Operater
Novartis
Operater
Job Description
Summary
Summary ~Operater opreme~Izvajanje dodeljenih proizvodnih nalog in dejavnosti v skladu s proizvodnim načrtom, da se omogoči pravočasno proizvodnjo proizvoda s kakovostjo in količino v skladu z ustreznimi smernicami GMP, varnosti in okolja.
~Servisni operater
~Izvajanje dodeljenih proizvodnih nalog in dejavnosti v skladu s proizvodnim načrtom v skladu z ustreznimi smernicami GMP, varnosti in okolja.
Izvajati rutinske operativne podporne dejavnosti v skladu s proizvodnim postopkom in razporedom ter omogočiti pravočasno proizvodnjo izdelka s kakovostjo in količino
~Specialist za dokumentacijo Admin
~The Documentation Specialist Admin upravlja spreminjanje, urejanje, distribucijo, pregled in arhiviranje GMP proizvodnih dokumentov in izdajo paketnih zapisov, da bi jih dostavili v Proizvodnjo v kakovosti in v rokih. Specialist za dokumentacijo Admin zagotavlja nabor administrativnih nalog, potrebnih za pravilno delovanje enote.
Locations
- Slovenia
Salary
Estimated Salary Rangemedium confidence
45,000 - 80,000 USD / yearly
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Execution of production tasksintermediate
- GMP complianceintermediate
- Safety protocol adherenceintermediate
- Environmental guideline complianceintermediate
- Routine operational supportintermediate
- Production planning adherenceintermediate
- Document managementintermediate
- Document editing and reviewintermediate
- Document distribution and archivingintermediate
- Batch record issuanceintermediate
- Administrative task managementintermediate
- Attention to detailintermediate
- Time managementintermediate
- Quality controlintermediate
Required Qualifications
- Knowledge of GMP guidelines (experience)
- Understanding of production procedures (experience)
- Experience in pharmaceutical manufacturing operations (experience)
- Administrative skills for documentation handling (experience)
Responsibilities
- Execute assigned production orders and activities according to the production plan
- Ensure timely production of product with required quality and quantity per GMP, safety, and environmental guidelines
- Perform routine operational support activities in accordance with production procedures and schedule
- Manage changes, editing, distribution, review, and archiving of GMP production documents
- Issue batch records and deliver them to Production in quality and on time
- Provide administrative tasks necessary for proper unit functioning
- Enable timely product production as a service operator
- Follow production schedule for all operator roles
Answer 10 quick questions to check your fit for Operater @ Novartis.
10 Questions
~2 Minutes
Instant Score
Operater
Novartis
Operater
Job Description
Summary
Summary ~Operater opreme~Izvajanje dodeljenih proizvodnih nalog in dejavnosti v skladu s proizvodnim načrtom, da se omogoči pravočasno proizvodnjo proizvoda s kakovostjo in količino v skladu z ustreznimi smernicami GMP, varnosti in okolja.
~Servisni operater
~Izvajanje dodeljenih proizvodnih nalog in dejavnosti v skladu s proizvodnim načrtom v skladu z ustreznimi smernicami GMP, varnosti in okolja.
Izvajati rutinske operativne podporne dejavnosti v skladu s proizvodnim postopkom in razporedom ter omogočiti pravočasno proizvodnjo izdelka s kakovostjo in količino
~Specialist za dokumentacijo Admin
~The Documentation Specialist Admin upravlja spreminjanje, urejanje, distribucijo, pregled in arhiviranje GMP proizvodnih dokumentov in izdajo paketnih zapisov, da bi jih dostavili v Proizvodnjo v kakovosti in v rokih. Specialist za dokumentacijo Admin zagotavlja nabor administrativnih nalog, potrebnih za pravilno delovanje enote.
Locations
- Slovenia
Salary
Estimated Salary Rangemedium confidence
45,000 - 80,000 USD / yearly
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Execution of production tasksintermediate
- GMP complianceintermediate
- Safety protocol adherenceintermediate
- Environmental guideline complianceintermediate
- Routine operational supportintermediate
- Production planning adherenceintermediate
- Document managementintermediate
- Document editing and reviewintermediate
- Document distribution and archivingintermediate
- Batch record issuanceintermediate
- Administrative task managementintermediate
- Attention to detailintermediate
- Time managementintermediate
- Quality controlintermediate
Required Qualifications
- Knowledge of GMP guidelines (experience)
- Understanding of production procedures (experience)
- Experience in pharmaceutical manufacturing operations (experience)
- Administrative skills for documentation handling (experience)
Responsibilities
- Execute assigned production orders and activities according to the production plan
- Ensure timely production of product with required quality and quantity per GMP, safety, and environmental guidelines
- Perform routine operational support activities in accordance with production procedures and schedule
- Manage changes, editing, distribution, review, and archiving of GMP production documents
- Issue batch records and deliver them to Production in quality and on time
- Provide administrative tasks necessary for proper unit functioning
- Enable timely product production as a service operator
- Follow production schedule for all operator roles
Answer 10 quick questions to check your fit for Operater @ Novartis.
10 Questions
~2 Minutes
Instant Score