Careers

"*" indicates required fields

Step 1 of 4

Career Openings

Document Control Clerk

Document Control Clerk

Department: Quality Assurance

Schedule: Mon-Thurs: 8:30 am – 4:30 pm, Fri: 8 am – 2 pm

Pay type: Hourly

Pay rate: $68,000 – $72,000 Yearly

Location: Farmingdale, NJ (Fulltime)

NutraStar is a fast-growing contract manufacturer specializing in the formulation and production of high-quality nutraceuticals. With more than 300 employees and a reputation built on customer service, precision, quality, and innovation, we serve some of the most respected brands in the health and wellness industry. Our continued investment in people, technology, and infrastructure drives our rapid growth and positions us as a leader in our field

About the role:

To develop, implement, and maintain effective document control procedures and systems that support organizational compliance, quality assurance, and operational efficiency. This role ensures consistent documentation practices across departments, manages the electronic document management system (EDMS), oversees the Standard Operating Procedures (SOP) system, and supports the Senior QA Manager in supplier qualification initiatives. 

Key Responsibilities:

  • Develop and implement document control procedures to ensure consistent and effective document management throughout the organization 
  • Collaborate with various departments to understand their document management needs and requirements 
  • Work closely with quality assurance, quality control and compliance team to align documentation with organizational goals 
  • Create and manage electronic document management systems 
  • Responsible for managing SOP system 
  • Assist Sr. QA Manager in supplier qualification program 
  • Maintain a clean and safe work environment. 
  • Show a desire and willingness to learn and succeed. 
  • Assist with Batch Record Control as needed.  
  • Assist with Customer Requests.  
  • Complete all required training activities. 
  • Demonstrate commitment to the organization by maintaining regular, on-site attendance, act in a reliable manner and follow through on responsibilities. 
  • Other duties as assigned. 

Education / Experience:

  • Bachelor’s degree – Food science degree preferred. 
  • 1-3 years of experience in a quality assurance environment. 
  • Knowledge of Microsoft Office/Excel applications/Smart sheet.
  • Strong attention to detail. 
  • Ability to work independently with minimal supervision. 
  • Excellent time management skills and ability to prioritize tasks effectively. 
  • Good communication skills and ability to work collaboratively as part of a team.
  • Bilingual, must be able to read and write English. 

NutraStar is an equal opportunity employer. Employment at our Company is based solely on job-related qualifications: we recruit, hire, train, promote and compensate our employees and provide all other conditions of employment including company sponsored events without regard to race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth and related medical conditions), gender identity or gender expression (including transgender status), sexual orientation, marital status, military service and veteran status, physical or mental disability, protected medical condition as defined by applicable state or local law, genetic information, or any other characteristic protected by applicable federal, state, or local laws and ordinances (referred to as “protected characteristics”).  Employment actions are based upon our operating needs and individual employee or applicant merit, including but not limited to: qualifications, experience, ability, availability, cooperation and job performance. 

Statements in this job description are not intended to be an exhaustive list of all duties, responsibilities, and skills required.  Management maintains the right to assign or reassign duties and responsibilities to this job at any time.   The Physical Requirements and Working Conditions section are intended to describe the nature of work and the minimum requirements of the job in general.  Physical Requirements and Working Conditions based on product(s) handled, equipment used and customer requirements.  

Published Date: May 7th, 2026

Employee Health and Safety Specialist

Employee Health and Safety Specialist

Location: Farmingdale, NJ   
Employment Type: Full-Time/On Site   

Schedule: Mon-Thurs 3:15 PM – 1:45 AM (2nd Shift) 
Pay Rate: $25-$30 per hour  
 

Company Overview:

NutraStar is a fast-growing contract manufacturer specializing in the formulation and production of high-quality nutraceuticals. With more than 300 employees and a reputation built on customer service, precision, quality, and innovation, we serve some of the most respected brands in the health and wellness industry. Our continued investment in people, technology, and infrastructure drives our rapid growth and positions us as leaders in our field.

