Start Date
Immediate
Expiry Date
11 Dec, 25
Salary
0.0
Posted On
12 Sep, 25
Experience
2 year(s) or above
Remote Job
Yes
Telecommute
Yes
Sponsor Visa
No
Skills
Method Transfer, Iso, Code, Uncertainty, Health, Communication Skills, Ethics, Regulatory Requirements, Regulatory Guidelines
Industry
Pharmaceuticals
For nearly 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.
POSITION SUMMARY
This role is responsible for ensuring the laboratory operations in accordance to ISO 17025 and cGMP
requirements. He/She will serve as analytical lead in variety of projects which includes but not
limited to method validation, method transfer, customized testing activities. In addition, this
individual is responsible for directing the day-to-day project activity through interaction with
technical personnel while gathering, analyzing and interpreting scientific data. He/She must ensure
accurate and precise results are being achieved and properly reported.
GENERAL REQUIREMENTS
Agreements, and regulatory requirements.
implement such improvements.
requirements.
QUALIFICATIONS:
laboratory environment
regulated laboratory
Uncertainty (MU)
on requirement of task on hand
study protocols, summary reports
Job Description: Senior Analyst
validation of new test procedures for incoming projects
client-driven projects
regulatory compliance
Customer site visits where required
study protocols, summary reports
deficiencies or concerns in a timely manner
and Regulatory Authorities
Job Description: Senior Analyst