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Batch Record Jobs (NOW HIRING)

Batch Record Reviewer I

Conshohocken, PA · On-site

$17.75 - $21.75/hr

Batch Record Reviewer SUMMARY Responsibilities include review of line documentation related to contract packaging. Will follow up on customer inquiries as they relate to same documentation and ...

Apply administrative and recordkeeping processes to support batch record document control * Committed to maintain excellent Food Safety Culture within the organization * Review production and QC ...

Batch Maker

Miami, FL · On-site

$20 - $30/hr

Familiarity with batch formulas, production records, and GMP procedures Responsibilities: * Prepare and mix cosmetic products according to formulas and batch instructions * Operate mixing and ...

Ability to read and interpret batch records and all company documents * Proficient in basic math and computer skills * Has experience leading a small group of team members Knowledge, Skills and ...

Keep detailed and accurate batch records, including materials used, process steps, and any deviations. * Work with batch sizes up to 4,000 gallons, ensuring proper mixing, timing, and process control.

Ability to read and interpret batch records and all company documents * Proficient in basic math and computer skills * Has experience leading a small group of team members Knowledge, Skills and ...

QA Specialist

Costa Mesa, CA · On-site

$65K - $75K/yr

Batch Record Review * Independently review executed batch records and associated documents (testing reports, equipment logs, deviations, cleaning records) for completeness, accuracy, clarity, and ...

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Batch Record information

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$12

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How much do batch record jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for batch record in the United States is $20.34, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $21.15 per hour, depending on experience, location, and employer.

What is a batch record?

Batch records are comprehensive documents used in pharmaceutical and manufacturing industries to record the production and processing details of each batch of a product. These records include information such as raw materials used, processing steps, equipment, in-process controls, and quality checks. Batch records ensure traceability, regulatory compliance, and product consistency by documenting every stage of production. They are critical for audits, investigations, and maintaining high-quality standards.

What are the key skills and qualifications needed to thrive as a batch record specialist?

To thrive as a Batch Record Specialist, you need a strong understanding of GMP regulations, meticulous attention to detail, and experience with documentation in pharmaceutical or biotech manufacturing, often supported by a degree in life sciences or a related field. Familiarity with electronic batch record (EBR) systems, LIMS, and quality management software is typically required. Strong organization, communication skills, and the ability to work accurately under tight deadlines are essential soft skills for this role. These skills ensure compliance, accurate record-keeping, and efficient batch release processes, which are critical for maintaining product quality and meeting regulatory standards.

What are some common challenges faced by professionals working with batch records, and how can they be addressed?

Professionals working with batch records often encounter challenges such as maintaining accuracy under tight deadlines, managing large volumes of documentation, and ensuring compliance with strict regulatory standards. To overcome these issues, it's essential to develop strong attention to detail, utilize robust organizational systems, and stay updated on current Good Manufacturing Practices (cGMP). Collaboration with quality assurance and production teams also helps ensure that discrepancies are identified and resolved efficiently, resulting in reliable and compliant batch documentation.

What is the difference between Batch Record vs Manufacturing Technician?

AspectBatch RecordManufacturing Technician
CredentialsTypically requires a degree in life sciences or related field, with knowledge of GMP regulationsOften requires a high school diploma or associate degree, with technical training in manufacturing processes
Work EnvironmentDocument review, compliance checks, and collaboration with production teams in pharmaceutical or biotech facilitiesHands-on production, equipment operation, and process monitoring in manufacturing plants
Industry UsageUsed across pharmaceutical, biotech, and regulated manufacturing sectorsCommonly employed in pharmaceutical, biotech, and manufacturing industries

The main difference is that Batch Records focus on documenting and ensuring compliance of manufacturing processes, while Manufacturing Technicians are involved in the hands-on production and operation of equipment. Both roles are essential in regulated manufacturing environments, but they serve different functions within the production process.

More about Batch Record jobs

What states have the most Batch Record jobs?

States with the most job openings for Batch Record jobs include:

What other helpful pages are available for Batch Record?

