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Quality Associate Ii Jobs in Indiana (NOW HIRING)

Quality Associate Pay rate based on experience! About Codis At Codis (formerly Particle Dynamics ... 2% - with immediate vesting * Clean, climate-controlled pharmaceutical environment * Growth ...

Quality Associate Pay rate based on experience! About Codis At Codis (formerly Particle Dynamics ... 2% - with immediate vesting * Clean, climate-controlled pharmaceutical environment * Growth ...

Quality Technician

Terre Haute, IN · On-site

$20.50 - $24.75/hr

What You'll Do As a Quality Associate Technician , you'll support manufacturing operations by ... Strong communication and organizational skills Preferred Qualifications * 1-2 years of quality ...

Quality Technician

Terre Haute, IN · On-site

$20.50 - $24.75/hr

What You'll Do As a Quality Associate Technician , you'll support manufacturing operations by ... Strong communication and organizational skills Preferred Qualifications * 1-2 years of quality ...

Warehouse Associate II

Plainfield, IN

$15.75 - $18.75/hr

The Warehouse Associate II is responsible for handling product safely and in accordance with best methods to maintain product quality. What You Will Do * Uses power equipment (e.g., forklift) to ...

Production Associate 2

Noblesville, IN · On-site

$14 - $17.75/hr

Follow quality system requirements, standard operating procedures, and Good Documentation Practices ... Minimum of 2 years experience working in a warehouse, logistics, supply chain, manufacturing, or ...

Production Associate 2

Noblesville, IN · On-site

$14 - $17.75/hr

Follow quality system requirements, standard operating procedures, and Good Documentation Practices ... Minimum of 2 years experience working in a warehouse, logistics, supply chain, manufacturing, or ...

Food Service Associate II, 1.0

Lafayette, IN · On-site

$13.50 - $17.50/hr

The Food Services Associate II may also be responsible for passing of patient food trays and other ... Our mission is to ensure that every patient receives the highest quality of care through innovation ...

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Quality Associate Ii information

What is the difference between Quality Associate Ii vs Quality Control Technician?

AspectQuality Associate IIQuality Control Technician
Required CredentialsTypically an associate degree or higher in a related fieldOften an associate degree or technical certification
Work EnvironmentOffice and manufacturing settings, supporting quality processesLaboratory and production environments, performing testing and inspections
Employer & Industry UsageCommon in manufacturing, pharmaceuticals, and biotechPrimarily in manufacturing and production sectors
Search & Comparison IntentUnderstanding roles, responsibilities, and career pathFocus on testing procedures and technical skills

The main difference between a Quality Associate II and a Quality Control Technician lies in their focus and responsibilities. Quality Associate II roles often involve supporting quality systems, documentation, and process improvements, while Quality Control Technicians primarily perform testing and inspections to ensure product quality. Both roles require similar educational backgrounds but differ in daily tasks and work environments.

What are some typical challenges a quality associate ii might face when working on cross-departmental projects?

As a Quality Associate II, you may frequently collaborate with teams from production, engineering, and regulatory affairs. One common challenge is ensuring clear communication and alignment on quality standards across departments, especially when project timelines are tight or priorities differ. You’ll often need to balance attention to detail with efficiency, managing documentation and compliance tasks while supporting process improvements. Developing strong working relationships and proactive communication skills can help you address these challenges effectively and contribute to smoother project execution.

What is a quality associate ii?

Quality Associate IIs are professionals who work in quality assurance or quality control, typically within manufacturing, pharmaceuticals, or other regulated industries. They are responsible for ensuring products and processes meet established standards and regulatory requirements. Their duties may include inspecting materials, reviewing documentation, conducting audits, and collaborating with other departments to resolve quality issues. Quality Associate IIs often have more experience than entry-level associates and may assist in training or supervising junior staff. Their work helps maintain product safety, consistency, and compliance.

