Batch Record Reviewer I
$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 ...
$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 ...
$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 ...
Miami, FL · On-site
The QA Batch Record Reviewer performs functions necessary to assure that all relevant manufacturing records are assembled, reviewed, and completed in a compliant efficient manner, and ultimately ...
Miami, FL · On-site
The QA Batch Record Reviewer performs functions necessary to assure that all relevant manufacturing records are assembled, reviewed, and completed in a compliant efficient manner, and ultimately ...
Miami, FL · On-site
The QA Batch Record Reviewer performs functions necessary to assure that all relevant manufacturing records are assembled, reviewed, and completed in a compliant efficient manner, and ultimately ...
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Miami, FL · On-site
The QA Batch Record Reviewer performs functions necessary to assure that all relevant manufacturing records are assembled, reviewed, and completed in a compliant efficient manner, and ultimately ...
Piscataway, NJ · On-site
$27 - $35/hr
The Batch Record Reviewer Group Lead is responsible for leading and overseeing batch record review activities across manufacturing, packaging, and related operations in a pharmaceutical manufacturing ...
Piscataway, NJ · On-site
$27 - $35/hr
The Batch Record Reviewer Group Lead is responsible for leading and overseeing batch record review activities across manufacturing, packaging, and related operations in a pharmaceutical manufacturing ...
Piscataway, NJ · On-site
$27 - $35/hr
The Batch Record Reviewer Group Lead is responsible for leading and overseeing batch record review activities across manufacturing, packaging, and related operations in a pharmaceutical manufacturing ...
Piscataway, NJ · On-site
$27 - $35/hr
The Batch Record Reviewer Group Lead is responsible for leading and overseeing batch record review activities across manufacturing, packaging, and related operations in a pharmaceutical manufacturing ...
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 ...
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 ...
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 ...
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 ...
Miami, FL · On-site
The QA Batch Record Reviewer performs functions necessary to assure that all relevant manufacturing records are assembled, reviewed, and completed in a compliant efficient manner, and ultimately ...
Miami, FL · On-site
The QA Batch Record Reviewer performs functions necessary to assure that all relevant manufacturing records are assembled, reviewed, and completed in a compliant efficient manner, and ultimately ...
Overview Wir suchen einen Batch Record Review Coordinator (m/w/d) fur unseren Produktionsstandort Dreieich bei Frankfurt am Main. In dieser Rolle unterstutzen Sie die fristgerechte und regelkonforme ...
Overview Wir suchen einen Batch Record Review Coordinator (m/w/d) fur unseren Produktionsstandort Dreieich bei Frankfurt am Main. In dieser Rolle unterstutzen Sie die fristgerechte und regelkonforme ...
Pharmaceuticals located in San Carlos is seeking a Quality Assurance Batch Record Reviewer / Person-In-Plant to support Quality oversight of manufacturing operations for the NIGHT SHIFT. This is a ...
Pharmaceuticals located in San Carlos is seeking a Quality Assurance Batch Record Reviewer / Person-In-Plant to support Quality oversight of manufacturing operations for the NIGHT SHIFT. This is a ...
Bloomington, IN · On-site
This role will be responsible for reviewing executed batch records and manufacturing documentation to ensure compliance with cGMP requirements, regulatory standards, and internal procedures. The ...
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Bloomington, IN · On-site
This role will be responsible for reviewing executed batch records and manufacturing documentation to ensure compliance with cGMP requirements, regulatory standards, and internal procedures. The ...
Quality Specialist II - Batch Record Review Raleigh, NC Pay: $22.00 - $24.00 per hour 26-07733 Job Summary The Quality Specialist II - Batch Record Review is responsible for reviewing manufacturing ...
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Quality Specialist II - Batch Record Review Raleigh, NC Pay: $22.00 - $24.00 per hour 26-07733 Job Summary The Quality Specialist II - Batch Record Review is responsible for reviewing manufacturing ...
Tustin, CA · On-site
$16.68 - $22.26/hr
You'll compile and review data, support manufacturing activity planning, and swiftly resolve issues. Coordinate controlled documents, training packets, and batch record preparation, while also ...
Tustin, CA · On-site
$16.68 - $22.26/hr
You'll compile and review data, support manufacturing activity planning, and swiftly resolve issues. Coordinate controlled documents, training packets, and batch record preparation, while also ...
Plymouth, MN · On-site
$20.50 - $28.50/hr
Review and complete production batch records to ensure accuracy and completeness in compliance with established procedures and timelines. * Verify all required documentation, approvals, and data ...
