Recipe Author (Italy)

JR Italy; Bari; In loco; USD 40.000 - 70.000; Tempo pieno

Descrizione del lavoro

A leading company in the pharmaceutical sector seeks a Recipe Author for freelance consultancy. Candidates must have strong expertise in pharmaceutical processes and a thorough understanding of documentation standards. The role involves collaborating with site experts to develop and validate electronic batch records while working in a dynamic team environment. Fluency in English and Italian is required, and interested applicants should apply promptly.

Competenze

• Speak English and Italian.
• Experience in pharmaceutical manufacturing and EBR documentation.
• Ability to work with SMEs.

Mansioni

• Understand manufacturing processes and assist in transitioning paper records to EBRs.
• Collaborate with SMEs and provide validation support.
• Configure and support EBR in various environments.

Conoscenze

Understanding of pharmaceutical manufacturing processes

Good Documentation Practices

Good Testing Practices

Ability to process map using software

Ability to work in agile team environment

Strumenti

Microsoft Visio

Rockwell Pharmasuite

Descrizione del lavoro

ADR Application Development Resources, Inc.

Location:

Job Category:

Other

-

EU work permit required:

Yes

Job Reference:

896182666188029952337117

Job Views:

2

Posted:

03.06.2025

Expiry Date:

18.07.2025

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

[e-mail]

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

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