Position Summary

The Safety & Environmental Specialist is responsible for developing, implementing, and maintaining workplace safety, environmental compliance, and risk management programs within a manufacturing facility. This role ensures compliance with all applicable federal, state, and local safety and environmental regulations while promoting a culture of safety, sustainability, and continuous improvement across the organization.

The ideal candidate is highly organized, detail-oriented, and experienced in manufacturing safety programs, regulatory compliance, incident investigation, and employee training.

Key Responsibilities

Safety Management

  • Develop, implement, and maintain site safety policies, procedures, and programs in compliance with regulatory requirements and company standards.
  • Ensure compliance with Occupational Safety and Health Administration (OSHA) standards and other applicable workplace safety regulations.
  • Conduct routine safety inspections, audits, and risk assessments throughout the manufacturing facility.
  • Identify workplace hazards and recommend corrective and preventive actions.
  • Lead incident, accident, near-miss, and injury investigations to determine root causes and implement corrective actions.
  • Manage safety documentation including injury logs, corrective action reports, and inspection records.
  • Oversee programs including Lockout/Tagout (LOTO), machine guarding, PPE compliance, confined space, hazard communication, and ergonomics.

Environmental Compliance

  • Ensure compliance with environmental regulations established by the Environmental Protection Agency (EPA), state agencies, and local authorities.
  • Manage waste disposal programs, recycling initiatives, and hazardous material handling procedures.
  • Coordinate with external agencies during inspections or compliance reviews.

Training & Employee Engagement

  • Develop and deliver safety orientation and ongoing training programs for employees, supervisors, and contractors.
  • Facilitate emergency response drills, evacuation procedures, and safety meetings.
  • Promote employee participation in safety committees and continuous improvement initiatives.
  • Create safety communications, alerts, and awareness campaigns.

Reporting & Continuous Improvement

  • Track and analyze safety metrics, incident trends, and environmental performance data.
  • Prepare monthly, quarterly, and annual EHS reports for leadership review.
  • Recommend improvements to reduce injuries, environmental impact, and operational risks.
  • Support sustainability initiatives and continuous improvement projects.

Qualifications

Education

  • Bachelor’s degree in Environmental Health & Safety, Environmental Science, Industrial Safety, Engineering, or related field preferred.
  • Equivalent combination of education and experience may be considered.

Experience

  • 3–5+ years of Environmental, Health, and Safety (EHS) experience in a manufacturing environment required.
  • Experience with regulatory inspections, audits, and compliance reporting.
  • Experience conducting incident investigations and root cause analysis.

Preferred Certifications

  • Board of Certified Safety Professionals certifications such as CSP, ASP, CHMM, or equivalent preferred.
  • First Aid/CPR certification preferred.

Technical Skills

  • Knowledge of OSHA, EPA, and state environmental regulations.
  • Experience with risk assessments, safety audits, and environmental reporting systems.
  • Proficiency in Microsoft Excel, Microsoft Word, and incident management systems.
  • Strong analytical, organizational, and problem-solving skills.

Core Competencies

  • Leadership and influence
  • Attention to detail
  • Regulatory compliance
  • Communication and training
  • Root cause analysis
  • Continuous improvement
  • Emergency preparedness

Physical Requirements

  • Ability to walk manufacturing floors for extended periods.
  • Ability to occasionally lift up to 25 pounds.
  • Ability to wear required PPE and work in production environments.

Work Environment

This position operates in both office and manufacturing settings with exposure to machinery, noise, forklifts, chemicals, and varying temperatures. Appropriate PPE must be worn when entering production areas.

Why Join NutraStar?

As a growing leader in the nutraceutical industry, NutraStar offers the opportunity to contribute to high-impact quality initiatives while working in a collaborative and safety-focused environment. You’ll play a vital role in ensuring product quality for customers worldwide.

NutraStar is an equal opportunity employer. Employment at our Company is based solely on job-related qualifications

Published Date: May 11th, 2026

ERP/DECOM Data Specialist

Location: Farmingdale, NJ

Employment Type: Full-Time/On Site

Schedule: Mon-Thurs 8:00 AM – 5:00 PM & Friday 8:00am-2:00pm

Pay Rate: $65,000-$85,000 Yearly

Company Overview:

NutraStar is a fast-growing contract manufacturer specializing in the formulation and production of high-quality nutraceuticals. With more than 300 employees and a reputation built on customer service, precision, quality, and innovation, we serve some of the most respected brands in the health and wellness industry. Our continued investment in people, technology, and infrastructure drives our rapid growth and positions us as leaders in our field.

