Sterilizer Operator I

About the Company

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.

In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.

Responsibilities

• Perform operator functions in the programming, loading, and unloading of EO Sterilizers.
• Complete work orders based on customer order requests/protocols.
• Perform testing of biological indicators and record results.
• Maintain a high level of communication skills when interfacing with customers.
• Perform inventory and reordering from suppliers.
• Receive both supplier and customer products.
• Create shipping documents when required.
• Maintain equipment and facility following daily cleaning procedures.
• Maintain documentation files and records.
• Interpret protocols and execute the PQ portion of a product validation process.
• Stay current with all regulations pertaining to EO sterilization.
• Comply with Quality Management (QMS) procedures and company policies.

Requirements

• Minimum High School Diploma or any related technical field (AA degree in biology or related field is a plus).
• Knowledge of QA/QC, document control, laboratory procedures, experimental and/or medical, and engineering/manufacturing design and development.
• Previous experience at a healthcare company in central supply preferred.

Skills

• High degree of organizational skills.
• Clear and precise written and verbal communication skills.
• Familiarity with FDA and ISO regulations pertaining to controlled documents.
• Administrative experience and/or background is a plus.

Benefits

• Excellent full-time benefits including comprehensive medical coverage, dental, and vision options.
• Life and disability insurance.
• 401(k) with company match.
• Paid vacation and holidays.

Pay

$23–25/hour

Schedule

Full-time. Candidates currently living within a commutable distance of San Jose, CA are encouraged to apply.