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Batch Engineer Jobs in Boston, MA (NOW HIRING)

Lead Data Engineer

Bedford, MA · On-site

$120K - $144K/yr

MITRE's Data Science and Engineering department is looking for qualified applicants to bring their ... Develop batch and streaming data-processing solutions for structured, semi-structured, and ...

Principal, Data Engineer

Woburn, MA · On-site

$170K - $213K/yr

  • Medical

  • Retirement

  • PTO

... batch and streaming use cases. * Design and implement end-to-end data pipelines, reusable ... Establish engineering standards for coding, testing, version control, documentation, and continuous ...

Data Platform Engineer

Boston, MA · On-site

$124K - $149K/yr

  • Medical

  • Life

We're looking for a Data Platform Engineer to join the team responsible for the infrastructure ... Basic understanding of data pipeline concepts - batch processing, scheduling, data modeling - and a ...

CQV/Validation Engineer

Holbrook, MA · On-site

$33 - $43/hr

The CQV/Validation Engineer is responsible for supporting the activities required to implement the ... Review and revise GMP documentation, including SOPs, batch records, protocols, reports, forms, and ...

Senior Data Engineer

Boston, MA

$115K - $156K/yr

Leverage Python and PySpark to enable real-time and batch processing of model outputs, enhancing ... Mentor junior engineers, establishing best practices in data engineering, DevOps, data science, and ...

Senior Automation Engineer

Norton, MA · On-site

$105K - $138K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

We're one of the largest engineering and system integration firms in the United States providing ... ISA S88 Batch standard * ISA S95 Controls System Architecture standard * GAMP 5 & cGMP * 21 CFR ...

Senior Data Engineer

Somerville, MA · On-site

$115K - $157K/yr

As a Senior Data Engineer at VIA, you will play a pivotal role in the growth of their solutions ... Develop, deploy, and maintain resilient ETL/ELT pipelines for both real-time streaming and batch ...

Senior Automation Engineer

Norton, MA · On-site

$105K - $138K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

We're one of the largest engineering and system integration firms in the United States providing ... ISA S88 Batch standard * ISA S95 Controls System Architecture standard * GAMP 5 & cGMP * 21 CFR ...

Senior Data Engineer

Somerville, MA · On-site

$115K - $157K/yr

As a Senior Data Engineer at VIA, you will play a pivotal role in the growth of their solutions ... Develop, deploy, and maintain resilient ETL/ELT pipelines for both real-time streaming and batch ...

Sr. Salesforce Developer

Roxbury Crossing, MA · On-site

$80 - $100/hr

  • Medical

  • Dental

  • Vision

  • Retirement

... Components, Apex triggers, batch processes, and flows Build and maintain integrations with ... Salesforce Platform Developer II certification Experience in higher education or large enterprise ...

Senior Automation Engineer

Plymouth, MA · On-site

$113K - $148K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

We're one of the largest engineering and system integration firms in the United States providing ... ISA S88 Batch standard * ISA S95 Controls System Architecture standard * GAMP 5 & cGMP * 21 CFR ...

Senior Automation Engineer

Norton, MA

$105K - $138K/yr

We're one of the largest engineering and system integration firms in the United States providing ... ISA S88 Batch standard * ISA S95 Controls System Architecture standard * GAMP 5 & cGMP * 21 CFR ...

Senior Automation Engineer

Andover, MA

$105K - $138K/yr

We're one of the largest engineering and system integration firms in the United States providing ... ISA S88 Batch standard * ISA S95 Controls System Architecture standard * GAMP 5 & cGMP * 21 CFR ...

As a Senior Data Engineer at VIA, you will play a pivotal role in the growth of their solutions ... Develop, deploy, and maintain resilient ETL/ELT pipelines for both real-time streaming and batch ...

Senior Automation Engineer

Plymouth, MA · On-site

$113K - $148K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

We're one of the largest engineering and system integration firms in the United States providing ... ISA S88 Batch standard * ISA S95 Controls System Architecture standard * GAMP 5 & cGMP * 21 CFR ...

Senior Automation Engineer

Plymouth, MA · On-site

$113K - $148K/yr

We're one of the largest engineering and system integration firms in the United States providing ... ISA S88 Batch standard * ISA S95 Controls System Architecture standard * GAMP 5 & cGMP * 21 CFR ...

Senior Automation Engineer

Boston, MA · On-site

$113K - $148K/yr

We're one of the largest engineering and system integration firms in the United States providing ... ISA S88 Batch standard * ISA S95 Controls System Architecture standard * GAMP 5 & cGMP * 21 CFR ...

Showing results 41-60

Batch Engineer information

See Boston, MA salary details

$14

$22

$36

How much do batch engineer jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for batch engineer in Boston, MA is $22.10, according to ZipRecruiter salary data. Most workers in this role earn between $18.80 and $22.98 per hour, depending on experience, location, and employer.

What is a batch engineer?

Batch engineers are professionals who design, implement, and optimize batch processing systems in manufacturing environments, particularly in industries like pharmaceuticals, chemicals, and food production. They are responsible for developing processes that produce products in discrete quantities or 'batches,' ensuring quality, efficiency, and safety standards are met. Batch engineers often work with automation systems, troubleshoot process issues, and collaborate with cross-functional teams to improve production workflows.

What are the key skills and qualifications needed to thrive as a batch engineer, and why are they important?