Position Description

The ERP / Data Specialist is responsible for maintaining the accuracy, integrity, and efficiency of data within the company’s Enterprise Resource Planning (ERP) system. This role supports cross-functional teams by managing data entry, system updates, reporting, and continuous improvement initiatives to optimize business processes.

Key Responsibilities

  • Lead end-to-end implementation of the DEACOM ERP system, including planning, configuration, testing, and deployment
  • Maintain and update data within the ERP system (items, BOMs, vendors, customers, pricing, etc.)
  • Ensure data accuracy, consistency, and integrity across all system modules
  • Perform regular data audits and resolve discrepancies
  • Support ERP implementation, upgrades, and system enhancements
  • Collaborate with departments such as Operations, Finance, Supply Chain, and Sales to gather data requirements
  • Generate and analyze reports to support business decisions
  • Assist in developing and documenting standard operating procedures (SOPs) for data management
  • Provide end-user support and basic training on ERP system usage
  • Troubleshoot data-related issues and escalate system concerns when needed
  • Support data migration, cleansing, and validation efforts
  • Monitor system workflows and recommend process improvements
  • Collaborate with stakeholders to gather and document business requirements
  • Translate business needs into system configurations and process improvements
  • Conduct system testing, validation, and troubleshooting to ensure accuracy and performance
  • Train end users and provide ongoing support post-implementation
  • Assist with data migration, system integration, and upgrades
  • Develop and maintain system documentation, SOPs, and training materials
  • Identify opportunities to improve workflows and increase system efficiency
  • Work closely with IT, operations, finance, and supply chain teams

Qualifications

  • Bachelor’s degree in information technology, Computer Science, or related field (or equivalent experience)
  • 3+ years of experience in IT roles with exposure to system decommissioning
  • 3+ years of experience with ERP systems, preferably DEACOM
  • Experience with ERP implementation and system configuration
  • Strong understanding of manufacturing, inventory, or distribution processes
  • Excellent problem-solving and analytical skills
  • Strong communication and stakeholder management skills
  • Ability to manage multiple projects and deadlines
  • Experience with data migration, archival, and lifecycle management
  • Experience with ERP implementation or system integration projects
  • Familiarity with data governance best practices
  • Experience with reporting tools (Power BI, Tableau, etc.)
  • Solid understanding of IT infrastructure, databases, and application dependencies
  • Strong attention to detail, ability to influence without authority, and patience in stressful situations.

Why Join NutraStar?

As a growing leader in the nutraceutical industry, NutraStar offers the opportunity to contribute to high-impact quality initiatives while working in a collaborative and safety-focused environment. You’ll play a vital role in ensuring product quality for customers worldwide.

NutraStar is an equal opportunity employer. Employment at our Company is based solely on job-related qualifications

Published Date: April 30th, 2026

Machine Operator Encapsulation

Location: Farmingdale, NJ  
Employment Type: Full-Time/On Site  
Schedule:  Mon-Thurs 3:30 PM – 2:00 AM 
Pay Rate: $18.50 per hour 

NutraStar is a fast-growing contract manufacturer specializing in the formulation and production of high-quality nutraceuticals. With more than 300 employees and a reputation built on customer service, precision, quality, and innovation, we serve some of the most respected brands in the health and wellness industry. Our continued investment in people, technology, and infrastructure drives our rapid growth and positions us as a leader in our field

About the Role

As Machine Operator, you will be responsible for setting up and operating tablet press equipment that produces dietary supplements in tablet and pill forms. You will also be responsible for cleaning the manufacturing equipment, utensils, and the room in which you operate.

