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Technical Responsible

por Ofertas de Emprego

Faro

Full-time

Data de publicação

Localização

Faro

Descrição da oferta

Join our dynamic and innovative team at Gro-Vida, a trailblazing cannabis facility committed to producing exceptional, high-quality products for our valued customers.
We are on the hunt for a passionate, experienced Technical Responsible to oversee and enhance our quality assurance processes, ensuring our products meet the highest standards of safety and efficacy. If you’re driven, meticulous, and eager to make a significant impact in a cutting-edge industry, Gro-Vida is the place for you!

Key Responsibilities:

Ensure all processes, from cultivation to final product, adhere to the highest quality standards.
Conduct regular audits and inspections to ensure compliance with internal policies and Infarmed regulations.
Stay abreast of all relevant regulatory requirements from Infarmed and other relevant bodies, ensuring company-wide compliance.
Liaise with Infarmed and other regulatory bodies, ensuring timely submission of required documentation.
Identify areas for process improvement and implement strategies to enhance product quality and operational efficiency.
Lead root cause analysis and corrective action initiatives to resolve quality issues.
Foster a culture of continuous improvement and quality excellence within the organisation.
Implement corrective actions and preventive measures to address non-compliance issues.

Defined in the following guidelines:
Registered Quality Assurance Professional. There is usually a regulatory body that they would report to and have to have particular education/courses.
This person must have knowledge of GACP and GMP but is only to work in a GACP environment.
GACP Guideline
GDP Guidelines
GMP Part II: Basic Requirements for Active Substances Used as Starting Materials;
GMP Part I: Good Manufacturing Practice for Medicinal Products for Human and Veterinary Use.

Ensuring at least the following:
That the quality management system is applied and maintained.
Giving priority to the management of authorised activities and to the accuracy and quality of records.
Coordinating and promptly carrying out any product recall operations.
Ensuring that customer complaints are handled effectively.
Ensuring that suppliers and customers are approved.
Approval of any subcontracted activities that may have an impact on GACP/GMP/GDP.
Ensuring that self-inspections are carried out at appropriate regular intervals, following a previously agreed program and that the necessary corrective measures are carried out.
Keeping adequate records of all delegated functions.
Deciding on the final destination of products returned, rejected or recalled from the distribution circuit.
Approval of any refund of products to marketable stocks.
Ensuring that all additional requirements imposed on certain products are met by national law.
Collaborate in technical activities relevant to the manufacture of active substances for medicinal products for human use.
Request official certificates for the import and export of controlled substances (psychotropic drugs and narcotic drugs) to the competent authorities.
Represent the manager in connections with external entities whenever required.
Monitor the latest developments and market trends and pharmaceutical regulation.
Participate in the evaluation of the technical feasibility of new projects.

Qualifications:
Fluent in English and Portuguese.
Higher education in Pharmaceutical Sciences, enrolled in the Order of Pharmacists, preferably with the title of specialist in the Pharmaceutical Industry.
Proven experience as a Quality Director or similar role in the cannabis industry or a related field.
In-depth knowledge of quality assurance and control principles, Infarmed regulations, and industry best practices.
Strong leadership and team management skills.
Excellent analytical, problem-solving, and decision-making abilities.
Effective communication and interpersonal skills.
Training in Good Agricultural and Collection Practices.
Training in Good Manufacturing Practices.
Training in Good Distribution Practices.

How to Apply:
Interested candidates should submit their resume and a cover letter detailing their relevant experience and qualifications via
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Join us at Gro-Vida and be part of a team that values quality, innovation, and teamwork. We look forward to welcoming you!