Job Description
We are seeking a detail-oriented and diligent
Data Entry Coordinator to join our client’s team in
New Brunswick, NJ . If you believe you are qualified, we would be excited to connect and discuss this opportunity in more detail.
Full-time Onsite
Contract
Pay Rate: DoE 1st shift Job Summary: · Data entry for CMA, CPP and CQA from the exhibited document.
Key Responsibilities: · Input data from Production Batch Records database into Microsoft Office (where applicable).
· Accurately and precisely enter all required data into Microsoft Office.
· Attend documentation review trainings (GMP, GDP, and other global document training courses annually).
· Provide weekly status updates on activity performed; escalate the issues if any which are holding up the data entry process.
· Evaluate and interpret trends from entered data.
· Present findings and trends on a weekly basis.
· Work with Cross Functional Teams to complete review and close out any documentation delays for designated area.
· Pulling of Batch Production records from archive and put it back
· Able to conduct retention sample inspection and documentation there of
· Pulling and Submission of product samples as per PQC/Stability /Misc etc.
· Review of Packaging batch records received from In house packaging or Contract Packagers
· Other duties as assigned by the supervisor.
Work Conditions: Office Environment
Lab Environment
Physical Requirements: While performing the duties of this job, the employee is frequently required to sit; use hands to finger, handle objects, or feel objects, tools, or controls; and reach with hands and arms. The employee is occasionally required to visit lab environment, stand, and stoop, kneel and crouch specific vision abilities required of this job include close vision, distance vision, color vision and the ability to adjust focus.
The employee must regularly lift and/or move up to 20 - 30 pounds.
Travel Estimate: Up to 5%
Qualifications: Minimum of a High School Diploma or equivalent. Highly skilled on Microsoft Office.
Minimum of two (2) years of experience in data entry within the pharmaceutical industry
The capability to understand the cGMPs as they relate to the job function.
Ability to follow defined instructions and scheduling in-process inspection and review of batch records in timely manner.
Strong communication skills; both verbal and written.
A self-starter with a hands-on approach and a can-do attitude.
The requirement for English language proficiency for this job role is Intermediate-B1+ (comparable to Global CEFR Independent B1) level based on the Common European Framework of Reference for Languages (CEFR).
About ProStaff We are a fast growing and successful agency that treats all its clients and candidates with a personal touch. ProStaff Workforce Solutions is a group of industry experts—many hailing from larger agencies—who know their business well and enjoy working in a more hands-on and flexible environment, with attention to detail. Our mission is to match quality people with quality jobs and quality companies to maximize productivity and profitability. We develop long-term relationships and provide a level of customer service and expertise that instill confidence and trust in our client companies and candidates.
Our Values • Integrity
• Commitment
• Quality
• Diversity
Benefits for eligible employees • Direct deposit
• Weekly pay
• Medical benefits
• 401(k) Plan
Please visit us at to explore all opportunities.
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Job Tags
Weekly pay, Full time, Contract work, Work at office, Flexible hours, Day shift,