Other pages related to Batch Record:

Infographic showing various Batch Record job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 82% Full Time, 14% Part Time, and 3% Contract. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $42,304 per year, or $20.3 per hour.

Batch Record Reviewer I

Conshohocken, PA • On-site

$17.75 - $21.75/hr

Full-time

Posted 22 days ago


Job description

Batch Record Reviewer Job Description

SUMMARY

Responsibilities include review of line documentation related to contract packaging. Will follow up on customer inquiries as they relate to same documentation and compliance issue. Complete final review and release for product distribution.The impact of review process directly impacts company compliance to regulatory requirements and customer satisfaction.

ESSENTIAL DUTIES AND RESPONSIBILITIES: The following is a list of responsibilities related to record review. Other duties may also be assigned.

  • Responsible for review of documentation related to primary, secondary, and clinical packaging after completion of reconciliation.
  • Responsible for critical review and logging of all above documentation for errors, omissions, over-writes and compliance to cGMPs, customer specifications, and internal SOP's.
  • Responsible for follow-up on all customer inquiries specific to documentation related to the packaging, testing and release of the work in-process or finished product.
  • Responsible for final release of work in-process or finished product.
  • Responsible for reviewing and maintaining the QAD Item Master Maintenance and Router Maintenance.
  • Responsible for logging and maintaining packaging process samples as well as coordinating shipment of samples to customers.
  • Responsible for maintaining and filing of documentation related to packaging in current appropriate status locations.
  • Responsible for entering lot specific information into the Quality Dashboard (Access Database).
  • Responsible for participating in internal, customer, and regulatory audits at the discretion of senior management.
  • Other responsibilities as required.

SUPERVISORY RESPONSIBILITIES: None

QUALIFICATIONS:

To perform this job successfully, an individual must be able to perform each essential duties and responsibilities satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

EDUCATION and/or EXPERIENCE:

High School Degree is required. One to two years related pharmaceutical experience and/or training; or equivalent combination of education and experience is preferred. Experience in pharmaceutical or related industry is desired.

- General knowledge of FDA regulations related to cGMPs required.

- General knowledge of cGDPs required.

- General knowledge of quality control/assurance required.

- General knowledge of DEA regulations preferred.

- Excellent detail skills as they apply to documentation review and compliance required.

- Good written and oral communication skills required.

- Good organizational and planning skills required.

- Excellent interpersonal skills required.

REQUIREMENTS:

Due to the nature of our work, all employees must be over the age of 18 and will be required to undergo a pre-employment drug test and background check.

MATHEMATICAL SKILLS:

Ability to apply moderately complex mathematical operations including an understanding of statistical sampling plans and the ability to calculate time, percentages, and decimals.Basic math skills (addition, subtraction, multiplication and division) are required.

LANGUAGE SKILLS:

Ability to respond to common inquiries or complaints from customers. Ability to respond to inquiries from peers and superiors. Ability to effectively present information to the following groups:

- Internal: Frequent contact with Quality Department, Project Managers, New Business Development, Material Management and Operations Department employees for information on quality documentation issues and cGMP issues.

- External: Occasional contact with customer representatives related to documentation.

REASONING ABILITY:

Ongoing contact with internal Sharp Operations, Project Managers, New Business Development, Material Management and Quality Department employees. Frequent contact with customer representatives concerning documentation issues, as well as cGMP's. A thorough understanding or each aspect of the job is required. Good organizational skills are necessary. Good reasoning skills for analysis and problem solving are needed.

COMPUTER SKILLS:

Must be proficient in Microsoft Office Suite, Adobe Acrobat, and QAD. Experience with Pilgrim SmartSolve system desired.

PHYSICAL DEMANDS:

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to use hands, speak and listen. The employee frequently is required to sit. The employee is occasionally required to stand, walk, and reach with hands and arms. The employee must occasionally lift and/or move up to 20 pounds. Specific vision abilities required by this job include close vision, distance vision, and ability to adjust focus.

WORK ENVIRONMENT: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.