FULL_TIME

FEED

YEAR

Associate’s degree or coursework in a scientific discipline (Biology, Chemistry, Food Science, or related field) preferred. This role ensures all products are manufactured in compliance with current Good Manufacturing Practices (cGMP) as outlined in 21 CFR Part 111.

<div style="border-bottom:solid #1b5e7b 1pt;padding:0in 0in 4pt 0in"><div style="border-bottom:solid #1b5e7b 1pt;padding:0in 0in 4pt 0in">SUN NUTRACEUTICALS Sun Nutraceuticals is a growing manufacturer of dietary supplements. We are seeking a reliable & motivated Quality Inspector to join our team. If you have a strong work ethic, a positive attitude, and a willingness to learn, this is an excellent opportunity to grow with a company that values hard work and promotes from within. POSITION SUMMARY The Quality Inspector is responsible for performing in-process and finished product inspections throughout the dietary supplement manufacturing facility. This role ensures all products are manufactured in compliance with current Good Manufacturing Practices (cGMP) as outlined in 21 CFR Part 111. The Quality Inspector plays a critical role in maintaining product quality, safety, and regulatory compliance.  ESSENTIAL DUTIES & RESPONSIBILITIES</div><ul style="margin-top:4px;margin-bottom:4px"><li>Conduct in-process inspections during manufacturing and packaging operations to ensure adherence to batch records and standard operating procedures (SOPs).</li><li style="margin-top:4px;margin-bottom:4px;margin-left:8px">Perform visual and physical inspections of incoming raw materials, in-process intermediates, and finished products for quality, and compliance with specifications.</li><li style="margin-top:4px;margin-bottom:4px;margin-left:8px">Verify line clearances and room clearances prior to the start of each production run to prevent cross-contamination.</li><li style="margin-top:4px;margin-bottom:4px;margin-left:8px">Review and verify batch production records, labels, and packaging materials for accuracy and completeness.</li><li style="margin-top:4px;margin-bottom:4px;margin-left:8px">Collect and submit samples for laboratory testing, including identity, potency, purity, and microbiological analysis.</li><li style="margin-top:4px;margin-bottom:4px;margin-left:8px">Initiate and support investigations for out-of-specification (OOS) results & deviations. </li><li style="margin-top:4px;margin-bottom:4px;margin-left:8px">Monitor environmental conditions (temperature, humidity) and sanitation practices within production areas.</li><li style="margin-top:4px;margin-bottom:4px;margin-left:8px">Verify that equipment calibration, cleaning, and maintenance records are current and complete.</li><li style="margin-top:4px;margin-bottom:4px;margin-left:8px">Communicate quality issues and trends to production staff and QA management in a timely manner.</li></ul><div style="border-bottom:solid #1b5e7b 1pt;padding:0in 0in 4pt 0in">QUALIFICATIONS & REQUIREMENTS</div>Education<ul style="margin-top:4px;margin-bottom:4px"><li style="margin-top:4px;margin-bottom:4px;margin-left:8px">High school diploma or GED required.</li><li style="margin-top:4px;margin-bottom:4px;margin-left:8px">Associate’s degree or coursework in a scientific discipline (Biology, Chemistry, Food Science, or related field) preferred.</li></ul>Experience<ul style="margin-top:4px;margin-bottom:4px"><li style="margin-top:4px;margin-bottom:4px;margin-left:8px">0–2 years of experience in a quality or manufacturing within a cGMP-regulated environment preferred.</li><li style="margin-top:4px;margin-bottom:4px;margin-left:8px">Dietary supplement, pharmaceutical, or food manufacturing experience is a plus.</li></ul>Knowledge & Skills<ul style="margin-top:4px;margin-bottom:4px"><li style="margin-top:4px;margin-bottom:4px;margin-left:8px">Basic understanding of cGMP regulations under 21 CFR Part 111 (training provided).</li><li style="margin-top:4px;margin-bottom:4px;margin-left:8px">Strong attention to detail and ability to follow written procedures accurately.</li><li style="margin-top:4px;margin-bottom:4px;margin-left:8px">Effective written and verbal communication skills for documentation and reporting.</li><li style="margin-top:4px;margin-bottom:4px;margin-left:8px">Ability to work independently and collaboratively in a fast-paced manufacturing environment.</li></ul><div style="border-bottom:solid #1b5e7b 1pt;padding:0in 0in 4pt 0in">PHYSICAL REQUIREMENTS & WORKING CONDITIONS</div><ul style="margin-top:4px;margin-bottom:4px"><li style="margin-top:4px;margin-bottom:4px;margin-left:8px">Ability to stand and walk for extended periods (up to 8 hours per shift).</li><li style="margin-top:4px;margin-bottom:4px;margin-left:8px">Ability to lift and carry up to 40 lbs.</li><li style="margin-top:4px;margin-bottom:4px;margin-left:8px">Work is performed on the manufacturing floor; exposure to powders, capsules, and cleaning agents is expected.</li><li style="margin-top:4px;margin-bottom:4px;margin-left:8px">Must be able to wear required personal protective equipment (PPE), including hairnets, gloves, safety glasses, and steel-toed shoes.</li><li style="margin-top:4px;margin-bottom:4px;margin-left:8px">May be required to work rotating shifts, weekends, or overtime based on production schedules.</li></ul></div>Powered by JazzHR

