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2 Sr. Regulatory Affairs Specialist Jobs in Center, PA

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B. Braun Medical Inc
Center, PA | Full Time
$90k-115k (estimate)
3 Months Ago
Aesculap Inc.
Center, PA | Full Time
$85k-110k (estimate)
6 Days Ago
Sr. Regulatory Affairs Specialist
Aesculap Inc. Center, PA
$85k-110k (estimate)
Full Time | Medical Technology 6 Days Ago
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Aesculap Inc. is Hiring a Sr. Regulatory Affairs Specialist Near Center, PA

You’re an important part of our future. Hopefully, we're also a part of your future! At B. Braun, we protect and improve the health of people worldwide. You support this vision, bringing expertise and sharing innovation, efficiency and sustainability as values. That’s why we would like to keep developing our company with you. Keeping your future in mind, we’re making a joint contribution to health care worldwide, with trust, transparency and appreciation. That's Sharing Expertise.
About B. BraunB. 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 .
Duties And Responsibilities
  • Position Summary:
  • Responsibilities: Essential Duties
  • Plans and prepares registration documents for marketing approval of drug and device products in the US and in foreign countries.
  • Serves as a regulatory liaison for new product development and make regulatory assessments of proposed changes to existing products for impact to regulatory documentation.
  • Provides strategic input and guidance to project teams in conjunction with supervisor.
  • Plans and prepares dossiers for registration of drug and device products.
  • Independently reviews and analyzes proposed modifications to drug and device products for regulatory impact.
  • Independently reads, reviews, interprets and keeps current with regulations and publications regarding drug and device products and communicate within the department.
  • May oversee and direct the work of other Regulatory Affairs professionals. The job function listed is not exhaustive and shall also include any responsibilities as assigned by the Supervisor from time to time.
  • 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.
  • Work under minimal supervision. Relies on experience and judgement to plan and accomplish assigned goals. May periodically assist in orienting, training, assigning and checking the work of lower level employees. Referring only complex problems and issues
  • Judgement is required in resolving complex problems based on experience.
  • Contacts are primarily with department supervisors, leads, subordinates, and peers. Frequent contact with external contractors/vendors.
Professional competencies
  • Expertise: Qualifications -Education/Experience/Training/Etc
  • Required:
  • Bachelor's degree required.
  • 06-08 years related experience required.
  • Applicable industry/professional certification required.
  • Regular and predictable attendance
  • Frequent business travel required, Secrecy and invention agreement and non-compete agreement, Ability to work non-standard schedule as needed
  • While performing the duties of this job, the employee is regularly required to sit and talk or hear. The employee frequently is required to use hands to handle or feel and reach with hands and arms. The employee is occasionally required to stand and walk. The employee must occasionally lift and/or move up to 20 pounds.
  • .
What We OfferB. 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.
Contact : B. Braun Medical Inc. | |

Job Summary

JOB TYPE

Full Time

INDUSTRY

Medical Technology

SALARY

$85k-110k (estimate)

POST DATE

06/23/2024

EXPIRATION DATE

07/17/2024

WEBSITE

aesculapbiologics.com

HEADQUARTERS

BREINIGSVILLE, PA

SIZE

<25

TYPE

Private

CEO

CHUCK DINARDO

REVENUE

$5M - $10M

INDUSTRY

Medical Technology

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