Production Technician jobs at Novartis

HTI is hiring Maintenance Technicians for our Client in Thomasville, NC. In addition, we have one position open at their Garner, NC facility as well. Pay is up to $38.03 Per Hour + $1.00 Per Hour Shift Differential, shift hours are 6:00 pm - 6:00 am, and Comprehensive Benefits Package Provided. What We Offer: Medical, Dental, and Vision Benefits PTO 401k Match HSA/FSA LTD/STD Life Insurance Telehealth Responsibilities: Complies with all company safety rules and procedures. Identifies warning signs of impending equipment failure. Performs basic troubleshooting for electrical problems with single phase and 3 phase motors, wiring and controls. 5+ years extensive experience in maintenance of a manufacturing environment. Ability to demonstration advanced knowledge of industrial control systems. Welding and Fabrication skills related to the modification of existing equipment is a plus. Intermediate experience with PLC's, VFD's and computers. Ability to work with automation, production, and computer systems. Ability to read and comprehend mechanical and electrical drawings/diagrams. Eduaation: HS Diploma or GED HTI is an Equal Opportunity Employer M/D/F/V/SO.

The main purpose of this role is to assist in all tasks associated with the production of Non-Marek's bulk vaccines and master these tasks as outlined in the departmental procedures. As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development, and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in several ways to foster a healthy working environment, meaningful work, mobility, networking, and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees. **Duties & Responsibilities** + Assists in the following areas of Non-Marek's vaccine production: TS-11, Cocci and Autogenous. + Performs all processes in accordance with Standard Operating Procedures. + Communicates any occurrences/deviations to SR Ops Process Leader / Team Leader / Group Leader immediately. + Always utilizes sterile technique and gowning technique. + Active knowledge of working under laminar flow hoods and HEPA filtered environment. + Responsible for keeping the lab area and all other working areas clean, sterile, and in compliance always. + Works well independently and within a team environment. + Works cooperatively with SR Ops Process Leader / Team Leader / Group Leader to train others. + Must be able to accurately measure liquid volume, convert units of measure, and perform moderately complex calculations. + Communicates well with fellow team members regarding daily tasks. Always is prepared for the day ahead. + Maintains accurate and timely manufacturing records, this includes all paperwork and files. + Actively promotes safety awareness in the lab, always acting in accordance with safety practices. + May assist in the candling of eggs at the incubation department. + Assists with washing, wrapping, and sterilizing glassware. + Assists with transporting raw materials and finished product in and out of the lab areas. + Completes daily/weekly job duties assigned monthly by SR Ops Process Leader. + Performs other duties as assigned. **Requirements** + B.S. in biology or science related field or 5 plus years of Marek's or Non-Marek's lab experience. + Required knowledge of non-Marek's technical processes. + Is fully trained and can work independently in the following areas of Non-Marek's vaccine production; Commercial Ovo culture ' Tissue Culture bulk production. + Ability to lift 50 pounds and carry 10 feet. + Must be a team player. + Must be able to lift 50 lbs. and carry it 10 ft. + Must be able to squat, bend, and stoop, as well as twisting and turning. + Manual dexterity and visual acuity are important. + Must be able to wear appropriate Personal Protective Equipment (PPE.) + Must be able to stand on feet for long periods of time and work in a sterile production environment. + Must be flexible with availability (able to work overtime as needed on short notice). This position requires weekend work. Regular attendance is a must. + Must possess the ability to work unsupervised, work well under time constraints, can think ahead to the next task, and be self-motivated. + Ability to think ahead to next task. + Ability to work well under time constraints. * Avian Biosecurity Policy:It is the responsibility of all Boehringer Ingelheim Animal Health, Inc. employees to take necessary steps to avoid contact with the avian species in general. This includes, but is not limited to, commercial poultry, yard chickens, turkeys, ducks, geese, wild birds, and pet birds.Should contact occur, precautions must be taken prior to entering a critical building or location: Anyone encountering the avian species should not enter a critical building or location for 24 hours unless they have showered, changed clothes and shoes. All qualified applicants will receive consideration for employment without regard to a person's actual or perceived race, including natural hairstyles, hair texture and protective hairstyles; color; creed; religion; national origin; age; ancestry; citizenship status, marital status; gender, gender identity or expression; sexual orientation, mental, physical or intellectual disability, veteran status; pregnancy, childbirth or related medical condition; genetic information (including the refusal to submit to genetic testing) or any other class or characteristic protected by applicable law.

By clicking the Apply button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takedas Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. Job DescriptionAbout the role: As a Manufacturing Technician II, you will implement all processes in production while strictly following cGMP, environmental health and safety guidelines and any applicable related regulations. You will have technical and administrative competence to organize and lead production activities. You will participate in both departmental projects and any quality working teams which may be applicable. Responsibilities include assisting with the movement of the product between the different stages of inspection to packaging within the value stream. In this role, you may act as line lead, and will ensure the line operates smoothly and keeps up with daily goals. In addition, you will document your process activities on routers or in the electronic batch management system (EBM). You will report to the Supervisor, Manufacturing. You will work 5am-5:30pm on a 2-2-3 rotating schedule. How you will contribute: Maintain a safe and quality working environment Participate in Continuous Improvement Teams. Support manufacturing operations. Lead Manufacturing Technicians I in daily tasks. Operate general production equipment (such as Downstream Automated Packaging {DAP} lines, forklifts, and hoists). Move pallets to different rooms within the value stream. Communicate and work cross-functionally with other departments. Receive and distribute supplies into the production area. Follow cGMP, environmental health and safety guidelines, and any other regulations. Complete relevant paperwork and electronic system prompts/tasks, following GDP/GMP guidelines. Perform daily cleaning of the production area to maintain in GMP fashion. Train new and existing employees/contractors on procedures. Communicate issues related to safety, quality, compliance and equipment to the manufacturing lead operator and supervisor. May perform other duties as assigned to enable team success and contribute toward professional development. What you bring to Takeda: High school diploma or GED 2+ years of experience or AA or higher and 1+ years of related work experience. Good interpersonal skills and ability to work effectively and efficiently in a team environment. Must be able to speak, read, write, and follow detailed written and oral instructions in English. Understanding of cGMP regulations in a pharmaceutical manufacturing environment Important Considerations: At Takeda, our patients rely on us to deliver quality products. As a result, we must follow strict rules in our manufacturing facilities to ensure we are not endangering the quality of the product. In this role, you may: Work in a controlled environment requiring special gowning and wear protective clothing over the head, face, hands, feet and body. This may include additional hearing protection for loud areas. Need to remove all make-up, jewelry, contact lenses, nail polish and/or artificial fingernails while in the manufacturing environment. Work in a cold, wet environment. Work multiple shifts, including weekends, or be asked to work supplemental hours, as necessary. Work around chemicals such as alcohol, acids, buffers and Celite that may require respiratory protection. In general, the position requires a combination of sedentary work and walking around observing conditions of the facility. Must be able to carry up to 30lbs, lift up to 30lbs, push/pull up to 30lbs (with assistance of material handling equipment). Must be able to stand and/or walk for an extended period over a 12-hour shift between rooms and across the site. May require bending, twisting, reaching overhead, and/or squatting motions to perform certain tasks. Repetitive motions with hands, wrists, turning head, bending at knees and waist. Must be able to walk within and between quality rooms and packaging rooms, as well as throughout the entire plant. 20/20 near and distance vision (Applies to roles performing visual inspection only) with or without glasses and/or contacts. May not be colorblind (Applies to roles performing visual inspection only). Indoor working conditions. Will work around moving equipment and machinery. May be required to work in confined spaces/areas. Some Clean Room and/or cool/hot storage conditions. (Applies to Filling Department only) May be exposed to and must not be allergic to cephalosporin. (Applies only to product touch roles) May work around chemicals such as alcohol, acids, buffers, and Celite that may require respiratory protection. Must be able to work on multiple shifts, including weekends, to support a 24/7 manufacturing operation as needed. Must be able to work non-traditional work hours, including weekends and holidays, as needed. Must be able to work a 12-hour shift (5:00am 5:30pm or 5:00pm 5:30am), in a 2-2-3 rotation. Must be able to work overtime as required. May require immunization before performing work within the manufacturing area. Requires flexibility to work during off shift hours and/or conduct activities in support of different shifts as needed. More about us: At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work. Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world. #GMSGQ #ZR1 #LI-MA1 Takeda Compensation and Benefits Summary We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. For Location: USA - IL - Round Lake - Drug Delivery U.S. Hourly Wage Range: $18.85 - $29.62 The estimated hourly wage range reflects an anticipated range for this position. The actual hourly wage offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job.The actual hourly wage offered will be in accordance with state or local minimum wage requirements for the job location. U.S. based employees may be eligible for short-term incentives. U.S. based employees may be eligible to participate in medical, dental, vision insurance, a 401(k) plan and company match, short-term and long-term disability coverage, basic life insurance, a tuition reimbursement program, paid volunteer time off, company holidays, and well-being benefits, among others. U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation. EEO Statement Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law. LocationsUSA - IL - Round Lake - Drug DeliveryWorker TypeEmployeeWorker Sub-TypeRegularTime TypeFull time Job Exempt No By applying, you consent to your information being transmitted by College Recruiter to the Employer, as data controller, through the Employers data processor SonicJobs. See Takeda Pharmaceutical Terms of Use at terms-of-use/ and Privacy Policy at privacy-notice/ and SonicJobs Privacy Policy at us/privacy-policy and Terms of Use at us/terms-conditions RequiredPreferredJob Industries Other

