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Process Associate Jobs in Quincy, MA (NOW HIRING)

Albertsons

Personnel Coordinator

Ipswich, MA · On-site

$21 - $28/hr

Maintain accurate personnel files, time and attendance records, and process associate data changes. * Serve as liaison between store associates and HR, Payroll, and Benefits teams. * Assist with ...

RoslinCT US

Lead Cell Processing Associate

Hopkinton, MA · On-site

$20 - $24.25/hr

The Lead Cell Processing Associate will also collaborate as needed with peers within Manufacturing ... Daily review of in-process cGMP documentation for completeness and accuracy * Other duties as ...

Tjx

Part Time Backroom Processing Associate

Westwood, MA · On-site

$16.25 - $16.75/hr

Accurately processes and prepares merchandise for the sales floor following company procedures and ... Associate discount; EAP; smoking cessation; bereavement; 401(k) Associate contributions; child care ...

Amazon

Process Assistant

Stoughton, MA · On-site

... floor as an associate resource, training associates and verifying SOP compliance - Ensuring ... process, including support for the interview or onboarding process, please visit for more ...

Amazon

Process Assistant

Stoughton, MA · On-site

... floor as an associate resource, training associates and verifying SOP compliance - Ensuring ... process, including support for the interview or onboarding process, please visit for more ...

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How much do process associate jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for process associate in Quincy, MA is $30.68, according to ZipRecruiter salary data. Most workers in this role earn between $28.56 and $34.13 per hour, depending on experience, location, and employer.

What is a process associate?

Process Associates are entry-level professionals who support the day-to-day operations of a business by handling administrative tasks, data processing, and workflow management. They often work in sectors like finance, healthcare, and business process outsourcing, ensuring processes run smoothly and efficiently. Their responsibilities include data entry, documentation, quality checks, and assisting with process improvements. Strong attention to detail, communication skills, and familiarity with relevant software are important for success in this role.

What does a process associate do?

A typical day for a Process Associate involves handling and processing transactions, managing data entry tasks, and ensuring that all assigned processes are completed within established timelines and quality standards. Process Associates frequently collaborate with team leads, quality analysts, and other associates to resolve issues or clarify process requirements. They may also participate in team meetings to discuss workflow improvements or share updates. This role requires strong attention to detail and effective communication with both colleagues and, occasionally, clients to ensure seamless operations.

What are the key skills and qualifications needed to thrive as a process associate?

To excel as a Process Associate, you typically need strong analytical abilities, attention to detail, and at least a high school diploma or bachelor’s degree, depending on the industry. Familiarity with process management software (such as SAP or Oracle), MS Office Suite, and sometimes Six Sigma certification are often valuable. Effective communication, time management, and adaptability help individuals stand out in this role. These skills ensure accuracy, efficiency, and smooth workflow execution, which are critical for supporting business operations and meeting organizational goals.

What is the difference between Process Associate vs Customer Service Executive?

AspectProcess AssociateCustomer Service Executive
Primary RoleSupports business processes, data entry, and operationsHandles customer inquiries, complaints, and support
Work EnvironmentBack-office, process-drivenFront-office, client-facing
Required SkillsAttention to detail, process knowledge, basic IT skillsCommunication skills, problem-solving, patience
Industry UsageBPO, finance, healthcare, ITBPO, retail, telecom, banking

While both roles are common in BPO and related industries, a Process Associate primarily supports operational processes behind the scenes, whereas a Customer Service Executive directly interacts with clients to resolve issues. Understanding these differences helps job seekers identify roles aligned with their skills and career goals.

Is a process associate a stressful job?

A process associate role can involve repetitive tasks, meeting deadlines, and attention to detail, which may contribute to stress levels. However, the job environment, workload, and support systems can influence how stressful the role feels for an individual.

Is a process associate job entry level?

A process associate position is often considered entry-level, suitable for candidates with basic skills in data entry, process management, or customer service. Many employers provide on-the-job training, and a high school diploma or equivalent is typically sufficient to start in this role.

What are the most commonly searched types of Process jobs in Quincy, MA?

The most popular types of Process jobs in Quincy, MA are:

What are popular job titles related to Process Associate jobs in Quincy, MA?

For Process Associate jobs in Quincy, MA, the most frequently searched job titles are:

What job categories do people searching Process Associate jobs in Quincy, MA look for?

The top searched job categories for Process Associate jobs in Quincy, MA are:

What cities near Quincy, MA are hiring for Process Associate jobs?

Cities near Quincy, MA with the most Process Associate job openings:

Process Associate jobs near you
Infographic showing various Process Associate job openings in Quincy, MA as of August 2026, with employment types broken down into 56% Full Time, and 44% Contract. Highlights an 100% In-person job distribution, with an average salary of $63,819 per year, or $30.7 per hour.

