QC Chemical Analyst

Work Schedule

Other

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Job Description

Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving sophisticated analytical challenges, growing efficiency in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global organization of more than 100,000 colleagues delivers an outstanding combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD. Monza site is an outstanding pharmaceutical contract manufacturing and development facility, specialized in aseptic injectable drugs, with a growing focus on biologics. Joining more than 1800 colleagues on site, the selected candidate will experience an excellent, international, and fast-growing environment.

We are looking for a QC Chemical Analyst!

Position Summary:

The ideal candidate will be responsible for conducting Quality Control testing of drug products in alignment with the shipping schedule and production requirements, ensuring the delivery of high-quality customer service.

Responsibilities:

• Conduct analysis on incoming, in-process, and release samples in compliance with GMP standards to support manufacturing processes, following the instructions provided by the Team Leader, SOPs, and analytical procedures.
• Prepare and handle documentation (protocols, reports, methods) in accordance with current GMP, SOPs, and guidelines, ensuring proper adherence to regulatory standards.
• Support instrument calibration following SOPs and protocols.
• Play an active role in the Company’s dedication to Process improvement and efficiency in QC operations to increase safety, quality and performance.
• Support other member of QA & QC team to achieve timelines set.
• Operate any equipment and conduct your day to duties according to current procedures and appropriate Health and Safety precautions.

Minimum Requirements/Qualifications:

• Degree in Chemistry, Biotechnology or other Scientific field.
• Previous experience in GMP QC Laboratory and in performing common chemical analysis (HPLC, UV, GC, TOC, PH, KF). Experience in performing biochemical analyses is a plus.
• Proficiency in English and Italian languages.
• Good knowledge of Office Suite and software Empower.

Soft Skills:

• Good time-management.
• Good attention to detail, accuracy and work to tight deadlines.
• Can multi-task and adapt to changing priorities.
• Efficient and self-motivated, willing to learn all aspects of Quality Control.
• Able to communicate effectively at all levels.
• Ability to work in a team.

Thermo Fisher Scientific is an Equal Opportunity Employer.

All qualified applicants will receive consideration for employment without regard to race, creed, religion, color, national or ethnic origin, citizenship, sex, sexual orientation, gender identity and expression, genetic information, veteran status, age or disability status.

Join us!

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