The main purpose of this role is to assist in all tasks associated with the production of Non-Marek’s bulk vaccines and master these tasks as outlined in the departmental procedures. As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development, and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in several ways to foster a healthy working environment, meaningful work, mobility, networking, and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees. Duties & Responsibilities Assists in the following areas of Non-Marek's vaccine production: TS-11, Cocci and Autogenous. Performs all processes in accordance with Standard Operating Procedures. Communicates any occurrences/deviations to SR Ops Process Leader / Team Leader / Group Leader immediately. Always utilizes sterile technique and gowning technique. Active knowledge of working under laminar flow hoods and HEPA filtered environment. Responsible for keeping the lab area and all other working areas clean, sterile, and in compliance always. Works well independently and within a team environment. Works cooperatively with SR Ops Process Leader / Team Leader / Group Leader to train others. Must be able to accurately measure liquid volume, convert units of measure, and perform moderately complex calculations. Communicates well with fellow team members regarding daily tasks. Always is prepared for the day ahead. Maintains accurate and timely manufacturing records, this includes all paperwork and files. Actively promotes safety awareness in the lab, always acting in accordance with safety practices. May assist in the candling of eggs at the incubation department. Assists with washing, wrapping, and sterilizing glassware. Assists with transporting raw materials and finished product in and out of the lab areas. Completes daily/weekly job duties assigned monthly by SR Ops Process Leader. Performs other duties as assigned. Requirements B.S. in biology or science related field or 5 plus years of Marek's or Non-Marek's lab experience. Required knowledge of non-Marek’s technical processes. Is fully trained and can work independently in the following areas of Non-Marek's vaccine production; Commercial Ovo culture ' Tissue Culture bulk production. Ability to lift 50 pounds and carry 10 feet. Must be a team player. Must be able to lift 50 lbs. and carry it 10 ft. Must be able to squat, bend, and stoop, as well as twisting and turning. Manual dexterity and visual acuity are important. Must be able to wear appropriate Personal Protective Equipment (PPE.) Must be able to stand on feet for long periods of time and work in a sterile production environment. Must be flexible with availability (able to work overtime as needed on short notice). This position requires weekend work. Regular attendance is a must. Must possess the ability to work unsupervised, work well under time constraints, can think ahead to the next task, and be self-motivated. Ability to think ahead to next task. Ability to work well under time constraints. * Avian Biosecurity Policy: It is the responsibility of all Boehringer Ingelheim Animal Health, Inc. employees to take necessary steps to avoid contact with the avian species in general. This includes, but is not limited to, commercial poultry, yard chickens, turkeys, ducks, geese, wild birds, and pet birds. Should contact occur, precautions must be taken prior to entering a critical building or location: Anyone encountering the avian species should not enter a critical building or location for 24 hours unless they have showered, changed clothes and shoes.

Job Title: Production Technician Type: Hourly, Non-Exempt Reports To: Operations Manager A Production Technician plays a crucial role in the healthcare system, specifically in the context of long-term care facilities such as nursing homes, assisted living facilities, and rehabilitation centers. The Production Technician processes and fills prescriptions. The Technician will also get the pharmacy environment ready for business by turning on equipment such as computers, printers, and scales; greet customers; measure and label medication; help take payment; help control inventory and stock shelves; and enter data into a computerized system. The Technician will work directly with a dispensing pharmacist and the Operations Manager to provide excellent customer service. Scope of Responsibilities Hayat Pharmacy is an innovative and compassionate company providing a variety of pharmacy services in Wisconsin. The company operates robust community-based pharmacies that offer award-winning services such as medication packaging, medication management, and free prescription delivery. Hayat Pharmacy focuses on providing opportunities for customers to achieve high-quality health outcomes through access, education, and in-home consultation, and on building and maintaining strong relationships with community medical providers and other external stakeholders. Position Responsibilities Accurately and efficiently dispense medications according to prescription orders and facility-specific protocols. Perform order entry and verification to ensure the correct medications, dosages, and administration instructions are provided. Prepare and label medications for individual patients, considering their specific needs and dosage forms. Monitor and manage pharmacy inventory, including restocking medications, conducting regular audits, and ensuring proper storage conditions. Work closely with pharmacists, healthcare providers, and facility staff to address any medication-related concerns, provide education, and ensure optimal patient outcomes. Adhere to state and federal regulations governing pharmacy practices, including maintaining patient confidentiality and ensuring compliance with controlled substance handling procedures. Participate in quality assurance programs to uphold the highest standards of medication safety and accuracy. Provide exceptional customer service to facility staff and healthcare professionals, addressing inquiries and resolving issues promptly. Required Knowledge and Skills Previous LTC pharmacy experience. State of WI Pharmacy Technician License. Strong analytical and critical thinking skills. Excellent written and verbal communication skills. Strong attention to detail. Strong organizational skills. Experience with PioneerRX and Framework software. Dedication to providing excellent customer service. Ability to work both independently and with limited supervision. Basic Qualifications 3-5 years work experience High School Diploma / GED PTCB Certification preferred

