NewRegulatory Specialist / Sr. Regulatory Specialist – Salty Snacks #26-19069 US Tech Solutions, Inc.Regulatory Specialist / Sr. Regulatory Specialist – Salty Snacks #26-19069Hershey, PAJob Description: This role supports Regulatory Affairs activities for Salty Snacks brands, ensuring compliance with U.S. food regulations across the product lifecycle—from ideation through commercialization and post launch. The position partners cross functionally with R&D, Marketing, Legal, Quality, Supply Chain to deliver compliant ingredients, formulas, labels, claims, and certifications for Salty products.
NewGRA CMC Specialist CSLGRA CMC SpecialistKing of Prussia, PASupport the collaboration with CSL’s Corporate & External Affairs organization to support legislative and statutory initiatives to allow CSL to take an active leadership role in shaping policy and regulatory frameworks that impact the development, registration, and life-cycle management of plasma-derived therapies. Ensures Accountability: Follows through on commitments and makes sure others do the same; Acts with a clear sense of ownership; Takes personal responsibility for decisions, actions, and failures; Establishes clear responsibilities and processes for monitoring work and measuring results; Designs feedback loops into work.
Revenue Cycle Operational Improvement Specialist St. Luke's Health Network, Inc.Revenue Cycle Operational Improvement SpecialistAllentown, PAFull timeContent includes but is not limited to the following: registration, insurance, online eligibility, address verification, financial clearance, financial counseling, price estimates, price transparency, business office procedures, work queue’s, customer service, scheduling, referral/authorizations, etc. Schedules and performs Revenue Cycle Workshop for hospital and SLPG new hire and existing employees to explain the impact various departments have on the revenue cycle and gain a stronger understanding of their individual roles within the revenue cycle.
Senior Regulatory Affairs Specialist PhilipsSenior Regulatory Affairs SpecialistMurrysville, PA$99,000–$157,000 / yearThe actual base pay offered may vary within the posted ranges depending on multiple factors including job-related knowledge/skills, experience, business needs, geographical location, and internal equity. Lead global regulatory intelligence initiatives, contribute to regulatory and product registration strategies, and help implement global regulatory roadmaps based on the competitive landscape and marketing objectives.
Regulatory Affairs Specialist, Global Quaker HoughtonRegulatory Affairs Specialist, GlobalConshohocken, PASupport chemical regulatory activities related to documentation including updating raw material information, communicating changes to raw material classifications, data management and updating the SDS system. Supports the Product Stewardship organization globally with responses to key stakeholders including regulatory inquiries, SDS authoring, and answering regulatory inquiries.
Senior Regulatory Affairs Specialist Integrated Resources, IncSenior Regulatory Affairs SpecialistWest Chester, PennsylvaniaContractorJob DescriptionClient: Direct ClientLocation: West Chester, PAJob Title: Senior Regulatory Affairs SpecialistDuration: 1 year + (Possible Extension)Job Summary:The Recall Regulatory Specialist III will be responsible for leading OUS (outside the US) field action execution activities including managing Field Action Strategy Team meetings, coordinating and preparing document packages to notify regulatory agencies of field action activities, drafting internal and external customer communications, providing updates to FDA and global regulatory agencies, processing and closing Field Actions in a timely manner, and act as support for FDA and regulatory inspections. Senior Regulatory Affairs SpecialistIntegrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms.
Senior Regulatory Affairs Specialist - Animal Health Cencora IncSenior Regulatory Affairs Specialist - Animal HealthPAYou will work closely with internal and client stakeholders across Regulatory Affairs, Quality, Manufacturing, Pharmacovigilance, Supply Chain, and Commercial teams to help ensure regulatory objectives are delivered efficiently and compliantly. This is an exciting opportunity for a regulatory professional who enjoys working across the full product lifecycle and partnering with cross-functional teams to deliver compliant, timely, and high-quality regulatory outcomes.
Regulatory Affairs Specialist Integrated Resources, IncRegulatory Affairs SpecialistPennsylvaniaFull timeResponsibilities will include:Partnering with global regulatory contacts to understand requirements for product registrations for new and modified productsPartnering with global regulatory contacts to plan, develop and submit product registration applications for new and modified productsObtaining and maintaining documents required for global registrations such as Certificates to Foreign Government and Certificates of Free Sale. Strong interpersonal, negotiation and problem solving skills; detail oriented• Ability to work independently and collaboratively with minimal supervision• Working knowledge of MS Office programs (Word, Excel, PowerPoint, Outlook) and electronic document management systems
Sr. Specialist Regulatory Affairs, Medical Devices West Pharmaceutical ServicesSr. Specialist Regulatory Affairs, Medical DevicesExton, PASpecialist is responsible for influencing department regulatory processes and procedures, developing strategies, authoring, reviewing, and supporting global registrations, including Premarket Notifications, Post Market Submissions, China NMPA Registrations, Technical Documentation for CE Marking, technical packages. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West's indelible mark on the healthcare industry has just begun.
Principal Specialist, Regulatory Affairs West Pharmaceutical Services IncPrincipal Specialist, Regulatory AffairsExton, PAPreferred Knowledge, Skills and Abilities: • Excellent oral communication and technical writing skills • Advanced knowledge of product life cycle, product development, design control and change control • International regulatory competency • Experience with administration and safety systems preferred • Minimum US Class I and EU Class IIa device experience and in-depth knowledge of US FDA regulations (Title 21CFR820) and EU MDD (93/42/EEC) and MDR (2017/745) • History of successful US 510(k) device and EU technical documentation submissions • Experience directly interacting with government agencies • Possesses technical leadership skills, as well as demonstrated understanding of related pharmaceutical operations (e.g., manufacturing, process development, analytical, quality assurance) • Experience reviewing product labeling and advertising/promotional material for medical devices • Strong negotiation and decision-making skills • Self-motivated with a proactive attitude and the ability to work effectively • Ability to manage multiple priorities. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West's indelible mark on the healthcare industry has just begun.