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

To thrive as a Quality Associate II, you need a solid understanding of quality assurance processes, regulatory compliance, and technical documentation, often supported by a bachelor's degree in a scientific or technical field. Familiarity with quality management systems (QMS), statistical analysis tools, and industry-specific standards such as ISO or GMP is typically required. Strong attention to detail, analytical thinking, and effective communication skills set outstanding candidates apart. These abilities are crucial to ensuring product quality, regulatory adherence, and continuous process improvement in a highly regulated environment.
What are popular job titles related to Quality Associate Ii jobs in Indiana? For Quality Associate Ii jobs in Indiana, the most frequently searched job titles are:
What cities in Indiana are hiring for Quality Associate Ii jobs? Cities in Indiana with the most Quality Associate Ii job openings:
Infographic showing various Quality Associate Ii job openings in Indiana as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 15% Part Time, 4% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution.

Quality Associate 2 - Batch Release

Singota Solutions

Bloomington, IN • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 13 days ago


Job description


Why join Team Singota?
We pride ourselves on a high-trust, high-accountability environment where we lift each other up. When you join Singota, you are a part of a team that respects, supports, and values its people. We celebrate wins together, brainstorm solutions together, and genuinely enjoy the work we do. The result? A team that's not just efficient, but also passionate, dedicated, and fun to work with.
Job Title: Quality Associate 2 - Batch Release
Department: QA
Reports to: Quality Assurance Supervisor
Location: Bloomington, IN (Onsite)
Position Type: Full-time, Exempt, 40 hr/wk
General Description:
The Quality Associate 2 - Batch Release is responsible for managing the workflow of records for Manufacturing and
QC/Development activities in accordance with company, client and regulatory quality standards, including the
appropriate disposition of materials or manufactured product. This position is responsible for reviewing records for
accuracy and completeness and for identifying discrepancies or issues that could result in product impact.
1. Responsible for the issuance, review, and release of batch records and protocols. Ensure records are executed in accordance with procedures and regulatory requirements.
2. Perform disposition of materials within the electronic inventory management system, issue appropriate release documentation.
3. Collaborate with various departments to ensure record specifications are accurate and related deviations are thoroughly investigated.
4. Interface with clients to provide support for review and release of records related to client material or product.
5. Author complex deviations, CAPAs, and change controls as needed.
6. Participate in the training of new Quality Assurance staff.
7. Support continuous improvement of the site's Quality Systems.
8. Generate and issue controlled labeling material for manufacturing operations. Review for legibility, accuracy, and compliance to company, client, and regulatory standards.
9. Review and disposition Quality Control/Development Laboratory records.
10. Write and review Standard Operating Procedures related to Quality Systems within Manufacturing and QC/Development.
11. Responsible for the development and issuance of Quality operational metrics.
12. Represent Quality Assurance at various project and technical meetings.
13. Must perform other duties as assigned by supervision. Responsible for notifying supervision when issues arise.
14. Comply with quality and safety management systems including requirements for documentation, training, system use, SOPs, processes, and procedures
Requirements
Skills and Physical Activity Requirements:
1. Excellent internal and external communication.
2. Demonstration of positive attitude and professional presence.
3. Good time management and organizational skills.
4. Detail orientated, must be able to perform thorough reviews of documentation.
Education and Work Experience Requirements:
1. Bachelor's degree or equivalent work experience - science related field preferred.
2. Minimum 3-5 years pharmaceutical experience, preferably in a Quality role.
3. Must possess knowledge of Good Documentation Practices (GDP).
4. Experience in an aseptic manufacturing and laboratory operations is desirable.
Benefits
  • Dental insurance - effective day one of employment
  • Health insurance - effective day one of employment
  • Vision insurance - effective day one of employment
  • Health savings account
  • Life & AD&D insurance
  • Short & long term disability
  • Paid time off & holidays
  • Employee Assistance Program
  • Tuition assistance
  • Sam's Club Basic membership reimbursement
  • 401(k) with company match

Singota Solutions is an Equal Opportunity Employer