Associate Operator, Production Tech I St. Louis, MO, US On-Site To set up machines to order specification for bottling. Fill and label products to order specification. Clean and sanitize equipment between orders. Strict attention to good manufacturing practices and plant safety and sanitation policies. At dsm-firmenich, being a force for good is not optional. Diversity, Equity & Inclusion is a shared responsibility woven into our daily work, benefiting to our People, Customers & Communities and driving business value. Equal access to opportunities is a given, belonging is a shared feeling, authenticity is celebrated. Your key responsibilities * Able to read and understand computer generated batch reports in order to set up machines to order specification. * Understand and follow Good Manufacturing Practices for the care, handling and storage of food products; and report any known or observed violations to management. Utilize HACCP philosophy and procedures in everyday work routine. * Must understand and follow all plant policies concerning safety/emergency, conduct, maintenance, sanitation and current procedures designed for the department. * Able to lift up to and including 50-pound packages in a safe manner as well as handling heavier packages including 55-gallon drums * Assist Team Leader and Production Supervisor in training new employees and performing competency reviews as needed * Must understand and follow procedures for pulling product samples for quality analysis We bring * Empowerment to make meaningful contributions while upholding ethical standards. * Recognition and celebration of your efforts and accomplishments * Opportunities for growth and advancement for those who embrace innovation and take initiative * Customer-first approach, working with world-renowned brands to turn ideas into impactful solutions * Responsibility and accountability in living company values and driving sustainable solutions * Supportive environment where individuals are empowered to progress and contribute to meaningful change You bring * High school diploma or equivalent * Ability to work independently and in accordance with company safety and sanitation standards is required * Must have 3-5 years related experience * Previous food plant experience helpful * Must possess and be able to demonstrate the knowledge, skills, and ability to perform the essential duties and responsibilities of a Production Tech I (kettle packing, serac, pail filler, drum line, flavor room 3 tank operations, label printing, and SAP) and Production Tech II (liquid compounding, emulsions, vanilla blending, vanilla still operation, and SAP * Willingness and ability to work in a facility with minimal temperature control, exposed to local temperature variations (hot & cold) About dsm-firmenich At dsm-firmenich, we don't just meet expectations - we go beyond them. Join our global team powered by science, creativity, and a shared purpose: to bring progress to life. From elevating health to making fortified food and sustainable skincare, the impact of your work here will be felt by millions - every single day. Whether it's fragrance that helps you focus, alternative meat that's better for the planet, or reducing sugar without losing flavor, this is where you help shape the future of nutrition, health, and beauty for everyone, everywhere. And while you're making a difference, we'll make sure you're growing too. With learning that never stops, a culture that lifts you up and the freedom to move across businesses, teams, and borders. Your voice matters here. And your ideas? They're essential to our future. Because real progress only happens when we go beyond, together. Inclusion, belonging and equal opportunity statement At dsm-firmenich, we believe being a force for good starts with the way we treat each other. When people feel supported, included, and free to be themselves, they do their best work - and that's exactly the kind of culture we're building. A place where opportunity is truly equal, authenticity is celebrated, and everyone has the chance to grow, contribute, and feel they belong. We're proud to be an equal opportunity employer, and we're serious about making our hiring process as fair and inclusive as possible. From inclusive language and diverse interview panels to thoughtful sourcing, we're committed to reflecting the world we serve. We welcome candidates from all backgrounds - no matter your gender, ethnicity, sexual orientation, or anything else that makes you, you. And if you have a disability or need any support through the application process, we're here to help - just let us know what you need, and we'll do everything we can to make it work. Agency statement We're managing this search directly at dsm-firmenich. If you're applying as an individual, we'd love to hear from you. We're not accepting agency submissions or proposals involving fees or commissions for this role.

Operator, Production Tech II St. Louis, MO, US On-Site To mix, blend, and formulate batches of raw ingredients and materials into finished product as specified on work orders to include liquid flavors and vanilla items according to formulas, procedures, and quality standards. At dsm-firmenich, being a force for good is not optional. Diversity, Equity & Inclusion is a shared responsibility woven into our daily work, benefiting to our People, Customers & Communities and driving business value. Equal access to opportunities is a given, belonging is a shared feeling, authenticity is celebrated. Your key responsibilities * Verify batch weights and quantities through mathematical calculations * Understand and follow Good Manufacturing Practices for the care, handling and storage of food products; and report any known or observed violations to management * Able to lift up to and including 50-pound packages in a safe manner as well as handling heavier packages including 55-gallon drums * Assist Team Leader and Production Supervisor in training new employees and performing competency reviews as needed * Properly and accurately sign off for raw materials retrieved, checking for foreign materials, rework generated, finished product produced, date and time completed on computer generated batch reports * Must understand and follow procedures for pulling product samples for quality analysis We bring * Empowerment to make meaningful contributions while upholding ethical standards. * Recognition and celebration of your efforts and accomplishments * Opportunities for growth and advancement for those who embrace innovation and take initiative * Customer-first approach, working with world-renowned brands to turn ideas into impactful solutions * Responsibility and accountability in living company values and driving sustainable solutions * Supportive environment where individuals are empowered to progress and contribute to meaningful change You bring * High school diploma or equivalent * Ability to work independently and in accordance with company safety and sanitation standards is required * Must have 3-5 years related experience * Previous food plant experience helpful * Must possess and be able to demonstrate the knowledge, skills, and ability to perform the essential duties and responsibilities of a Production Tech I (kettle packing, serac, pail filler, drum line, flavor room 3 tank operations, label printing, and SAP) and Production Tech II (liquid compounding, emulsions, vanilla blending, vanilla still operation, and SAP * Willingness and ability to work in a facility with minimal temperature control, exposed to local temperature variations (hot & cold) About dsm-firmenich At dsm-firmenich, we don't just meet expectations - we go beyond them. Join our global team powered by science, creativity, and a shared purpose: to bring progress to life. From elevating health to making fortified food and sustainable skincare, the impact of your work here will be felt by millions - every single day. Whether it's fragrance that helps you focus, alternative meat that's better for the planet, or reducing sugar without losing flavor, this is where you help shape the future of nutrition, health, and beauty for everyone, everywhere. And while you're making a difference, we'll make sure you're growing too. With learning that never stops, a culture that lifts you up and the freedom to move across businesses, teams, and borders. Your voice matters here. And your ideas? They're essential to our future. Because real progress only happens when we go beyond, together. Inclusion, belonging and equal opportunity statement At dsm-firmenich, we believe being a force for good starts with the way we treat each other. When people feel supported, included, and free to be themselves, they do their best work - and that's exactly the kind of culture we're building. A place where opportunity is truly equal, authenticity is celebrated, and everyone has the chance to grow, contribute, and feel they belong. We're proud to be an equal opportunity employer, and we're serious about making our hiring process as fair and inclusive as possible. From inclusive language and diverse interview panels to thoughtful sourcing, we're committed to reflecting the world we serve. We welcome candidates from all backgrounds - no matter your gender, ethnicity, sexual orientation, or anything else that makes you, you. And if you have a disability or need any support through the application process, we're here to help - just let us know what you need, and we'll do everything we can to make it work. Agency statement We're managing this search directly at dsm-firmenich. If you're applying as an individual, we'd love to hear from you. We're not accepting agency submissions or proposals involving fees or commissions for this role.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. Job Description * Works and communicates effectively with team members. * Maintains consistent quality and efficiency in all assigned work processes. * Keeps equipment and work environment clean and organized. * Understands and follows documents relevant to responsibilities, e.g., work instructions, checklists, batch records, logs. * Maintains accurate production records according to requirements and in compliance with established quality system standards. * Organizing, sorting and prioritizing DNA samples that come in daily. * Pipetting DNA sequencing reactions. * Performing DNA purification on sequencing reactions, loading and scheduling 3730xl ABI Sequencers. * Will work with and under the supervision of a Lab Team Lead. * Operating lab equipment: Thermocyclers, ABI 3730xl sequencers, centrifuges, automated liquid handlers. * Follows all company safety and regulatory policies, including handling hazardous materials and wearing of PPE that are relative to assigned work. Qualifications The ideal candidate would possess: * Experience with biology techniques and using basic lab equipment. * Capacity to perform under pressure in a fast paced production environment * Experience in oligonucleotide manufacturing highly desirable. * Experience with DNA Sequencing using 3730xl highly desirable. * Previous experience working in an ISO-9000 or cGMP environment. * Microsoft Windows and Excel proficiency. * Previous experience working with Hazardous Chemicals. * Strong computer, scientific, and organizational skills * Excellent communication (oral and written) and attention to detail * Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude * Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Basic Minimum Qualifications: * Bachelor's degree in biology, chemistry, or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major) * Annual RCRA awareness training. * Ability to lift 35+ pounds. * Authorization to work in the United States indefinitely without restriction or sponsorship Additional Information Position is part-time, between the hours of 2:00am and 6:00am. Candidates currently living within a commutable distance of Louisville, KY are encouraged to apply. What we offer: * Excellent full time benefits including comprehensive medical coverage, dental, and vision options * Life and disability insurance * 401(k) with company match * Paid vacation and holidays Eurofins USA Genomic Services is a Disabled and Veteran Equal Employment Opportunity employer.

