Description
Position Summary:
We are seeking a Pharmaceutical Chemist to lead regulatory processes, manage quality, and ensure regulatory compliance within a pharmaceutical company.
Key Responsibilities:
1. Lead sanitary registration processes and regulatory compliance.
2. Manage the quality management system and supervise operations.
3. Participate in strategy and development of new products.
Our client, a leading pharmaceutical company specializing in the importation and commercialization of medical devices and over-the-counter (OTC) products, is seeking the following profile:
**REQUIREMENTS:**
* Professional degree in Pharmaceutical Chemistry (Mandatory).
* Valid professional license (Mandatory).
* More than 2 years of experience as Technical Director or in similar positions (e.g., Regulatory Affairs or Quality Management Head) in pharmacies or pharmaceutical laboratories. (Desirable)
* Experience managing sanitary registrations for medical devices and/or pharmaceutical products (OTC). (Desirable)
* Solid knowledge of Good Storage Practices (GSP) and Good Distribution and Transportation Practices (GDTP).
* Proficiency in applicable Peruvian health regulations (Law No. 29459 and current regulations).
* Knowledge of DIGEMID regulations for medical devices and pharmaceutical products.
* Experience with quality management systems (ISO 9001, ISO 13485\).
* Intermediate-level proficiency in MS Office: Word, Excel, PowerPoint.
* Familiarity with pharmacovigilance and technovigilance software. (Desirable).
**RESPONSIBILITIES:**
* Lead processes related to obtaining, renewing, modifying, and canceling sanitary registrations with regulatory authorities.
* Manage required technical and legal documentation, ensuring compliance and validity.
* Represent the company before health authorities during audits and inspections.
* Supervise compliance with labeling, leaflet, and promotional material regulations.
* Ensure compliance with GSP and GDTP across the entire supply chain.
* Design, implement, and maintain the quality management system.
* Supervise storage, inventory, and distribution processes, guaranteeing optimal conditions.
* Manage quality deviations, non-conforming products, returns, and market withdrawals.
* Participate in supplier selection and evaluation.
* Conduct internal and external quality audits.
* Lead, train, and supervise the technical and warehouse teams.
* Participate in strategic planning and development of new product lines.
* Evaluate regulatory requirements for new products and business opportunities.
* Provide technical and regulatory support in the development of proprietary products.
* Ensure compliance with all applicable legal regulations.
**WORK LOCATION**: Miraflores
**WORK MODALITY**: 100% on-site
**WORK HOURS**: Monday to Friday, 8:00 a.m. to 6:00 p.m.
**BENEFITS**:
* Formal employment under the General Regime \- Statutory benefits
Please send your updated CV to: cv(arroba)selekto\-rrhh.com with subject line: Technical Director
Workplace: On-site employment