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Batch Disposition Specialist Jobs (NOW HIRING)

SAB

Senior Quality Assurance Specialist

Sioux Falls, SD · On-site

$79K - $109K/yr

The Sr. QA Specialist leads key quality system functions to ensure compliance with cGMP and ... Perform batch disposition activities by reviewing batch records, in-process and release testing ...

MSD

Senior Specialist, Quality Assurance (Hybrid)

Rahway, NJ · On-site

$83K - $115K/yr

The Senior Specialist, Quality Assurance BDQR is responsible for providing Quality oversight and ... batch disposition. * Provide Quality oversight of an evolving biologics clinical space by ...

INCOG

QA Specialist for IQC

Fishers, IN · On-site

QA Specialist will be instrumental in ensuring site compliance with Regulations, ISO Standards ... Dispose of Filled Inspected Product (FIP) rejects following batch disposition. Exemplify and take ...

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Batch Disposition Specialist information

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$31.5K

$71.3K

$117K

How much do batch disposition specialist jobs pay per year?

As of Aug 11, 2026, the average yearly pay for batch disposition specialist in the United States is $71,279.00, according to ZipRecruiter salary data. Most workers in this role earn between $57,000.00 and $84,500.00 per year, depending on experience, location, and employer.

What are the primary challenges faced by batch disposition specialists in ensuring timely product release?

Batch Disposition Specialists often face the challenge of balancing strict regulatory compliance with tight production schedules. Ensuring all documentation is accurate and complete, investigating deviations, and coordinating with quality assurance, manufacturing, and regulatory teams require strong attention to detail and effective communication skills. Delays may occur if discrepancies arise, so proactive problem-solving and collaborative teamwork are essential for timely batch release. This role is crucial in maintaining product quality and patient safety, making it both challenging and rewarding.

What is the difference between Batch Disposition Specialist vs Quality Control Technician?

AspectBatch Disposition SpecialistQuality Control Technician
CredentialsTypically requires a high school diploma or equivalent; certifications in quality or manufacturing are a plusHigh school diploma or equivalent; certifications in quality assurance or laboratory testing are common
Work EnvironmentManufacturing or pharmaceutical facilities, handling batch approvals and documentationLaboratories or production lines, performing tests and inspections
Industry UsageUsed in manufacturing, pharmaceuticals, and food production for batch releaseCommon in quality assurance, manufacturing, and laboratory settings

The Batch Disposition Specialist focuses on approving and releasing manufacturing batches, ensuring compliance and documentation. In contrast, the Quality Control Technician performs testing and inspections to verify product quality. Both roles are essential in manufacturing industries but differ in their primary responsibilities and work focus.

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

To excel as a Batch Disposition Specialist, you should have a background in life sciences or quality assurance, with knowledge of GMP regulations and batch record review. Familiarity with quality management systems (QMS), electronic documentation systems, and regulatory compliance tools is typically required. Strong attention to detail, analytical thinking, and effective communication are vital soft skills for this role. These skills ensure that product batches meet strict quality and regulatory standards, safeguarding product integrity and patient safety.

What is a batch disposition specialist?

Batch Disposition Specialists are professionals responsible for reviewing and deciding the final status of manufactured product batches in industries such as pharmaceuticals, biotechnology, and food production. They ensure that all required quality control tests and documentation are complete and compliant with regulatory standards before a batch is released, rejected, or quarantined. Their work is critical to maintaining product safety, quality, and adherence to industry regulations. These specialists often collaborate with quality assurance, production, and regulatory teams to resolve any issues before making disposition decisions.
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What cities are hiring for Batch Disposition Specialist jobs? Cities with the most Batch Disposition Specialist job openings:
What states have the most Batch Disposition Specialist jobs? States with the most job openings for Batch Disposition Specialist jobs include:
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Batch Disposition Specialist jobs near you
Infographic showing various Batch Disposition Specialist job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 13% Part Time, and 3% Contract. Highlights an 90% Physical, 3% Hybrid, and 7% Remote job distribution, with an average salary of $71,279 per year, or $34.3 per hour.

Senior Quality Assurance Specialist

SAb Biotherapeutics, Inc

Sioux Falls, SD • On-site

$79K - $109K/yr

Full-time

Posted 26 days ago

Job description

The Sr. QA Specialist leads key quality system functions to ensure compliance with cGMP and regulatory standards in a biotech environment. With over five years of experience, this role manages complex investigations, oversees change control and CAPA processes, supports regulatory inspections, and mentors junior QA staff. The specialist drives continuous improvement and cross-functional collaboration to uphold product quality and operational excellence.
NOTE: Some relocation assistance available for this role.
Duties and Responsibilities (Responsibilities include but are not limited to):
  • Lead and execute quality oversight of manufacturing and QC operations, including executed batch record review, deviation, investigations, risk assessments, change control, SOPs and cross-functional liaison to ensure compliance with cGMP and internal quality standards.
  • Independently lead quality-driven projects and present key quality metrics, training initiatives, and validation documentation reviews to leadership and cross-functional teams.
  • Drive ownership of quality systems, including change control, CAPA, and document management, with accountability for process improvement and regulatory alignment.
  • Author, review, and approve controlled documentation, including SOPs, batch records, and work instructions, ensuring accuracy, completeness, and adherence to applicable regulatory standards.
  • Perform batch disposition activities by reviewing batch records, in-process and release testing results, Environmental monitoring records, Certificates of Analysis (CoAs), deviation investigations, and quality event closures to determine and document batch approval or rejection decisions.
  • Inspect and approve raw materials, packaging components, and in-process materials against approved specifications and/COA, ensuring compliance with internal standards, regulatory expectations, and release criteria prior to use in manufacturing operations.
  • Provide QA floor support during manufacturing process as needed.
  • Other duties/responsibilities as assigned.
Supervisory Responsibilities:
This position does not have supervisory responsibilities.
Education/Experience/Skills:
  • BS/BA in life sciences
  • 5+ years of quality assurance experience in a regulated manufacturing environment required (FDA, EMA, MHRA, Health Canada). Pharmaceutical or related industry experience is highly preferred.
  • Must have strong communication skills. Demonstrated proficiency in Microsoft Office software (Word, Excel, PowerPoint and Outlook).
  • Ability to effectively present information in one-on-one, small groups and company meetings.
  • Must be able to occasionally aseptically gown to support QA on the floor activities in ae clean rooms and practice aseptic behavior in controlled areas
  • Utilizes established mathematical and scientific techniques to compile and analyze data.
  • Familiar with eQMS functionality. Experience implementing an eQMS is highly desirable.
  • Demonstrates self-motivation, initiative, and accountability in managing priorities, completing assignments, and proactively identifying opportunities for process improvement.
Working Environment and Travel:
While performing the duties of this job, the employee is regularly required to walk, stand and sit. The employee must regularly lift and/or move up to 10 pounds. Specific vision abilities required by this job include close vision, peripheral vision, and the ability to adjust focus.
Normal office environment with some exposure to lab areas. The noise level in the working environment is usually moderate.
Occasional travel may also be expected, as needed.
ADA:
The employer will make reasonable accommodations in compliance with the Americans with Disabilities Act of 1990.
This job description will be reviewed periodically as duties and responsibilities change with business necessity. Primary and additional duties and responsibilities are subject to modification.
SAB BIO is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. SAB BIO is committed to the principle of equal employment opportunity for all employees and does not discriminate based on race, religion, color, sex, gender identify, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other legally protected status. EOE/AA/Vets

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