Key Responsibilities:

  • Operate and clean manufacturing encapsulation and/or room and equipment
  • Transport blended materials from staging area to encapsulation and/or compression room
  • Verify all blend materials for accuracy and quantities received
  • Operate encapsulation and/or tablet press machines as per product batch record following Standard Operating Procedures
  • Document all process readings in the manufacturing batch record
  • Perform changeover and set-up of designated manufacturing equipment
  • Practice Good Manufacturing procedure as trained in cGMP training
  • Required to wear appropriate safety equipment and adhere to safety procedures and Federal and State regulations
  • Monitor encapsulation machine operation and report any abnormal conditions to the immediate Supervisor
  • Assist manufacturing supervisor in the collection of information to conduct investigations
  • Follow procedures described in SOP’s and report deviations to the immediate supervisor
  • Facilitate and cooperate with any Continuous Improvement Program
  • Perform other duties as assigned by supervisor

Requirements:

  • Must be able to read, write, and speak English.
  • Highschool diploma or equivalent
  • Entry level position, Experience is not required
  • At least 1 year in manufacturing or production environment a plus
  • Physical ability to: Lift/push/pull up to 25 lbs frequently and up to 50 lbs occasionally. Stand for extended periods. Work in an environment with powders, chemicals, and common allergens.

Why Join NutraStar?

As a growing leader in the nutraceutical industry, NutraStar offers the opportunity to contribute to high-impact quality initiatives while working in a collaborative and safety-focused environment. You’ll play a vital role in ensuring product quality for customers worldwide.

NutraStar is an equal opportunity employer. Employment at our Company is based solely on job-related qualifications

Published Date: January 15th, 2026

Porter

Location: Farmingdale, NJ  
Employment Type: Full-Time/On Site  
Schedule: 7:00 AM – 3:00 PM (Monday – Thursday) / 8:00 AM – 2:00 PM (Friday)
Pay Rate: $16.00 – $18.00 Hourly

NutraStar is a fast-growing contract manufacturer specializing in the formulation and production of high-quality nutraceuticals. With more than 300 employees and a reputation built on customer service, precision, quality, and innovation, we serve some of the most respected brands in the health and wellness industry. Our continued investment in people, technology, and infrastructure drives our rapid growth and positions us as leaders in our field.

About the Role:

The porter is responsible for maintaining the cleanliness and safety of our offices, production, and packaging areas. The person in this role will safely perform manual tasks with speed and efficiency, ensuring work environments are healthy and safe for all employees. The porter may also assist with basic maintenance, deliveries, and support tasks as needed. 

Key Responsibilities:

  • Maintain cleanliness and sanitation in assigned areas, including offices, hallways, restrooms, production, packaging, and public spaces. 
  • Sweep, mop, vacuum, and dust floors and surfaces regularly. 
  • Collect garbage, trash, and recyclables, and assist in transporting them to disposal or management areas. 
  • Dispose of trash and recycling in accordance with company policies. 
  • Perform cleaning and maintenance tasks, including dumpster cleaning, bathroom cleaning, mopping tile, vacuuming carpets, and other assigned duties. 
  • Assist with moving furniture, equipment, and supplies as required. 
  • Stock and replenish cleaning supplies and other necessary items. 
  • Carry out routine inspections and document maintenance and cleaning activities. 
  • Perform deep cleaning tasks and special projects as assigned. 
  • Report maintenance issues, safety hazards, or damaged equipment to supervisors. 
  • Support events, deliveries, or other operational activities as needed. 
  • Follow all safety guidelines and procedures, including proper use of Personal Protective Equipment (PPE), to maintain a safe working environment.

Qualifications:

  • Porter Experience
  • Bilingual in both Spanish and English 
  • Ability to effectively communicate to keep others informed of progress and changes in work status
  • Physical ability to lift and carry up to 50 pounds
  • Knowledge and practice of safety procedures and proper PPE usage

Why Join NutraStar?

As a growing leader in the nutraceutical industry, NutraStar offers the opportunity to contribute to high-impact quality initiatives while working in a collaborative and safety-focused environment. You’ll play a vital role in ensuring product quality for customers worldwide.

