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