Quality assurance technician jobs in West Palm Beach, FL

Title: 2nd Shift QA/QC Technician Reports To: QA/QC Supervisor Type: Full-Time | Onsite | Non-Exempt Pero Family Farms is a market share leader with over a century of dedication, commitment and integrity. Operating since 1908, Pero is the farm trusted by retailers and consumers alike. We are a fully integrated farming operation, with departments that specialize in organic farming, logistics, global supply chain management, national sales operations, food processing operations, and strategic marketing functions. Our operation includes over 35,000 acres spanning across the East Coast of the United States from Florida to New York, with distribution and production facilities in several different states. We pride ourselves in maintaining a strong family heritage and tradition that has been dedicated to quality, innovation, and excellent customer service that has been feeding America's families for over a century. Our family's passion for farming remains unwavering, with a vision to continue the tradition for many generations to come, whilst maintaining the reverence and trust it has established with the American consumer. As we expand our offering to include an assortment of organic vegetable options; we have become one of the largest organic vegetable growers in the country and we are looking to grow our workforce family. Join us in continuing and strengthening our position as a market share leader dedicated and trusted by retailers and consumers alike. JOB SUMMARY It is the Quality Assurance/Quality Control Technician's responsibility to ensure compliance with all relevant regulatory requirements and guidelines, ensure compliance with all customer expectations, internal quality, and Food Safety Standards and Policies. Requirements PRIMARY FUNCTIONS Inspect inbound/outbound product Take temperature and cultures of product Document all inspections and data as needed Perform assigned tasks related to quality and food safety The QA/QC Technician will be responsible for making sure company products are safe and meet or exceed company quality standards, and fully comply with food regulations. Monitor and enforce organic handling practices. Critical Control Point testing of HACCP program To effectively operate PAA pumps, sanitizing outlets, and performs testing to ensure Organic wash requirements are met To effectively operate chlorine pumps, sanitizing outlets, and performance of testing to ensure chlorination wash requirements are met Sample pulling for shelf life, microbiological, and customer requirements Pre-Operational testing of sanitation to include: ATP testing of surfaces, and evaluations of cleaning practices To effectively monitor and test all metal detection units for assurance of metal free production Packaging and seal testing, relative to container type - such as vacuum, pressure, or bubble testing Calibrations on weight scaled, thermometers, and all applicable testing tools or detectors GMP (Good manufacturing Practices) monitoring of operations to ensure foods safe environment Color code enforcement; sanitation, organics, allergens, others as required Hold and release program Rework program Shelf-life evaluation and sensory testing as required Paperwork filing Work with soap's other cleaning chemicals Schedule: 4PM to 2AM/when business ends Must be available on Holidays and Weekends Other duties as required PHYSICAL REQUIREMENTS Required to stand, sit, walk for long periods of time Frequent use of hands for simple firm, grasping and writing Occasional bending, stopping, reaching, and climbing Occasional Lifting, carrying 5 pounds to 50 pounds Occasionally using cutting utensils (I.E Knives, peeler, etc.) Exposure to product fumes such as onions, peppers etc. Exposure to varying temperatures of 45 degrees or less Exposure to chemicals such as chlorine, etc. Works overtime as required Other duties as required SKILLS & REQUIREMENTS Food Quality inspection experience, produce experience preferred Good communication skills, including basic written and spoken English, to ensure understanding of safety procedures and documentation Computer skills - Basics: Microsoft Excel, Word, PowerPoint, Office Industry Specific: Famous HACCP certification or have participated in HACCP training Must be able to follow complex verbal and written instructions and be able to work independently to evaluate and resolve Quality-related problems and identify and communicate short term remedial actions. Must have a high level of problem-solving skills. COMPANY BENEFITS/PERKS 401(k) Health, Dental, Vision Insurance and more Paid Time Off (PTO) The company (Pero) reserves the right to alter, amend, expand or contract these duties and responsibilities as the companies needs evolve.

