Quality and Regulatory Affairs
KvalitaVe společnosti ARaymond vytváříme špičkové upevňovací a montážní systémy pro stroje a výrobky, které udržují svět v pohybu.
Společnost byla založena v Grenoblu v roce 1865 a dodnes zde má sídlo. Jsme rodinný podnik s bohatou historií inovací, na které jsme hrdí – včetně vynálezu druku (patentky).
Již více než 158 let jsou hnacím motorem našeho úspěchu lidské hodnoty, které ztělesňuje náš model řízení, tzv. Servant leadership. Ten podporuje samostatnost zaměstnanců a prioritou je jejich spokojenost .
Dnes zaměstnáváme více než 8 500 lidí ve 25 zemích světa a jsme odhodláni stát se lídrem v oblasti udržitelnosti pro celosvětový trh s upevňovacími a montážními prvky.
Propojte části, které posouvají svět vpřed
Při práci v čistém, ekologickém a technologicky vyspělém výrobním prostředí budete pomáhat vytvářet špičkové upevňovací a montážní systémy pro inovace, na které se všichni denně spoléháme.
Co u nás budete dělat?
- Write, analyze, and edit technical documents to support country specific regulatory submissions and compile submissions in a format consistent with applicable guidance documents, including investigational device submissions in USA, Canada, Europe and India.
- Work with other departments and communicate the submission requirements when documents are needed for regulatory submission.
- Maintain regulatory files.
- Maintain and update regulatory authorizations, such as IDEs, 510(k)s, Canadian medical device licenses, and CE dossiers for EU, NRTL certifications etc.
- Maintain Compliance with respect to Combination products and 21CFR Part 820
- Assure that appropriate maintenance of registrations occurs including renewals, device listings, site registrations, supplements for changes and annual reports.
- Support approval in other regions as required.
- Assist in preparing response to regulatory authorities questions within assigned timelines.
- Stay abreast of regulatory procedures and changes in regulatory climate.
- Assess device related incidents/complaints for medical device reporting requirements.
- Compile and submit reportable events to relevant regulatory authorities in timely manner.
- Handle recalls and field actions, if required.
- Review and create product labels and review promotional material for compliance with applicable regulations and technical standards.
- Support external regulatory agency audits, providing regulatory input to minimize potential for findings of non-compliance.
- Assist in preparing clinical trial site ethics review board applications for investigational device trials. Prepare interim or final reports for trial site ethics boards as required
- Other duties as assigned.
Key Attributes
- Self & Team Management
- Minimum of 2 years regulatory or equivalent experience within a device or pharmaceutical company, CRO, or similar organization
- Scientific knowledge, must be able to digest complex data while keeping the big picture through good analytical skills
- Excellent written and Verbal communication skills with the ability to listen, articulate and advocate
- Proactive, high performance, result oriented and manage projects with ethical integrity
- Technical system skills (e.g. MS office applications, databases, efficient online research)
- Manage multiple projects and deadlines
- Ability to identify compliance risks and escalate when necessary
Demonstrate both creative and critical thinking skill
ISO 27K-
- Maintaining awareness and adherence about applicable information security policies and procedures
- Maintaining compliance with contractual requirements
- Ensuring information, they use or information under their custody is adequately protected as per ARaymond information security expectations.
- Reporting any noted suspicious behavior, vulnerability, and incidents to authority
Co od vás potřebujeme?
Graduation/ Post Graduation in with Specialization in Pharma/ Engineering along with 15- 20 Years of experience
Skills
- Knowledge of 5S methodology
- Team-Working
- Environment, Health, and Safety Risk Management
- Customer Service Orientation
- Workplace Emergency Preparedness
- Decision Making
- Knowledge of EHS Standards and Procedures
- Communication Skills
- Knowledge of ergonomic working conditions
- Accountability and Ownership
- Root cause analysis
- Knowledge of Plastic Raw Material
Knowledge of Steel Raw Material