20 annunci per il ruolo di monitoring specialist - milano, lom (recruiting in corso)

Equipment Validation Compliance Specialist
Thermo Fisher Scientific —Monza, Lombardia
- Tempo pieno
- Inglese
- Microsoft Office
- Laurea magistrale
(Senior) Short-Term Flex Optimisation Analyst – Automated Flexibility Trading (m/f/d)
Statkraft —Milano, Lombardia
- 50.000 € - 70.000 € all'anno
- Tempo pieno
- Inglese
- Laurea triennale
- Python
- Congedo parentale
Candidatura rapida
Global Data Factory Specialist
Amplifon —Milano, Lombardia
- 35.000 € - 49.000 € all'anno
- Tempo pieno
- Remoto
- Gestionale
- Ingegneria
- Inglese
Curricular Internship - Trade & Working Capital Products
UniCredit S.p.A —Milano, Lombardia
- Tempo pieno
- Microsoft Powerpoint
- Microsoft Excel
- Gestionale
Sr. Associate, Trade Marketing
Alcon —Milano, Lombardia
- 41.650 € all'anno
- Tempo pieno
- Microsoft Excel
- Vendite
- Inglese
Pricing Specialist
Zimmer Biomet —Segrate, Lombardia
- Da 28.982 € all'anno
- Tempo pieno
- Microsoft Excel
- Inglese
- Competenze analitiche
Sustainability Specialist, Solutions, Italy
DSV —Settala, Lombardia
- Tempo pieno
- Microsoft Powerpoint
- Microsoft Excel
- Gestionale
Specialist - Milano
Sephora —Milano, Lombardia
- Tempo pieno
- Gestionale
- Inglese
Global IT Manager Network Services
Campari Group —Sesto San Giovanni, Lombardia
- 69.000 € - 92.000 € all'anno
- Informatica
- Azure
- Gestionale
Investment Banking – M&A Analyst Intern
Azimut Holding —Milano, Lombardia
- 900 € al mese
- Microsoft Powerpoint
- Microsoft Excel
- Inglese
14 giorni
Digital Performance Marketing Specialist
Moncler —Milano, Lombardia
- 26.000 € - 31.000 € all'anno
- Gestionale
- Inglese
- Laurea triennale
Product Specialist Urologia
Ambu —Milano, Lombardia
- Tempo pieno
- Inglese
- Leadership
Internship - Credit Risk | Milan
KPMG —Milano, Lombardia
- 800 € - 1.000 € al mese
- Inglese
- Microsoft Office
- Tirocinio formativo/stage
Application Expert (Temporary)
Sealed Air —Rho, Lombardia
- Laurea triennale
- Ingegneria elettrica
- Tirocinio formativo/stage
Social media graphic & content intern
VIBRAM SPA —Milano, Lombardia
- 600 € al mese
- Gestionale
- Social media management
- Inglese
Candidatura rapida
Service Desk Operator | Space Programmes
Etinars —Milano, Lombardia
- Microsoft Outlook
- Inglese
- Microsoft Office
Candidatura rapida
Business Development Manager
Ropes & Gray LLP —Milano, Lombardia
- Gestionale
- Inglese
- Microsoft Office
Specialist Corporate Finance (f/w/x)
Bayerische Landesbank —Milano, Lombardia
- Tempo pieno
- Inglese
- Competenze analitiche
- Laurea triennale
Customer Salesforce Senior Consultant
KPMG —Milano, Lombardia
- 30.000 € - 37.000 € all'anno
- Gestionale
- Vendite
- Salesforce
Sales Specialist- Motion Drives Lombardia
ABB S.p.A. —Sesto San Giovanni, Lombardia
- Da 48.000 € all'anno
- Gestionale
- Vendite
- Inglese
Candidatura rapida
2 giorni

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Equipment Validation Compliance Specialist

