QC Operation data Review

at  Thermo Fisher Scientific

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. With revenues exceeding $24 billion and the largest investment in R&D in the industry, we give our people the resources and chances to create meaningful contributions to the world.

Responsibilities:

• to perform GMP data review quality control analytical testing of intermediates and finished product under GMP conditions for QC chemical and biochemical analysis release or as part of stability studies.
• to review paper and electronic data according to ALCOA+ pillar
• to maintain own training record and support other team members as require
• to participate in continuous improvement activities and look for further opportuniites to progress the team/department.

EH&S:

• Understand emergency procedures and comply with safe systems of work.
• ensure compliance with environmental
• prompt reporting any near misses and breaches of rules

Minimum requirement:

• degree in Chemistry or biochemical or strongly related scientific discipline would be an advantage
• previous experience as analyst in chemical/biochemical (ELISA test, HPLC)
• ability to work under critical timelines
• effective communication skills at all internal and external levels
• excellent attention to detail
• excellent organization skills

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

• to perform GMP data review quality control analytical testing of intermediates and finished product under GMP conditions for QC chemical and biochemical analysis release or as part of stability studies.
• to review paper and electronic data according to ALCOA+ pillar
• to maintain own training record and support other team members as require
• to participate in continuous improvement activities and look for further opportuniites to progress the team/department