Summary/objective The Quality Technician II plays a pivotal role in ensuring the effective, efficient, compliant, and proactive support of new product launches and the continuous quality of existing products. Essential Functions • Monitor and maintain the state of inventory, quality, equipment, maintenance, calibration and facilities and ensure they comply with QS and cGMP requirements. • Drive quality and compliance, adhering to all Quality Systems documentation requirements and establishing/supporting plans to exceed Niowave's goals for Quality, including Safety, Compliance, Six Sigma Quality, On-Time Delivery (OTD), and financial objectives. • Support internal and external audits. • Support validation of test methods, monitoring processes, and equipment. • Support production teams in product/material hold, release, disposition, and traceability assessments, and implement improvements to reduce recurring deviations that lead to rework or scrap. • Support new product introduction (NPI) quality activities including prototype testing, process validation, and technology transfer ensure successful product launches. • Collaborate with cross-functional teams to support and solve production and quality challenges. • Collect, monitor, analyze and communicate data to provide insight on quality metrics set by the management team. Specific Job Functions (Production) • Support product/material hold, release, disposition, and traceability assessments, and implement improvements to reduce recurring deviations. • Support teams throughout tolerance, nonconformances, deviations, complaints, and CAPA investigations. • Support teams through document revisions or change control procedures that support continuous improvement and other needs. • Support Quality Assurance Specialists (QAS) with completing quality checks and approvals on production records. Working Title Quality Technician II (Production) Market Title TBD Reports To Director of Quality FLSA Classification Hourly/Non-exempt Competencies: • Embraces and models the Niowave Values of Teamwork, Courage, Integrity, and Upright Zeal. • Understands how to integrate into a new team/organization - appreciates the history of current state, know how and when to make suggestions, as well as using just the right pace to reach the improved future state. • Understands their own communication and learning styles, can assess others' styles, and is able to find the right path to connect the two. • Demonstrates excellent organizational and analytical skills, complemented by strong computer literacy. • Demonstrates effective interpersonal, written, and oral communication skills. • Develops and maintains good relationships, gains the confidence of others and works effectively in a multidisciplinary matrix environment. • Resilient self-starter, who learns and acts quickly within a rapidly evolving environment. Required Education and Experience •ssociate degree or equivalent in science or another related field. • 2+ years related experience, with a solid understanding of regulatory compliance related to operations and quality procedures. • Experience in quality assurance or quality control roles within a manufacturing or industrial environment. • Knowledge and experience in eQMS and/or Inspection, Measuring and Test Equipment (IMTE) management. Preferred Education and Experience • Bachelor's degree or equivalent in science, engineering, or another related field. • 3+ years related experience, with a solid understanding of regulatory compliance related to operations and quality procedures. • Experience in a facility with radiation regulatory requirements and or quality assurance experience with pharmaceuticals or medical devices. • Experience with Minitab, JMP or other analytical tools. • Experience in audits (internal, NRC, FDA, etc.). • Knowledge of any of the following: ISO 13485, 21 CFR 820, 21 CFR 210/211, Nuclear Regulatory Commission (NRC) regulations or similar regulatory compliance experience. 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. • Use hands to finger, handle, or feel objects, tools, or controls • Reach with hands and arms • Climb stairs • Walk throughout all locations of the company • Talk and hear • Wear safety glasses, goggles, gloves, lab coat and/or Tyvek suit. • Occasionally lift or move office products and supplies, up to 25 pounds. • Stand and sit for prolonged periods. Position Type/Expected Hours of Work • Full-time position. • The company's standard operating hours are Monday through Friday 6a - 6p with production related activities requiring 24/7/365 shifts. • This position will have working hours during M - F and will be assigned to a production shift. • Niowave has multiple locations within the Lansing area. Travel between locations is expected in the role. Other duties Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.

Join a fast-growing, high-tech research and manufacturing company located next to beautiful Old Town Lansing. Niowave is a leader in the development of superconducting particle accelerators for the production of medical and industrial radioisotopes. The team is now scaling up to meet a worldwide demand for critical radioisotopes. These include the most-commonly used nuclear medicine tracer, molybdenum-99, and the revolutionary cancer-killing actinium-225. Summary/Objective Full-time position for electronics technicians to operate, install, and maintain superconducting particle accelerators. Collaborate with controls engineers to keep systems running and test new hardware. Job Duties Participate in operation of particle accelerators for research, development, and production runs Work with technicians, accelerator operators, engineers, and physicists to build, test, and deploy system components, including magnet coils and associated power supplies for focusing and steering electron beams high-voltage hardware radio-frequency systems, including vacuum-tube and solid-state amplifiers, high-power coax industrial PLC controls Diagnose failures and assist in repair, replacement, and improvements Work with vendors of mechanical and electrical equipment during troubleshooting Routing and terminating electrical controls and power wiring Assist manufacturing and assembly groups in the construction of new accelerator installations Desired Skills and Qualifications Electrical circuit soldering and debugging Familiarity with use of common electrical tools (multimeters, oscilloscopes) Familiarity with common mechanical hardware and hand tools Ability to read electrical schematics and wiring diagrams Familiarity with PLCs and microwave electronics desired Associate's Degree in Electronics or related field, or equivalent technical experience Job Conditions Participation in shift operation of accelerators including evening, night and weekend hours, and related on-call time Move between offices and buildings to access accelerator hardware and prototypes Operate computers and diagnostic hardware like multimeters and oscilloscopes Safely lift equipment and move supports into place up to 50 lbs (and more using appropriate rigging) Extract and communicate information from design documents, test reports, electrical schematics and manufacturing prints *Please include a cover letter with your resume and application.