Plymouth, MN · On-site
$20.50 - $28.50/hr
Review and complete production batch records to ensure accuracy and completeness in compliance with established procedures and timelines. * Verify all required documentation, approvals, and data ...
$57K - $107K/yr
Reviews all batch documentation for accuracy and completeness according to cGMP's to ensure timely release. * Ensures deviations are initiated for any batch record review related events Find ...
$57K - $107K/yr
Reviews all batch documentation for accuracy and completeness according to cGMP's to ensure timely release. * Ensures deviations are initiated for any batch record review related events Find ...
Minneapolis, MN · On-site
$20.50 - $28.50/hr
Review and complete production batch records to ensure accuracy and completeness in compliance with established procedures and timelines. * Verify all required documentation, approvals, and data ...
Minneapolis, MN · On-site
$20.50 - $28.50/hr
Review and complete production batch records to ensure accuracy and completeness in compliance with established procedures and timelines. * Verify all required documentation, approvals, and data ...
A Day in the Life • Perform comprehensive batch record review to support product release in compliance with GMP and regulatory requirements • Ensure all documentation, deviations, and ...
A Day in the Life • Perform comprehensive batch record review to support product release in compliance with GMP and regulatory requirements • Ensure all documentation, deviations, and ...
Review completed batch records, routers, inspection records, equipment logs, and supporting documentation for completeness, legibility, accuracy, required signatures, dates, and compliance with ...
Review completed batch records, routers, inspection records, equipment logs, and supporting documentation for completeness, legibility, accuracy, required signatures, dates, and compliance with ...
Review completed batch records, routers, inspection records, equipment logs, and supporting documentation for completeness, legibility, accuracy, required signatures, dates, and compliance with ...
Review completed batch records, routers, inspection records, equipment logs, and supporting documentation for completeness, legibility, accuracy, required signatures, dates, and compliance with ...
Are you resilient? The Master Batch Record (MBR) Designer will be presented with hard work ... Subject to motor vehicle report review. * Maintain valid driver's license and endorsements as ...
Are you resilient? The Master Batch Record (MBR) Designer will be presented with hard work ... Subject to motor vehicle report review. * Maintain valid driver's license and endorsements as ...
$12.98 - $14.86
1% of jobs
$14.86 - $16.74
15% of jobs
$17.31 is the 25th percentile. Wages below this are outliers.
$16.74 - $18.62
31% of jobs
The median wage is $18.86 / hr.
$18.62 - $20.50
28% of jobs
$20.54 is the 75th percentile. Wages above this are outliers.
$20.50 - $22.38
12% of jobs
$22.38 - $24.26
8% of jobs
$24.26 - $26.14
4% of jobs
$26.14 - $28.02
1% of jobs
$28.02 - $29.90
0% of jobs
$29.90 - $31.77
0% of jobs
$31.77 - $33.65
0% of jobs
$12
$20
$33
A Batch Record Reviewer is responsible for reviewing manufacturing and production records to ensure compliance with regulatory standards and internal quality procedures. They verify that all documentation is complete, accurate, and meets Good Manufacturing Practices (GMP) requirements. Their role helps maintain product quality and ensures that any discrepancies or deviations are identified and addressed before product release. Batch Record Reviewers typically work in industries such as pharmaceuticals, biotechnology, and food manufacturing.
A typical day for a Batch Record Reviewer involves meticulously examining batch records, manufacturing documentation, and supporting data to ensure compliance with regulatory and company standards. Reviewers frequently interact with production staff, quality assurance teams, and sometimes laboratory personnel to clarify discrepancies or gather additional information. Attention to evolving priorities and deadlines is common, especially when batches are ready for product release. This role offers valuable exposure to multiple departments and can serve as an excellent pathway to higher-level quality or regulatory positions within the company.
To thrive as a Batch Record Reviewer, you need a keen attention to detail, strong analytical skills, and a solid understanding of Good Manufacturing Practices (GMP), often supported by a degree in life sciences or related fields. Familiarity with electronic documentation systems, quality management software, and sometimes certifications like Six Sigma or GMP training is highly valued. Excellent organization, communication, and problem-solving abilities are important soft skills for ensuring thorough and compliant record review. These competencies are crucial for maintaining product quality, regulatory compliance, and operational efficiency in pharmaceutical or biotech manufacturing environments.
Cities with the most Batch Record Reviewer job openings:
The most popular types of Batch Record Reviewer jobs are:
States with the most job openings for Batch Record Reviewer jobs include:
For Batch Record Reviewer jobs, the most frequently searched job titles are:

Conshohocken, PA
$17.75 - $21.75/hr
Full-time
Posted 20 days ago
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.
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.