Data Entry Coordinator

Sun Pharmaceutical Industries • New Brunswick, NJ

273d

About The Position

Sun Pharma is the world's fourth largest generics company with presence in Specialty, Generics and Consumer Healthcare products. Supported by more than 40 manufacturing facilities, we provide high-quality medicines, trusted by healthcare professionals and patients, to more than 100 countries across the globe. Over the last two decades, Sun Pharma has established itself as a leading player in the generics market in the U.S., and we are rapidly ramping up our presence in the specialty branded market with a focus on dermatology, ophthalmology and onco-dermatology. The position is responsible for data entry for CMA, CPP and CQA from the exhibited document.

Requirements

• Minimum of a High School Diploma or equivalent.
• Highly skilled on Microsoft Office.
• 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).
• Minimum of two (2) years of experience in data entry.

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.
• Archival of Batch Records and maintaining the required log for batch records.
• 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 thereof.
• 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.
• Should be flexible in working both 1st and 2nd shifts as per business requirement.

Benefits

• Medical coverage
• Dental coverage
• Vision coverage
• Life insurance
• Disability insurance
• 401(k) savings plan
• Flexible spending accounts
• Employee assistance program
• Paid time off benefits, including vacation time and sick time

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Industry: Chemical Manufacturing
• Education Level: High school or GED