Specialist Data Review – Mycoplasma Services

You'll be crucial in ensuring clients receive quality data by meticulously reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations.

Essential Duties and Responsibilities

• Apply GMP/GLP in all areas of responsibility, as appropriate.
• Demonstrate and promote the company vision.
• Ensure 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 for which review is being performed.
• Use MS Windows applications such as Excel, Word, Access, and Outlook email.
• Conduct all activities in a safe and efficient manner.
• Perform other duties as assigned.

Qualifications

• Education/Experience: Master's degree in a science-related field (Biochemistry / Biotechnology / Microbiology) with 3-7 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.

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 judgment.
• Science background/education and/or laboratory experience.
• Strong Math Skills.
• Logical Thinking, Good Reasoning Ability.
• Motivation to excel.
• Coaching/mentoring of peers.