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:
Packaging Shift Supervisor _ Avlona BU
(Ref:PSS_AVL _04.2023)
SUMMARY:
The position holder will be required to coordinate the effective operation of Packaging teams of his/her shift in order to:
Implement successfully packaging plan
Achieve daily targets
Ensure compliance with GMP rules
DUTIES AND RESPONSIBILITIES:
The Packaging Shift Supervisor, reporting directly to the Head of Packaging, is responsible for the overall coordination of Packaging Team at Avlona BU, and in particular shall:
Supervise and coordinate all packaging processes on a daily shift basis, to ensure required quality and quantity
Responsible for the implementation of H&S guidelines within the department
Ensure and coordinate continuous training of personnel within the department
Participate in the preparation and coordination of packaging validation process
Participate in Inspections (Internal, Health Authorities, and Customers) as requested
Responsible of continuous improvement actions
Ensure that all relative documentation is properly recorded and signed by QP before sent to Quality Assurance department
Monitor packaging lines and equipment’s maintenance
Participate in the Packaging Plan composition
Identify process improvement opportunities
In collaboration with Quality Assurance department, the Production Shift Supervisor shall also:
Participate in definition and approval of packaging written processes
Monitor and report deviation from current procedures, root cause analysis and evaluation of impact on production
Implement corrective actions according to company’s policies and regulations, within respective timelines
Ensure that products are produced according to production plan in the frame of quality and quantity
PROFILE / SKILLS: Languages:
Fluent in English (advanced oral and written skills).
Academic Background
University Science Degree
Special Knowledge
Advanced PC skills: (excellent MS skills- especially word, excel, PowerPoint)
Qualifications
Minimum 1 years of Pharmaceutical industry experience at a relative role.
Work in rotational shifts
Soft skills on continuous improvement, problem solving, results oriented, time management
Demonstrated teamwork and collaboration skills
Good communication skills (oral and written) to convey production guidelines/targets in an inspiring manner highly acceptable and understandable to the team
Good negotiation skills
Working effectively within deadlines
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