Recipe Author (Europe or Italy)

JR Italy; Treviso; Remoto; USD 30.000 - 50.000; Tempo pieno

Descrizione del lavoro

A leading company is seeking a Recipe Author for a freelance contract role, primarily focused on pharmaceutical manufacturing documentation. The position requires fluency in English and Italian, alongside expertise in documentation and the ability to work within cross-functional teams. Ideal candidates will possess a good understanding of manufacturing processes and agile methodologies.

Competenze

• Fluency in English and Italian is essential.
• Experience with pharmaceutical processes and documentation is required.

Mansioni

• Understand and design documentation for pharmaceutical manufacturing.
• Work with SMEs to convert batch records into electronic records.
• Participate in fit gap analysis and process modeling.

Conoscenze

Understanding of pharmaceutical manufacturing processes

Expertise in Good Documentation Practices

Ability to process map site requirements

Ability to work in a fast paced agile team environment

Fluency in English and Italian

Strumenti

Microsoft Visio

Rockwell Pharmasuite

Descrizione del lavoro

Social network you want to login/join with:

Recipe Author (Europe or Italy), treviso

col-narrow-left

Client:

ADR Application Development Resources, Inc.

Location:

Job Category:

Other

-

EU work permit required:

Yes

col-narrow-right

Job Reference:

896182666188029952337115

Job Views:

2

Posted:

03.06.2025

Expiry Date:

18.07.2025

col-wide

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]