Planet Pharma
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https://www.propharmagroup.com
https://www.propharmagroup.com
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Target PR: 53-68/h depending on experience
HM's Top Needs:
1. minimum 3 years direct experience in international registration
2. time management and project management skills, and abilities of quickly learning how to navigate the Medtronic systems and maintain registration database/tracker in a timely manner
3. understanding of business urgencies and priorities
Education Required: Bachelor of Engineering/Science as minimum; Master preferred
Years’ Experience Required: 4-5 years as independent RA specialist in US/EU/Global registration
Top 3 technical skills or experience requiredL: good time management and project management; experience on global regulatory strategies and working with RA teams in different regions for product registration; familiar with medical device design control process and follow up with design/manufacturing sites on additional documents required by global regulations
Responsibilities may include the following and other duties may be assigned. Directs or performs coordination and preparation of document packages for regulatory submissions from all areas of company internal audits and inspections. Leads or compiles all materials required in submissions license renewal and annual registrations. Recommends changes for labeling manufacturing marketing and clinical protocol for regulatory compliance. Monitors and improves tracking / control systems. Keeps abreast of regulatory procedures and changes. May direct interaction with regulatory agencies on defined matters. Recommends strategies for earliest possible approvals of clinical trials applications.
SPECIALIST CAREER STREAM: Typically an individual contributor with responsibility in a professional discipline or specialty. Delivers and/or manages projects assigned and works with other stakeholders to achieve desired results. May act as a mentor to colleagues or may direct the work of other lower level professionals. The majority of time is spent delivering and overseeing the projects from design to implementation while and adhering to policies using specialized knowledge and skills normally acquired through advanced education typically University.
DIFFERENTIATING FACTORS
Autonomy: Seasoned individual contributor. Works independently under limited supervision to determine and develop approach to solutions. Coaches and reviews the work of lower level specialists may manage projects / processes.
Organizational Impact: May be responsible for entire projects or processes within job area. Contributes to the completion of work group objectives through building relationships and consensus to reach agreements on assignments.
Innovation and Complexity: Problems and issues faced are difficult and may require understanding of multiple issues job areas or specialties . Makes improvements of processes systems or products to enhance performance of the job area. Analysis provided is indepth in nature and often provides recommendations on process improvements.
Communication and Influence: Communicates with senior internal and external customers and vendors. Exchange information of facts statuses ideas and issues to achieve objective and influence decisionmaking.
Leadership and Talent Management: May provide guidance coaching and training to other employees within job area. May manage projects requiring delegation of work and review of others' work product .
Required Knowledge and Experience: Requires advanced knowledge of job area combining breadth and depth typically obtained through advanced education combined with experience. May have practical knowledge of project management. Requires a University Degree and minimum of 4 years of relevant experience or advanced degree with a minimum of 2 years relevant experience.
Remote Sr Regulatory Affairs Spec
Remote Carlsbad, CA 92008 US
Posted: 08/28/2024
2024-08-28
2024-10-11
Employment Type:
Contract
Job Category: Regulatory Sciences and Medical Writing
Job Number: 614157
Is job remote?: Yes
Country: United States
Job Description
Target PR: 53-68/h depending on experience
HM's Top Needs:
1. minimum 3 years direct experience in international registration
2. time management and project management skills, and abilities of quickly learning how to navigate the Medtronic systems and maintain registration database/tracker in a timely manner
3. understanding of business urgencies and priorities
Education Required: Bachelor of Engineering/Science as minimum; Master preferred
Years’ Experience Required: 4-5 years as independent RA specialist in US/EU/Global registration
Top 3 technical skills or experience requiredL: good time management and project management; experience on global regulatory strategies and working with RA teams in different regions for product registration; familiar with medical device design control process and follow up with design/manufacturing sites on additional documents required by global regulations
Responsibilities may include the following and other duties may be assigned. Directs or performs coordination and preparation of document packages for regulatory submissions from all areas of company internal audits and inspections. Leads or compiles all materials required in submissions license renewal and annual registrations. Recommends changes for labeling manufacturing marketing and clinical protocol for regulatory compliance. Monitors and improves tracking / control systems. Keeps abreast of regulatory procedures and changes. May direct interaction with regulatory agencies on defined matters. Recommends strategies for earliest possible approvals of clinical trials applications.
SPECIALIST CAREER STREAM: Typically an individual contributor with responsibility in a professional discipline or specialty. Delivers and/or manages projects assigned and works with other stakeholders to achieve desired results. May act as a mentor to colleagues or may direct the work of other lower level professionals. The majority of time is spent delivering and overseeing the projects from design to implementation while and adhering to policies using specialized knowledge and skills normally acquired through advanced education typically University.
DIFFERENTIATING FACTORS
Autonomy: Seasoned individual contributor. Works independently under limited supervision to determine and develop approach to solutions. Coaches and reviews the work of lower level specialists may manage projects / processes.
Organizational Impact: May be responsible for entire projects or processes within job area. Contributes to the completion of work group objectives through building relationships and consensus to reach agreements on assignments.
Innovation and Complexity: Problems and issues faced are difficult and may require understanding of multiple issues job areas or specialties . Makes improvements of processes systems or products to enhance performance of the job area. Analysis provided is indepth in nature and often provides recommendations on process improvements.
Communication and Influence: Communicates with senior internal and external customers and vendors. Exchange information of facts statuses ideas and issues to achieve objective and influence decisionmaking.
Leadership and Talent Management: May provide guidance coaching and training to other employees within job area. May manage projects requiring delegation of work and review of others' work product .
Required Knowledge and Experience: Requires advanced knowledge of job area combining breadth and depth typically obtained through advanced education combined with experience. May have practical knowledge of project management. Requires a University Degree and minimum of 4 years of relevant experience or advanced degree with a minimum of 2 years relevant experience.
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Although this hasn't been an issue at Planet Pharma, the staffing industry has seen an increase in people falsely representing themselves as recruiters to gather personal information from job seekers. For your safety, do not provide sensitive data to anyone you have not spoken with thoroughly and never provide banking information during the application process. Candidate safety is a top priority at Planet Pharma.