Pay Type: Salary 61,0000 - 63,000 Amrize is building North America. From bridges and railways to data centers, schools, offices and homes, our solutions are inside the buildings and infrastructure that connect people and advance how we live. And we invite you to come and build with us. As the partner of choice for professional builders, we offer advanced branded solutions from foundation to rooftop. Wherever our customers are, whatever their job, we're ready to deliver. Our 19,000 colleagues work across 1,000 sites supported by an unparalleled distribution network. Infrastructure, commercial and residential, new build, repair and refurbishment: We're in every construction market. Amrize listed on the New York Stock Exchange and the SIX Swiss Exchange on June 23, 2025, following our spinoff as an independent company. Join us and build _your_ ambition. Learn more at ********************** (****************************************** Description: Join the Duro-Last team, a brand of Amrize Building Envelope and the world's largest manufacturer of custom-fabricated commercial roofing solutions. Were seeking a Roof Inspector -QA Tech Rep I - FL who's ready to be part of an innovative, people-first brand shaping the future of the roofing industry. **ABOUT THE ROLE** Duro-Last Roofing, the world's largest manufacturer of prefabricated roofing systems, has an opening for a **Quality Assurance Technical Representative (Roofing Inspector)** in the **Pompano Beach, Florida** area. This is a full-time, year-round, salary-based position with a company vehicle, cell phone, tablet and expense account provided. **WHAT YOU'LL ACCOMPLISH** + Physically inspect roof installations for quality and workmanship. + Issue the roof warranty in accordance with the Duro-Last specifications. + Make repairs to Duro-Last roofs. + Conduct on-site training classes and offer guidance to contractors in proper roof installation. + Provide support to Duro-Last contractors and sales reps in territory. + Schedule inspections and repairs and prepare reports for warranties. + This is a physically challenging position that requires bending, lifting, pulling, climbing, etc. + Other job duties as assigned. **WHAT WE ARE LOOKING FOR** + Two to four years of experience in commercial low slope roofing, construction, roof inspection or quality assurance is highly desirable. + Individual must be equipped with strong motivation, organization, time management, documentation and communication skills (both orally and written). + Must have excellent attention to detail and the ability to multi-task and prioritize. + Demonstration of strong work ethics (punctual, dependable, and trustworthy) is necessary. + The ability to complete responsibilities and operate equipment conforming to company production, personnel and safety procedures is needed. + The ability to read and comprehend roofing specifications. + Must be able to communicate and handle conflict in a professional manner. + Valid driver's license and an acceptable driving record (MVR). + Must be willing to do **extensive regional travel** . + Must be computer literate. + Must be able to pass a physical agility test, drug screen & criminal background check. **WHAT WE OFFER** + Competitive salary + 401(k) retirement plan with company contribution + Medical, Dental, Vision, Disability and Life Insurance + Holistic Health & Well-being programs + Health Savings Accounts (HSA) & Flexible Spending Accounts (FSA) + Paid time off + 12 paid holidays + Paid Parental Leave (maternity & paternity) + Educational Assistance Program + Bonus Incentive Company vehicle and expense account provided \#Duro-Last **BUILDING INCLUSIVE WORKSPACES** At Amrize, there is endless opportunity for you to play your part. Whether you're in a technical, managerial, or frontline role, you can shape a career that works for you. We're seeking builders, creative thinkers and innovators. Come put your expertise to work while developing the knowledge and skills to drive your career forward. With us you'll have the chance to build your ambition! Amrize North America Inc. takes pride in our hiring processes and our commitment that all qualified applicants will receive consideration for employment without regard to age, race, color, ethnicity, religion, creed, national origin, ancestry, gender, gender identity, gender expression, sex, sexual orientation, marital status, pregnancy, parental status, genetic information, citizenship, physical or mental disability, past, current, or prospective service in the uniformed services, or any other characteristic protected by applicable federal, state or local law. Amrize North America Inc, and its respective subsidiaries are Equal Opportunity Employers, deciding all employment on the basis of qualification, merit and business need. Amrize Canada Inc. is committed to the principles of employment equity and encourages the applications from women, visible minorities, and persons with disabilities. In compliance with the ADA Amendments Act (ADAAA), if you have a disability and would like to request accommodation in order to apply for a position with us, please email recruiting-accommodations@amrize.com . This email address should only be used for accommodations and not general inquiries or resume submittals. In Ontario, our organization/business is committed to fulfilling our requirements under the Accessibility for Ontarians with Disabilities Act. Under the Act, accommodations are available on request for candidates taking part in all aspects of the selection process. While we sincerely appreciate all applications, only candidates selected for an interview will be contacted.