NutraStar is an equal opportunity employer. Employment at our Company is based solely on job-related qualifications

Published Date: January 15th, 2026

QC Chemist

Location: Farmingdale, NJ  
Employment Type: Full-Time/On Site  
Schedule: 10:00 AM – 7:00 PM (Monday – Thursday) / 8:00 AM – 2:00 PM (Friday)
Pay Rate:  $65,000.00 – $75,000.00 Annually

About the Role:

Are you a meticulous and proactive analytical chemist with a passion for quality? We are seeking a dedicated QC Chemist to join our Quality Control Laboratory team. You will play a crucial role in ensuring the quality of our raw materials and finished products through precise laboratory testing and diligent adherence to quality standards.

Key Responsibilities:

  • Performing analytical testing of raw materials and finished products in accordance with established procedures and specifications. Techniques may include HPTLC, UV-Vis, FTIR, and Performing analytical testing of raw materials and finished products in accordance with established procedures and specifications. Techniques may include HPTLC, UV-Vis, FTIR, and Wet Chemistry.
  • Operating and maintaining laboratory equipment.
  • Conducting and managing ‘Out of Specification’ (OOS) and ‘Awaiting Disposition’ Investigations, including root cause analysis and corrective action planning.
  • Assisting with out of specification investigations. Bench-level OOS investigation experience is strongly preferred.
  • Method development, validation, and implementation. Experience with method development and validation is desirable.
  • Managing samples, including receipts, processing, archival, and maintenance of tracking tools.
  • Preparation and review of test records associated with raw material release and Certificates of Analysis (COA).
  • Routine laboratory maintenance, including inventory, waste management, equipment verification, and coordination of services.
  • Adhering to laboratory safety protocols and maintaining a clean and organized work environment.
  • Supporting swing shift operations or after-hours testing to manage critical testing outside standard hours (Mon-Thu 10:00am-7:00pm; Friday 8:00am-2:00pm flexibility is required).

Qualifications:

  • Education/Experience: Bachelor’s degree in a related field.
  • Specialized Knowledge (Preferred): Proficiency in analytical chemistry, ideally within the nutraceutical or pharmaceutical industry.
  • HPTLC and metals testing experience is strongly desired.
  • Familiarity with cGMP, FDA, ISO/IEC 17025, and food safety regulations.
  • Experience with laboratory document control systems.
  • Proficiency in Microsoft Office, Excel, SharePoint, and laboratory data entry systems.

Other Requirements:

  • Strong attention to detail.
  • Excellent time management and prioritization skills.
  • Ability to work independently with minimal supervision and collaboratively as part of a team.

Why Join NutraStar?

As a growing leader in the nutraceutical industry, NutraStar offers the opportunity to contribute to high-impact quality initiatives while working in a collaborative and safety-focused environment. You’ll play a vital role in ensuring product quality for customers worldwide.

Published Date: April 27th, 2026

Quality Release Specialist

Quality Control Release Specialist
Location: Farmingdale, NJ  
Employment Type: Full-Time/On Site 

Schedule:  Mon-Thurs 8:00 AM – 5:00 PM, Fri 8:00 AM – 2:00 PM

Pay Rate:  $65,000.00 – $70,000.00 Hourly

Hour Per Week: 40 hours per week

 
 
NutraStar is a fast-growing contract manufacturer specializing in the formulation and production of high-quality nutraceuticals. With more than 300 employees and a reputation built on customer service, precision, quality, and innovation, we serve some of the most respected brands in the health and wellness industry. Our continued investment in people, technology, and infrastructure drives our rapid growth and positions us as a leader in our field
 
About the role
 
The Quality COA Specialist plays a critical role in ensuring the quality and compliance of products and services by preparing, reviewing, and maintaining accurate and complete Certificates of Analysis (COAs) and Batch Production Records (BPRs) for manufactured batches in accordance with cGMP. This role involves collaborating with various departments to ensure that COAs are generated and maintained in accordance with industry standards and company policies. In addition to performing the QA review of batch records for final products and reviews and evaluates QC data to ensure that lots meet applicable cGMP requirements prior to release.
 