Our Production Technician I - Label Printing plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. Once you complete our training, your responsibilities will include printing of labels for compounded sterile products (CSPs), bulk bags and non-sterile solutions in accordance with current Good Manufacturing Practices and Operating Procedures and communicates functions and duties necessary to operate the label printing equipment. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US. This is a full-time role for our 2nd Shift working Monday through Friday from 2:00 PM to 10:30 PM. This is a set, consistent schedule with minimum overtime requirements and based on site in our Bloomsbury, NJ location. This is a safety sensitive position that may be subject to random drug testing, in accordance with applicable laws. What the Production Technician I - Label Printing Does Each Day: * Operates label printing/verification equipment to print product labels * Safely transports label rolls from storage to printing area and back to printed label storage * Performs Batch specific cleaning of room and equipment and fill out appropriate preventative maintenance forms and checklists * Documents in a timely manner all tasks requiring written records * Maintains a smooth flow of production and monitors equipment * Escalates any equipment or process deviation Our Most Successful Production Technician I - Label Printing: * Approach others in a tactful manner * React well under pressure * Follow through on commitments * Carefully follows clear directions to ensure safety and accuracy * Are detail-oriented and take careful notes * Take initiative to identify problems and opportunities Minimum Requirements for this Role: * A High School diploma or equivalent * Able to successfully complete a background check * Able and willing to walk, stoop, stand, bend, and lift up to 50 lbs. throughout each shift, with or without reasonable accommodation * Familiarity with and comfortable using mobile devices such as smartphones, tablets, handhelds * 18+ years of age * Must be currently authorized to work in the United States on a full-time basis; Quva will not sponsor applicants for work visas * Minimum of 1 year reliable and sustained performance as Production Technician (ILP, Post Compounding, Formulation, Warehouse) OR relevant work experience * Label printing CAs as per Label Printing training curriculum Any of the Following Will Give You an Edge: * College Degree with an emphasis in Chemistry, Biochemistry or equivalent * Pharmaceutical experience * Experience operating printing equipment, computer software & hardware * Working knowledge of cGMPs and regulatory requirements as well as all applicable SOPs Benefits of Working at Quva: * Set, full-time, consistent work schedule * Comprehensive health and wellness benefits including medical, dental and vision * 401k retirement program with company match * 17 paid days off plus 8 paid holidays per year * Occasional weekend and overtime opportunities with advance notice * National, industry-leading high growth company with future career advancement opportunities * The base compensation for this role is estimated to be within the range described below. The compensation offered may vary depending on relevant factors such as experience, skills, training, education, certifications, geographic location, and market conditions * Range: $19.00-$23.00/hour About Quva: Quva is a national, industry-leading provider of compounded injectable medicines and software solutions that help power the business of hospital and health-system pharmacy. Quva Pharma produces and distributes injectable medicines required by health care providers and critical to patient care. Quva BrightStream partners with health-systems to analyze large amounts of data and through AI and machine learning, develops software solutions that turns the data into insights that are used to better run their pharmacy operation. Quva's overall product and technology offerings help health-systems achieve greater value and deliver the highest-quality patient care. Quva is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. Quva's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with Quva is "at will." California Consumer Privacy Act (CCPA) Notice for Applicants and Employees

TITLE: Production Technician Title: Production Technician Reports To: Production Supervisor Indivior is a global pharmaceutical company working to help change patients' lives by developing medicines to treat opioid use disorder (OUD). Our vision is that all patients around the world will have access to evidence-based treatment for OUD and we are dedicated to transforming OUD from a global human crisis to a recognized and treated chronic disease. Building on its global portfolio of OUD treatments, Indivior has a pipeline of product candidates designed to expand on its heritage in this category. Headquartered in the United States in Richmond, VA, Indivior employs approximately 800 individuals globally. Visit **************** to learn more. Connect with Indivior on LinkedIn by visiting ********************************** POSITION SUMMARY: The Production Technician will be responsible to setup/run/improve the dispensing/compounding and filling process and will also be the individual that train and certify new employees in these areas to make sure we have the same level of knowledge between our teams. ESSENTIAL FUNCTIONS: The responsibilities of this role include, but are not limited to, the following: * Adhere to plant safety policies and procedures, contribute to a safe work environment. * Setup and operate highly automated equipment in the PFS Suite. * Adhere to standard operating procedures and current Good Manufacturing Practices to ensure quality of product. * Provide customer-oriented service and support in fast-paced manufacturing environment. * Document process steps on appropriate batch documentation. * Attain and maintain qualification for the operation of assigned process equipment and duties in the area. * Perform preventative and corrective maintenance of assigned process equipment. * Collaborate with Maintenance and Engineering personnel to troubleshoot equipment problems. * Proactively monitor documentation and product quality, properly documenting all activities and reporting issues to supervision. * Contribute to the achievement of key departmental objectives including improving safety performance, reducing deviations, improving productivity, and training compliance. MINIMUM QUALIFICATIONS: * High school diploma/GED with minimum five (5) years of experience in pharmaceutical Pre-Filled Syringe (PFS) manufacturing required OR * Associate degree with minimum four (4) years of experience in pharmaceutical Pre-Filled Syringe (PFS) manufacturing * High technical knowledge of GMP manufacturing in a manufacturing environment. * Demonstrated proficiency in Pre-Filled Syringe (PFS) manufacturing operations related to all functions of the filling process * Knowledge of current Good Manufacturing Practices (cGMPs) * Previous experience with Manufacturing Execution Systems and electronic batch release is preferred. COMPETENCIES/CONDUCT: In addition to the minimum qualifications, the employee will demonstrate: * Strong ability to multitask * Ability to demonstrate attention to detail * Ability to develop independence in performing daily tasks * Collaborative work ethic with a strong bias for action * Demonstrated ability to train and coach others * Ability to effectively communicate (written and verbal) * Flexibility and problem-solving skills * Knowledge of lean manufacturing principles * Ability to wear personal protective equipment (safety glasses, safety shoes, protective gloves etc. BENEFITS: Indivior is committed to providing a culture driven by guiding principles and top-tier benefits that match the importance of the work we do. The Indivior experience includes: * 3 weeks' vacation plus floating holidays and sick leave, plus company closure from December 24th- January 1st * 401(k) and Profit Sharing Plan- Company match of 75% on your first 6% of contributions and profit sharing contribution equal to 4% of your eligible pay * U.S. Employee Stock Purchase Plan- 15% Discount * Comprehensive Medical, Dental, Vision, Life and Disability coverage * Health, Dependent Care and Limited Purpose Flex Spending and HSA options * Adoption assistance * Tuition reimbursement * Concierge/personal assistance services * Voluntary benefits including Legal, Pet Insurance and Critical Illness coverage * Gym, fitness facility and cell phone discounts GUIDING PRINCIPLES: Indivior's guiding principles are the foundation for each employee's success and growth. Each employee is expected to demonstrate understanding and adherence to our guiding principles in their everyday performance. COMPLIANCE OBLIGATIONS: Indivior is committed to maintaining a workplace where employees are committed to compliance and feel comfortable raising concerns about potential violations of policies or unethical behaviour. As part of your responsibilities, you are expected to: Employee Obligations: * Have unquestionable ethics and integrity with the willingness to stand firm on these principles even under significant pressure * Risk IQ: Know what policies apply to your role and function and adhere to them. * Speak Up: If you see something, say something. Manager Obligations: * Have unquestionable ethics and integrity with the willingness to stand firm on these principles even under significant pressure * Reinforce risk awareness with your team, with accountability and oversight for ongoing review and mitigation. * Model and reinforce a Speak Up culture on your team. The duties and responsibilities identified in this position description are considered essential but are not limited to only those outlined. The employee may perform other functions that may be assigned. Management retains the discretion to add or change the duties of this position at any time. EQUAL EMPLOYMENT OPPORTUNITY EOE/Minorities/Females/Vet/Disabled