Job Requirements: include the following essential duties and responsibilities: Develop a thorough knowledge of CHAUVET DJ Product range and a working knowledge of Pro Product including both operation and multiple unit connectivity. Visually and physically inspect all products to determine they meet specification in regard to Packaging and Presentation, Physical Appearance, Performance and Functionality, using a range of necessary tools for testing. Safely and responsibly handle / operate hand tool such as calipers, power drills, screw drivers, laser testers, light meters, heat guns, box cutters and others as may be required. Document and report all issues to QC Supervisor that could lead to customer dissatisfaction, contribute to recurring defects and potential loss of sales. Provide timely feedback to Supervisor regarding product failures or performance concerns. Make sure Labeling, Barcoding and Silk Screening are accurate and correctly placed. Participate in department wide training, cross training and mentoring programs for new and existing team members with a view to increasing personal knowledge of Chauvet Products and Control systems specifically DMX protocol and ShowXpress. Develop skills that aid is successful diagnosis of errors related to product operation or functions. Partner with Customer Service. Repair Technicians, Sales and Shipping personnel to meet and exceed Chauvet Customer experience. Other duties as assigned. Education and/or Experience: High school diploma or general education degree (GED); 2-4 years or more experience in repair/service of lighting, small electronics or technical products. Ability to interpret technical instructions, follows established procedures, and keeps accurate records. Good observation and analytical skills. Attention to detail. Excellent communication and time-management skills with the ability to work independently with little supervision in a fast- paced environment. Physical Demands: While performing the duties of this job, the employee is regularly required to use hands to finger, handle, or feel; reach with hands and arms; and talk or hear. The employee frequently is required to stand; walk; and stoop, kneel, crouch or crawl. The employee is occasionally required to sit and climb or balance. The employee must regularly lift and/or move up to ten pounds, frequently lift and/or move up to fifty pounds, and occasionally lift and/or move more than one hundred pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus. Ability to perform physical work and wear the proper safety equipment at the same time. Working Conditions: Work may be performed outside of a climate controlled environment.

At STERIS, we help our Customers create a healthier and safer world by providing innovative healthcare and life science product and service solutions around the globe. The Quality Technician is responsible for assisting in administration of the quality functions at a site to assure adherence to ISO 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable regulatory standards. You will support manufacturing and servicing operations by assisting in performing and documenting problem-solving investigations and conducting in-process sub-assembly and final QC product acceptance testing. Quality Technicians assist in identifying and documenting process and product non-conformances. They work with operations team members to perform and document problem-solving investigations. In addition, Quality Technicians may review device history records, authorize release of finished product/processes and execute calibration and environmental monitoring processes. This is a day shift position; Mon-Fri, 9am - 6pm. What You'll Do as a Quality Technician * Assist in production line Quality investigations and associated problem-solving activities. * Will coordinate and conduct in-process and final QC product acceptance testing, depending on facility. * Investigates production line stoppages to identify corrective actions. * Participates on a Material Review Board to review and process non-conformance reports. * Enters and retrieves Quality data from local and global systems. * Verifies calculations, dose ranges, dosimeter placements and special instructions prior to processing and part of final product release. * Complete other duties as assigned. The Experience, Skills and Abilities Needed Required: * Minimum of three (3) years of experience in a manufacturing or repair environment or other technical production tasks with a high school diploma or equivalent. * Minimum of one (1) year of experience in a manufacturing or repair environment or other technical production tasks with an associate degree. * Familiarity working with and using a microscope. * Experience working with a Quality Management System (ISO 13485). * Experience using basic hand tools i.e., utility knife, screwdrivers, hammers. * Proficiency using MS Office including Work, Excel and Outlook. * High level of professionalism, good communication skills, able to work individually and as part of a team. Preferred: * Knowledge of metrology (mics, calipers, gauges). Ability to sit and stand for long periods of time. What STERIS Offers We value our employees and are committed to providing a comprehensive benefits package that supports your health, well-being and financial future. Here is a brief overview of what we offer: * Market Competitive Pay * Extensive Paid Time Off and (9) added Holidays * Excellent Healthcare, Dental and Vision Benefits * Long/Short Term Disability Coverage * 401(k) with a company match * Maternity and Paternity Leave * Additional add-on benefits/discounts for programs such as Pet Insurance * Tuition Reimbursement and continued education programs * Excellent opportunities for advancement in a stable long-term career #LI-KL1 Pay range for this opportunity is $19.00 - $22.00/hour. This position is eligible for bonus participation. Minimum pay rates offered will comply with county/city minimums, if higher than range listed. Pay rates are based on a number of factors, including but not limited to local labor market costs, years of relevant experience, education, professional certifications, foreign language fluency, etc. STERIS offers a comprehensive and competitive benefits portfolio. Click here for a complete list of benefits: STERIS Benefits STERIS is an Equal Opportunity Employer. We are committed to equal employment opportunity and the use of affirmative action programs to ensure that persons are recruited, hired, trained, transferred and promoted in all job groups regardless of race, color, religion, age, disability, national origin, citizenship status, military or veteran status, sex (including pregnancy, childbirth and related medical conditions), sexual orientation, gender identity, genetic information, and any other category protected by federal, state or local law. We are not only committed to this policy by our status as a federal government contractor, but also we are strongly bound by the principle of equal employment opportunity.