 
Key Responsibilities:
 
Prepare and review COAs for various products and services, ensuring accuracy, completeness, and compliance with relevant regulations and standards. 
Gather and analyze data from testing and inspection activities to support COA generation. ·
Maintain a comprehensive understanding of product specifications, testing protocols, and acceptable limits.
 Conduct routine inspections and quality checks to ensure products meet established quality standards.
Maintain accurate and organized records of COAs, test results, and other relevant documentation.
Ensure QA checklist is adequate and comprehensive to enable batch disposition
Writes, reviews and revises SOPs as required
Perform duties as assigned by QA Management
Collaborate with other departments, including production, laboratory, and sales, to ensure smooth COA processes.
Prepare and present quality reports and summaries to management and other stakeholders.
Communicate quality issues and concerns effectively to relevant personnel.
Strong Communication, both verbal and written
Flexible and open to change
Team skills and tolerance
Attention to detail.
Patience and the ability to remain calm in stressful situations.
Ability to work well with others.
Must be able to read, analyze and review batch records and lab reports.
Process Improvement approach to responsibilities
 
Qualifications
 
Bachelor’s degree (preferred) in Food Science or related field.
2+ years’ experience in GMP or FDA regulated industry.
Basic math and computer skills.
Ability to work as part of team and adapt to changes in work duties.
Detail-oriented, thorough, and methodical, and able to follow timeline.
Ability to handle multiple tasks and priorities with excellent time management.
Must be able to influence others without authority.
 
Additional Requirements
 
Proficiency in a specific laboratory software or data analysis tool.
Microsoft Office Suite, Outlook
Trained and well versed on the DEACOM (ERP) application.
21 CFR 111 cGMP in Manufacturing, Packaging, or Holding Operations for Dietary Supplements
FSSC 22000 Food Safety Management System
7 CFR 205 National Organic Program (NOP)
 
Why Join NutraStar?

NutraStar is an equal opportunity employer. Employment at our Company is based solely on job-related qualifications: we recruit, hire, train, promote and compensate our employees and provide all other conditions of employment including company sponsored events without regard to race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth and related medical conditions), gender identity or gender expression (including transgender status), sexual orientation, marital status, military service and veteran status, physical or mental disability, protected medical condition as defined by applicable state or local law, genetic information, or any other characteristic protected by applicable federal, state, or local laws and ordinances (referred to as “protected characteristics”).  Employment actions are based upon our operating needs and individual employee or applicant merit, including but not limited to: qualifications, experience, ability, availability, cooperation and job performance. 
 
Statements in this job description are not intended to be an exhaustive list of all duties, responsibilities, and skills required.  Management maintains the right to assign or reassign duties and responsibilities to this job at any time.   The Physical Requirements and Working Conditions section are intended to describe the nature of work and the minimum requirements of the job in general.  Physical Requirements and Working Conditions based on product(s) handled, equipment used and customer requirements.  
 
 
 
 

Published Date: May 7th, 2026

Quality Control Inspector 

Quality Control Inspector 

Location: Farmingdale, NJ  

Employment Type: Full-Time/On Site  

Schedule: Mon-Thurs 5:00 AM – 3:30 PM (1st Shift); 3:30 PM – 2:00 AM (2nd Shift)  

Pay Rate: $20.50-$23.50 Hourly  

Company Overview: 

NutraStar is a fast-growing contract manufacturer specializing in the formulation and production of high-quality nutraceuticals. With more than 300 employees and a reputation built on customer service, precision, quality, and innovation, we serve some of the most respected brands in the health and wellness industry. Our continued investment in people, technology, and infrastructure drives our rapid growth and positions us as a leader in our field. 

Position Description 

We are currently looking for a bilingual Quality Control Inspector to join our team, with openings available for both our 1st and 2nd shifts. This role is essential to our Quality Control Compliance, involving the review of batch records and the inspection of production at every stage—from blending and encapsulation to packaging. The ideal candidate will thrive in a team-oriented environment and ensure our products meet the highest standards of quality, integrity, and safety.  