To thrive as a Batch Engineer, you need a strong background in chemical or process engineering, with experience in batch processing operations and often a relevant engineering degree. Familiarity with Distributed Control Systems (DCS), batch automation software like DeltaV or Siemens PCS 7, and knowledge of industry standards such as ISA-88 are typically required. Strong problem-solving, attention to detail, and effective communication skills help in optimizing processes and collaborating with cross-functional teams. These skills and qualifications are crucial for ensuring efficient, safe, and compliant batch production in manufacturing environments.

What are some common challenges a batch engineer may face when managing large-scale batch processing systems?

Batch Engineers often encounter challenges such as optimizing job scheduling to maximize resource utilization while minimizing processing time. Handling job failures and troubleshooting data inconsistencies are also frequent issues, as large-scale systems can be sensitive to small errors. Additionally, they must ensure that batch jobs integrate smoothly with upstream and downstream systems, requiring strong communication with development, operations, and data teams. Staying updated with automation tools and best practices is crucial for efficiently managing these complex workflows.

What is the difference between Batch Engineer vs Process Engineer?

AspectBatch EngineerProcess Engineer
CredentialsBachelor's in Chemical, Mechanical, or Industrial EngineeringBachelor's in Chemical, Mechanical, or Industrial Engineering
Work EnvironmentManufacturing plants, chemical facilities, pharmaceutical productionManufacturing plants, chemical facilities, process optimization settings
Industry UsageFood, pharmaceuticals, chemicals, manufacturingChemical, petrochemical, manufacturing, process industries
Primary FocusDesign, operation, and optimization of batch production processesDesign and improvement of continuous or batch processes for efficiency

Both Batch Engineers and Process Engineers work in manufacturing and chemical industries, often sharing similar educational backgrounds. Batch Engineers focus on managing and optimizing batch production processes, while Process Engineers work on designing and improving overall manufacturing processes. Understanding these distinctions helps in choosing the right career path or job role.

$33 - $43/hr

Full-time

Re-posted 15 days ago


Job description

Sebela Pharmaceuticals is a U.S. pharmaceutical company with a market-leading position in Gastroenterology and a focus on innovation in Women’s Health. Our Vision is to build the leading Gastroenterology company in the U.S., with a complementary focus on innovation in Women’s Health, premised on our expertise in pharmaceutical development and commercialization. Braintree Laboratories, Inc., a part of Sebela Pharmaceuticals, has its contract development and manufacturing organization (CDMO) in Holbrook, MA, offering pharmaceutical-development and in-house manufacturing services for specialty gastroenterology products.
We value dedication, energy, and enthusiasm, and we focus on innovation and results while striving to achieve our corporate mission and vision. Sebela Pharmaceuticals is committed to cultivating an inclusive environment where all employees are treated with respect. We accomplish this by fostering a culture of diversity, equity and inclusion, which is essential to innovation and continuous improvement. Sebela operates from three locations in Roswell, Georgia, Braintree and Holbrook, MA and headquarters in Dublin, Ireland.
The CQV/Validation Engineer is responsible for supporting the activities required to implement the Holbrook site’s validation plan in compliance with current industry and regulatory expectations. This role supports the development, review, execution, and completion of qualification, validation, and related cGMP documentation.
PRINCIPAL DUTIES AND RESPONSIBILITIES
  • Participate in validation, qualification, and commissioning activities for pharmaceutical manufacturing equipment, utilities, facilities, processes, cleaning programs, and computerized systems.
  • Participate in validation and CQV projects from planning through documentation, execution, discrepancy resolution, approval, and closeout.
  • Develop, review, and/or execute validation documentation such as change control, test scripts, protocols, reports, User Requirements Specifications, risk assessments, traceability matrices, and related supporting documents.
  • Support equipment, utility, facility, process, cleaning, and computerized system validation activities, as assigned.
  • Document and assist in resolving protocol discrepancies, deviations, incidents, nonconformances, and validation issues, including impact assessments and corrective actions/CAPA.
  • Collaborate with Manufacturing, Engineering, Quality Assurance, Quality Control, Technical Operations, IT, and external vendors to support validation deliverables and project timelines.
  • Review and revise GMP documentation, including SOPs, batch records, protocols, reports, forms, and related controlled documents.
  • Complete GMP documentation and validation records accurately, clearly, and contemporaneously in accordance with company procedures and good documentation practices.
QUALIFICATIONS
To perform this job successfully, an individual must be able to perform each essential function satisfactorily, be flexible in terms of work hours, and have knowledge and experience in Equipment and Utility Qualification, Process Validation, Cleaning Validation and/or Computerized System Validation. The requirements listed below are representative of the knowledge, skills and/or abilities required. Equivalent combination of education and relevant experience will be considered.
  • Bachelor’s degree or higher in Engineering, Life Sciences or related discipline.
  • 3+ years relevant FDA regulated industry/validation experience or an equivalent amount of validation experience.
  • Experience with validation, qualification, commissioning, CQV, manufacturing support, quality systems, engineering documentation, or technical project execution.
  • Familiarity with one or more of the following areas is preferred: equipment qualification, facility qualification, utility qualification, cleaning validation, process validation, computerized system validation, or commissioning.
  • Ability to write, review, or execute technical documents such as protocols, test scripts, reports, SOPs, batch records, specifications, risk assessments, or deviation investigations.
  • Strong problem-solving, communication, and technical writing skills.
  • Knowledge of good documentation practices and cGMPs required.
  • Knowledge of 21 CFR Part 11, validation lifecycle principles, or risk-based validation approaches preferred.
  • Auto CAD experience preferred.
  • Flexible to work overtime (paid) as needed.
Pay Range: $33.00 - $43.00 per hour/annualized at $68-89K not including any overtime pay (this reflects our reasonable and good faith estimate of what will be paid at the time of posting). Competitive benefits package included.