Premier Stoneworks, LLC in Delray Beach, FL, is seeking a Quality Assurance Technician to join our dedicated team. As a key player in our company, you will ensure that our products meet the highest standards of quality and safety. Your attention to detail and commitment to excellence will be instrumental in maintaining our reputation for top-notch craftsmanship. With a competitive hourly salary ranging from $26 to $30, you will have the opportunity to grow and thrive in a dynamic work environment where your skills are valued and recognized. Join us at Premier Stoneworks, LLC, where you can showcase your expertise, drive improvements, and contribute to the success of our thriving business. Be part of a team that prioritizes quality and innovation, and take your career to new heights in the heart of Delray Beach, FL. Conduct regular inspections and audits of production processes to identify areas for improvement and ensure compliance with regulations. Analyze data to track quality performance metrics and develop reports for management review. Collaborate with production teams to address quality issues and implement corrective actions. Provide training and support to employees on quality standards and procedures to maintain a culture of quality excellence. 3+ years of experience in quality assurance roles. Strong background in the concrete industry. Excellent attention to detail and analytical skills. Proficient in conducting quality audits and creating detailed reports. U.S. work Authorization and familiarity with relevant regulations.

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 Description The Cleaning Authority of Fort Lauderdale is looking for experienced professional cleaners who are ready to take the next step in their career - becoming trainers for our growing team! We're a trusted and well-established company, and with demand increasing, we need leaders who can coach, motivate, and guide new hires to deliver the high-quality cleanings our customers expect. What You'll Do Train new employees in the field (on-site and hands-on) Demonstrate and enforce our Detail-Clean Rotation System Ride along with new hires during their first 3 days Provide ongoing coaching and performance feedback Support office management in maintaining team standards Who We're Looking For Minimum 1 year of residential cleaning experience Strong communication and leadership skills Reliable transportation & valid driver's license Positive, team-first attitude Bilingual (English and Spanish) Pay & Benefits $17-$19/hr based on experience Paid travel time & mileage Weekly pay via direct deposit No nights or weekends Paid holidays & vacation time Career advancement opportunities (Team Leader & Supervisor roles) Why Work With Us? We value our employees and believe great training starts with great people. You'll be respected, rewarded, and a key part of our leadership team as we continue growing in Fort Lauderdale. Ready to lead and grow with us? Apply now and let's build a team that shines! Job Type: Full-time Pay: $18.00 - $20.00 per hour Expected hours: 38 - 40 per week Benefits: Fuel reimbursement Mileage reimbursement On-the-job training Paid time off Paid training Schedule: Monday to Friday Supplemental Pay: Performance bonus Tips Language: English (Preferred) Spanish (Preferred) License/Certification: Driver's License and reliable car (Required) Ability to Commute: Fort Lauderdale, FL 33312 (Required) Work Location: In person

Primo Brands is a leading branded beverage company in North America with a focus on healthy hydration. We are proud to offer an extensive and iconic portfolio of highly recognizable, sustainably sourced, and conveniently packaged branded beverages distributed across more than 150,000 retail outlets. Compensation: $23.50 Location: Ft Lauderdale, FL Shift: Friday- Sunday 4:00am-4:00pm **_Shift differential: 6%-8% of base hourly rate paid for applicable hours worked_** Responsibilities + This position is responsible for quality control testing of raw source water, water processing and finished bottled water products to ensure regulatory compliance with the applicable Food and Drug Administration (FDA), State, Local, International Bottled Water Association (IBWA), and Primo Water North America (PWNA) bottled water and beverage safety and quality standards. + Perform microbiological and wet chemistry testing on source water, process and finished product samples in accordance with Standard Methods and PWNA requirements (standard operating procedures and policies). + Maintain detailed and accurate documentation of all analyses and inspections concerning incoming raw materials, water processing treatment equipment and production processes. + Monitor and maintain manufacturing plant quality assurance programs to ensure adherence to established FDA, State, local, IBWA and PWNA standards. + Contribute as a member of the Food Safety team to ensure compliance with all applicable bottled water and beverage safety and quality standards. + Work with production and maintenance departments on various projects as necessary and appropriate. + Assist with cleaning and sanitization (Clean-In-Place (CIP) duties for the water processing equipment and production areas as necessary and appropriate, according to regulatory standards. + Manage multiple tasks and priorities while maintaining detailed and accurate records, quality and safety standards. + Understand and use water processing and mineral batching computer controls to effectively changeover production lines for different bottled water type production runs ensuring all quality control testing is within Primo Water North America specification (s). + Maintain an organized and clean work environment. + Perform other tasks as directed. Qualifications + Microbiology, Food Science, Biology, Chemistry or related field experience. + Excellent analytical and problem-solving skills with strong written and oral communication skills. + Ability to make quality decisions independently and works well with limited supervision, both individually and as a team. + Understanding Food Safety principles and Current Good Manufacturing Practices (cGMP). + Understanding of Good Laboratory Practices (GLPs) and aseptic sampling and handling techniques to collect samples for microbiological analysis including: E. coli, Total Coliform and Heterotrophic Plate count (HPC). + Ability to pass the International Bottled Water Association (IBWA) Certified Plant Operator (CPO) exam and maintain the certification. + Ability to become a Preventive Controls Qualified Individual (PCQI) as part of the FDA Food Safety Modernization Act (FSMA) requirements. + Ability to become a Safe Quality Food (SQF) Practitioner (Only required in MV & CAN). + Ability to support regulatory and internal audits. + Ability to stoop, bend, lift and twist on a regular basis. + Ability to work overtime as needed. + Ability to stand for long periods of time. + Ability to repeatedly lift 50 pounds. + Working knowledge of MS Word, Excel and PowerPoint. Primo Brands' established portfolio includes billion-dollar brands Poland Spring and Pure Life , premium brands like Saratoga and Mountain Valley , regional leaders such as Arrowhead , Deer Park , Ice Mountain Ozarka , and Zephyrhills , purified brands, Primo Water and Sparkletts , and flavored and enhanced brands like Splash and AC+ION . Our extensive direct-to-consumer offerings and industry-leading line-up of innovative water dispensers create consumer connectivity through recurring water purchases across Water Direct, Water Exchange, and Water Refill. At Primo Brands, our more than 11,000 associates are at the heart of what we do and deliver on our mission to provide healthy hydration to consumers wherever, however and whenever they want it. We believe in fostering a respectful culture, which values our associates who are deeply invested in quality hydration, our communities, and the sustainability of our packaging and water sources for generations to come. Primo Brands is proud to be an Equal Opportunity and Affirmative Action employer, seeking to create a welcoming and diverse environment. We do not discriminate based on race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender, gender identity, gender expression, transgender status, sexual stereotypes, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics. We also consider qualified applicants with criminal histories, consistent with applicable federal, state, and local law. Salary Range Disclaimer: The salary range provided for this position is an approximation based on market research, internal compensation data and the candidate's qualifications and experience. Final salary offers are determined through a comprehensive evaluation of candidate qualifications and may vary depending on factors such as skills, experience, and geographic location of the position. Other components of the compensation package, including benefits and bonuses, will also be considered. We are committed to fair and equitable compensation practices, and we encourage open dialogue about compensation during the interview process. Candidates must possess strong English language skills to effectively communicate with customers and provide exceptional service. Proficiency in English is essential for understanding customer needs, resolving inquiries, and collaborating with team members.

