Senior Analyst

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.

**Duties and Responsibilities**:

- Provides strong, independent technical leadership to technical personnel
- Leads, designs and performs method development (i.e. bioassay and mycoplasma) and validation of new test procedures for incoming projects
- Functions as Technical Reviewer for A2LA accredited tests and non-accredited tests
- Evaluates analytical results to form interpretations of data and renders scientific opinions for client-driven projects
- Serves as technical liaison with Customers with regards to technical services and performs Customer site visits where required
- Prepares documents including methods, procedures, standard operating procedures (SOP), study protocols, summary reports
- Assures that SOPs are in accordance to ISO 17025, cGMP and other regulatory requirements
- Provides problem-solving skills for test procedures and investigations within laboratory unit
- Responsible for notifying Quality Assurance and Senior Management of any compliance deficiencies or concerns in a timely manner
- Monitors all proficiency-based testing and ensures compliance
- Participates in internal Quality Audits, System Audits, Audits conducted by external agencies and Regulatory Authorities
- Participates in quarterly management review
- Drives process, quality and safety improvement initiatives within the department
- Provides coaching and mentoring to Technical personnel
- Supports the Laboratory Manager in all relevant functions

**Qualifications**:

- Bachelor of Science or any related field; MSc. preferred but not essential
- Minimum 2-6 years of relevant QC microbiological experience working in an ISO17025 / GMP laboratory environment
- Experience in method validation and development, method transfer, qualification activities in regulated laboratory
- Good knowledge of ISO 17025, cGMP and other regulatory guidelines
- Good understanding/working knowledge of Project Management and Measurement Uncertainty (MU)
- Good technical understanding and judgement
- Good interpersonal and communication skills across cultures
- Team player with ability to work in cross-functional teams as well as independently depending on requirement of task on hand

**About Discovery**

**About Charles River**
Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.

At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.

227222