Our Production Technician I - Prep plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. Once you complete our training, your responsibilities will include supporting the preparation of up-front processes of the manufacturing of compounded sterile preparations (CSPs) in accordance with established procedures. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US. This is a full-time role for our 1st shift, working Monday through Friday from 6AM to 2:30PM. This is a set, consistent schedule with minimum overtime requirements and based on site in our Bloomsbury, NJ location. This is a safety sensitive position that may be subject to random drug testing, in accordance with applicable laws. What the Production Technician I - Prep Does Each Day: * Support cleanrooms, formulations, ILP, and compounding * Assist in preparation, transportation, labeling, production, and processing of materials * Daily/weekly/monthly cleaning of rooms and equipment while adhering to standards * Maintain Aseptic Gowning Qualification to support cleaning * Complete necessary documents for accountability and traceability of product following Good Documentation Practices (GDPs) * Manage FEFO of chemicals, pulling expired ones monthly * Complete documentation of activities in accordance with established procedures * Perform sterile filter integrity testing as required Our Most Successful Production Technicians I - Prep: * Promote active listening with team members and enjoys collaboration * Effectively and productively engages with others and establishes trust, credibility, and confidence with others * Are Customer Oriented * Take initiative to identify problems and opportunities Minimum Requirements for this Role: * High school Diploma or GED from recognized institution or organization * Able to successfully complete a background check * 18+ years of age * Able and willing to walk, stoop, stand, bend, and lift up to 50 lbs. throughout each shift, with or without reasonable accommodation * Familiarity with and comfortable using mobile devices such as smartphones, tablets, handhelds * Must be currently authorized to work in the United States on a full-time basis; Quva is not able to sponsor applicants for work visas Any of the Following Will Give You an Edge: * Experience in a role requiring repetitive tasks * Experience in a pharmaceutical manufacturing environment * Experience with Good Documentation Practices (GDPs) * At least 1 year hospital or retail pharmacy experience * At least 1-year pharmaceutical manufacturing * CPhT Certification * ACPE Sterile Certification Benefits of Working at Quva: * Set, full-time, consistent work schedule * Comprehensive health and wellness benefits including medical, dental and vision * 401k retirement program with company match * 17 paid days off plus 8 paid holidays per year * Occasional weekend and overtime opportunities with advance notice * National, industry-leading high growth company with future career advancement opportunities * The base compensation for this role is estimated to be within the range described below. The compensation offered may vary depending on relevant factors such as experience, skills, training, education, certifications, geographic location, and market conditions * Range: $18.00-$21.00/hour About Quva: Quva is a national, industry-leading provider of compounded injectable medicines and software solutions that help power the business of hospital and health-system pharmacy. Quva Pharma produces and distributes injectable medicines required by health care providers and critical to patient care. Quva BrightStream partners with health-systems to analyze large amounts of data and through AI and machine learning, develops software solutions that turns the data into insights that are used to better run their pharmacy operation. Quva's overall product and technology offerings help health-systems achieve greater value and deliver the highest-quality patient care. Quva is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. Quva's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with Quva is "at will." California Consumer Privacy Act (CCPA) Notice for Applicants and Employees

Our Production Technician I - ILP plays a vital role within our organization. Once you complete our training, your responsibilities will include supporting execution of product visual inspection, labeling and packaging (ILP) operations at the Quva facility in accordance with established processes and procedures. At Quva, you will be an essential part of a mission-driven organization dedicated to expanding critical access to quality, affordable medication and data insights while promoting a culture of innovation, collaboration, and continuous improvement. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US. This is a full-time role for our 1st Shift, working Monday through Friday from 6:30 AM to 3:00 PM. This is a set, consistent schedule with minimum overtime requirements and based on site in our Bloomsbury, NJ location. This is a safety sensitive position that may be subject to random drug testing, in accordance with applicable laws. Watch this video to learn more What the ILP Technician Does Each Day: * Assists preparation of inspection and packaging room materials supplies * Conducts labeling and the processing of production materials as required * Daily/ Bi-Weekly/Monthly cleaning of room and equipment and fills out appropriate preventative maintenance forms and checklists in accordance with SOP's * Conduct and complete line and room clearances as per established procedures * Completes necessary documents for accountability and traceability of products following Good Documentation Practices (GDPs); comply with cGMPs, and company ISO standards * Complies with 503B guidelines; cGMPs, standard operating procedures and company policies * Performs equipment calibration checks and troubleshoots production equipment as needed * Completes documentation of activities in accordance with established procedures * Immediately notifies production management of deviations to established processes or procedures * Assists other areas as needed (cleaning; non-sterile filling; kitting and preparation operations, etc.) * Primary, secondary, and tertiary labeling of products * Secondary and final packaging of product * Requires visual inspection of product * Maintains inspection ready environment and supports internal / external audits Our Most Successful ILP Technicians: * Promotes active listening with team members; Contributes appropriately to conversations; Strong verbal and written communication skills with the ability to work effectively with other departments within the organization and with people at all levels of the organization * Understands how various issues affect each other and the outcome of projects; Improves upon existing approaches by seeking opportunities to creatively transform; mechanical aptitude a plus * Effectively and productively engages with others and establishes trust, credibility, and confidence with others * Listens to internal customers, ensures commitments are met, sets appropriate internal customer expectations * Has working knowledge of cGMPs and regulatory requirements as well as all applicable SOPs * Follows policies and procedures; completes administrative tasks correctly and on time * Approaches others in a tactful manner; reacts well under pressure; treats others with respect and consideration regardless of their status or position; accepts responsibility for own actions; follows through on commitments * Has strong attention to detail * Is flexible and can adapt to support multiple production areas and shifts as needed Minimum Requirements for this Role: * High school Diploma or GED from recognized institution or organization required * Will be required to undergo a color perception exam and must be able to produce a passing test result * Will be required to undergo a vision exam and must be able to produce 20/20 vision with or without correction * Able to successfully complete a drug and background check * 18+ years of age * Must be currently authorized to work in the United States on a full-time basis; Quva will not sponsor applicants for work visas Any of the Following Will Give You an Edge: * Pharmaceutical experience Benefits of Working at Quva: * Set, full-time, consistent work schedule * Comprehensive health and wellness benefits including medical, dental and vision * 401k retirement program with company match * 17 paid days off plus 8 paid holidays per year * Occasional weekend and overtime opportunities with advance notice * National, industry-leading high growth company with future career advancement opportunities * The base compensation for this role is estimated to be within the range described below. The compensation offered may vary depending on relevant factors such as experience, skills, training, education, certifications, geographic location, and market conditions * Range: $18.00 - $21.00 / Hour or Year About Quva: Quva is a national, industry-leading provider of compounded injectable medicines and software solutions that help power the business of hospital and health-system pharmacy. Quva Pharma produces and distributes injectable medicines required by health care providers and critical to patient care. Quva BrightStream partners with health-systems to analyze large amounts of data and through AI and machine learning, develops software solutions that turns the data into insights that are used to better run their pharmacy operation. Quva's overall product and technology offerings help health-systems achieve greater value and deliver the highest-quality patient care. Quva is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. Quva's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with Quva is "at will." California Consumer Privacy Act (CCPA) Notice for Applicants and Employees