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.

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.

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.

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 Dec 8, 2025. 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.

Forgen is dedicated to building a better future - for generations. Seasonal Position. The Quality Control Technician conducts daily inspections to ensure compliance with company and customer quality standards. They possess the authority to enforce corrective actions for any deficiencies in work, equipment, or materials. Their duties encompass maintaining quality assurance protocols, conducting material testing, and analyzing test results. They execute quality assessments, perform inspections, calibrate equipment, and communicate findings. Furthermore, they manage project document control, prepare submissions meeting project specifications, and interpret plans to ensure project compliance. Forgen Overview Forgen is a leading geotechnical and specialty civil construction company operating across North America. We are dedicated to delivering innovative solutions for complex civil, geotechnical, and environmental challenges, guided by our core values of integrity, passion, teamwork, and smart work. Key Responsibilities This role will include temporary night shift periods. Inspecting the work in progress to assure compliance with the quality control plan and quality criteria as specified in the Contract Documents. Performing quality control sampling and testing during construction or ensuring that outside companies are performing tests according to the specifications. Verifying that the equipment used in testing meets test requirements, that tests are conducted according to procedures and best management practices, and that testing equipment and procedures remain consistent over the duration of the project. Identifying work that does not meet acceptance criteria, documenting defective work, and reporting to the QC Manager. Administering the Inspection Test Plans (ITP). Completing the daily field logs. Taking daily field photographs. Maintaining quality control document files. Inspect all delivered materials to document there are no defects in workmanship, they have the proper identification, are not damaged and delivery is complete. Visual inspection will also include the correct quantity, completeness evidence of compliance with approvals, and proper documentation in accordance with manufacturer's requirements and the contract documents. Monitor delivery, handling, and storage of materials per specifications. Observe that storage facilities are applicable, protective, and secure to prevent damage or contamination to equipment and materials per specifications. Review and maintain any manufacturer material certifications. Pertinent information will be entered, and any non-conformances identified during material inspections will be recorded on a Material Delivery Receipt. Basic Qualifications Degree in an engineering discipline (civil, mechanical, electrical, structural), preferred. Knowledge of mathematics - arithmetic, geometry, calculus, and statistics and their relevant applications. Computer skills especially in the use of Microsoft Word and PowerPoint and the ability to manage files and records effectively. Valid Driver's License and ability to drive on behalf of company business. Preferred Qualifications The following safety training is preferred, but not mandatory. Company will provide additional training, as necessary. 40-Hour HAZWOPER Training 8-Hour OSHA Refresher. Competent Person Safety Training. 30-Hour OSHA Construction Safety Training. EM 385-1-1 Training Physical Demands & Work Environment This role requires lifting up to 50 pounds, extended standing or walking on project sites, climbing in and out of equipment, and working in confined spaces or at heights. Work conditions and demands may vary, with possible exposure to heavy machinery, chemicals, dust, fumes, noise, and extreme weather. Proper PPE, including protective eyewear, gloves, a hard hat, and steel-toed boots, is required. Effective communication, tool use, and adherence to safety protocols are essential. This job description outlines the general scope of work and is not exhaustive. Employees may be assigned additional duties as needed. Requirements may be adjusted to accommodate disabilities, except where they pose a direct safety risk. Equal Opportunity Forgen is an equal-opportunity employer and prohibits discrimination based on any legally protected status. Privacy Policy At Forgen, we are committed to protecting your privacy. We collect and use your personal data to manage the recruitment process, including assessing your application, verifying information, and, if applicable, entering into an employment contract. Your information may be shared with authorized third parties who perform services on our behalf, such as background checks, and only where permitted by law. We implement appropriate security measures to safeguard your information and retain it only as long as necessary for recruitment and legal purposes. You have the right to access, correct, or request deletion of your data, and to withdraw your consent at any time where applicable. For questions or to exercise your rights, please contact *************. California Privacy Policy Agency Policy

