Specialist Data Review MD-MV Analytical Chemistry

3 weeks ago

Bengaluru, India Eurofins Full time

Position 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

Basic Minimum Qualifications (BMQ):

To perform this job successfully, the individual must be able to perform each essential duty satisfactorily. The requirements below are representative of the knowledge, skill or ability required.

Education/Experience (BMQ):

Masters degree in a science-related field with 4-7 years of experience in Pharmaceutical Chemistry drug product/substance testing with knowledge of regulatory requirements.

Key Candidate Attributes:

  • Self-motivation; excellent quality of work and attention to detail
  • Ability to communicate effectively with coworkers and internal/external clients
  • Ability to learn new tasks quickly and to move easily from task to task
  • Ability to handle prioritization and multiple tasks simultaneously
  • Ability to use a personal computer and learn necessary programs
  • Good communication skills (oral and written)
  • Organizational ability and good judgement
  • Science background/education and/or laboratory experience
  • Strong Math Skills
  • Logical Thinking, Good Reasoning Ability
  • Motivation to excel
  • Coaching/mentoring of peers

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