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Quality Systems Officer (QSOA_05.2024)

Κωδικός Θέσης : QSOA_05.2024
Ημερομηνία ανάρτησης αγγελίας : 27/5/2024




FAMAR is a European contract manufacturing and development partner, for the pharmaceutical and health & beauty industry. Building on our 70 years’ expertise, we deliver flexible solutions, from development to production and distribution. Driven by our customer-care mindset, we offer services covering the majority of pharmaceutical forms, while providing a particularly strong expertise in Liquids, Ointments and Creams. Through the outstanding knowledge and commitment of our 1850 employees and with a network of 6 production sites, we supply a wide range of 1800 products in 125 international markets.

We are looking to recruit in Anthoussa BU:

    

                                                          QUALITY SYSTEMS OFFICER
                                                                 (QSOA_05.2024)
 

ΤHE POSITION HOLDER WILL BE REQUIRED TO:

Contribute to the implementation of quality systems of the BU and to report on and assist in ensuring all processes and services are in accordance with Famar Guidelines, industry standards/requirements and GMP requirements
 
DUTIES AND RESPONSIBILITIES:
The holder of the position will refer to the Quality Systems Manager and will have the following responsibilities:
• Authoring and reviewing of assigned Quality Written Procedures
• FAMAR Quality System as applicable by opening, reviewing and/or approving relevant records (e.g. deviations, CAPAs, Change Controls).
• Review equipment qualification protocols (facility and utility systems, computer systems, process equipment and GMP processes).
• Participate in internal audits (self-audits - customer GMP and HA audits).
• Training personnel on procedures and processes.
• Integrate risk management principles into quality systems s.
• Collaborating with internal departments for continuous improvement of procedures and product quality

•Monitor pest controls.

•Monitor production practices to ensure compliance with GMP standards.

PROFILE/ SKILLS:            
Languages:
• Fluent in English (advanced oral and written skills).
 
Academic Background:
• University Degree in Chemistry/Chemical Engineering/Pharmacy/Biology.
Special Knowledge
• Advanced PC skills: (excellent MS skills- especially word, excel, PowerPoint), Good knowledge of Intranet applications like SharePoint as a plus.

Qualifications:
• 1-3 years’ experience in Quality management, preferably within the pharmaceutical/healthcare industries.
• Knowledge both theoretical and practical aspects of EU Regulations & Directives, Quality Management Systems and processes (ISO 9001)  as well as international GMP regulations of medicinal products, will be considered as a plus
• Highly credible – both professionally and personally, with an engaging and action orientated approach.
• Soft skills on change management, time management, listening & communication, autonomy, self-confidence, problem solving, results oriented, able to work under remote management.
• Demonstrated teamwork, collaborative and consensual – A colleague that people turn to for advice and want to work with.


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