a related scientific discipline required; Master's degree preferred.
- 4+ years of analytical laboratory experience in pharmaceutical, medical device, biotechnology, or other regulated industries.
- Strong experience operating analytical instrumentation, including HPLC and GC.
- Experience with Empower chromatography software and data analysis.
- Experience with analytical method validation, method transfer, and assay and/or impurity testing.
- Working knowledge of FDA, USP, EP, ICH, ISO, and GMP requirements.
- Strong technical writing, problem-solving, and laboratory investigation skills.
PREFERRED EXPERIENCE INCLUDES
- Experience developing, implementing, or maintaining drug stability programs.
- Experience writing stability protocols, reports, and regulatory documentation.
- Experience supporting laboratory compliance and audit readiness activities.
- Applicable industry or professional certifications.
COMPENSATION
- Salary Range: $70,000 - $78,300 Annually
The targeted range for this role takes into account a range of factors that are considered when making compensation and hiring decisions, including skill sets, experience and training, licensure and certifications, and other business and organizational needs. The disclosed range estimate has not been adjusted for any 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.
B. Braun offers an excellent benefits package, which includes healthcare, a 401(k) plan, and tuition reimbursement.
LOCATION
Job Posting Location: Allentown, Pennsylvania, United States
EEO STATEMENT
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.
TN Medical Devices Job Roles in Pennsylvania
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Search Medical Devices Jobs in PennsylvaniaMedical Devices TN Sponsorship Jobs in Pennsylvania: Frequently Asked Questions
Which medical devices companies sponsor TN visas in Pennsylvania?
Several major medical devices employers in Pennsylvania have established international hiring programs. Siemens Healthineers maintains a significant presence in Malvern, West Pharmaceutical Services is headquartered in Exton, and Teleflex operates from Wayne. Smaller contract manufacturers and device startups in the Philadelphia suburbs and Lehigh Valley also sponsor TN visas, particularly for engineers, scientists, and regulatory affairs professionals with specialized credentials.
Which cities in Pennsylvania have the most medical devices TN sponsorship jobs?
The Philadelphia metropolitan area, particularly the western suburbs including Malvern, Wayne, Exton, and King of Prussia, concentrates the highest number of medical devices employers in Pennsylvania. Pittsburgh has a growing health technology sector tied to its university and hospital networks. The Lehigh Valley, anchored by Allentown and Bethlehem, also hosts established device manufacturers with recurring international hiring needs.
What types of medical devices roles typically qualify for TN sponsorship?
TN visa eligibility in medical devices generally requires the position to fall within an eligible TN occupation category and the candidate to hold a qualifying degree in a relevant field. Roles that commonly align include mechanical or biomedical engineers, quality and regulatory affairs specialists, scientists in R&D, and computer systems engineers working on embedded or software-driven devices. The position must require professional-level credentials, not just technical experience.
How do I find medical devices TN sponsorship jobs in Pennsylvania?
Migrate Mate is built specifically for this search. You can filter by TN visa, the medical devices industry, and Pennsylvania to see roles where employers have indicated sponsorship willingness. This saves significant time compared to manually reviewing job postings that rarely specify visa support. Migrate Mate focuses on connecting Canadian and Mexican professionals with U.S. employers actively open to TN arrangements, including in Pennsylvania's device sector.
Are there state-specific or industry-specific considerations for TN sponsorship in Pennsylvania medical devices?
Pennsylvania does not impose state-level visa sponsorship requirements, but the medical devices industry adds regulatory complexity that shapes hiring. Employers in FDA-regulated device manufacturing often require candidates to demonstrate familiarity with quality management systems such as ISO 13485 or FDA 21 CFR Part 820. Roles tied to clinical or lab environments may also require specific licensure under Pennsylvania state law, which is separate from and in addition to TN visa eligibility.