Top 5 Quality control associate Jobs in West Babylon Ny

GMP Quality Associate (Overnight Role 06:00 pm - 06:00 am)
Kedrion Biopharma Inc. —Melville, NY
- $23 - $25 an hour
- Weekends as needed
- Mid-level
- Continuous improvement
- US work authorization
- AD&D insurance
- Paid holidays
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Quality Assurance Associate (Daytime Role 06:00 am - 06:00 pm)
Kedrion Biopharma Inc. —Melville, NY
- $23 - $25 an hour
- Weekends as needed
- Mid-level
- Continuous improvement
- US work authorization
- AD&D insurance
- Paid holidays
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Manufacturing Quality Associate (Overnight Role 06:00 pm - 06:00 am)
Kedrion Biopharma Inc. —Melville, NY
- $23 - $25 an hour
- Weekends as needed
- Continuous improvement
- US work authorization
- Experience equivalent to degree accepted
- AD&D insurance
- Paid holidays
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Quality Operations Associate (Daytime Role 06:00 am - 06:00 pm)
Kedrion Biopharma Inc. —Melville, NY
- $23 - $25 an hour
- Weekends as needed
- Mid-level
- Analysis skills
- Continuous improvement
- AD&D insurance
- Paid holidays
Quick Apply

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GMP Quality Associate (Overnight Role 06:00 pm - 06:00 am)

Kedrion Biopharma Inc. -
Melville, NY

Quick Apply

Job Details

Full-time
$23 - $25 an hour

Benefits

AD&D insurance
Paid holidays
Health insurance
Dental insurance
Paid time off
Vision insurance

Qualifications

Quality records maintenance
Document control experience within pharmaceutical industry
Procedural guides
Labeling
Production deviation management
Metrics Reporting
Mid-level
Inspection reporting and documentation
Manufacturing standard operating procedures
Quality control data reporting
Manufacturing facility experience
Key Performance Indicators
Maintenance records management
Continuous improvement
Pharmaceutical company experience
Quality assurance experience within pharmaceutical industry
Compliance documentation
Regulatory/legal compliance standards in production
Collaboration with manufacturing teams
Quality control experience within pharmaceutical industry
Productivity software
Investigating compliance violations
Production batch record review
Quality control communication
Safety standard operating procedures
Standard operating procedures (SOPs)
Communication skills
Cross-functional communication
Pharmaceutical manufacturing facility experience

Full Job Description

Kedrion Biopharma Inc. is an international company that collects and fractionates blood plasma to produce and distribute plasma-derived therapeutic products for us in treating and preventing serious diseases, disorders and conditions such as Hemophilia, Primary Immune System Deficiencies and Rh-Sensitization.

Job Summary

Be at the forefront of quality and compliance in pharmaceutical manufacturing.

The GMP Quality Associate supports quality oversight activities across manufacturing operations to help ensure products are manufactured safely, consistently, and in compliance with regulatory requirements. Working directly on the production floor, this role partners with Manufacturing and Quality teams to monitor operations, review documentation, perform routine inspections, and help resolve quality issues in real time. This is an excellent opportunity for individuals who are passionate about quality, compliance, and continuous improvement in a highly regulated environment.

What you'll do

Provide quality oversight and GMP support for daily manufacturing operations.
Monitor batch processing activities to ensure compliance with approved procedures, batch records, and cGMP requirements.
Conduct routine inspections of production activities, manufacturing areas, utilities, systems, and facilities.
Review production logbooks, batch records, and supporting documentation for completeness, accuracy, and compliance.
Verify critical manufacturing parameters and support in-process quality reviews.
Support plasma and component inspection activities.
Identify, document, and communicate compliance observations and quality concerns in a timely manner.
Track and trend quality observations to support site performance metrics and continuous improvement initiatives.
Initiate and document minor non-conformance events.
Support Return to Service activities and associated quality documentation.
Review utility alarms, maintenance records, work orders, and calibration documentation to ensure compliance requirements are met.
Assist with the revision and maintenance of SOPs and other GMP-controlled documents.
Support investigations, deviations, corrective actions, and change control activities as assigned.
Collaborate with Manufacturing, Quality, Engineering, and other cross-functional teams to support operational excellence.
Maintain accurate records and documentation in accordance with GMP and GDP requirements.
Follow all safety policies, procedures, and regulatory standards.
Perform additional duties and project work as required to support site objectives.

Over Night Role: 06:00 pm - 06:00 am (Alternating days including weekends)

Qualifications and need-to-know

College degree preferred or equivalent combination of education and relevant experience required.
Experience in pharmaceutical manufacturing, Quality Assurance, Quality Operations, or production environments preferred.
Knowledge of GMP and GDP regulations and experience working in a regulated environment.
Experience with biologics manufacturing, plasma fractionation, aseptic filling, or labeling operations is a plus.
Experience supporting investigations, deviations, non-conformances, or quality systems is preferred.
Strong attention to detail and ability to review technical documentation accurately.
Effective verbal and written communication skills.
Demonstrated problem-solving and organizational abilities.
Proficiency with Microsoft Office applications and email systems.
Ability to work effectively in a team-oriented manufacturing environment.
Commitment to safety, quality, regulatory compliance, and continuous improvement.

Employment eligibility verification will be required at the time of hire. This position does not offer visa sponsorship now or in the future.

Kedrion Biopharma Inc. is committed to providing equal employment opportunities to all employees and applicants. We prohibit discrimination and harassment based on race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. This policy applies to all employment terms, including recruitment, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

Please note that salary ranges are calculated based off levels of: relevant experience, education, and certifications.

Kedrion Biopharma Inc. offers numerous benefits to our qualifying employees, including:

Medical, vision and dental insurance
Life and AD&D insurance
Paid holidays
PTO accrual
and much more!

Please let us know if you would like further details regarding the benefits that we offer to our qualifying employees, and we would be glad to provide you with our full benefits guide, as well as answering any questions you may have!

If you require assistance with your employment application or need reasonable accommodations to perform job duties, please contact our Talent Acquisition team at [email protected].

Kedrion Biopharma Inc. participates in E-Verify and provides the federal government with Form I-9 information to confirm employment authorization. For more information, please contact the Department of Homeland Security.

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Refine Your Search

quality control associate jobs in west babylon ny

GMP Quality Associate (Overnight Role 06:00 pm - 06:00 am)

Quality Assurance Associate (Daytime Role 06:00 am - 06:00 pm)

Manufacturing Quality Associate (Overnight Role 06:00 pm - 06:00 am)

Quality Operations Associate (Daytime Role 06:00 am - 06:00 pm)

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