Recipe Author (Italy)

JR Italy; Catania; In loco; EUR 10.000 - 30.000; Tempo pieno

Descrizione del lavoro

A leading company in pharmaceutical documentation seeks a Recipe Author for a freelance position based in Catania, Italy. The role involves authoring technical documents and converting paper records into electronic formats, requiring expertise in pharmaceutical processes and language skills in English and Italian. Suitable candidates must have experience in good documentation practices and agile team environments.

Competenze

• Expertise in pharmaceutical manufacturing processes, preferably solid oral dose and packaging.
• Fluent in English and Italian languages.

Mansioni

• Understand pharmaceutical manufacturing processes.
• Collaborate with site SMEs to convert paper batch records into EBRs.
• Configure EBRs in different environments and support validation.

Conoscenze

Pharmaceutical manufacturing processes

Good Documentation Practices

Good Testing Practices

Microsoft Visio

Process mapping

Agile methodology

Collaboration

Descrizione del lavoro

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Recipe Author (Europe or Italy), Catania

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Client:

ADR Application Development Resources, Inc.

Location:

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

896182666188029952337122

Job Views:

2

Posted:

03.06.2025

Expiry Date:

18.07.2025

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Job Description:

Title: Recipe Author (Europe or Italy)

Location: Remote, Europe/India

This is a Freelance Contract Consultant job and will be paid in US dollars

There are 3 openings and I need one person who speaks English and Italian

Please send CV in English

Job Responsibilities:

• Understanding of pharmaceutical manufacturing processes (Solid oral dose and packaging preferred)
• Possesses expertise in Good Documentation and Good Testing Practices
• Ability to process map site requirements using Microsoft Visio or similar software
• Collaborate with site SMEs to convert paper batch records into EBRs in Rockwell Pharmasuite using existing functionality
• Convert existing EBRs in legacy systems (P2C2, PMX, etc.) into Rockwell Pharmasuite EBRs
• Design reusable Building Blocks for multiple processes
• Author requirements, specifications, and validation documents
• Test EBR full functionality in a compliant manner
• Work efficiently in a fast-paced agile team environment
• Participate in fit-gap analysis, process modeling, and standardization with Area lead & Process SME
• Coordinate with lead RA to develop BB requirements
• Provide estimates, user story points, and status updates for assigned stories
• Author and support validation documents for EBRs
• Configure EBRs in Development, Stage, & Production environments
• Address site-specific questions, use cases, and ERs from site EBR and PO
• Collaborate across teams to develop ER requirements
• Provide HyperCare and go-live support

If interested, please send your CV in English to me immediately or contact me via WhatsApp at [phone].