Johnson & Johnson companies are equal opportunity employers.
DIRECTOR 1 (MD), MEDICAL SAFETY-4776130328
Description
Johnson & Johnson Consumer Products Company, a member of Johnson & Johnson's Family of Companies, is recruiting for a Director of Medical Safety, within the division of Medical Affairs, located in Fort Washington, PA or Skillman, NJ.
Johnson & Johnson Family of Consumer Companies develops and markets OTC drugs, nutritional products, baby care, wound care and skin care products that address the needs of consumers and health care professionals and incorporate the latest innovations. The portfolio includes heritage brands JOHNSON'S® Baby and BAND-AID® Brand, TYLENOL® and MOTRIN ®products, ZYRTEC® and BENADRYL® allergy medicines, NEUTROGENA®, as well as leading skin care brands such as AVEENO® and CLEAN & CLEAR®.
This position will provide safety expertise to Johnson & Johnson Family of Consumer Companies and is part of the Medical Affairs Safety team and will report to the North America Regional Safety Officer. This position supports the North America Regional Safety Officer in oversight of pharmacovigilance activities for JJFCC products and in ensuring compliance with local and global regulations and company policies. This position provides medical input to and execution of health hazard assessments, and works collaboratively with Quality Assurance, Regulatory Affairs, Consumer Medical Safety and others on the assessment of potential safety issues with regard to manufacturing quality. This position will also work in collaboration with Global Medical Safety (GMS), Regulatory Compliance, Office of Consumer Medical Safety (OCMS), and MCH business/functional units to identify, evaluate and communicate safety and/or compliance issues. Under limited supervision and in accordance with all applicable federal, state and local laws/regulations, the Companies' policies, procedures and guidelines, the responsibilities for this position include, ensure safety reporting activities are conducted in accordance with company policies, regulatory requirements and good clinical and manufacturing standards. Providing medical input to and oversight of the execution of the safety section of the McNeil Manufacturing Quality Assurance Annual Product Reviews, working collaboratively with Quality Assurance, Regulatory Affairs, Consumer Medical Safety and others on the assessment of potential safety issues with regard to manufacturing quality. Leading and performing medical safety assessments and health hazard evaluations of new and existing products. Supporting other safety related activities such as review of periodic adverse event reviews (PADERs/PSURs), clinical trial protocols, surveillance reports, and safety-related labelling changes. Collaborating with internal and external safety experts to identify process improvements, to ensure that safety reporting activities are conducted in accordance with company policies, regulatory requirements, and good clinical and manufacturing standards. Communicating/translating medical safety/technical knowledge to scientists and non-scientists. Training and mentoring other company scientists and healthcare professionals. Provide support on pharmacovigilance audits and inspections.
Qualifications
A minimum of a MD/DO degree is required. Board eligibility or certification is also required. Certification in primary care specialty (example: internal medicine, emergency medicine, family practice or pediatrics) with post- residency patient care experience is preferred. Clinical pharmacology, toxicology, epidemiology and academic experience is a plus. A minimum of 7 years experience within the pharmaceutical industry is required. 4 years experience in Safety/Pharmacovigilance is required. An understanding of regulatory requirements, product quality management and Good Manufacturing Practices is preferred. Experience with pharmacovigilance of OTC products is a plus. The ability to manage multiple competing priorities; navigation of a matrix environment; leadership as well as team member skills; strong written, oral and interpersonal skills; and sound medical judgment. Minimal travel is required between Fort Washington, PA and Skillman, NJ. This position is located in Ft. Washington, PA or Skillman, NJ.
BE VITAL in your career, Be seen for the talent you bring to your work. Explore opportunities within the Johnson & Johnson Family of Companies.
J2W:LI
Primary Location:North America-United States-New Jersey-Skillman
Other Locations:North America-United States-Pennsylvania-Fort Washington
Organization: Johnson & Johnson Consumer Inc. (6071)
Job: Medical Affairs
Certain sites within the Johnson & Johnson family of companies participate in E-Verify as appropriate in accordance with Company guidelines and federal or state law. To learn more about the government sponsored program and to see a list of the sites that are currently enrolled, please click here.
