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Data Entry In Jobs in Irmo, SC (NOW HIRING)

Accounts Payable Clerk

West Columbia, SC ยท On-site

$20 - $22/hr

Maintain clear and accurate financial records through consistent data entry, filing, and account ... Previous experience in an accounts payable position with responsibility for invoice entry and ...

... in the Reentry Coordinators. -Knowledge:Building client/customer rapportBusiness planning - how to organize prospect data, develop and follow an approach, and organize time -Skills:Objective setting ...

Conduct in-person interviews (phone interviews for e-campus) * Initiate student re-enrollment ... Business planning - how to organize prospect data, develop and follow an approach, and organize ...

Conduct in-person interviews (phone interviews for e-campus) * Initiate student re-enrollment ... Business planning - how to organize prospect data, develop and follow an approach, and organize ...

Be Seen First

Data Entry: Enter and update client information into our client database system, ensuring accurate ... Proficiency in Microsoft Office; experience with Red Tail Client Tracking Software is a plus.

New

Be Seen First

Data Entry: Enter and update client information into our client database system, ensuring accurate ... Proficiency in Microsoft Office; experience with Red Tail Client Tracking Software is a plus.

New

Guest Services Associate-Overnight

Columbia, SC ยท On-site

$12 - $14.75/hr

... data entry, record-keeping, and other common reception duties. * Become proficient in all aspects of Oliver Gospel's HMIS and other required systems. * Communicate effectively with program members ...

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Data Entry In information

See Irmo, SC salary details

$9

$15

$23

How much do data entry in jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for data entry in in Irmo, SC is $15.90, according to ZipRecruiter salary data. Most workers in this role earn between $13.37 and $17.88 per hour, depending on experience, location, and employer.

What is a data entry in?

Data Entry In jobs involve inputting, updating, and maintaining information in computer systems or databases. Employees in these roles are responsible for ensuring data accuracy, organizing records, and sometimes verifying information from various sources. These positions are essential in many industries, as accurate data is crucial for operations, reporting, and decision-making. Data Entry In professionals need good attention to detail, typing skills, and basic computer proficiency.

What are the key skills and qualifications needed to thrive as a data entry in?

To thrive as a Data Entry In, you need strong attention to detail, fast and accurate typing skills, and a high school diploma or equivalent. Familiarity with spreadsheet software like Microsoft Excel, data management systems, and sometimes basic knowledge of database tools is typically required. Excellent organizational skills, time management, and the ability to maintain confidentiality help individuals stand out in this role. These skills ensure data accuracy, efficiency, and trustworthy handling of sensitive information, which are critical for business operations.

What are some common challenges faced in a data entry in, and how can they be effectively managed?

Data Entry professionals often encounter challenges such as handling large volumes of repetitive information, maintaining high accuracy, and meeting tight deadlines. To manage these effectively, it's important to develop strong attention to detail, establish efficient workflows, and take regular breaks to reduce fatigue and maintain focus. Utilizing keyboard shortcuts and data management tools can also help streamline the process and minimize errors, ensuring that data is entered quickly and accurately.

What is the difference between Data Entry In and Data Entry Clerk?

AspectData Entry InData Entry Clerk
CredentialsHigh school diploma or equivalentHigh school diploma or equivalent
Work EnvironmentOffice, remote, or data centersOffice, remote, or data centers
Industry UsageCommonly used in logistics, warehouse, and inventory sectorsWidely used across various industries including healthcare, finance, and administration
Job FocusEntering data related to shipments, inventory, or logisticsInputting various types of data into systems, often administrative

Data Entry In typically refers to roles focused on inputting logistics or inventory data, often in warehouse or supply chain settings. Data Entry Clerk is a broader role found across many industries, emphasizing general administrative data input. Both roles require similar skills and credentials but differ mainly in their specific industry focus and work environment.

Is data entry hard to learn?

Data entry is generally straightforward to learn, especially with basic computer skills and familiarity with spreadsheet or database software. It involves tasks like inputting, updating, and managing information, which can be mastered through practice and training. Many roles require attention to detail and accuracy but do not demand advanced technical knowledge.

Is data entry well paid?

Data entry jobs typically offer hourly wages that are close to minimum wage or slightly above, with pay varying based on experience, location, and complexity of tasks. Advanced skills, such as proficiency with specific software or fast typing speeds, can lead to higher pay. Overall, data entry is generally considered an entry-level position with moderate pay.

What exactly do data entry jobs do?

Data entry jobs involve inputting, updating, and managing information in computer systems or databases. Workers typically use tools like spreadsheets and data management software, and accuracy and attention to detail are essential skills for this role.

What cities near Irmo, SC are hiring for Data Entry In jobs?

Cities near Irmo, SC with the most Data Entry In job openings:

Infographic showing various Data Entry In job openings in Irmo, SC as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 15% Part Time, and 3% Contract. Highlights an 84% Physical, 4% Hybrid, and 12% Remote job distribution, with an average salary of $33,074 per year, or $15.9 per hour.