Sun Nutraceuticals

Quality Inspector - Dietary Supplement Manufacturing

Analysis Skills

Biology

Biotech and Pharmaceutical

Calibration

Capsules

Chemistry

Cleaning Equipment

Code of Federal Regulations

Communication Skills

Current Good Manufacturing Practice (cGMP)

Detail Oriented

Documentation

Environmental Monitoring

Food Production

Food Science

High School Diploma

Housekeeping/Cleaning

Laboratory Testing

Lift/Move 40 Pounds

Maintain Compliance

Manufacturing

Manufacturing Operations

Microbiology

People Management

Physical Demands

Presentation/Verbal Skills

Process Manufacturing

Product Packaging

Product Safety

Quality Assurance

Quality Control

Quality Management

Record Keeping

Regulatory Compliance

Safety Compliance

Sanitation

Specimen Collection

Standard Operating Procedures (SOP)

Time Management

Writing Skills

partner JazzHR

OTHER

UNKNOWN

Monitor the behavior and activities of clients by patrolling the perimeter and dorms, reporting any concerns to clinical staff regarding the health, safety, or wellbeing of clients. House of Hope, a non-profit organization, is seeking a part-time weekends only Behavioral Health Technician (BHT) to join our team!

Benefits: <ul><li>Free uniforms</li></ul> 

 A passion for helping others, the ability to adapt in diverse settings, possess strong interpersonal skills and looking to join an amazing team. Are these the characteristics that are often used to describe you?  If your answer is yes, this could be the opportunity you’ve been searching for! House of Hope, a non-profit organization, is seeking a part-time weekends only Behavioral Health Technician (BHT) to join our team! The Behavioral Health Technician (BHT) position involves ensuring the provision of a safe and therapeutic environment for clients. Part-time shifts currently available Weekends Only Friday, Saturday and Sunday (Required) - 7am-3pm & 3pm-11pm  Experience, Knowledge, and Skills: ·         High School Diploma or equivalent required. ·         One year of BHT experience preferred. ·         Experience working with the substance abuse population preferred. ·         Excellent verbal and written skills. ·         Computer literate. Duties and Responsibilities: <ul><li>Monitor the behavior and activities of clients by patrolling the perimeter and dorms, reporting any concerns to clinical staff regarding the health, safety, or wellbeing of clients.</li><li>Provide clients with training or assistance with basic daily living skills and personal hygiene services as needed.</li><li>Provide positive reinforcement and support clients.</li><li>Performs other BHT responsibilities as assigned.</li></ul>

House of Hope Inc

Behavioral Health Technician (BHT) - Part-time Friday-Sunday Only

Behavioral Health

Computer Skills

Customer Support/Service

Interpersonal Skills

Nonprofit

Safety/Work Safety

Substance Abuse

Training/Teaching

The successful candidate will bring deep validation expertise, the ability to build and continuously improve systems, and a proven track record of technical problem-solving in cosmetic and OTC drug manufacturing operations. Maintain and demonstrate expertise in applicable regulatory requirements GMP, FDA regulations (21 CFR Parts 11/210/211), and ISO 22716 for cosmetics and OTC drug products.