Key Responsibilities: 

  • Adhere to Standard Operating Procedures (SOPs) and Good Manufacturing Practices (cGMP).  
  • Conduct thorough inspections of staged raw materials, in-process components, and finished products.  
  • Perform routine in-process checks and inspect lines or room clearances for pharmacy, blending, and packaging.  
  • Review batch records and reconciliation data across all phases of the manufacturing process.  
  • Accurately document inspection results, deviations, and quality control activities (sample logs, retains, cleaning logs).  
  • Monitor facility temperatures and ensure the correct retention of all process samples.  
  • Communicate quality defects promptly to supervisors and collaborate with cross-functional teams.  
  • Assist in investigations for customer complaints, deviations, or CAPA by providing necessary information or samples.  
  • Maintain a clean and safe work environment and follow all biohazard safety standards and OSHA precautions.  
  • Demonstrate a commitment to the organization through regular on-site attendance and reliable follow-through.  

Qualifications: 

  • Bilingual; must be able to read and write English.  
  • At least 1 year of experience in production batch record review and/or incoming inspection.  
  • Experience in Quality or Manufacturing within a cGMP environment.  
  • Proficient in Microsoft Office, with strong experience in Excel.  
  • Knowledge of quality systems, Good Documentation Practice (GDP), and relevant regulations (21 CFR 111, FSSC 22000).  
  • Strong organizational skills, attention to detail, basic math, and the ability to multitask in a fast-paced environment.  
  • Physical: Ability to stand for extended periods and lift, push, or pull products.  

Why Join NutraStar? 

As a growing leader in the nutraceutical industry, NutraStar offers the opportunity to contribute to high-impact quality initiatives while working in a collaborative and safety-focused environment. You’ll play a vital role in ensuring product quality for customers worldwide. 

NutraStar is an equal opportunity employer. Employment at our Company is based solely on job-related qualifications 

Published Date: May 6th, 2026

Quality Control Microbiologist

Quality Control Microbiologist

Location: Farmingdale, NJ  

Employment Type: Full-Time/On Site  

Pay Rate:  $65,000.00 – $75,000.00 Annually

NutraStar is a fast-growing contract manufacturer specializing in the formulation and production of high-quality nutraceuticals. With more than 300 employees and a reputation built on customer service, precision, quality, and innovation, we serve some of the most respected brands in the health and wellness industry. Our continued investment in people, technology, and infrastructure drives our rapid growth and positions us as a leader in our field

About the Role:

NutraStar is seeking a highly skilled and detail-oriented QC Microbiologist to join our Quality Control Laboratory team. This role is responsible for performing a broad range of microbiological tests to ensure the quality, safety, and compliance of raw materials, components, and finished products. The QC Microbiologist plays a key role in maintaining laboratory compliance with cGMP, FDA, ISO/IEC 17025, and food safety standards.

This position requires strong analytical skills, excellent documentation practices, and the ability to support after-hours testing when necessary.

Key Responsibilities

•            Perform microbiological testing of raw materials and finished products following established SOPs and specifications.

•            Conduct microbial enumeration and identification, water quality testing, method development, and validation activities.

•            Manage sample receipt, handling, tracking, and archival.

•            Lead and support Out of Specification (OOS) and Awaiting Disposition investigations, including root cause analysis and corrective actions.

•            Prepare and review test records and Certificates of Analysis (COAs).

•            Maintain laboratory documentation, inventory, equipment, and biosafety compliance.

•            Prepare and coordinate samples requiring external microbiological testing.

•            Operate and maintain laboratory equipment, including autoclaves, incubators, and other analytical systems.

•            Follow all safety protocols, including PPE requirements and biohazard procedures.

•            Support after-hours sample processing and critical testing as needed.

•            Collaborate with cross-functional teams across Quality, Production, and R&D.

Qualifications

•            Bachelor’s degree in microbiology, Biology, or a related field.

•            Proficiency in microbiology; nutraceutical or pharmaceutical experience preferred.

•            Experience conducting OOS investigations required; bench-level microbiology strongly preferred.

•            Experience with microbial identification methods (plating, microscopy, rapid ID systems) is a plus.

•            Familiarity with cGMP, FDA, ISO/IEC 17025, and food safety regulations.

•            Strong attention to detail, documentation accuracy, and time management skills.

•            Ability to work independently and collaboratively.