Our Production Technician I - Prep/Cleanroom Support Technician plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. Once you complete our training, your responsibilities will include assisting in Prep/Cleanroom operations at QuVa Pharma in accordance with established processes and procedures. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US. This is a full-time role for our 2nd shift, working Monday through Friday from 2:00 PM to 10:30 PM CST. This is a set, consistent schedule with minimum overtime requirements and based on site in our Sugar Land, TX location. This is a safety sensitive position that may be subject to random drug testing, in accordance with applicable laws. What the Production Technician I - Prep/Clean Room Support Does Each Day: * Support cleanrooms, formulations, ILP, and compounding * Assist in preparation, transportation, labeling, production, and processing of materials * Daily/weekly/monthly cleaning of rooms and equipment while adhering to standards * Maintain Aseptic Gowning Qualification to support cleaning * Complete necessary documents for accountability and traceability of product following Good Documentation Practices (GDPs) * Manage FEFO of chemicals, pulling expired ones monthly * Complete documentation of activities in accordance with established procedures * Perform sterile filter integrity testing as required Our Most Successful Production Technicians I - Prep/Clean Room Support: * Promote active listening with team members and enjoys collaboration * Effectively and productively engages with others and establishes trust, credibility, and confidence with others * Are Customer Oriented * Take initiative to identify problems and opportunities Minimum Requirements for this Role: * A High School diploma or equivalent * Able to successfully complete a background check * Able and willing to walk, stoop, stand, bend, and lift up to 50 lbs. throughout each shift, with or without reasonable accommodation * Familiarity with and comfortable using mobile devices such as smartphones, tablets, handhelds * Able and willing to follow strict clothing and accessory rules to support our sterile operating environment * 18+ years of age * Must be currently authorized to work in the United States on a full-time basis; Quva will not sponsor applicants for work visas Any of the Following Will Give You an Edge: * Experience in a role requiring repetitive tasks * Experience in a pharmaceutical manufacturing environment * Experience with Good Documentation Practices (GDPs) * 1-year of pharmaceutical manufacturing * CPhT Certification * ACPE Sterile Certification Benefits of Working at Quva: * Set, full-time, consistent work schedule * Comprehensive health and wellness benefits including medical, dental and vision * 401k retirement program with company match * 17 paid days off plus 8 paid holidays per year * Occasional weekend and overtime opportunities with advance notice * National, industry-leading high growth company with future career advancement opportunities About Quva: Quva is a national, industry-leading provider of compounded injectable medicines and software solutions that help power the business of hospital and health-system pharmacy. Quva Pharma produces and distributes injectable medicines required by health care providers and critical to patient care. Quva BrightStream partners with health-systems to analyze large amounts of data and through AI and machine learning, develops software solutions that turns the data into insights that are used to better run their pharmacy operation. Quva's overall product and technology offerings help health-systems achieve greater value and deliver the highest-quality patient care. Quva is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. Quva's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with Quva is "at will." California Consumer Privacy Act (CCPA) Notice for Applicants and Employees

Our Production Technician I - ILP plays a vital role within our organization. Once you complete our training, your responsibilities will include supporting execution of product visual inspection, labeling and packaging (ILP) operations at the Quva facility in accordance with established processes and procedures. At Quva, you will be an essential part of a mission-driven organization dedicated to expanding critical access to quality, affordable medication and data insights while promoting a culture of innovation, collaboration, and continuous improvement. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US. This is a full-time role for our 1st shift, working Monday through Friday from 6:00 AM to 2:30 PM CST. This is a set, consistent schedule with minimum overtime requirements and based on site in our Sugar Land location. This is a safety sensitive position that may be subject to random drug testing, in accordance with applicable laws. Watch this video to learn more What the Production Technician I - ILP Does Each Day: * Assists preparation of inspection and packaging room materials supplies * Conducts labeling and the processing of production materials as required * Daily/ Bi-Weekly/Monthly cleaning of room and equipment and fills out appropriate preventative maintenance forms and checklists in accordance with SOP's * Conduct and complete line and room clearances as per established procedures * Completes necessary documents for accountability and traceability of products following Good Documentation Practices (GDPs); comply with cGMPs, and company ISO standards * Complies with 503B guidelines; cGMPs, standard operating procedures and company policies * Performs equipment calibration checks and troubleshoots production equipment as needed * Completes documentation of activities in accordance with established procedures * Immediately notifies production management of deviations to established processes or procedures * Assists other areas as needed (cleaning; non-sterile filling; kitting and preparation operations, etc.) * Primary, secondary, and tertiary labeling of products * Secondary and final packaging of product * Requires visual inspection of product * Maintains inspection ready environment and supports internal / external audits Our Most Successful Production Technician I - ILP: * Promotes active listening with team members; Contributes appropriately to conversations; Strong verbal and written communication skills with the ability to work effectively with other departments within the organization and with people at all levels of the organization * Understands how various issues affect each other and the outcome of projects; Improves upon existing approaches by seeking opportunities to creatively transform; mechanical aptitude a plus * Effectively and productively engages with others and establishes trust, credibility, and confidence with others * Listens to internal customers, ensures commitments are met, sets appropriate internal customer expectations * Has working knowledge of cGMPs and regulatory requirements as well as all applicable SOPs * Follows policies and procedures; completes administrative tasks correctly and on time * Approaches others in a tactful manner; reacts well under pressure; treats others with respect and consideration regardless of their status or position; accepts responsibility for own actions; follows through on commitments * Has strong attention to detail * Is flexible and can adapt to support multiple production areas and shifts as needed Minimum Requirements for this Role: * High school Diploma or GED from recognized institution or organization required * Will be required to undergo a color perception exam and must be able to produce a passing test result * Will be required to undergo a vision exam and must be able to produce 20/20 vision with or without correction * Able to successfully complete a drug and background check * 18+ years of age * Must be currently authorized to work in the United States on a full-time basis; Quva will not sponsor applicants for work visas Any of the Following Will Give You an Edge: * Pharmaceutical experience Benefits of Working at Quva: * Set, full-time, consistent work schedule * Comprehensive health and wellness benefits including medical, dental and vision * 401k retirement program with company match * 17 paid days off plus 8 paid holidays per year * Occasional weekend and overtime opportunities with advance notice * National, industry-leading high growth company with future career advancement opportunities About Quva: Quva is a national, industry-leading provider of compounded injectable medicines and software solutions that help power the business of hospital and health-system pharmacy. Quva Pharma produces and distributes injectable medicines required by health care providers and critical to patient care. Quva BrightStream partners with health-systems to analyze large amounts of data and through AI and machine learning, develops software solutions that turns the data into insights that are used to better run their pharmacy operation. Quva's overall product and technology offerings help health-systems achieve greater value and deliver the highest-quality patient care. Quva is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. Quva's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with Quva is "at will." California Consumer Privacy Act (CCPA) Notice for Applicants and Employees