Titan Florida has an excellent opportunity for a concrete Quality Control Technician for its Ready-Mix division, located in Tri-County. This salaried non-exempt position reports directly to the Quality Manager. The primary functions of this position are to ensure high quality ready-mix product and provide industry related technical assessments. Responsibilities Responsibilities: * Perform sample testing and monitoring of our concrete production and procedures for the region. * Observe job site testing and perform comparative testing with independent testing agencies. * Communicate with customers, testing laboratories, and dispatch and plant supervisors regarding mix utilization and admixture dosage rates. * Perform plant inspections of our facilities and recommend corrective action to ensure compliance with project specifications, DOT, Federal specifications, and Titan America's QA guidelines * Perform visual inspection assessments of jobsite conditions, solutions, and recommendations to correct problems if they occur. * Monitor test report data and plant records to help determine specification compliance in accordance with project, Federal and State specifications * Perform all pertinent ASTM, ACI and DOT testing procedures and evaluations. * Supports Sales and Production departments in resolving quality-based customer queries and complaints. * Participates in the analysis of customer claims and supports the investigation of the causes linked to process or production conditions. Qualifications Required Skills: * FDOT Plant, ACI Field Testing, Aggregate, and Lab Technician Certifications preferred or able to obtain within the first six months of hire. * Minimum one -year experience in Ready Mix Concrete, quality control, or related industry * H.S. Diploma or equivalent required, college degree preferred. * Must have excellent interpersonal, verbal, and written communication skills. * Must be computer literate in Windows, Excel, Adobe, and MS Office. Knowledge of other software programs and computer functionality a plus * Excellent data entry skills and ability to multi-task under pressure. Working Environment * Display a professional and courteous attitude to co-workers, supervisors, and the general public at all times. * Willingness to work in a team environment and assist co-workers or supervisors with other duties as required. * Working outdoors with exposure to extreme heat, extreme cold and other outdoor environmental conditions, constant standing, and walking, climbing, working from heights and lifting up to 50 lbs. * Ability to work flexible shifts including nights, weekends, and overtime. * Job requires the following motions: climbing, stretching, driving/steering, sitting, twisting, vibration, riding on rough terrain, and exposure to extremes of heat or cold weather. * Ability to pass pre-employment processes including criminal background check, physical, and drug screen. * Travel between sites as needed. Titan America is a leading employee centric company that is an environmentally and socially progressive heavy building materials company located in the eastern United States. Titan America is a part of the TITAN Group, an independent, multi‐regional producer of cement and other related building materials headquartered in Athens, Greece. Our products include cement, aggregate, ready‐mixed concrete, and fly ash beneficiation. TITAN Group has a track record of continuous growth since its establishment in 1902. It has expanded its production and distribution operations into 13 countries, employing more than 5,500 people. Our products protect human life and personal property, improve the quality of life, generate economic prosperity, and connect society. Titan America is an Equal Employment Opportunity (EEO) / Affirmative Action employer and welcomes all qualified applicants. Applicants will receive fair and impartial consideration without regard to race, sex, color, religion, national origin, age, disability, veteran status, genetic data, or other legally protected status. #LI-DNI

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!

