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Quality Control Associate Two Jobs in Rhode Island

Careers | CET

Quality Associate

Bristol, RI · On-site

Summary The Quality Associate supports both quality assurance and quality control initiatives regarding Production and Operations to ensure that customer requirements are met, and any discrepancies ...

Proterial America

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Lead Quality Compliance Inspector - Defense

Ashaway, RI · On-site

$28 - $32/hr

Associates degree or technical education preferred. * Past leadership or lead inspector experience ... Quality Control Standards * Strong analytical, decision making and problem-solving skills * Basic ...

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All JobsQuality Control Associate Two JobsQuality Control Associate Two Jobs in Rhode Island

Quality Control Associate Two information

What is the difference between Quality Control Associate Two vs Quality Control Associate One?

AspectQuality Control Associate TwoQuality Control Associate One
Required CredentialsHigh school diploma or equivalent; some roles may require certifications in GMP or ISO standardsHigh school diploma or equivalent; basic understanding of quality standards
Work EnvironmentManufacturing or laboratory settings, often in regulated industriesSimilar environments, typically in labs or production areas
Employer & Industry UsageUsed in pharmaceutical, biotech, and manufacturing companiesCommonly used in similar industries, often as entry-level roles
Common Search & Comparison IntentYes, often compared to associate level roles to understand responsibilities and requirementsNo, usually the starting point for quality roles

Quality Control Associate Two typically requires more experience or certifications than Quality Control Associate One. It involves more responsibilities in quality inspections and compliance, making it suitable for those with some industry experience. Both roles are common in manufacturing and laboratory environments within regulated industries.

Is quality control a good career path?

Quality Control Associate Two is a role focused on inspecting products, ensuring standards are met, and documenting quality issues. It offers opportunities for skill development in inspection techniques, attention to detail, and familiarity with quality management systems, making it a stable career choice in manufacturing and production industries.

What does a quality control associate do?

A Quality Control Associate is responsible for inspecting products and materials to ensure they meet quality standards and specifications. They perform tests, document findings, and may use tools like calipers or microscopes, often working in manufacturing or laboratory environments. Attention to detail and knowledge of quality procedures are essential for this role.

What cities in Rhode Island are hiring for Quality Control Associate Two jobs?

Cities in Rhode Island with the most Quality Control Associate Two job openings:

Quality Control Associate Two jobs near you

Quality Assurance Associate I (Cumberland, RI)

CEDENT

Cumberland, RI • On-site

Full-time

Re-posted 13 days ago

Job description

SUMMARY/OBJECTIVE This position supports activities of the Quality Assurance Department regarding pharmaceutical manufacturing, testing and packaging to ensure compliance with all relevant pharmaceutical regulatory requirements: FDA, GMP. Provides QA oversight to operations under direction of the QA Manager. Provides review, impact/risk assessment analysis, detailed improvement plans for change controls, deviations, investigations and CAPA.

Adheres to Client compliance initiatives, including following all quality and division/company policy requirements. Helps to ensure that all Client products meet quality requirements by supporting all assigned quality aspects of product approval. The QA Associate II/III independently conducts quality assurance audits of production records (manufacturing, analytical and quality control records) and facility records assuring company standards are maintained and product integrity is preserved.

RESPONSIBILITIES 1. Provide support to GMP investigations, validation documentation review and approval, identify gaps within existing Quality Systems and propose solutions for functional management; 2. Participates/leads internal/external audits, prepare and issue audit reports.

Recommend remediation actions and follow up on implementation of the plan. 3. Supports resolution of technical and compliance issues/gap analysis.

4. Aides implementation of Quality Systems/System Improvements. 5.

Supports and assists with Quality systems-related training, including compliance with cGMP and SOPs. 6. Interface with key quality, manufacturing, customers and coordinate documentation impacting quality areas.

7. Review/approval of all cGMP documents generated across site to include (but not limited to): SOPs, technical reports, validation documents, QA assessment, APRs, audit documents, change control, deviation & document revisions, etc. 8.

Participates in activities associated with primary batch record review, non-conformances investigation and CAPA. 9. Work in coordination with regulatory affairs group in support of ANDA submissions.

10. Provides QA review/approval of all cGMP documents associated with manufacture of product. 11.

Communicates with contractors and internal manufacturing/technical groups regarding compliance and quality issues (i.e., batch documentation, investigations, timelines and data related issues). 12. Authors or revises SOPs as necessary

13. Actively engaged in the training of staff with lesser experience or knowledge of quality assurance processes. Educate and instruct QA and plant personnel in quality best practices for sampling, labeling, good documentation practices, equipment sanitation.

Confirm these procedures are being adhered to, taking corrective actions when non-conformances are observed. 14. Routinely provide input to quality and operations management for better operational procedures to improve overall efficiency and regulatory compliance.

15. Assist in development of special department projects and work in conjunction with quality management. 16.

Other duties as assigned. COMPETENCIES 1. Project Management 2.

Technical Capacity. 3. Discretion.

4. Problem Solving/Analysis. 5.

Decision Making. 6. Communication Proficiency.

7. Collaboration Skills. 8.

Learning Agility 9. Managing Changing Priorities POSITION TYPE/EXPECTED HOURS OF WORK This is a full-time position requiring 40 or more hours of work per week.

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About Cedent

Sourced by ZipRecruiter

CEDENT strives to attract and retain the best people and provide an environment where they can all develop professionally and build a rewarding career. As a result, we create an inclusive environment that is rich in diversity, acknowledges each individual's uniqueness and promotes respect, personal achievement and stewardship. Our clients are global and so is CEDENT. We build and maintain a global workforce that includes people from different backgrounds, with a vast range of skills and experience all united by a common culture and commitment to help our clients achieve high performance. Cultivating a diverse workforce and inclusive work environment makes business sense. Our peoples varied skills are the talent engine that powers CEDENT, enabling it in turn to deliver the innovative solutions that help our clients outperform competitors.

Industry

It services

Company size

11 - 50 Employees

Headquarters location

Plano, TX, US

Year founded

2008

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