DIRECTOR 1 (MD), MEDICAL SAFETY-4776130328
Description
Johnson & Johnson Consumer Products Company, a member of Johnson & Johnson's Family of Companies, is recruiting for a Director of Medical Safety, within the division of Medical Affairs, located in Fort Washington, PA or Skillman, NJ.
Johnson & Johnson Family of Consumer Companies develops and markets OTC drugs, nutritional products, baby care, wound care and skin care products that address the needs of consumers and health care professionals and incorporate the latest innovations. The portfolio includes heritage brands JOHNSON'S® Baby and BAND-AID® Brand, TYLENOL® and MOTRIN ®products, ZYRTEC® and BENADRYL® allergy medicines, NEUTROGENA®, as well as leading skin care brands such as AVEENO® and CLEAN & CLEAR®.
This position will provide safety expertise to Johnson & Johnson Family of Consumer Companies and is part of the Medical Affairs Safety team and will report to the North America Regional Safety Officer. This position supports the North America Regional Safety Officer in oversight of pharmacovigilance activities for JJFCC products and in ensuring compliance with local and global regulations and company policies. This position provides medical input to and execution of health hazard assessments, and works collaboratively with Quality Assurance, Regulatory Affairs, Consumer Medical Safety and others on the assessment of potential safety issues with regard to manufacturing quality. This position will also work in collaboration with Global Medical Safety (GMS), Regulatory Compliance, Office of Consumer Medical Safety (OCMS), and MCH business/functional units to identify, evaluate and communicate safety and/or compliance issues. Under limited supervision and in accordance with all applicable federal, state and local laws/regulations, the Companies' policies, procedures and guidelines, the responsibilities for this position include, ensure safety reporting activities are conducted in accordance with company policies, regulatory requirements and good clinical and manufacturing standards. Providing medical input to and oversight of the execution of the safety section of the McNeil Manufacturing Quality Assurance Annual Product Reviews, working collaboratively with Quality Assurance, Regulatory Affairs, Consumer Medical Safety and others on the assessment of potential safety issues with regard to manufacturing quality. Leading and performing medical safety assessments and health hazard evaluations of new and existing products. Supporting other safety related activities such as review of periodic adverse event reviews (PADERs/PSURs), clinical trial protocols, surveillance reports, and safety-related labelling changes. Collaborating with internal and external safety experts to identify process improvements, to ensure that safety reporting activities are conducted in accordance with company policies, regulatory requirements, and good clinical and manufacturing standards. Communicating/translating medical safety/technical knowledge to scientists and non-scientists. Training and mentoring other company scientists and healthcare professionals. Provide support on pharmacovigilance audits and inspections.
Qualifications
A minimum of a MD/DO degree is required. Board eligibility or certification is also required. Certification in primary care specialty (example: internal medicine, emergency medicine, family practice or pediatrics) with post- residency patient care experience is preferred. Clinical pharmacology, toxicology, epidemiology and academic experience is a plus. A minimum of 7 years experience within the pharmaceutical industry is required. 4 years experience in Safety/Pharmacovigilance is required. An understanding of regulatory requirements, product quality management and Good Manufacturing Practices is preferred. Experience with pharmacovigilance of OTC products is a plus. The ability to manage multiple competing priorities; navigation of a matrix environment; leadership as well as team member skills; strong written, oral and interpersonal skills; and sound medical judgment. Minimal travel is required between Fort Washington, PA and Skillman, NJ. This position is located in Ft. Washington, PA or Skillman, NJ.
BE VITAL in your career, Be seen for the talent you bring to your work. Explore opportunities within the Johnson & Johnson Family of Companies.
J2W:LI
Primary Location:North America-United States-New Jersey-Skillman
Other Locations:North America-United States-Pennsylvania-Fort Washington
Organization: Johnson & Johnson Consumer Inc. (6071)
Job: Medical Affairs
Certain sites within the Johnson & Johnson family of companies participate in E-Verify as appropriate in accordance with Company guidelines and federal or state law. To learn more about the government sponsored program and to see a list of the sites that are currently enrolled, please click here.