Thermo Fisher Scientific -
Monza, Lombardia

Candidati adesso

Dettagli della posizione

Tempo pieno

Qualifiche

Inglese
Microsoft Office
Laurea magistrale
Competenze analitiche
Laurea triennale
FMEA
Produzione

Descrizione completa della posizione

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office

Job Description

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

DESCRIPTION
Join us as a Equipment Validation Compliance Specialist at Thermo Fisher Scientific, where you'll contribute to ensuring product quality and regulatory compliance. In this position, you'll be responsible for reviewing and approving qualification protocols, qualification reports and technical documentation related to equipment and systems requiring qualification, ensuring compliance with applicable regulatory requirements and company procedure. Working with cross-functional teams, you'll help maintain our high standards of quality while supporting continuous improvement initiatives. This role offers excellent opportunities for professional growth within an established leader in serving science.

KEY RESPONSIBILITIES

Review technical documentation related to equipment and systems requiring qualification, ensuring compliance with current regulatory requirements (cGMP, FDA, and other applicable regulations) and internal procedures.
Review and approve qualification protocols and reports (IQ/OQ/PQ), ensuring their accuracy, completeness, and compliance with applicable GMP regulations and company standards.
Support equipment qualification activities by providing quality oversight and evaluating technical issues to ensure proper execution of IQ/OQ/PQ protocols in accordance with approved procedures.
Support the Team Leader during customer and regulatory inspections by preparing and providing the required documentation and information, and participating in audits when needed, ensuring compliance with current GMP requirements.
Ensure adherence to company quality standards by monitoring the implementation of procedures within the area of responsibility, in line with corporate quality policies and procedures.
Maintain and continuously update Standard Operating Procedures (SOPs), operating procedures, methods, and validation documentation related to the area of responsibility through document preparation and periodic review, ensuring ongoing compliance with current GMP requirements.

REQUIREMENTS

Education:

Bachelor's or Master's Degree required.

Preferred Fields of Study: Pharmaceutical Chemistry and Technology (CTF), Pharmacy, Chemistry, Biotechnology, Biology, Engineering or related scientific field.

Professional experience

At least 5 years of experience in the pharmaceutical industry, preferably within Quality Assurance and Equipment Validation.

Technical knowledge

Experience in sterile pharmaceuticals manufacturing environments.

Knowledge of equipment and system validation principles, including IQ/OQ/PQ.

Knowledge of FDA/EMA validation regulations and industry standards.
Good knowledge of cGMP regulations.

Knowledge of data integrity requirements and 21 CFR Part 11 compliance.

Experience with risk assessment methodologies (FMEA).
Expertise in Microsoft Office suite.

Language

English: Intermediate (written and spoken).

Personal skills

Ability to work independently and as part of cross-functional teams.
Quality-oriented mindset.

Critical thinking and analytical skills.

High attention to detail and accuracy.

Ability to manage multiple priorities effectively.

Additional information

Travel between sites may be required.
Flexible schedule may be necessary for time-sensitive validation activities.

Candidati adesso

Perfeziona la tua ricerca

monitoring specialist offerte - milano, lom

Equipment Validation Compliance Specialist

(Senior) Short-Term Flex Optimisation Analyst – Automated Flexibility Trading (m/f/d)

Global Data Factory Specialist

Curricular Internship - Trade & Working Capital Products

Sr. Associate, Trade Marketing

Pricing Specialist

Sustainability Specialist, Solutions, Italy

Specialist - Milano

Global IT Manager Network Services

Investment Banking – M&A Analyst Intern

Digital Performance Marketing Specialist

Product Specialist Urologia

Internship - Credit Risk | Milan

Application Expert (Temporary)

Social media graphic & content intern

Service Desk Operator | Space Programmes

Business Development Manager

Specialist Corporate Finance (f/w/x)

Customer Salesforce Senior Consultant

Sales Specialist- Motion Drives Lombardia

Voglio ricevere gli ultimi avvisi Job Alert per il ruolo di monitoring specialist nella seguente località: milano, lom

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