Recipe Author (Italy)

JR Italy; Mantova; In loco; USD 50.000 - 80.000; Part-time

Descrizione del lavoro

A leading company in pharmaceutical consulting is seeking a Recipe Author to work remotely in Europe or India. This freelance role focuses on understanding pharmaceutical manufacturing processes and requires expertise in documentation practices. The candidate should possess strong skills in process mapping, agile collaboration, and authoring requirements. Proficiency in English and Italian is essential for effective communication in this role.

Competenze

• Experience in the pharmaceutical industry with solid dose and packaging preferred.
• Fluency in English and Italian is essential.

Mansioni

• Understand and document pharmaceutical processes, including EBRs.
• Participate in agile team activities and fit gap analysis.
• Author validation documents and configure EBRs in environments.

Conoscenze

Pharmaceutical manufacturing processes

Good Documentation Practices

Good Testing Practices

Process mapping

Agile team collaboration

Documentation authoring

Strumenti

Microsoft Visio

Rockwell Pharmasuite

P2C2

PMX

Descrizione del lavoro

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Recipe Author (Europe or Italy), mantova

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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:

896182666188029952337124

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 Description:

• 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 alike software

• Ability to work with site SMEs to turn paper batch records into EBRs in Rockwell Pharmasuite utilizing existing functionality

• Ability to work with site SMEs to turn existing EBRs in legacy systems (P2C2, PMX, etc.) into Rockwell Pharmasuite EBRs utilizing existing functionality

• Ability to design Building Blocks that can be reused in multiple processes

• Ability to author requirements, SPEC, and validation documents

• Ability to test an EBR full functionality in a compliant manner

• Ability to work in a fast paced agile team environment

• Participates in fit gap analysis & Process Modeling & process standardization with Area lead & Process SME

• Works with lead RA to develop BB requirements

• Provide times, user story point estimates, and status for all stories assigned to them

• Authors and performs documents supporting validation of EBRs

• Configures EBR in Development, Stage, & Production Environment

• Address Site specific questions, use cases and ER from Site EBR and PO

• Works across the teams to put requirement together for ER development

• Provide HyperCare and Go-live support

If you are interested in this position, please send your CV in English to me immediately at

or Call me on my What's app # [phone]