Quality Technician Quality Inspector OVERVIEW: The Quality Technician is responsible for ensuring that all quality related documents are completed to allow for product approval and on-time delivery. ESSENTIAL DUTIES AND RESPONSIBILITIES: Setup And Monitor SPC Collecting Activities Release all Jobs Prior to Manufacturing Comply with ISO and Customers QC Standards, Procedures and Specifications Prepare First Article Inspection packages, IAW AS9102 Develop Quality Inspection Plans. Develop PFMEA, control plans, flow charts and any APQP, as required. Track and upkeep PPAP requirements Participate in root cause and corrective action items utilizing 8D methodology Train Quality Inspectors on proper inspection techniques Follow Routers Instructions Perform First Piece, In process and Final Inspections using CMM/Layout Inspection SUPERVISORY RESPONSIBILITIES: This job has no supervisory responsibilities. COMPETENCIES Language Skills Ability to read, analyze and interpret documents such as safety rules, operating and maintenance instructions and procedural manuals. Ability to write reports and correspondence. Ability to speak effectively before groups of customers or employees of the organization. Mathematical Skills Ability to work with mathematical concepts such as probability and statistical inference, and fundamentals of plane and solid geometry and trigonometry. Ability to apply concepts such as fractions, percentages, ratios, and proportions to practical situations. Reasoning Skills Ability to apply common sense, understanding to carry out instructions furnished in written, oral or diagram form. Ability to deal with problems involving several concrete variables in standardized situations. EDUCATION, EXPERIENCE, and TRAINING: · High School Diploma or general education degree (GED) and/or 5 years of experience in Quality Assurance. · Working Knowledge of common Drawing Standards and Interpretation · Knowledge of Inspection Methods and Techniques · Knowledge of basic GD&T CERTIFICATES, LICENSES, REGISTRATIONS: There are no specific requirements for this position. COMPUTER SKILLS: Word Processing and Spreadsheet Software TRAVEL REQUIREMENTS: There are no specific travel requirements for this position. PHYSICAL DEMANDS - The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The employee must regularly lift and/or move up to 10 pounds. The employee must occasionally lift and/or move up to 100 pounds. The employee must frequently stand, walk, sit, use hands to finger, handle or feel, reach with hands and arms and talk or hear. The employee must occasionally climb or balance and stoop, kneel, crouch or crawl. VISION REQUIREMENTS: Snellen 14/18, (20/30) or Jaeger 2 - employee will be tested in at least one eye, either corrected or uncorrected Color Vision Requirements: Individuals shall be capable of adequately distinguishing and differentiating colors used in the method for which certification is required, the process being performed or inspection activity. Color Perception testing is required one time only. Note: Vision tests may be substituted for the options listed above providing the equivalence is verified and documented by a licensed optometrist or ophthalmologist. WORK ENVIRONMENT The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. This position regularly works in an environment near moving mechanical parts. This position occasionally works in an environment with fumes or airborne particles. This position works in an environment with moderate noise level (Examples: business office with computers and printers, light traffic) EOE

Job Details Entry Oxygen Development, LLC Deerfield Beach - Deerfield Beach, FL Full Time High School $16.00 - $20.00 Hourly Not Applicable Any NutritionDescription Missions Comply with Good Manufacturing Practices (GMP) and relevant laws and regulations for cosmetics and OTC products. Guarantee quality at each Bill of Material level (RAW, PKG, BULK, WIP, FG). Scope Packaging, Pressed Pans, Hot Pours and Finished Products. Functions GMP: Follow GMP training. Report and coach where necessary. Issue the batch code and expiration date according to customers' requirements. Set up work orders to ensure that all specifications are met by validating the first ten pieces (TBOM, Spectrum, Standard) - Correct items received, Torque test, Jacomex, Fill Weight, Appearance, Bulk Temperature, Bulk Color, Pan/Compact Compatibility, Date Code - Expiration Date Printing… Support production in the assessment of quality aspects necessary to complete the production in accordance with the specifications established. Create sample number in Oracle for any products requiring micro testing. Provide retains, micro, pre-shipment and OTC samples (if applicable) to Quality Assurance. Incoming components: inspect to supplier drawing, artwork, and color standards. Report any deviations to the QC Manager and reject or raise nonconformance as appropriate. Work with Customer Service Representative and Purchasing by reporting all issues regarding CSCs and Direct Buy / Turnkey, Respectively. Outgoing Inspection: Inspect Finished Goods and WIP's (Part finished items / work in progress) to ISO-2859. Record results on the inspection sheet. Reworks: When reworks resulting from quarantine inspection or customer complaint are required, support production by checking that reworks are done in accordance with the instructions from Quality. Perform a gazebo with all involved departments for any non-conformances or red zone issues. Document each non-conformance by following the Non-Conforming SOP (Issuance of a Non-Conformance number, description of the non-conformance, and corrective action / reworks instruction if applicable). Send pre-ship samples and OFA submissions to the customer in timely manner (24 hours) as required. Edit logs and submission forms accordingly. Update the status in Oracle for Packaging, PPOs, and Finished Goods as required. Ensure all issues are communicated to QC Manager and that any deviations are documented. Key Performance Indicators % FG RFT. % WIP RFT. % Rej PKG lots. Qualifications Education High School Diploma or equivalent. Some education in mathematics and English. A formal qualification in mechanical engineering would be advantageous. Experience in Cosmetics Manufacturing and assembly or similar FMCG. Work Experience Knowledge of Quality Assurance. Experience in related industries: Cosmetics, Personal Care, Consumer Goods, Pharmaceutical, Food & Beverage. Skills Analytical skills. Employee management skills. Business and functional expertise. Strategic thinking. High performer under pressure. Excellent written and verbal communication skills (Spanish a plus). Proven problem solving and analytical skills. Demonstrate creativity, flexibility, and use of innovative approaches. Abilities Positive & Communicative. Questioning & Challenging. Accountable & Transparent. Team Oriented. “Can do” problem solving attitude. Process Focused. Results oriented. Quality focused. Lack of blame attitude. Working Conditions Perform repetitive tasks. Regularly working in a noisy environment. Sitting for long periods of time. Frequently working in normal office environment. Physical Demands Light physical activity as necessary. Climbing stairs. May require prolonged sitting at desk. Vertical and Horizontal Footbridges VERTICAL - QC Manager. HORIZONTAL - Purchasing, NPD, Production.

