Specialist Data Review MD-MV Analytical Chemistry

Position Summary:

Ensure that clients receive high-quality data by reviewing laboratory data for accuracy, clarity, and compliance with GMP and/or GLP regulations.

Essential Duties and Responsibilities:

• Apply GMP/GLP standards in all areas of responsibility, as appropriate.
• Review laboratory documentation, generated data, calculated results, and final reports to ensure they meet departmental, corporate, and client SOPs.
• Gain a technical understanding of the analytical techniques relevant to the data being reviewed.
• Read and interpret analytical procedures accurately.
• Utilize MS Windows applications including Excel, Word, Access, and Outlook for documentation and communication.
• Demonstrate and promote the company's vision in all interactions and activities.
• Maintain regular attendance and punctuality.
• Conduct all activities in a safe, compliant, and efficient manner.
• Perform other related duties as assigned.

Basic Minimum Qualifications (BMQ):

• Master's degree in a science-related field.
• 4–7 years of experience in pharmaceutical chemistry (drug product or drug substance testing).
• Knowledge of regulatory requirements and industry best practices in a GMP/GLP environment.

Key Candidate Attributes:

• Strong self-motivation and consistent delivery of high-quality, detail-oriented work.
• Excellent communication skills (verbal and written) to interact effectively with coworkers and clients.
• Ability to learn quickly and switch between tasks efficiently.
• Strong organizational skills and sound judgment in handling priorities.
• Competence in using personal computers and standard applications.
• Solid science background with relevant laboratory experience.
• Proficiency in mathematics, logical thinking, and data reasoning.
• Motivation to excel and continually improve.
• Willingness to coach or mentor peers.