Job Summary: Validation Quality Engineer will serve as the subject matter expert (SME) and technical owner of the Master Validation Program for PML’s manufacturing facilities. This role is responsible for authoring, executing, and overseeing validation protocols, reports, and supporting documentation to ensure facilities, utilities, manufacturing processes and equipment are qualified and compliant with OTC drug and cosmetic manufacturing regulatory standards. The successful candidate will bring deep validation expertise, the ability to build and continuously improve systems, and a proven track record of technical problem-solving in cosmetic and OTC drug manufacturing operations. This individual will play a critical role in ensuring inspection readiness, regulatory compliance, and continuous improvement across validation programs. The ideal candidate will monitor systems, equipment and processes, often collaborating with process engineers, operations, or quality personnel, to assess processes and parameters against industry standards, establish validation standards, and develop performance testing and quality control measures to ensure compliance with FDA regulations and GMP standards. This hands-on leadership role combines strategic and risk-based quality system management with operational oversight to ensure product safety, efficacy, and regulatory compliance throughout equipment, systems and process lifecycles. This position requires a detail-oriented leader who can balance operational excellence with regulatory requirements in a fast-paced, client-focused manufacturing environment. Essential Duties and Responsibilities:<ul><li style="text-align:justify">Develop, implement, and maintain PML’s Master Validation Program at PML’s facilities.</li><li style="border:none;text-align:justify">Lead and support commissioning, qualification, and validation (IQ/OQ/PQ) activities for facilities, utilities, manufacturing processes and equipment </li><li style="border:none;text-align:justify">Author, review, and execute validation documentation including protocols, reports, project plans, risk assessments, CAPAs, deviations, and change controls.</li><li style="border:none;text-align:justify">Serve as SME for validation within the change control process, providing technical oversight and guidance across cross-functional teams.</li><li style="border:none;text-align:justify">Assist in management and continuous improvement of calibration programs, ensuring adherence to schedules and regulatory requirements.</li><li style="border:none;text-align:justify">Develop and report on key metrics related to areas of responsibility, including statistical analysis as needed.</li><li style="text-align:justify">Lead and/or assist in investigations and resolution of quality issues through root cause analyses and determined corrective/preventive action (CAPA) initiatives</li><li style="border:none;text-align:justify">Assist in developing, monitoring, and acting on process data to drive continuous improvement.</li><li style="border:none;text-align:justify">Support audit and inspection readiness by presenting validation activities to regulatory authorities and customers; lead responses and corrective actions as required.</li><li style="border:none;text-align:justify">Partner with Quality, Manufacturing, Engineering, and site leadership to resolve technical issues, support process improvements, and foster a culture of compliance.</li></ul><ul><li style="text-align:justify">Maintain and demonstrate expertise in applicable regulatory requirements GMP, FDA regulations (21 CFR Parts 11/210/211), and ISO 22716 for cosmetics and OTC drug products.</li><li style="text-align:justify">Develop, review, write, and implement SOPs for quality validation functions.</li><li style="text-align:justify">Drive collection, analysis and trending of validation data, reports or Quality metrics </li><li style="text-align:justify">Aids in internal audit program, as well as regulatory and customer audit inspection readiness.</li><li style="text-align:justify">Provides training for other departments as needed.</li><li style="text-align:justify">Train and mentor cross-functional teams on validation and best practices.</li><li style="text-align:justify">Willingness to travel to company facilities as needed, up to 50%.</li></ul> Qualifications:<ul><li style="border:none;margin-left:8px;text-align:justify">Bachelor’s degree in Engineering or related field.</li><li style="border:none;text-align:justify">Minimum 3 years as a validation engineer in a regulated manufacturing environment preferred (cosmetics or OTC drugs a plus).</li><li style="border:none;text-align:justify">Extensive experience in equipment calibration and performance testing, advanced proficiency in data analysis tools and project management software, and in-depth knowledge of production processes and standards.</li><li style="border:none;text-align:justify">Exceptional analytical and problem-solving abilities, excellent leadership, communication and technical writing skills, and strong organizational abilities</li><li style="border:none;text-align:justify">Proven ability to work in a fast-paced, client-focused environment.</li></ul> Preferred Skills:<ul><li style="border:none;text-align:justify">Working knowledge of quality systems and regulatory requirements (21 CFR Part 11/ 210 / 211), including data integrity practices.</li><li style="border:none;text-align:justify">Experience working with cross-functional technology teams and enterprise systems.</li><li style="border:none;text-align:justify">Exceptional problem-solving skills, attention to detail, and the ability to manage multiple priorities in a fast-paced environment.</li><li style="border:none;text-align:justify">Strong attention to detail and organizational skills.</li><li style="border:none;text-align:justify">Effective written and verbal communication skills.</li><li style="border:none;text-align:justify">Proficiency in Microsoft Office and familiarity with electronic quality systems.</li></ul> Physical Requirements:<ul><li style="border:none;margin-left:2px;text-align:justify">Ability to lift and move objects weighing up to 25 pounds regularly and occasionally heavier items with assistance.</li><li style="border:none;margin-left:2px;text-align:justify">Ability to stand, walk, bend, stoop, push, and pull for extended periods during shifts.</li></ul><ul><li style="border:none;margin-left:2px;text-align:justify">Good understanding of safety protocols and practices.</li><li style="border:none;margin-left:2px;text-align:justify">Willingness to work flexible hours, including shifts and weekends.</li><li style="border:none;margin-left:2px;text-align:justify">Ability to work in a fast-paced environment and adapt to changing priorities.</li></ul> At Prime, we believe that a diverse, equitable and inclusive workplace makes us a more relevant, more competitive, and more resilient company. We welcome people from all backgrounds, ethnicities, cultures, and experiences. Prime is an equal opportunity employer.  Powered by JazzHR

Weekend Manufacturing Jobs in Lighthouse Point, FL

Resume Resources

Get noticed by top employers!

Weekend Manufacturing Jobs in Lighthouse Point, FL

Quality Inspector - Dietary Supplement Manufacturing Sun Nutraceuticals

Behavioral Health Technician (BHT) - Part-time Friday-Sunday Only House of Hope Inc

Validation Quality Engineer- Miami Gardens, Fl. Prime Matter Labs

Resume Resources