At STERIS, we help our Customers create a healthier and safer world by providing innovative healthcare and life science product and service solutions around the globe. The Quality Technician is responsible for assisting in administration of the quality functions at a site to assure adherence to ISO 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable regulatory standards. You will support manufacturing and servicing operations by assisting in performing and documenting problem-solving investigations and conducting in-process sub-assembly and final QC product acceptance testing. Quality Technicians assist in identifying and documenting process and product non-conformances. They work with operations team members to perform and document problem-solving investigations. In addition, Quality Technicians may review device history records, authorize release of finished product/processes and execute calibration and environmental monitoring processes. This is a day shift position; Mon-Fri, 9am - 6pm. What You'll Do as a Quality Technician • Assist in production line Quality investigations and associated problem-solving activities. • Will coordinate and conduct in-process and final QC product acceptance testing, depending on facility. • Investigates production line stoppages to identify corrective actions. • Participates on a Material Review Board to review and process non-conformance reports. • Enters and retrieves Quality data from local and global systems. • Verifies calculations, dose ranges, dosimeter placements and special instructions prior to processing and part of final product release. • Complete other duties as assigned. The Experience, Skills and Abilities Needed Required: • Minimum of three (3) years of experience in a manufacturing or repair environment or other technical production tasks with a high school diploma or equivalent. • Minimum of one (1) year of experience in a manufacturing or repair environment or other technical production tasks with an associate degree. • Familiarity working with and using a microscope. • Experience working with a Quality Management System (ISO 13485). • Experience using basic hand tools i.e., utility knife, screwdrivers, hammers. • Proficiency using MS Office including Work, Excel and Outlook. • High level of professionalism, good communication skills, able to work individually and as part of a team. Preferred: Knowledge of metrology (mics, calipers, gauges). Ability to sit and stand for long periods of time. What STERIS Offers We value our employees and are committed to providing a comprehensive benefits package that supports your health, well-being and financial future. Here is a brief overview of what we offer: • Market Competitive Pay • Extensive Paid Time Off and (9) added Holidays • Excellent Healthcare, Dental and Vision Benefits • Long/Short Term Disability Coverage • 401(k) with a company match • Maternity and Paternity Leave • Additional add-on benefits/discounts for programs such as Pet Insurance • Tuition Reimbursement and continued education programs • Excellent opportunities for advancement in a stable long-term career #LI-KL1 Pay range for this opportunity is $19.00 - $22.00/hour. This position is eligible for bonus participation. Minimum pay rates offered will comply with county/city minimums, if higher than range listed. Pay rates are based on a number of factors, including but not limited to local labor market costs, years of relevant experience, education, professional certifications, foreign language fluency, etc. STERIS offers a comprehensive and competitive benefits portfolio. Click here for a complete list of benefits: STERIS Benefits STERIS is an Equal Opportunity Employer. We are committed to equal employment opportunity and the use of affirmative action programs to ensure that persons are recruited, hired, trained, transferred and promoted in all job groups regardless of race, color, religion, age, disability, national origin, citizenship status, military or veteran status, sex (including pregnancy, childbirth and related medical conditions), sexual orientation, gender identity, genetic information, and any other category protected by federal, state or local law. We are not only committed to this policy by our status as a federal government contractor, but also we are strongly bound by the principle of equal employment opportunity.

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 Coconut Creek, 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 Coconut Creek,FL. Application Deadline This position is anticipated to close on Dec 8, 2025. 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.