Regulatory Affairs Specialist, EHS, North America Henry Schein IncRegulatory Affairs Specialist, EHS, North AmericaPA$56,604–$88,443 / yearDevelop and deliver employee environmental, health, and safety (EHS) awareness and training programs to ensure compliance with applicable federal, state, and international regulations, including OSHA, OSHA State Plans (e.g., Cal/OSHA), DOT, IATA, IMO, and EPA requirements. Proficient in Microsoft Office applications, including PowerPoint, and experienced with project management methodologies and tools commonly used in the medical device or pharmaceutical industries.
Product Stewardship and Regulatory Affairs Sp AGC IncProduct Stewardship and Regulatory Affairs SpExton, PAEssential Functions: Supports new product registrations for Americas region, e.g., TSCA PMN/LVE/Polymer Exemptions, and Canadian DSL/NDSL notifications in close collaboration with R&D and global product stewardship teams. The position is part of a global highly interactive, diverse, and supportive team and will manage product stewardship activities to enable sales of new products and maintain the right to operate with existing products.
NewRegulatory Specialist Sr. Regulatory Specialist Salty Snacks TekWissen LLCRegulatory Specialist Sr. Regulatory Specialist Salty SnacksHershey, PA$39–$44.86Regulatory Specialist Salty Snacks Location: Hershey, PA 17033 Duration: 12 Months Job Type: Temporary Assignment Work Type: Onsite Shift: 08:00am 04:30pm Job Description: This role supports Regulatory Affairs activities for Salty Snacks brands, ensuring compliance with food regulations across the product lifecycle-from ideation through commercialization and post launch. The position partners cross functionally with R&D, Marketing, Legal, Quality, Supply Chain to deliver compliant ingredients, formulas, labels, claims, and certifications for Salty products.
Medical Affairs Specialist West Pharmaceutical ServicesMedical Affairs SpecialistRadnor, PAWest solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West's indelible mark on the healthcare industry has just begun. The role will also support clinical consultation and medical affairs by ensuring that clinical regulatory technical documentation, and testing validation are aligned with clinical work flow, real-world clinical practices and patient needs, ultimately enhancing the development of safe and effective medical products.
Administrative Specialist - Podiatry: Educational Affairs Temple UniversityAdministrative Specialist - Podiatry: Educational AffairsPhiladelphia, Pennsylvania$32,000–$51,000Reporting to the Assistant Dean for Educational Affairs in the School of Podiatric Medicine (TUSPM), the Administrative Specialist provides academic, administrative, clerical and facilities related support services to TUSPM's Office of Educational Affairs and to the basic sciences curriculum and instruction, including faculty members of the Lewis Katz School of Medicine, in an accurate, timely and courteous manner. Compliance Statement:In the performance of their functions as detailed in the position description employees have an obligation to avoid ethical, legal, financial and other conflicts of interest to ensure that their actions and outside activities do not conflict with their primary employment responsibilities at the institution.
NewSr Regulatory Affairs Specialist Globus MedicalSr Regulatory Affairs SpecialistAudubon, PennsylvaniaPrepares and maintains regulatory pre-market submissions and other pre-market filings to assist in acquiring appropriate commercial distribution clearances. Coordinates and prepares document packages for regulatory submissions for new and mature products, ensuring compliance with local and regional registration requirements.
Clinical Affairs Specialist, Interventional Coronary (REMOTE) Teleflex IncClinical Affairs Specialist, Interventional Coronary (REMOTE)Philadelphia, PARemote$92,800–$139,200 / yearOur portfolio includes a broad range of clinically relevant products, such as the GuideLiner and Turnpike Catheters; the Orsiro Mission Drug-Eluting Stent; the PK Papyrus Covered Coronary Stent; the Ringer Perfusion Balloon Catheter; the Pulsar -18 T3 Self-Expanding Stent; Passeo Balloon Catheters; and the OnControl Powered Bone Access System. Collaborate cross-functionally with Marketing, Sales, Engineering, and other internal teams on strategic initiatives and product-related activities, applying critical thinking and clinical judgment to evaluate information, address challenges, and support informed decision-making within established.
Clinical Affairs Specialist, Interventional Oncology (REMOTE) Teleflex IncClinical Affairs Specialist, Interventional Oncology (REMOTE)Philadelphia, PARemote$110,000–$120,000 / yearOur portfolio includes a broad range of clinically relevant products, such as the GuideLiner and Turnpike Catheters; the Orsiro Mission Drug-Eluting Stent; the PK Papyrus Covered Coronary Stent; the Ringer Perfusion Balloon Catheter; the Pulsar -18 T3 Self-Expanding Stent; Passeo Balloon Catheters; and the OnControl Powered Bone Access System. Collaborate cross-functionally with Marketing, Sales, Engineering, and other internal teams on strategic initiatives and product-related activities, applying critical thinking and clinical judgment to evaluate information, address challenges, and support informed decision-making within established company policies and practices.
NewRegulatory Specialist / Sr. Regulatory Specialist Salty Snacks #26-19069 US Tech Solutions, Inc.Regulatory Specialist / Sr. Regulatory Specialist Salty Snacks #26-19069Hershey, PARemote$40–$45.17 / hourJob Description: This role supports Regulatory Affairs activities for Salty Snacks brands, ensuring compliance with U.S. food regulations across the product lifecycle—from ideation through commercialization and post launch. The position partners cross functionally with R&D, Marketing, Legal, Quality, Supply Chain to deliver compliant ingredients, formulas, labels, claims, and certifications for Salty products.
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