QC Chemistry Operations Supervisor

Nephron Pharmaceuticals

West Columbia, SC โ€ข On-site

Full-time

Posted 11 days ago


Job description

Description:

Corporate Statement:

Nephron Pharmaceuticals is a privately-owned global leader in the manufacturing of generic drug products, over-the-counter (OTC) drug products and medical devices. Nephron’s products are sterile, preservative and additive free and proudly made in the USA! We are headquartered in West Columbia, South Carolina. Our location provides the ability to develop new devices and medications including respiratory therapies, ophthalmic, and injectables, for in-house or contract manufacturing opportunities. The facility utilizes completely automated manufacturing, packaging, and distribution systems, in addition to high volume and redundant utility systems, to ensure production system availability. Nephron specializes in Blow-Fill-Seal (BFS) manufacturing, a niche technology that allows a vial of medication to be formed, filled and sealed in a continuous process, in a sterile, enclosed environment and without human intervention.

As an industry leader in product safety and quality, Nephron produces a variety of inhalation solutions, suspensions, injectables, and ophthalmics. Nephron is currently working on research and development projects that include over 50 new products. The company’s longstanding relationships with major drug wholesalers allow us to distribute our products to retail pharmacies, mail order pharmacies, hospitals, home care companies, and long-term care facilities. Nephron has a sales force that covers all fifty states and some international territories. Nephron exists to provide top-quality, affordable medications to everyone. Our quality first culture is built on: Transformation, Execution and Trust.

Job Purpose:

• Assist in overseeing the day-to-day operations of the QC Chemistry Laboratory in a high-growth, fast-paced, dynamic work environment while ensuring compliance with FDA and DEA regulations.

• Assist in the implementation of practical process improvements to reduce lead times and improve turn- around times for lab testing.

• Help maintain a flexible organization to allow fast changing manufacturing priorities to occur with minimum disruption and avoid back logs.

• Ensure the Quality Control group is fully compliant with all cGMP requirements including adequate maintenance and cleanliness of equipment and laboratories.

• Recruit, train, manage, and mentor direct reports.

• Performs other duties as assigned or apparent.

Essential Duties and Responsibilities:

• Plans, organizes, and manages resources for sample testing to maintain laboratory workflow and schedule adherence.

• Verify notebooks, raw data, and COA’s before final QC approval.

• Verify data entry in the Laboratory Information Management Systems conform to final product specifications.

• Provide management approval for final product release.

• Assist in establishing, maintaining, and reporting key performance indicators for the department with respect to daily operations.

• Assist in overseeing the QC Chemistry lab operations and assure operations are conducted in accordance with regulatory requirements and expectations.

• Responsible for drafting, editing, and approving SOPs related to Analytical Services functions, equipment, documentation, and/or processes.

• Assist with the day-to-day process of laboratory investigations including, but not limited to OOT and OOS investigations.

• Develop and approve methods and results including: product specifications; protocols, SOPs, and reports for analytical method validation and stability studies; IQ/OQ/PQ protocols and reports for equipment; master production records.

• Direct, perform and resolve out-of-specification investigations and implement corrective and preventative actions

· Day to day employee personnel management including, but not limited to time card approvals, performance reviews, and addressing personnel matters.

· Capable of defining strategic objectives for the Analytical Services department as well as generating and implementing initiatives that improve the department efficiency and the quality of the results and processes.

Knowledge & Skills:

  • Knowledge of FDA manufacturing/regulatory quality systems regulations, qualification, facilities and investigation requirements.
  • Must be detailed oriented and have excellent organizational skills.

• Must possess effective written and oral communication skills and be able to handle multiple projects within limited time frames.

• Must have skills in HPLC, GC, and mass spectroscopy detection technologies.

• Must have excellent communication and technical writing skills.

• Expected to be a leader in the technology area and to train others for more routine and specific project-oriented applications.

• The ability and willingness to change direction and focus to meet shifting organizational and business demands.

• The ability to create and contribute environment that values people, encourages trust, teamwork, and open communication, and provides participation, learning, feedback and recognition.

• The ability to effectively manage one self, demonstrates integrity, be productive under pressure, and achieve development goals.

• The ability to manage a multitude of resources and to be accurate and current with data and information.

Education/Experience:

  • Minimum Bachelor’s degree and/or 5 years of experience working in Quality Control Chemistry and/or Research & Development.
  • Experience with cGMP documentation systems and with implementation of quality control systems.
  • Preferred experience in analytical method development, transfer and validation.
  • Must possess a strong experience base in product QC testing and release procedures and documentation.
  • Salary Range: Based on experience

Working Conditions / Physical Requirements:

• Position requires bending, typing, climbing, lifting, reaching, vision, standing, sitting (10%), walking, and hearing.

Requirements: