Quality technician jobs in Boynton Beach, FL - 175 jobs

Job DescriptionRo is a direct-to-patient healthcare company with a mission of helping patients achieve their health goals by delivering the easiest, most effective care possible. Ro is the only company to offer nationwide telehealth, labs, and pharmacy services. This is enabled by Ro's vertically integrated platform that helps patients achieve their goals through a convenient, end-to-end healthcare experience spanning from diagnosis, to delivery of medication, to ongoing care. Since 2017, Ro has helped millions of patients, including one in every county in the United States, and in 98% of primary care deserts. Ro has been recognized as a Fortune Best Workplace in New York and Health Care for four consecutive years (2021-2024). In 2023, Ro was also named Best Workplace for Parents for the third year in a row. In 2022, Ro was listed as a CNBC Disruptor 50. As a Quality Control (QC) Pharmacy Technician, you will be the on-site subject matter expert for quality control activities at our 503a compounding pharmacy located in Boynton Beach, FL. This role is responsible for quality oversight activities that ensure compounded processes are well documented and that products are handled and tested per facility SOPs. This position will be responsible for record review, raw material receipt and testing, product retains, product sampling and testing, lot release, and environmental monitoring. You will partner closely with pharmacy operations to ensure the pharmacy location maintains a high level of quality and compliance. This role will report to the Manager, Corporate Quality - Pharmacy on the Clinical team.What You'll Do Support QC oversight for compounding operations. Assist with development, support implementation, and maintain SOPs, Forms, Work Instructions and other required controlled documents. Own the finished product retain program, ensuring a sample of each compounded lot is retained per SOP. Conduct reviews of cleaning logs, compounding records, and other controlled records created throughout the facility. Assist in root cause investigations and continuous quality improvement initiatives. Assist in the execution of training on quality topics, functioning as the on-site SME for quality. Provide Pharmacy Compliance with requests arising from pharmacy inspections. Ensure the highest quality and cleanliness of the facility and equipment, leading our environmental monitoring program. Conduct Quality Assurance checks on relevant product batches according to predefined guidelines, reviewing final test results to perform lot release. What You'll Bring to the Team Bachelor's degree in any science discipline, preferred. Current pharmacy technician license in Florida or the ability to obtain pharmacy technician licensure, preferred. At least 3 years experience working in a manufacturing production environment or a high volume compounding pharmacy required. Experience working in a cGMP or 503B facility where PPE, cleanliness, and sterile sampling techniques are part of daily routine, required. Experience identifying need for and assisting in the creation of SOPs and other controlled documents. Knowledge of environmental monitoring in cGMP environments. Experience with Good Documentation Practices, preferred. Experience training others, preferred. Strong attention to detail and ability to think strategically and tactically. Outstanding written and verbal communication skills. Irrational passion for building the future of healthcare with an emphasis on quality processes to drive successful patient outcomes. We've Got You Covered Full medical, dental, and vision insurance + OneMedical membership Healthcare and Dependent Care FSA 401(k) with company match Flexible PTO Wellbeing + Learning & Growth reimbursements Paid parental leave + Fertility benefits Pet insurance Student loan refinancing Virtual resources for mindfulness, counseling, and fitness We welcome qualified candidates of all races, creeds, genders, and sexuality to apply. The target hourly rate for this position ranges from $30.43 to $36.78, in addition to a competitive equity and benefits package (as applicable). When determining compensation, we analyze and carefully consider several factors, including location, job-related knowledge, skills and experience. These considerations may cause your compensation to vary. Ro recognizes the power of in-person collaboration, while supporting the flexibility to work anywhere in the United States. For our Ro'ers in the tri-state (NY) area, you will join us at HQ on Tuesdays and Thursdays. For those outside of the tri-state area, you will be able to join in-person collaborations throughout the year (i.e., during team on-sites). At Ro, we believe that our diverse perspectives are our biggest strengths - and that embracing them will create real change in healthcare. As an equal opportunity employer, we provide equal opportunity in all aspects of employment, including recruiting, hiring, compensation, training and promotion, termination, and any other terms and conditions of employment without regard to race, ethnicity, color, religion, sex, sexual orientation, gender identity, gender expression, familial status, age, disability and/or any other legally protected classification protected by federal, state, or local law. See our California Privacy Policy here.

Cresco Labs is one of the largest public, vertically integrated, multistate operators in the cannabis industry. Our portfolio of in-house cultivated and manufactured brands features some of the highest quality, most awarded and most popular cannabis products in America. With dozens of locations nationwide, our owned and operated Sunnyside dispensaries provide a welcoming, positive, judgement-free place to shop for anyone at any point on their cannabis journey. Founded in 2013, Cresco Labs' mission is to normalize and professionalize cannabis through our passionate employees. As stewards of the cannabis industry, our teams are constantly focused on supporting the needs of our fellow colleagues, consumers, customers, and communities alike. With a focus on Social Equity and Educational Development, our SEEDTM initiative ensures that our company reflects the communities in which we serve, ensuring equal opportunity for all to have the knowledge and resources to work in and own businesses in cannabis. At Cresco Labs, we aim to revolutionize and lead the nation's cannabis industry with a focus on quality and consistency of product, and to bring legitimacy to the industry with the highest level of integrity and professionalism. If you're interested in joining our mission, click the below links to join our team today! MISSION STATEMENT At Cresco, we aim to lead the nation's cannabis industry with a focus on regulatory compliance, product consistency, and customer satisfaction. Our operations bring legitimacy to the cannabis industry by acting with the highest level of integrity, strictly adhering to regulations, and promoting the clinical efficacy of cannabis. As Cresco grows, we will operate with the same level of professionalism and precision in each new market we move in to. SCHEDULE Monday - Friday, 7:00AM - 3:30PM JOB SUMMARY Cresco Labs is seeking a detail-oriented Extraction Technician to join our manufacturing team. This role is responsible for supporting the preparation, processing, and formulation of cannabis products in compliance with state regulations and Cresco Labs' quality standards. The ideal candidate is motivated, safety-focused, and comfortable working in a fast-paced production environment. CORE JOB DUTIES Manufacturing: Prepare and maintain extraction areas in accordance with Cresco Labs SOPs and state compliance regulations. Process biomass and perform solvent-based and solventless extractions. Conduct lab bench work, including product filtration and formulation. Operate and monitor high-RPM machinery such as centrifuges and Cup 15 systems. Safely handle solvents (ethanol, butane) and materials under extreme hot and cold conditions. Perform quality control checks to ensure consistency, safety, and efficacy of finished products. Maintain accurate documentation, batch records, and compliance logs. Assist other departments with production tasks as needed. Work in temperature-controlled, loud environments while adhering to all safety protocols. Flexibility to work extended hours when production requires. Facility Cleaning: Perform all assigned tasks to maintain a clean, safe, and compliant production facility. Follow Cresco Labs' hygiene standards before beginning any production activities, including proper handwashing, use of hairnets, and changing into appropriate work attire. Complete sanitation of all production areas, equipment, tools, containers, and appliances in accordance with company SOPs and regulatory requirements. Ensure cleanliness and organization are upheld to support product safety, quality, and operational efficiency. REQUIRED EXPERIENCE, EDUCATION AND SKILLS Prior experience in a laboratory, food production, pharmaceutical, nutraceutical, or manufacturing environment preferred. Strong attention to detail with a proven commitment to safety protocols and quality standards. Ability to safely lift, move, and operate heavy equipment as required. Comfortable working with solvents, high-powered machinery, and in varying environmental conditions (temperature-controlled, loud, hot/cold). Effective time-management skills with the ability to prioritize, multi-task, and adapt in a fast-paced, evolving environment. Strong teamwork, communication, and problem-solving skills. Proficiency with Windows-based software; experience with point-of-sale or inventory management systems a plus. BENEFITS Cresco Labs is proud to offer eligible employees a robust offering of benefits including, major medical, dental and vision insurance, a 401(K)-match program, FSA/HSA programs, LTD/STD options, life insurance and AD&D. We also offer eligible employees paid holidays and paid time off. Other rewards may include annual discretionary bonuses, stock options as well as participation in our employee discount program. Benefits eligibility for permanent positions may vary by full-time or part-time roles, location, or position. In accordance with any local and state compensation laws, the compensation listed is the current estimated range for the position. Final offer details and future compensation may be determined by multiple factors including but not limited to, geographic location, market compensation data, skills, experience, and other relevant factors. For questions about this please discuss with your recruiter during the interview process. Pay Range$19-$19 USD ADDITIONAL REQUIREMENTS Must be 21 years of age or older to apply Must comply with all legal or company regulations for working in the industry Cresco Labs is an Equal Opportunity Employer and all applicants will be considered without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status. California Consumer Privacy Act ("CCPA") Notice to Applicants:Please read the California Employee Privacy Notice ("CA Privacy Notice") regarding Sunnyside* and its affiliate Cresco Labs' policies pertaining to the collection, use, and disclosure of personal information. This CA Privacy Notice supplements the information contained in the Sunnyside* Privacy Policy and applies to California resident employees and job applicants. Applicants with disabilities may access this notice in an alternative format by contacting ************************* Reporting a Scam: Cresco Labs is aware of fictitious employment offers being circulated from various sources. Many of these schemes consist of an alleged offer of employment with Cresco Labs with the intention of gaining personal information, including payment and/or banking information. Be aware that fraudulent job offers and correspondence may appear legitimate: they may feature a Cresco Labs logo, they may appear to originate from an official-looking email address or web site, or they may be sent by individuals purporting to represent Cresco Labs or an entity which includes the word Cresco Labs in its name. Please note that Cresco Labs does not ask for payment or personal banking information as a condition of employment. Any personal information is requested for payroll or state badging purposes only. Applications can be securely submitted through our career's pages.We are working diligently to block this from happening. Beware if an offer of employment looks too good to be true. Never divulge personal and banking information or send money if you are unsure of the authenticity of an email or other communication in the name of Cresco Labs.If you are in doubt, please contact us at **************************** with questions.

Job Description Job Title: Quality Regulatory Technician - Labeling Compliance Department: Quality Assurance / Regulatory Affairs Employment Type: Monday - Friday 8:30am - 5pm $19 - $22/ HR We are seeking a detail-oriented Quality Regulatory Technician to join our Quality Assurance team, specializing in labeling compliance. This role ensures that all product labels and packaging meet internal standards and adhere to local, state, federal, and international regulatory requirements. The ideal candidate is highly organized, collaborative, and experienced in dietary supplement labeling and packaging. MUST BE BILINGUAL ENGLISH/SPANISH. Key Responsibilities Apply style guidelines and branding standards to new and revised product labels. Ensure compliance of all labeling with applicable local, state, and federal regulations. Create and revise label items in the company's document control system; draft and release engineering change orders. Support continuous improvement initiatives within the Labeling department. Provide daily regulatory support for labeling strategies and operations across multiple projects. Interpret and apply regulatory guidance to labeling within the dietary supplement industry for domestic and international markets. Collaborate cross-functionally with teams including Engineering, Marketing, Quality, and R&D to support label and packaging updates and new product development. Interface with distributors and stakeholders to resolve labeling/packaging issues. Oversee the development and review of advertising and promotional materials for regulatory compliance. Conduct proofreading and side-by-side reviews of primary and secondary labels, including multilingual inserts, for final artwork approval. Manage and track labeling/packaging timelines and documentation for regulatory submissions and audits. Communicate regulatory updates and interpret compliance directives for internal teams, offering solutions and guidance. Provide support to Regulatory and Design teams and assist with additional regulatory duties as assigned. Qualifications 2+ years of experience in regulatory labeling or packaging, preferably in the dietary supplement or consumer goods industry. Strong knowledge of FDA regulations, FTC advertising guidelines, DSHEA, and international labeling standards. Experience with document control systems and engineering change orders. Excellent proofreading skills and attention to detail. Strong organizational, multitasking, and communication skills. Ability to collaborate in a fast-paced, cross-functional environment.

Overview Summary: The Quality Control Technician will implement and comply with quality assurance methods and procedures to ensure products and materials are produced in accordance with specifications in a safe and efficient manner. Principal Duties and Responsibilities: Quality Control Analysis: • Conduct tests and inspect concrete to evaluate quality or conformance to specifications • Sample and evaluate quality of materials related to concrete • Monitor equipment operation to ensure that concrete is within tolerance • Record inspection or test data, such as slump, air content, unit weight, temperature, or moisture content • Input test data into company quality control software • Test hardened concrete for compressive strength • Input strength results into company quality control software • Analyze, evaluate, and resolve customer concerns involving specific conditions, situations, quantities, and other influences associated with product • Manage and maintain quality control software for assigned area Production and processing: • Perform aggregates and batch plants tests including aggregate gradation and moisture tests for State and spec projects as required Communication Skills: • Provide information to supervisors, co-workers, and contractors via phone, e-mail or in person • Effectively communicate with dispatch office to successfully ship and test concrete Global Responsibilities: • Regular attendance and physical presence at work is an essential function of this position • This job may require additional duties not listed above and the employee may be asked to perform those duties to meet business needs Qualifications: Education/Specialized Knowledge/Professional Certifications: • High School Diploma or equivalent required • Bachelor's degree in related field preferred • ACI Level 1, NICET Certified or NRMCA Short Course completion on aggregates or concrete are required • Valid driver's license required •I DOT PCC Level I or WDOT PCCTEC I certification(s) or higher are preferred(IL South, IL North, and WI region only) • Knowledge of raw materials, production processes and quality control are preferred Experience: • Experience in related field preferred Skills/Abilities: • Able to read, write, and speak English preferred • Able to operate a smart phone/device • Proficient in Microsoft Office Suite Working Conditions: • Operation within a fast-paced environment • Exposed to moving mechanical parts, vehicles, heavy construction equipment, toxic or caustic chemicals, and outside weather conditions • Noise level is usually moderate, but can be high and requires personal hearing protection on occasion at job sites, plants and laboratories • Must be able to work through stressful situations while maintaining professionalism and composure • Local travel required Physical Requirements: • Regularly required to talk or hear; frequently is required to stand; walk; use hands to finger, handle or feel; and reach with hands and arms • Occasionally required to sit; climb or balance; and stoop, kneel, crouch or crawl • Must be able to stand and move about job sites with uneven and unpaved ground while managing concrete delivery onsite • Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus • Must be able to frequently bend in order to obtain samples from stockpiles or ground, climb ladders with buckets of admixtures, and push wheelbarrows of concrete • Must be able to operate buttons, levers, and other controls located on various equipment • Must be able to work long and flexible hours as necessary • Must be able to maneuver in and around our plants, yards and jobsites as necessary • Lift/Carry up to 55pounds frequently • Lift up to 100 pounds occasionally Ozinga is an Equal Opportunity Employer. We consider applications for all positions without regard to race, color, religion, creed, gender, national origin, age, disability, sexual orientation, citizenship status, genetic information, or any other legally protected status.

Lupin is comprised of a fast growing, innovative and robust team of manufacturing, Research and Development and commercial divisions. Together these entities make up the generic and branded U.S. business. Lupin has a significant generic pipeline, and a branded focus on women's health. Our first Research and Development facility in the US is located in Coral Springs, Florida which focuses on generic and branded orally inhaled and nasal drug products. Somerset, New Jersey is home to one of Fifteen commercial manufacturing sites globally and the only commercial manufacturing facility in the United States for Lupin, as well as additional Research and Development teams. Lupin is prided on being people-focused and centered around how impactful we are with our customers. Dollars are not a measure of success but rather the people we help along the way. Responsibilities Role Summary Quality Assurance Associate independently performs tasks with minimal supervision ensuring compliance with LIRC Quality Assurance programs and procedures, and all applicable predicate rules. Assists in the maintenance of Quality Systems and develops new controls and procedures that are appropriate and effective as part of continuous Quality Improvement activities at the site. Ensures that Laboratory and Manufacturing functions are operating in full compliance with the Current Good Manufacturing Practices (cGMPs), regulatory requirements, company procedures and continuous improvement. Essential Duties and Responsibilities Participate in the design and development of Lupin's Quality Systems and provide support of continuous improvement and management of Quality Systems. Issuance of GMP documents i.e. logbooks, notebooks, batch records, etc. Release of cleanrooms after cleaning activities. Inspection and release of GMP area prior to manufacturing activities. Inspection of incoming materials, in process and finished products. Provide support in the review of cGMP documentation, including, but not limited to specifications, standard operating procedures/ test methods, and batch records. Support internal and to 3rd party audits at LIR site. Facilitate quality-related training and mentoring, where required. Partnership with other functional areas (Operations, Product Development, Quality Control, Engineering and Facilities, Manufacturing, and Supply Chain) to ensure site continuous compliance. Support employee training program. Management of QA retain samples and archival of GMP documents. Provide support in the documentation of investigations and Root Cause Analysis. Perform other QA duties as assigned. Qualifications Education & Experience A Bachelor's Degree (B.S.) in Chemistry, Biology, Microbiology or Pharmacy related field is preferred. A minimum of 1-3 years' experience in an FDA-regulated or Pharmaceutical/Medical Device manufacturing environment. A thorough knowledge of cGMP regulations as they apply to Drugs and Medical Devices is required. Relevant experience with laboratory and manufacturing functions along with GMP quality assurance functions is required. Ability to enforce adherence to internal quality policies, procedures and cGMP. Ability to interface and work with a diverse group of departments and individuals is required. Must be team oriented with excellent interpersonal skills. Must have the ability to express regulatory requirements clearly and understandably. Must possess good oral and written skills in the English language. Availability to work in second shift. Lupin is an equal opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, color, national origin, gender, religion, age, disability, veteran's status, or any other classification as required by applicable law. Physical Requirements The physical requirements of the position generally include: standing, walking, sitting, using hands and fingers, reaching with hands and arms, talking and hearing. In some circumstances, bending, kneeling, crouching, stooping, and crawling may apply. This position may require lifting up to 15 pounds occasionally. Generally work is performed in an office environment. Search Firm Representatives Please Read Carefully Lupin USA, and its Affiliates does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms for any current openings at our company without a valid written search agreement in place will be deemed the sole property of Lupin. No fee will be paid in the event a candidate is hired by Lupin as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, No phone calls or emails

Job DescriptionAbout Us At The Pharmacy Hub, we collaborate with pharmaceutical brands, manufacturers, health brands, telemedicine providers, and healthcare companies to deliver essential products directly to patients. Our expertise allows us to seamlessly distribute pharmaceuticals, medical devices, and other healthcare products to consumers, ensuring greater accessibility and convenience. Core Values The Pharmacy Hub is dedicated to breaking barriers in healthcare by championing access, intervention and affordability. Customer-first mindset - we develop strong partnerships with telehealth platforms and healthcare companies to enhance access and understand their specific needs Innovation for intervention in care - we develop advanced compounding solutions and products to better support patient health outcomes Continuous improvement - we continuously improve our processes and offerings through intelligent, honest and transparent practices to deliver cost-effective solutions that truly benefit our clients and their patients. You will play a pivotal role in maintaining these values and contributing to the company's mission of redefining healthcare delivery through superior pharmacy services. Job Summary We are seeking a detail-oriented Quality Control Technician to support quality assurance and compliance activities within a non-sterile compounding pharmacy environment. This role supports day-to-day quality control functions, documentation accuracy, and regulatory compliance related to compounded preparations, controlled substances, and pharmacy operations. Key Responsibilities Perform routine quality control checks in a non-sterile compounding environment Verify compounding documentation, batch records, logs, and labels for accuracy and completeness. Assist with tracking deviations, errors, or quality issues related to compounded preparations. Assit with CAPA activities by collecting data, maintaining logs, and confirming that corrective actions are completed Maintain accurate and organized quality and compliance records. Assist with internal audits, inspections, and preparation of supporting documentation. Work closely with pharmacists, compounding technicians, and compliance staff. Follow and reinforce quality assurance and documentation standards. Participate in quality, safety, and compounding-related training. Collect and document quality data related to compounding operations and pharmacy workflows. Assist in identifying trends or recurring issues and escalate concerns to the Quality team. Support basic reporting and tracking of quality metrics. Qualifications High School Diploma or GED. 1-2 years of experience in a compounding pharmacy, pharmaceutical lab, healthcare, or regulated production environment Strong attention to detail and ability to follow written procedures Basic understanding of quality control principles and regulated workflows. Hands-on experience with non-sterile compounding. Familiarity with USP , FDA guidance, and state pharmacy regulations. Experience supporting quality assurance or compliance functions What We Offer Competitive salary. Bonus program based on productivity and efficiency. Flexible scheduling options. Opportunities for growth in a rapidly expanding telepharmacy practice. Collaborative and innovative work environment focused on patient safety and compliance. Work Schedule Evening: 3:00 p.m. - 12:00 a.m Overnight: 9:00 p.m. - 6:00 a.m This is a full-time position, working 40 hours per week, Monday through Friday This is a 100% onsite role; remote or hybrid work is not available. The hourly rate will vary based on experience Pay Range$20-$25 USD Benefits: 401(k) with up to 4% matching Medical, dental, vision and life insurance Paid time off Paid public holidays At The Pharmacy Hub, we don't just offer jobs-we offer opportunities for career growth and development. We take pride in our fast-paced, team-driven culture and are committed to supporting our employees in achieving success. If you're ready to join a company that values hard work, dedication, and teamwork, apply today! We look forward to welcoming you to The Pharmacy Hub and working together to deliver top-tier pharmacy fulfillment solutions.

Job Title: Quality Regulatory Technician - Labeling Compliance Department: Quality Assurance / Regulatory Affairs Employment Type: Monday - Friday 8:30am - 5pm $19 - $22/ HR We are seeking a detail-oriented Quality Regulatory Technician to join our Quality Assurance team, specializing in labeling compliance. This role ensures that all product labels and packaging meet internal standards and adhere to local, state, federal, and international regulatory requirements. The ideal candidate is highly organized, collaborative, and experienced in dietary supplement labeling and packaging. MUST BE BILINGUAL ENGLISH/SPANISH. Key Responsibilities Apply style guidelines and branding standards to new and revised product labels. Ensure compliance of all labeling with applicable local, state, and federal regulations. Create and revise label items in the company's document control system; draft and release engineering change orders. Support continuous improvement initiatives within the Labeling department. Provide daily regulatory support for labeling strategies and operations across multiple projects. Interpret and apply regulatory guidance to labeling within the dietary supplement industry for domestic and international markets. Collaborate cross-functionally with teams including Engineering, Marketing, Quality, and R&D to support label and packaging updates and new product development. Interface with distributors and stakeholders to resolve labeling/packaging issues. Oversee the development and review of advertising and promotional materials for regulatory compliance. Conduct proofreading and side-by-side reviews of primary and secondary labels, including multilingual inserts, for final artwork approval. Manage and track labeling/packaging timelines and documentation for regulatory submissions and audits. Communicate regulatory updates and interpret compliance directives for internal teams, offering solutions and guidance. Provide support to Regulatory and Design teams and assist with additional regulatory duties as assigned. Qualifications 2+ years of experience in regulatory labeling or packaging, preferably in the dietary supplement or consumer goods industry. Strong knowledge of FDA regulations, FTC advertising guidelines, DSHEA, and international labeling standards. Experience with document control systems and engineering change orders. Excellent proofreading skills and attention to detail. Strong organizational, multitasking, and communication skills. Ability to collaborate in a fast-paced, cross-functional environment.

We are seeking to recruit a Surface Quality Inspector for our location in Jupiter, Florida Strong attention to detail by visually looking at the surface quality of polished optics by using both hands to hold the optic to look thru (transmission) and in reflection to perform the visual inspection of Ø 5mm to Ø 200mm parts. Perform a visual inspection of the optical (glass) lenses against applicable standards ( i.e. ISO10110 and MIL-PRF-13830) using a high intensity light source, or indirect lighting with eye loupes, and/or microscope to identify and find any surface defects (scratches, stains, chips, fractures, etc.) on the lens after polishing or coating. Use the applicable standard to determine if the depth/width of the defect is acceptable or rejected based on the drawing specification. Visual inspection of low/moderate (standard/commercial) grade surface quality requirements (80-50, 60-40 scratch dig equivalent) which are a commonly acceptable cosmetic standards. Perform the inspection of raw glass blanks with documentation and release of material to production. Must be able to use cleaning solvents (alcohol, acetone and others) with special cloth wipes to clean, wipe, and to dissolve and remove any contaminants from the lens before and after inspection. After inspection of the optics, must be able to wrap the lens to protect from scratches, stains, chips, etc. Must be able to follow written and verbal instructions in a reliable and consistent manner. Must accurately document the description of lenses that do not meet the surface quality requirements, segregate the nonconforming parts from acceptable lenses, and to protect the rejected lens before sending to rework (internally or externally) or transferring acceptable lenses to inventory. May use various measuring instruments to measure physical dimension (in mm and inches). Must be able to escalate observed or potential lens quality or process defects to team lead or department supervisor. Must be organized, meticulous and a conscientious worker to minimize mishandling. Lenses inspected are finished product to be built into assemblies that must be handled with utmost care. Maintain contamination control and cleanliness of the area at all times. Proper safety procedures and process controls will be followed at all times when working with solvents, sharp edges and high intensity light sources. Should be an independent worker who can be focused on their responsibilities under minimal supervision with handling and processing parts quickly and efficiently before sending the lenses to coating (outside process), inventory, or to the customer. Work instructions and inspection training to be provided but individual must be able listen and ask questions, refer to the instructions and notes taken, and retain the information provided to reference back. REQUIREMENTS: High School Diploma, some college preferred. General knowledge of reading mechanical or optical blueprints/drawings. Use of measuring equipment such a caliper or dial indicators (mm and inch units). General computer skills and aptitude. Experienced in an ISO 9000 quality system work environment is preferred.

We are seeking a dedicated Quality Assurance Specialist to ensure that all product quality complaints are handled efficiently and in accordance with our rigorous company procedures. This role involves collaborating with external partners and internal departments to conduct thorough root cause analyses and enhance procedural compliance. Responsibilities * Ensure all product quality complaints are properly initiated, investigated, and responded to following company procedures. * Work with external partners and customers to gather necessary information for robust root cause analysis. * Collaborate with functional departments to identify additional procedural controls for compliance improvement. Essential Skills * Proficiency in quality assurance and data entry. * Experience with Electronic Quality Management Systems such as TrackWise, Master Control, Veeva. * Ability to use Microsoft Word and Excel effectively. Additional Skills & Qualifications * Associate's Degree in a Scientific Field. * Good understanding of current regulatory requirements related to market complaints. * Strong working knowledge of market complaints and root cause analysis processes. * Excellent technical writing skills with a strong command of the English language. Work Environment This role operates within a lab environment regulated by FDA and GMP standards. The position is a first shift role, Monday through Friday, from 8 am to 5 pm. This opportunity is within a large pharmaceutical company, offering the potential for hands-on lab experience and possible long-term opportunities contingent on openings post-assignment completion. Job Type & Location This is a Contract to Hire position based out of Fort Lauderdale, FL. Pay and Benefits The pay range for this position is $25.00 - $26.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Fort Lauderdale,FL. Application Deadline This position is anticipated to close on Jan 21, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Who we are: Cosmetic Solutions is a leading manufacturer of cosmetic and OTC products, committed to innovation, quality, and continuous improvement. Our Quality Control team plays a vital role in ensuring our products meet the highest standards of safety, efficacy, and compliance. We are seeking a detail-oriented and proactive Quality Control Technician to join our Raw Materials team. This role is essential to maintaining product integrity and regulatory compliance through rigorous testing and documentation practices. Quality Control Lab Technician Major Responsibilities Sample all incoming raw material for Quality control testing Conduct daily quality control testing Water Maintain the raw material standards library Conduct routine and non-routine testing of raw materials, in-process items, and finished goods. Maintain retained sample inventory and storage area. Calibrate and maintain lab equipment (pH meter, viscometer, balances). Review and follow SOPs, specifications, and related documentation. Compile, interpret, and report analytical data. Troubleshoot instruments and initiate investigations for anomalies and deviations. Ensure compliance with GLP, GMP, and SOPs. Document test results accurately in lab notebooks and databases. Collaborate with cross-functional teams to resolve quality issues and implement corrective actions. Participate in writing SOPs, OOS reports, deviations, CAPAs, and investigations. Support sample testing, data entry, and coordination with external labs/vendors. Promote and demonstrate company core values and participate in 6S lean initiatives. Maintain a clean and organized lab environment. Perform other duties as assigned by management. Support the daily execution of the Quality Management System QUALIFICATIONS: Written/oral communication skills required. 2-3 years of experience in the Cosmetic or pharmaceutical industry preferred. Associate's degree or higher in Chemistry, Biology, or a related scientific discipline. Experience & Skills: Experience in cosmetics, pharmaceuticals, or other FDA-regulated industries. Strong knowledge of GLP, GMP, and regulatory standards. Experience in a regulated laboratory environment. Excellent attention to detail and organizational skills. Strong problem-solving and analytical abilities. Effective communication and teamwork skills. Proficiency in Microsoft Office and laboratory data systems. Ability to work independently and manage multiple priorities. Cosmetic Solutions LLC. is committed to equal employment opportunity for all employees and applicants for employment without regard to age, color, creed, disability status, gender, national origin, race, religion, sexual orientation or veteran status, or any other legally protected status.

Requirements Required Skills & Qualifications Ability to understand, speak, read and write English Self-starter and/or team player with strong verbal, written, and communication skills. Courteous professional manner when interacting with all employees. Solid technology skills with ability to utilize and learn various types of technology. Strong interpersonal skills to handle sensitive and confidential situations while demonstrating poise, tact, and diplomacy Efficient and high standards of accuracy and organization in performing tasks Strong decision making skills and ability to prioritize work; effective time management skills Analytical and problem-solving skills to find solutions to various problems; good vision, and mathematical competency Proficient in Microsoft Office, including Word, Excel, internet and email Ability to interact with all levels of the organization while maintaining integrity and strict confidentiality regarding sensitive information Solid knowledge of workplace safety regulations and procedures to ensure compliance with health and safety standards. Experienced with production tracking systems and software to monitor performance, optimize processes, and ensure efficient operations. High School Diploma or equivalent 2 years' experience in manufacturing setting Mittera is a leading-edge company that provides commercial and digital printing, finishing, graphic design, data analytics, direct mail processing, and fulfillment services. Mittera's full-service approach connects data-driven revelations, bar-raising creative, and expertly printed materials to give our customers' brand recognition it deserves. Competitive compensation and robust benefits plans are offered. Benefits include: Medical Dental Vision Life and AD&D Policies Short and Long-Term Disability 401K with Company Match Paid Time Off Paid Volunteer Time Off Location specific benefits should go here! Mittera is proud to be an equal opportunity workplace. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, or Veteran status. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements. All applicants must be 18 years of age or older. Visit us today at mittera.com or stop by and fill out an application at Mittera location near you!

Job Title: QC Lab Tech Department: Lab/QC - Asphalt Plant Reports To: Lab Supervisor Who is OHLA USA? We are a company who believes in building a better, safer, more sustainable world for generations to come. We are committed to making a difference within our communities, who depend on the safety and reliability of the structures we build and is possible with our main asset, our people! OHLA USA brings together the construction industry's most diverse talent who thrive in a collaborative work environment and appreciate challenges and opportunities. Community Asphalt, founded in 1980 as an asphalt paving contractor, based in Miami, Florida, and part of OHLA USA since 2006, has since become specialized in general road construction and transportation infrastructure. From its four operation and plant facilities in Miami-Dade, Fort Myers, Vero Beach and West Palm Beach, the company boasts extensive geographic coverage throughout South Florida, focusing on all aspects of transportation infrastructure development, primarily for state and local authorities. Community Asphalt continues to provide traditional paving services which include grading and paving, pavement milling, surveying, excavation, on and off-road hauling, drainage, utilities, base finishing, and highway sweeping. The company also provides engineering, contracting, design and build and finance and more complex PPP contracts services. These projects include parking lots, industrial and retail complexes, road and highway construction, and airport runways. Summary Our company has an immediate opening for QC Lab Tech in Miami, Fl. The QC Lab Tech is responsible for conducting quality control sampling and testing of asphalt mixes and aggregates produced at the plant. This role ensures compliance with FDOT standards, project specifications, and company quality goals, while supporting production teams with timely feedback and accurate documentation. Essential Duties and Responsibilities include the following: Perform daily quality control sampling and testing in accordance with FDOT, ASTM, and AASHTO standards. Conduct laboratory testing including: Gradations, asphalt content, bulk specific gravity, and theoretical maximum specific gravity (Rice test). Compaction and volumetric analysis of asphalt mixes. Moisture content and temperature testing. Document and report test results through FDOT-approved systems (e.g., MAC, LIMS). Monitor plant production and provide feedback to operators for adjustments as needed. Assist with FDOT mix design verifications, trial batches, and adjustments. Maintain laboratory cleanliness, calibrations, and equipment in compliance with FDOT Quality Control program requirements. Submit daily reports and maintain all required FDOT documentation for project compliance. Follow company and FDOT safety protocols at all times. Perform other duties as assigned by supervisor. Qualifications: Education & Experience High school diploma or equivalent required. Prior experience in asphalt materials testing, quality control, or construction materials laboratory work preferred. Familiarity with FDOT Standard Specifications for Road and Bridge Construction is strongly preferred. Certifications FDOT Quality Control Certifications preferred (or ability to obtain): Asphalt Plant Level I & II Must adhere to all company safety policies and procedures. Reliable transportation to and from the job site. Ability to lift up to 50 lbs. and work in laboratory and outdoor asphalt plant environments. Physical Requirements: Requires the following motions: climbing, bending, squatting, lifting, stretching, pushing, pulling, twisting, kneeling, standing, walking, sitting and reaching. Occasional lifting of up to 50 pounds. Working Conditions: Capability to work in varying outdoor weather conditions and perform physically demanding tasks. Exposure to construction site hazards. Testing: Must pass a drug and physical test and criminal background. Schedule: Ability to work long hours, including nights and weekends. Flexible. Driver's License - Regular Class E. Application Process: Interested candidates should submit a resume and cover letter through our online recruiting platform via: Job Openings - OHLA USA (applicantstack.com). Applications will be reviewed on a rolling basis until the position is filled. BENEFITS WE OFFER: Medical, Dental, Vision, Life Insurance, Critical Illness Insurance, Accident Insurance, Hospital Indemnity Insurance, Short-Term Disability, Long-Term Disability, Legal Insurance, Tuition Reimbursement, Employee Referral Program, Employee Discounts, Paid Holidays, PTO & 401k Program Match! Equal Opportunity, Affirmative Action, Veteran's Preference, E-Verify Statement and Drug-Free Workplace OHLA USA is an Equal Opportunity Employer, committed to an inclusive and diverse workforce. We uphold an Affirmative Action Program (AAP) and actively seek to recruit veterans in accordance with the Vietnam Era Veterans' Readjustment Assistance Act (VEVRAA). We participate in the E-Verify program, confirming the employment eligibility of all our newly hired employees. We are a drug-free workplace.

Description Job Title Quality Control Inspector Company Snapshot: Born in Miami more than a quarter of a century ago, Tuuci is the global leader in premium shade and placemaking products for hospitality, commercial, and residential outdoor settings. From locations in North America, Europe and Asia, our teams strive to meet and exceed the Tuuci vision: to help people live their best life outdoors through inspiring design, enduring performance, and convivial service. We work in a fun, fast-paced, and diverse environment in which close collaboration and the spirited exchange of ideas are encouraged. Our culture supports our vision by encouraging creativity, driving excellence, and supporting personal growth and development. Tuuci is searching for a team member who embodies passion and performance in the Quality Control department. The Quality Control Inspector position inspects raw materials, finished products and the procedures of the entire production cycle to ensure efficiency and consistency. Other responsibilities include but not limited to: Essential Duties and Responsibilities: Conduct audit inspection on the in-process, process procedure and finished goods products by confirming specifications using drawings and procedures. Approve or reject raw materials with respect to quality standards. Document inspection results by completing reports and logs. Assist in determining the root cause and the implementation of a corrective action. Organize the disposition of rejected materials and log all rejected materials. Measure products with rulers, calipers, gauges, or micrometers. Monitor operations to ensure that they meet production standards; recommend adjustments to the production process. Document the QC results by preparing reports of the findings; ensure materials are checked in with the required paperwork and is in proper condition. Maintain safe and healthy work environment by following standards and procedures. Assist in the development of SOPs. Other tasks as assigned. Education and Qualifications: We prefer candidates with 2 years of quality control, receiving and inspection experience. Experience working in warehouse or manufacturing environment. Experience with reading engineering drawings, measuring tools and proficiency in MS Word and Excel. Lift up to 45lbs. Must be Fluent in English and Spanish. This is a full-time, night shift position hours are Monday through Friday from 3:30pm to 12:00am and occasionally require overtime up to 2:30am and Saturdays. Tuuci is an equal opportunity employer. All applicants and employees are to be treated equally with the same rights and privileges with respect to recruiting, hiring, promotions, demotions, transfers, separations, compensation, and benefits regardless of their age, race, color, creed, religion, or ethnic origin, sex, sexual orientation, pregnancy-related status, marital status, veteran status, physical or mental disability, where the individual is otherwise qualified, or any other category protected by applicable law. This employer participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. If E-Verify cannot confirm that you are authorized to work, this employer is required to give you written instructions and an opportunity to contact Department of Homeland Security (DHS) or Social Security Administration (SSA) so you can begin to resolve the issue before the employer can take any action against you, including terminating your employment. Employers can only use E-Verify once you have accepted a job offer and completed the Form I-9. *************

Funky Buddha Brewery, located in Oakland Park, Florida, is seeking a full-time Entry-Level Quality Control Lab Technician to join its growing team. Established in 2010 at its Boca Raton brewpub, Funky Buddha is known for pushing the boundaries of traditional brewing methods with culinary-inspired recipes utilizing all-natural, food-centric ingredients. The brewery has since expanded into alternative beverage production, including THC-infused products, while maintaining a strong commitment to quality, safety, and compliance. This position is ideal for someone early in their laboratory or quality career who is eager to learn, detail-oriented, and interested in working in both traditional brewery quality control and regulated THC beverage testing. The role will work closely with and under the guidance of the Senior QC Lab Technician and Quality Manager. JOB DESCRIPTION The Entry-Level Quality Control Lab Technician supports quality assurance and quality control activities across both beer and THC-infused beverage production. EXAMPLE OF DUTIES: ESSENTIAL FUNCTIONS Beer Quality Control Assist with aseptic sampling of beer, wort, yeast, water, and brewery environments Prepare microbiological media and assist with plating and basic microbial analysis Perform routine yeast cell counts and viability testing under supervision Support chemical analysis including pH, alcohol %, bitterness, and color measurements Enter and maintain quality data in brewery software systems THC Product Quality Control Assist with sampling and testing of THC-infused beverages Support potency, homogeneity, and stability testing preparation Maintain chain-of-custody documentation and compliance records Follow all SOPs and safety procedures related to THC handling SUPPORTIVE FUNCTIONS In addition to performance of the essential functions, this position may be required to perform a combination of the following supportive functions, with the percentage of time performing each function to be solely determined by the supervisor based upon the particular requirements of the company. Assist with R&D trials and quality improvement projects Support production and operations teams as needed Perform other duties and special projects as assigned PHYSICAL REQUIREMENTS Near Vision Constant Far Vision Constant Hearing Constant Talking Constant Sitting Frequent Walking Frequent Computer Use Frequent Crouching, Bending, Stooping Frequent Reaching Occasional Grasping Occasional Pushing/Pulling Occasional Lifting/Carrying up to 55 lbs Occasional Climbing Stairs Occasional SAFETY REQUIREMENTS OSHA laws require the use of the following Personal Protective Equipment (PPE) when performing work duties that have the potential of risk to your health or safety: Safety goggles when walking through the Production area Steel Toe rubber boots Hearing Protection in loud environments Safety gloves when handling industrial strength chemicals Employees will be trained in the proper use and care of assigned PPE. Funky Buddha Brewery provides the required PPE. It is your responsibility to report defective, damaged or lost PPE, or equipment that does not fit properly to your Manager. ORGANIZATIONAL RELATIONSHIPS No positions directly report to this position. SPECIFIC JOB KNOWLEDGE, SKILL AND ABILITY The individual must possess the following knowledge, skills and abilities and be able to demonstrate that he or she can perform the essential functions of the job, with or without reasonable accommodation, using some other combination of skills and abilities. Entry-level laboratory or manufacturing experience preferred Strong attention to detail and documentation skills Proficiency with Microsoft Office Willingness to learn laboratory techniques and regulatory requirements Ability to work safely with hazardous chemicals Ability to work safely in a wet, noisy, and non-temperature-controlled environment Ability to work safely in confined spaces and around complex machinery Ability to stoop, squat, kneel, and crawl for purposes of collecting samples, gathering data, and cleaning Ability to work independently on multiple projects at one time, maintaining attention to detail with each project Ability to meet production, quality and safety standards Open mind for cross-training and covering other department's tasks related to beer production and quality QUALIFICATION STANDARDS EDUCATION Four-year college degree in natural sciences (e.g., microbiology, biochemistry, food science, etc.) preferred. LICENSES OR CERTIFICATES No special licenses or certificates required. GROOMING All employees must maintain a neat, clean and well-groomed appearance. Integrity, loyalty and a good sense of humor are all factors in who we hire. We are a rapidly expanding company with growth potential within. Funky Buddha Brewery is an Equal Opportunity Employer

Duda Farm Fresh Foods, Inc. is a wholly-owned subsidiary of DUDA, established in 2006 to manage the company's legacy fresh produce operations. Capitalizing on a tradition begun in 1926 of growing healthy fresh fruits and vegetables, Duda Farm Fresh Foods offers year-round availability of a wide range of products packed under the Dandy brand. A full-service grower, packer, shipper, marketer, importer and exporter of farm fresh fruits and vegetables and fresh-cut vegetables, its operations are geographically diversified. The Florida-based corporation has production and shipping operations in Florida, California, Arizona, Michigan and Georgia with additional domestic and international locations. Duda Farm Fresh Foods is seeking a FSQA/QC Technician to support food safety and quality programs at our Belle Glade facility. This role ensures compliance with food safety practices, verifies product meets customer specifications, and confirms processing rooms meet standards prior to start-up and throughout production. Key Responsibilities Conduct food safety and quality inspections during production Enforce GMPs and food safety procedures; document non-compliance and corrective actions Verify product quality, labeling, packaging, and date accuracy Perform inventory age reports and collect product samples Calibrate QA tools; monitor water systems, ATP swabs, and metal detection Maintain accurate and organized food safety documentation Collect environmental, equipment, water, and field samples as needed Assist with investigations and follow-up on unusual occurrences Support QA/QC operations at other Duda locations as needed Qualifications High school diploma required 6+ months QA/QC or food safety experience preferred Strong attention to detail and time management skills Basic computer and documentation skills Ability to work independently and in a fast-paced team environment English required; bilingual Spanish preferred Valid driver's license Physical & Work Requirements Ability to lift, push, or pull 50-80 lbs Repetitive bending, standing, and walking Field and facility work required Travel to other locations may be required If you are reliable, detail-oriented, and ready to contribute to a team focused on quality and efficiency, apply and grow with us at Duda Farm Fresh Foods. All applicants must be able to pass a physical, drug test, criminal background check and have valid driver license. The individual should have a great attitude and the ability to learn new things while keeping the interest of our company a priority. We offer an excellent benefit package as part of our total compensation including medical, dental and vision insurance, 401K, flexible spending accounts, paid time off, holiday pay and much more. For more information about A. Duda and Sons, Inc., please visit our website *************