Associate Engineer/Scientist, Process & Product Transfer

SpearBio

Woburn, MA • On-site

$95K/yr

Full-time

Posted 19 days ago

Job description

Spear Bio, founded in 2021, is a well-funded and rapidly growing biotech start-up headquartered in Woburn, Massachusetts. Our proprietary technology, Successive Proximity Extension Amplification Reaction (SPEAR), is a novel wash-free immunoassay platform, offering unprecedented sensitivity. We are dedicated to revolutionizing early disease diagnosis and monitoring by providing scalable, ultrasensitive solutions that deliver unparalleled accuracy in measuring low-abundant biomarkers, enabling clinicians and researchers to improve patient outcomes and advance global health.
Associate Engineer/Scientist, Process & Product Transfer
Spear Bio is seeking a dedicated and experienced Associate Engineer/Scientist, Process & Product Transfer to join our Product Transfer team. This role will support the transfer of new products from Assay Development to Manufacturing prior to commercialization, with responsibility for design transfer activities, process documentation, scaled reagent builds, and cross-functional execution. The ideal candidate will bring hands-on experience in immunoassay development or manufacturing within the diagnostics industry, along with a strong understanding of regulated product development and manufacturing practices.
Responsibilities:
-Product Transfer
  • Lead new product introduction (NPI) design transfer activities and ensure all required deliverables are completed in alignment with Product Development Process requirements.
  • Develop specifications and acceptance criteria for raw materials or in-process materials to ensure product quality.
  • Translate assay designs into manufacturing work instructions and in-process test instructions that can be easily understood by manufacturing operators.
  • Build assay reagents at scale during feasibility and design verification phases while ensuring batch records are completed in accordance with cGMP requirements.
  • Plan and execute process verification experiments to demonstrate the robustness and reproducibility of assays being transferred.
  • Ensure material transactions are completed in a timely manner to maintain accurate inventory control.

-Compliance and Continuous Improvement
  • Drive lean manufacturing, process improvement, and supply chain initiatives to improve cost of goods, efficiency, yield, and quality.
  • Lead investigations during design transfer and provide resolutions for product and process issues.
  • Develop electronic records for manufacturing work instructions and create data analysis templates to improve efficiency and reduce errors.
  • Maintain detailed records of manufactured materials during the transfer process and complete batch records following cGMP requirements.
  • Review executed batch records and work with QA to address any quality issues prior to release (deviation, NCMR, CAPA, change control).
  • Ensure all process documentation is accurate, complete, and compliant with regulatory standards (e.g., FDA, ISO).
  • Support regulatory submissions, audits, and inspections as required.

Education & Experience:
  • Bachelor's or Master's degree in Bioengineering, Chemical Engineering, Biochemical Engineering, Chemistry, Biochemistry, or a related field.
  • If Bachelor's degree, must also have 3+ years of relevant industry experience (see below). If Master's degree, must also have 1+ years of relevant industry experience (see below).
  • Relevant experience includes product or technology transfer, IVD or RUO diagnostic assay manufacturing, or manufacturing sciences in other regulated industry.

Qualifications:
  • Experience in product or technology transfer within the diagnostics industry under cGMP requirements to support product launches.
  • Experience with IVD or RUO diagnostic assay kit manufacturing.
  • Experience with process validation, statistical analysis, and continuous improvement methodologies.
  • Demonstrated project management skills.
  • Familiarity with design controls during the product development process.
  • Familiarity with Good Documentation Practices, cGMP requirements, FDA and/or ISO quality standards for medical device and IVD products.
  • Familiarity with CLSI guidelines is a plus.
  • High attention to detail to ensure accuracy and consistency in documentation and batch record execution.
  • Strong analytical and problem-solving skills to address and resolve technical issues.
  • Excellent communication skills to effectively collaborate with cross-functional teams.
  • Proficiency in Excel for creating manufacturing records and data analysis templates.
  • Experience leveraging AI tools to support process automation is a plus, with appropriate human-in-the-loop oversight.

We offer competitive compensation, meaningful stock ownership, comprehensive benefits, and a great work environment. This is an opportunity to enter an innovative, high-growth startup at an early stage and play an integral role in the company's growth and success. We are focused on identifying candidates who have demonstrated leadership and excellence throughout their careers and are excited by the prospect of building an industry-leading company.
Spear Bio Inc. provides equal opportunity in employment to all persons. No person shall be denied equal access because of race, creed, color, religion, national origin, sex, sexual orientation, gender identity, age, or physical/mental disability.
Spear Bio does not accept resume submissions from external recruiting agencies. Any unsolicited resumes or candidate information submitted without prior written agreement will be deemed the property of Spear Bio, and no placement fees will be paid.

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