•            Proficiency in Microsoft Office Suite, SharePoint, and laboratory information systems.

•            Ability to work in a laboratory environment exposed to powders, chemicals, and potential allergens.

Physical Requirements

•            Ability to stand for extended periods.

•            Ability to occasionally lift, push, or pull up to 50 lbs.

•            Capability to work in a manufacturing plant environment and perform repetitive motions.

Why Join NutraStar?

NutraStar is an equal opportunity employer. Employment at our Company is based solely on job-related qualifications: we recruit, hire, train, promote and compensate our employees and provide all other conditions of employment including company sponsored events without regard to race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth and related medical conditions), gender identity or gender expression (including transgender status), sexual orientation, marital status, military service and veteran status, physical or mental disability, protected medical condition as defined by applicable state or local law, genetic information, or any other characteristic protected by applicable federal, state, or local laws and ordinances (referred to as “protected characteristics”).  Employment actions are based upon our operating needs and individual employee or applicant merit, including but not limited to: qualifications, experience, ability, availability, cooperation and job performance. 

Published Date: May 14th, 2026

Quality Control Supervisor

Location: Farmingdale, NJ

Employment Type: Full-Time/On Site

Schedule: Mon-Thurs 5:00 AM – 3:30 PM (1st Shift)

Pay Rate: TBD

Company Overview:

NutraStar is a fast-growing contract manufacturer specializing in the formulation and production of high-quality nutraceuticals. With more than 300 employees and a reputation built on customer service, precision, quality, and innovation, we serve some of the most respected brands in the health and wellness industry. Our continued investment in people, technology, and infrastructure drives our rapid growth and positions us as a leader in our field.

Position Description

The Quality Control Supervisor is responsible for ensuring that products and services meet established standards set by the customer. This role involves training plant operators to maintain strong overall quality control during staging, blending, production, and packaging. The Supervisor ensures all products adhere to regulations, performance requirements, and customer expectations while overseeing the performance of Quality Control Coordinators and Inspectors.

Key Responsibilities

  • Instruct and train quality inspectors and operators on inspection procedures and audit processes.
  • Ensure all plant operators are trained in the quality expectations of their specific roles.
  • Manage personnel availability to ensure inspection coverage for every production line and shift.
  • Complete and retain all training records in accordance with company procedures.
  • Support and conduct annual SOP/GMP/GDP training across all departments.
  • Assist in investigations for Customer Complaints by providing required quality data.
  • Review production batch records in a timely manner to ensure accuracy and compliance.
  • Systematically manage the hold and release process for items and communicate status to facility leadership.
  • Communicate quality defects directly to management as needed.
  • Adhere to Standard Operating Procedures (SOPs) and Good Manufacturing Practices (GMP).
  • Oversee the sample process to the Quality Lab and manage the OOS (Out of Specification) investigation process.
  • Ensure the maintenance and management of all retain samples.
  • Support and develop team members through leadership and coaching.
  • Maintain regular, on-site attendance and follow through on all professional responsibilities.
  • Reduce customer complaints related to product defects, bottle counts, and case packing.
  • Improve the overall accuracy and completion of Batch Records.

Qualifications

  • Bachelor’s degree in Food Science or a related field preferred.
  • 2+ years of experience in a GMP or FDA-regulated industry.
  • Basic math, Microsoft Office Suite (Outlook), and proficiency in DEACOM (ERP) applications.
  • Strong attention to detail, ability to influence without authority, and patience in stressful situations.
  • Adhere to all company safety policies, wear required PPE, and report unsafe conditions immediately.
  • Must adhere to 21 CFR 111 (cGMP), 7 CFR 205 (National Organic Program), and 9 CFR 417 (HACCP).

Why Join NutraStar?

As a growing leader in the nutraceutical industry, NutraStar offers the opportunity to contribute to high-impact quality initiatives while working in a collaborative and safety-focused environment. You’ll play a vital role in ensuring product quality for customers worldwide.

NutraStar is an equal opportunity employer. Employment at our Company is based solely on job-related qualifications

Published Date: April 23rd, 2026

Position You're Applying For*