Cresco Labs is one of the largest public, vertically integrated, multistate operators in the cannabis industry. Our portfolio of in-house cultivated and manufactured brands features some of the highest quality, most awarded and most popular cannabis products in America. With dozens of locations nationwide, our owned and operated Sunnyside dispensaries provide a welcoming, positive, judgement-free place to shop for anyone at any point on their cannabis journey. Founded in 2013, Cresco Labs' mission is to normalize and professionalize cannabis through our passionate employees. As stewards of the cannabis industry, our teams are constantly focused on supporting the needs of our fellow colleagues, consumers, customers, and communities alike. With a focus on Social Equity and Educational Development, our SEEDTM initiative ensures that our company reflects the communities in which we serve, ensuring equal opportunity for all to have the knowledge and resources to work in and own businesses in cannabis. At Cresco Labs, we aim to revolutionize and lead the nation's cannabis industry with a focus on quality and consistency of product, and to bring legitimacy to the industry with the highest level of integrity and professionalism. If you're interested in joining our mission, click the below links to join our team today! MISSION STATEMENT At Cresco, we aim to lead the nation's cannabis industry with a focus on regulatory compliance, product consistency, and customer satisfaction. Our operations bring legitimacy to the cannabis industry by acting with the highest level of integrity, strictly adhering to regulations, and promoting the clinical efficacy of cannabis. As Cresco grows, we will operate with the same level of professionalism and precision in each new market we move in to. SCHEDULE Monday - Friday, 7:00AM - 3:30PM JOB SUMMARY Cresco Labs is seeking a detail-oriented Extraction Technician to join our manufacturing team. This role is responsible for supporting the preparation, processing, and formulation of cannabis products in compliance with state regulations and Cresco Labs' quality standards. The ideal candidate is motivated, safety-focused, and comfortable working in a fast-paced production environment. CORE JOB DUTIES Manufacturing: * Prepare and maintain extraction areas in accordance with Cresco Labs SOPs and state compliance regulations. * Process biomass and perform solvent-based and solventless extractions. * Conduct lab bench work, including product filtration and formulation. * Operate and monitor high-RPM machinery such as centrifuges and Cup 15 systems. * Safely handle solvents (ethanol, butane) and materials under extreme hot and cold conditions. * Perform quality control checks to ensure consistency, safety, and efficacy of finished products. * Maintain accurate documentation, batch records, and compliance logs. * Assist other departments with production tasks as needed. * Work in temperature-controlled, loud environments while adhering to all safety protocols. * Flexibility to work extended hours when production requires. Facility Cleaning: * Perform all assigned tasks to maintain a clean, safe, and compliant production facility. * Follow Cresco Labs' hygiene standards before beginning any production activities, including proper handwashing, use of hairnets, and changing into appropriate work attire. * Complete sanitation of all production areas, equipment, tools, containers, and appliances in accordance with company SOPs and regulatory requirements. * Ensure cleanliness and organization are upheld to support product safety, quality, and operational efficiency. REQUIRED EXPERIENCE, EDUCATION AND SKILLS * Prior experience in a laboratory, food production, pharmaceutical, nutraceutical, or manufacturing environment preferred. * Strong attention to detail with a proven commitment to safety protocols and quality standards. * Ability to safely lift, move, and operate heavy equipment as required. * Comfortable working with solvents, high-powered machinery, and in varying environmental conditions (temperature-controlled, loud, hot/cold). * Effective time-management skills with the ability to prioritize, multi-task, and adapt in a fast-paced, evolving environment. * Strong teamwork, communication, and problem-solving skills. * Proficiency with Windows-based software; experience with point-of-sale or inventory management systems a plus. BENEFITS Cresco Labs is proud to offer eligible employees a robust offering of benefits including, major medical, dental and vision insurance, a 401(K)-match program, FSA/HSA programs, LTD/STD options, life insurance and AD&D. We also offer eligible employees paid holidays and paid time off. Other rewards may include annual discretionary bonuses, stock options as well as participation in our employee discount program. Benefits eligibility for permanent positions may vary by full-time or part-time roles, location, or position. In accordance with any local and state compensation laws, the compensation listed is the current estimated range for the position. Final offer details and future compensation may be determined by multiple factors including but not limited to, geographic location, market compensation data, skills, experience, and other relevant factors. For questions about this please discuss with your recruiter during the interview process. Pay Range $19-$19 USD ADDITIONAL REQUIREMENTS * Must be 21 years of age or older to apply * Must comply with all legal or company regulations for working in the industry Cresco Labs is an Equal Opportunity Employer and all applicants will be considered without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status. California Consumer Privacy Act ("CCPA") Notice to Applicants: Please read the California Employee Privacy Notice ("CA Privacy Notice") regarding Sunnyside* and its affiliate Cresco Labs' policies pertaining to the collection, use, and disclosure of personal information. This CA Privacy Notice supplements the information contained in the Sunnyside* Privacy Policy and applies to California resident employees and job applicants. Applicants with disabilities may access this notice in an alternative format by contacting ************************* Reporting a Scam: Cresco Labs is aware of fictitious employment offers being circulated from various sources. Many of these schemes consist of an alleged offer of employment with Cresco Labs with the intention of gaining personal information, including payment and/or banking information. Be aware that fraudulent job offers and correspondence may appear legitimate: they may feature a Cresco Labs logo, they may appear to originate from an official-looking email address or web site, or they may be sent by individuals purporting to represent Cresco Labs or an entity which includes the word Cresco Labs in its name. Please note that Cresco Labs does not ask for payment or personal banking information as a condition of employment. Any personal information is requested for payroll or state badging purposes only. Applications can be securely submitted through our career's pages. We are working diligently to block this from happening. Beware if an offer of employment looks too good to be true. Never divulge personal and banking information or send money if you are unsure of the authenticity of an email or other communication in the name of Cresco Labs. If you are in doubt, please contact us at **************************** with questions.

