Since its creation in 1957, Huckert’s International Laboratory’s mission has been to offer high-level disinfectants that protect professionals from both the risks of contamination and any side effects. An expert in bio-decontamination and high-level disinfection, Huckert’s Laboratory produces and develops two ranges, UMONIUM38 for disinfecting instruments, benches and equipment, and PHYTOGEL By Huckert’s for skin care. We produce disinfectants that comply with and are validated according to European normative application standards. Our products are stable, safe and effective in all circumstances, even under adverse conditions. We do not compromise on quality, so our products are fast, active on a very wide spectrum of germs, without toxicity or corrosion effect. For us, a disinfectant should not replace a biological hazard with a chemical hazard. ISO 9001 and ISO 13485 certified – medical devices. Huckert’s Laboratory, with its 60 years of know-how in the disinfection of protected environments, can assist you in controlling infectious risks.
Laboratoire Huckert’S International SPRL

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Sales representative
✓ You have a successful experience of more than 2 years in sales.
✓ You have a good knowledge of the scientific community.
✓ You know how to translate your commercial talent into an effective, convincing and customer-oriented approach.
✓ You are a born salesperson working in an autonomous and organized way.
✓ You are optimistic, eager to learn, communicative and you seek solutions.
✓ Your work is professional and results-oriented.
✓ You are flexible, efficient, organized, autonomous, dynamic, motivated.
✓ You have an excellent presentation and you contribute to a positive image of the company

Sales Assistant Trinlingual FR-EN-DU
✓ You are dynamic and motivated.
✓ Proactive, versatile, you take initiatives and are involved in your work.
✓ You have a perfect command of word, Excel, Outlook software
✓ You are a good French-Dutch-English trilingual.
✓ Knowledge of Odoo is a strong asset.
✓ You are organized and enjoy working in a team.
✓ You have an excellent presentation in relation to the position you hold.

QUALITY ASSISTANT (M/F)
Under the responsibility of the Quality Manager, your missions are:
QUALITY SYSTEM
✓ Respect and enforce the quality policy
✓ Drafting, implementation and management of quality documents in accordance with applicable standards
✓ Equipment and premises: participation in the qualification of equipment
✓ Improvement of the Quality System
✓ Monitoring and participation in the internal audit program.
QUALITY CONTROL
✓ Quality control upon receipt of the various products
✓ Release of batches of Medical Devices.
✓ Management & monitoring of anomalies
✓ Monitoring and management of CAPAs
✓ Follow-up of the sample library.
✓ Monitoring of control, measurement and test equipment
✓ Quality control on new products, comparative studies on test performance of different suppliers.
REGULATORY
✓ Contribution to the creation and updating of the documents constituting the EC files
✓ Team QA/QC Back-Up
✓ Support for monitoring and updating risk analyzes

PRODUCTION OPERATOR (M/F)
FUNCTION
✓ You join a team responsible for the production, packaging and shipping of products.
✓ You participate in the cleaning of the premises, respecting the procedures.
✓ You are in charge of the maintenance-preparation-assembly-dismantling of the shows.
✓ You participate in the maintenance of the various installations related to the entire building and all work relating to the proper functioning of the company.

REGULATORY MANAGER (M/F)
Your mission :
You are in charge of Regulatory Affairs
✓ Participate in quality monitoring and ISO9001:2015 and IS013485:2016 certification
✓ Ensure compliance with the various regulations in force
✓ Submit the registration and variation files for Laboratoire Huckert’s International products to the competent authorities, in accordance with the regulatory procedures and the legislation in force
✓ Ensure the maintenance of marketing authorizations/notifications (renewals, variations, payment of fees if applicable)
✓ Enter the files and regulatory documents in the company’s databases;
✓ Prepare and validate the packaging information as well as the promotional documents according to the regulations in force;
✓ Monitor submission and approval dates and escalate any questions about a product raised by a local authority;
✓ Organize the traceability and archiving of documents and local files;
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