Data Entry Operator III

About Prism Data Consulting

Prism Data Consulting is dedicated to assisting data professionals in discovering their ideal career paths. We function as an analysis and verification service, not a staffing agency, connecting candidates with employers seeking data expertise. We are not the Employer of Record for this position; our role is to facilitate connections between exceptional candidates and leading employers.

Employer Industry: Biotechnology and Pharmaceutical

Why Consider This Job Opportunity

• Gain opportunities for career advancement and professional growth within the organization.
• Work in a supportive and collaborative team environment.
• Contribute positively to manufacturing operations through precise data management.
• Participate in essential processes that uphold compliance and data integrity.
• Develop valuable skills in data collection systems and analytical tools.

What To Expect (Job Responsibilities)

• Accurately enter and validate extensive batch record data, ensuring high levels of consistency.
• Systematically manage and monitor workload to guarantee all necessary process data is located, gathered, and entered.
• Perform timely and precise data entry to aid in daily process monitoring and associated tasks.
• Engage regularly with data users to facilitate efficient data utilization and resolve any issues.
• Adhere strictly to all facility training, policies, and current Good Manufacturing Practice (cGMP) requirements.

What Is Required (Qualifications)

• Possess a High School Diploma or equivalent.
• Have 0-3 years of relevant experience in the biotech, pharmaceutical, or similar sectors.
• Demonstrate exposure to data collection systems or manufacturing data environments.
• Exhibit strong computer proficiency, including advanced skills in Microsoft Office Suite.
• Be highly detail-oriented, self-motivated, and capable of working autonomously.

How To Stand Out (Preferred Qualifications)

• Previous experience with data collection systems or analytical tools is advantageous.
• Familiarity with cGMP standards and the associated documentation requirements is preferred.
• Prior experience in a manufacturing or production setting is a plus.
• Show an ability to quickly adapt to new technologies and evolving processes.

Additional Information

We are committed to candidate privacy and promoting equal-opportunity employment. Our partnerships are with companies that share these values, aiming to create a hiring environment that is fair, transparent, and secure. Please report any employer found not adhering to these principles.