About Us At The Pharmacy Hub, we collaborate with pharmaceutical brands, manufacturers, health brands, telemedicine providers, and healthcare companies to deliver essential products directly to patients. Our expertise allows us to seamlessly distribute pharmaceuticals, medical devices, and other healthcare products to consumers, ensuring greater accessibility and convenience. Core Values The Pharmacy Hub is dedicated to breaking barriers in healthcare by championing access, intervention and affordability. Customer-first mindset - we develop strong partnerships with telehealth platforms and healthcare companies to enhance access and understand their specific needs Innovation for intervention in care - we develop advanced compounding solutions and products to better support patient health outcomes Continuous improvement - we continuously improve our processes and offerings through intelligent, honest and transparent practices to deliver cost-effective solutions that truly benefit our clients and their patients. You will play a pivotal role in maintaining these values and contributing to the company's mission of redefining healthcare delivery through superior pharmacy services. Job Summary We are seeking a detail-oriented Quality Control Technician to support quality assurance and compliance activities within a non-sterile compounding pharmacy environment. This role supports day-to-day quality control functions, documentation accuracy, and regulatory compliance related to compounded preparations, controlled substances, and pharmacy operations. Key Responsibilities Perform routine quality control checks in a non-sterile compounding environment Verify compounding documentation, batch records, logs, and labels for accuracy and completeness. Assist with tracking deviations, errors, or quality issues related to compounded preparations. Assit with CAPA activities by collecting data, maintaining logs, and confirming that corrective actions are completed Maintain accurate and organized quality and compliance records. Assist with internal audits, inspections, and preparation of supporting documentation. Work closely with pharmacists, compounding technicians, and compliance staff. Follow and reinforce quality assurance and documentation standards. Participate in quality, safety, and compounding-related training. Collect and document quality data related to compounding operations and pharmacy workflows. Assist in identifying trends or recurring issues and escalate concerns to the Quality team. Support basic reporting and tracking of quality metrics. Qualifications High School Diploma or GED. 1-2 years of experience in a compounding pharmacy, pharmaceutical lab, healthcare, or regulated production environment Strong attention to detail and ability to follow written procedures Basic understanding of quality control principles and regulated workflows. Hands-on experience with non-sterile compounding. Familiarity with USP , FDA guidance, and state pharmacy regulations. Experience supporting quality assurance or compliance functions What We Offer Competitive salary. Bonus program based on productivity and efficiency. Flexible scheduling options. Opportunities for growth in a rapidly expanding telepharmacy practice. Collaborative and innovative work environment focused on patient safety and compliance. Work Schedule Evening: 3:00 p.m. - 12:00 a.m Overnight: 9:00 p.m. - 6:00 a.m This is a full-time position, working 40 hours per week, Monday through Friday This is a 100% onsite role; remote or hybrid work is not available. The hourly rate will vary based on experience Pay Range$20-$25 USD Benefits: 401(k) with up to 4% matching Medical, dental, vision and life insurance Paid time off Paid public holidays At The Pharmacy Hub, we don't just offer jobs-we offer opportunities for career growth and development. We take pride in our fast-paced, team-driven culture and are committed to supporting our employees in achieving success. If you're ready to join a company that values hard work, dedication, and teamwork, apply today! We look forward to welcoming you to The Pharmacy Hub and working together to deliver top-tier pharmacy fulfillment solutions.

We are seeking to recruit a Surface Quality Inspector for our location in Jupiter, Florida Strong attention to detail by visually looking at the surface quality of polished optics by using both hands to hold the optic to look thru (transmission) and in reflection to perform the visual inspection of Ø 5mm to Ø 200mm parts. Perform a visual inspection of the optical (glass) lenses against applicable standards ( i.e. ISO10110 and MIL-PRF-13830) using a high intensity light source, or indirect lighting with eye loupes, and/or microscope to identify and find any surface defects (scratches, stains, chips, fractures, etc.) on the lens after polishing or coating. Use the applicable standard to determine if the depth/width of the defect is acceptable or rejected based on the drawing specification. Visual inspection of low/moderate (standard/commercial) grade surface quality requirements (80-50, 60-40 scratch dig equivalent) which are a commonly acceptable cosmetic standards. Perform the inspection of raw glass blanks with documentation and release of material to production. Must be able to use cleaning solvents (alcohol, acetone and others) with special cloth wipes to clean, wipe, and to dissolve and remove any contaminants from the lens before and after inspection. After inspection of the optics, must be able to wrap the lens to protect from scratches, stains, chips, etc. Must be able to follow written and verbal instructions in a reliable and consistent manner. Must accurately document the description of lenses that do not meet the surface quality requirements, segregate the nonconforming parts from acceptable lenses, and to protect the rejected lens before sending to rework (internally or externally) or transferring acceptable lenses to inventory. May use various measuring instruments to measure physical dimension (in mm and inches). Must be able to escalate observed or potential lens quality or process defects to team lead or department supervisor. Must be organized, meticulous and a conscientious worker to minimize mishandling. Lenses inspected are finished product to be built into assemblies that must be handled with utmost care. Maintain contamination control and cleanliness of the area at all times. Proper safety procedures and process controls will be followed at all times when working with solvents, sharp edges and high intensity light sources. Should be an independent worker who can be focused on their responsibilities under minimal supervision with handling and processing parts quickly and efficiently before sending the lenses to coating (outside process), inventory, or to the customer. Work instructions and inspection training to be provided but individual must be able listen and ask questions, refer to the instructions and notes taken, and retain the information provided to reference back. REQUIREMENTS: High School Diploma, some college preferred. General knowledge of reading mechanical or optical blueprints/drawings. Use of measuring equipment such a caliper or dial indicators (mm and inch units). General computer skills and aptitude. Experienced in an ISO 9000 quality system work environment is preferred.

Mittera is looking for a Quality Inspector to join our growing team! The Quality Inspector will be responsible for developing, implementing, and maintaining comprehensive quality management systems that ensure our products consistently meet and exceed the highest industry standards. This role is critical in maintaining our reputation for excellence in our printing and collectible card production. Key Responsibilities Perform inspections (in process, incoming and final) per procedures. Release all acceptable finished goods, quarantine problematic finished goods for QA analysis. Collect, review, and distribute Customer Samples based on Customer requirements Collect, review, and file Retains. Conducts WIP quality checks in each production department Quarantine tag production that is outside of normal Mittera quality standards. Sorts nonconforming product when required. Notify Management immediately when any quality issue jeopardizes the completion of the order specified quantity. Ensures tests and procedures are properly followed during production Provides other assistance to the Quality Assurance Manager as requested Works proactively to promote teamwork at all levels of the company Conforms with and abides by all regulations, policies, work procedures, safety rules, security procedures and instructions Performs all duties according to established safety policy, including wearing any required PPEs to perform duties as applicable Willing to work flexible hours as needed Ensure security of confidential Customer records and data Special projects as assigned, working independently and/or within a team And other job duties as assigned. Requirements Required Skills & Qualifications Ability to understand, speak, read and write English Self-starter and/or team player with strong verbal, written, and communication skills. Courteous professional manner when interacting with all employees. Solid technology skills with ability to utilize and learn various types of technology. Strong interpersonal skills to handle sensitive and confidential situations while demonstrating poise, tact, and diplomacy Efficient and high standards of accuracy and organization in performing tasks Strong decision making skills and ability to prioritize work; effective time management skills Analytical and problem-solving skills to find solutions to various problems; good vision, and mathematical competency Proficient in Microsoft Office, including Word, Excel, internet and email Ability to interact with all levels of the organization while maintaining integrity and strict confidentiality regarding sensitive information Solid knowledge of workplace safety regulations and procedures to ensure compliance with health and safety standards. Experienced with production tracking systems and software to monitor performance, optimize processes, and ensure efficient operations. High School Diploma or equivalent 2 years' experience in manufacturing setting Mittera is a leading-edge company that provides commercial and digital printing, finishing, graphic design, data analytics, direct mail processing, and fulfillment services. Mittera's full-service approach connects data-driven revelations, bar-raising creative, and expertly printed materials to give our customers' brand recognition it deserves. Competitive compensation and robust benefits plans are offered. Benefits include: Medical Dental Vision Life and AD&D Policies Short and Long-Term Disability 401K with Company Match Paid Time Off Paid Volunteer Time Off Location specific benefits should go here! Mittera is proud to be an equal opportunity workplace. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, or Veteran status. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements. All applicants must be 18 years of age or older. Visit us today at mittera.com or stop by and fill out an application at Mittera location near you!