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QUALITY SYSTEMS OFFICER

Κωδικός Θέσης : QSOAVL_09 2020
Ημερομηνία ανάρτησης αγγελίας : 21/9/2020




 

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 seek to recruit for BU in Avlonas site:

QUALITY SYSTEMS OFFICER
(Ref: QSOAVL_09 2020)


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 of personnel regarding procedures and processes.
• Integrate risk management principles into quality systems across proactive and reactive processes.
• Work with internal departments to ensure continuous improvement of procedures and quality of products

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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