Microbiological Lab Analyst

TN Italy; Brindisi; In loco; EUR 30.000 - 50.000; Tempo pieno

Descrizione del lavoro

Join a leading pharmaceutical ingredients company as a Lab Analyst in Brindisi. This role involves performing microbiological analyses and ensuring compliance with GMP standards. You'll work within a collaborative team, contributing to the development and validation of analytical methods while fostering a culture of career development and inclusion. With a commitment to sustainability and innovation, this forward-thinking company offers a dynamic environment for professionals eager to make a difference in the pharmaceutical industry.

Servizi

Annual Bonus

Company cantine

Training & Development

Competenze

• Knowledge of microbiological techniques and laboratory instrumentation.
• Experience in a GMP environment or quality control is a plus.

Mansioni

• Perform microbiological analyses and environmental monitoring.
• Record and formalize results following GMP procedures.

Conoscenze

Bioburden analysis

Microbiological techniques

Laboratory instrumentation

GMP standards

Teamwork

Organizational skills

Communication skills

Proficiency in English

Formazione

High school diploma in chemistry

Degree in biology or related fields

Strumenti

SAP

Descrizione del lavoro

Join Euroapi Team as a Lab Analyst

We are looking for a Lab Analyst to join our microbiology laboratory within the QC department, aiming to strengthen our team.

Responsibilities

• Perform analyses in the Microbiological Laboratory, including:
• Bioburden analysis of Finished Products
• Microbiological analyses of water and primary packaging samples
• Environmental monitoring analyses
• Preparation and validation of culture media for microbiological analysis

Record, formalize, and analyze results following GMP procedures, using specific software like SAP.

Participate in developing and validating analytical methods, as well as implementing new techniques and instrumentation.

Contribute to formalizing or revising procedures related to Quality Control activities.

This is a fixed-term 12-month contract, and we are looking for someone to join as soon as possible.

About Our Company

EUROAPI focuses on active ingredient solutions to meet global customer and patient needs. We are a leading pharmaceutical ingredients company with around 200 products and a broad technological portfolio, developing innovative molecules through our Contract Development and Manufacturing Organization (CDMO).

The EUROAPI Italy facility, located in Brindisi, has a rich history since 1966 and specializes in developing and manufacturing Active Pharmaceutical Ingredients (APIs) under GMP conditions.

Requirements

• High school diploma or higher in chemistry, biology, or related fields
• Knowledge of biological and microbiological techniques, laboratory instrumentation, and cGMP standards
• GMP environment or quality control experience is a plus
• Teamwork and good organizational skills
• Proficiency in English (written and spoken)
• Good communication skills

Benefits

• Annual Bonus
• Company cantine
• Training & Development

Our Culture & Values

We foster a culture that promotes career development and talent management, emphasizing how we work as much as what we achieve, guided by our core values.

Diversity & Inclusion

We are committed to a diverse and inclusive environment, valuing transparency, respect, and equal treatment, and protecting against discrimination.

Environmental, Social, and Governance Responsibility

We believe our success depends on adapting to future challenges, ensuring sustainability and resilience in the pharmaceutical supply chain.