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You will be updated with latest job alerts via emailPosition Summary:
Ensuring that the client receives quality data by reviewing laboratory data for accuracy clarity and adherence to GMP and/or GLP regulations
Essential Duties and Responsibilities:
Applies GMP/GLP in all areas of responsibility as appropriate
Demonstrate and promote the company vision
Regular attendance and punctuality
Read and understand analytical procedures
Review documentation generated data calculated results and final reports according to departmental corporate and client SOPs
Gain a technical understanding of the techniques in which review is being performed
Use MS Windows applications such as EXCEL Word Access Outlook email
Conducts all activities in a safe and efficient manner
Performs other duties as assigned
Qualifications :
Education/Experience (BMQ):
Masters degree in a sciencerelated field (Biochemistry / Biotechnology / Microbiology) with 37 years of experience in Bio/Pharmaceutical drug product/substance testing with knowledge of regulatory requirements.
Experience with analytical techniques such as qPCR microbiological techniques knowledge of USP/EP/JP compendia and laboratory software applications such as PCR analysis software bioinformatics tools and LIMS is preferred
Additional Information :
Key Candidate Attributes:
Remote Work :
No
Employment Type :
Fulltime
Full-time