Our Production Technician I - Formulation plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical product. Once you complete our training, your responsibilities will include supporting daily manufacturing activities for non-sterile and sterile bulk/CSP operations. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US. This is a full-time role for our 3rd shift, working Monday through Friday from 10:00 PM to 6:30 AM. This is a set, consistent schedule with minimum overtime requirements and based on site in our Sugar Land, TX location. This is a safety sensitive position that may be subject to random drug testing, in accordance with applicable laws. What the Production Technician I - Formulation Does Each Day: * Weighing of chemicals to support product formulation * Formulation of bulk intermediate solutions * Sterile filter integrity testing * Clean Room cleaning and disinfection * Perform equipment calibration checks * Daily Supply list for respective area turned into receiving by scheduled time * Open/close Formulation pods and ILP in accordance with work instructions and daily task lists Our Most Successful Production Technician I - Formulation: * Approach others in a tactful manner * React well under pressure * Follow through on commitments * Carefully follows clear directions to ensure safety and accuracy * Are detail-oriented and take careful notes * Take initiative to identify problems and opportunities * Have strong math skills Minimum Requirements for this Role: * A High School diploma or equivalent * Able to successfully complete a drug and background check * Familiarity with and comfortable using mobile devices such as smartphones, tablets, handhelds * Able and willing to walk, stoop, stand, bend, and lift throughout each shift, with or without accommodation * 18+ years of age * Must be currently authorized to work in the United States on a full-time basis; QuVa will not sponsor applicants for work visas * Requires extensive training and qualification including but not limited to: gown training; aseptic technique; competency assessments; direct observation; and media fill qualification for each compounding process * Strong math skills Any of the Following Will Give You an Edge: * College Degree with an emphasis in Chemistry, Biochemistry or equivalent * 1 year of pharmaceutical manufacturing experience * Working knowledge of cGMPs and regulatory requirements as well as all applicable SOPs Benefits of Working at QuVa: * Set, full-time, consistent work schedule * Comprehensive health and wellness benefits including medical, dental and vision * 401k retirement program with company match * 17 paid days off plus 8 paid holidays per year * Occasional weekend and overtime opportunities with advance notice * National, industry-leading high growth company with future career advancement opportunities About QuVa: QuVa Pharma is a national, industry-leading, FDA registered 503B outsourcing services company that provides hospitals with essential medications in ready-to-administer injectable formats that are critical for effective patient care. We are leading the way with unmatched expertise in current Good Manufacturing Practices and sterile pharmaceutical manufacturing, and the highest quality and safety standards so hospitals can more confidently and reliably focus on patient care nationwide. As a leader in sterile compounding, we continue to invest in automation and integrated technologies to improve our production processes, safety, consistency, and product quality. As part of our team, you'll experience being at the forefront of groundbreaking solutions, collaborating with brilliant minds, and making a tangible impact in healthcare delivery. QuVa is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. QuVa's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with QuVa is "at will." California Consumer Privacy Act (CCPA) Notice for Applicants and Employees

**About Us:** Cordis is an independent, customer-focused global provider of interventional cardiovascular medical technologies. During our 60+ year history we've established a legacy of pioneering breakthrough technologies, including the first guiding catheters and coronary drug eluting stents. Cordis has built a strong global footprint that spans over 70 countries. We're teammates, not just employees. Our culture empowers you to act like an owner and unleash your full potential in the process. With diverse teams on a global scale, we foster an inclusive atmosphere where everyone is embraced for who they are, their unique perspective, and what they bring to the table. We believe the richness of our experiences and backgrounds enhances the careers of our teammates, the service to our customers, and ultimately, the lives of our patients. If you love a challenge and are ready to have a direct, positive impact on the lives of millions, then Cordis is just the place for you. Join us, and let's improve the wellbeing of millions, together. **We are the people behind the people who keep saving lives.** The 1 st shift Sr Tech Production Set-up and Maintenance coordinates and perform the calibration and preventative maintenance activities for equipment in the Operations and R&D areas. **Responsibilities** + Perform routine calibration, preventative maintenance, and repair on manufacturing/R&D equipment and systems (including mechanical, pneumatic, and electrical systems). + Repair equipment/fixtures as requested by the equipment/fixture owner(s). + Possess basic knowledge of a wide range of equipment and the ability to provide technical support to Manufacturing, R&D, and other departments. + Ability to review results to ensure that it complies with predetermined requirements/criteria (such as visual, dimensional criteria, etc.). + Perform simple calibration activities (as required, with training). + Responsible for adhering to all hygiene and safety standards. + Responsible for following all company SOPs, cGMPs, WIs, and Quality policies. + Work with support groups to troubleshoot and repair equipment. + Must be able to work effectively with other department personnel. + Responsible for communicating business related issues or opportunities to next management level. + Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures. + Responsible for ensuring compliance with Quality Procedures, Laws and Regulations of the applicable markets. + Performs other duties assigned as needed. **Qualifications** + High school diploma or equivalent (AA degree preferred) and 5-10years related work experiencerequired. + 5+ years working with production related equipment within a Controlled Environment Room (Clean Room) is preferred. + Experience or training in hazardous material emergency response is desirable. + Experience in a regulated industry where documentation compliance is enforced is preferred. + Knowledge of use of hand-tools. **Pay / Compensation** The expected pre-tax pay rate for this position is $27.11 - $40.67 per hour Actual pay may fluctuate outside of the range depending on skills, education, experience, job-related knowledge and location. Cordis is proud to be an equal opportunity employer and is committed to providing equal opportunity for all teammates and applicants. At Cordis, our teammates all bring different strengths, experiences, and backgrounds, who share a passion for improving people's lives. Diversity not only includes race and gender identity, but also age, disability status, veteran status, sexual orientation, religion, and many other parts of one's identity. All our teammate's points of view are key to our success, and we believe inclusion is everyone's responsibility. Together, we strive to create and maintain working and learning environments that are inclusive, equitable and welcoming. **JOIN OUR TALENT COMMUNITY** Joining our Talent Community is a great way to receive company news and updates, as well notifications on career opportunities and events that interest you! Please tell us more about yourself so we can align you with future opportunities that match your background, skills and interests. **Job Locations** _US-CA-Santa Clara_ **ID** _2025-3504_ **Category** _Operations_ **Position Type** _Regular Full-Time_ CORDIS is proud to be an equal opportunity employer, values diversity in all its forms is and committed to fostering an inclusive work environment. We are committed to advancing our culture of belonging, where all teammates feel seen, heard, and appreciated and encouraged to be their authentic selves. Our team is invested in attracting, retaining and growing top talent. Our Teammates are the core of our innovation and success. Cordis is an inclusive, engaging place to work and grow a career. CORDIS is committed to offering reasonable accommodations, upon request, to job applicants with disabilities. If you need assistance or an accommodation due to a disability, please contact *******************

Job Description This position functions primarily in a classified ISO-8 environment and requires the individual to wear appropriate PPE. This position will perform dispensing and formulation operations and perform other duties, such as cleaning, restocking, visual inspection, and labeling, as required and/or assigned. All assigned tasks must be conducted in adherence with all applicable procedures, cGMPs, company policies and any other quality or regulatory (Ex: OSHA, DEA, FDA, etc.) requirements. Facility is a multiple shift operation where variable shifts, including weekends, may be required. Schedule: Tuesday to Friday 3 PM Until 1:30 AM (or until work is completed) Pay: $25/hour SAFETY Strictly adhere to all cGMP, health and safety requirements, procedures, and corporate policies. Authorized to immediately stop any task that is determined to be an imminent hazard. Always promote and demonstrate safe work practices and adhere to PPE requirements. Safely handle chemicals, corrosives, solvents, and other pharmaceutical compounds. Demonstrate physical ability to lift a minimum of 50 lbs. and push/pull pallets, product cans, etc. multiple times per shift. PRIMARY RESPONSIBILITIES: Perform ISO-8 dispensing and formulation operations consistent with established protocols, procedures, and regulatory/cGMP requirements. Learn to utilize all relevant equipment/technology for formulation operations. Complete and document required training to gain proficiency for all assigned job tasks. Accurately and contemporaneously document all actions performed per GDP standards. Assist with classified and non-classified area cleaning and maintenance as required. Perform visual inspection, labeling, and additional support tasks as required. Make recommendations for process improvements. Possess the ability to master multiple processes across different areas. Recognize and respond appropriately to equipment/documentation issues and deviations; obtain appropriate clarification and guidance from leadership before proceeding. Maintain a quality focused, “Right First Time”, attitude. Arrive for work on-time, prepared to work in the classified environment for the majority of each shift. Operate with Integrity by maintaining high ethical standards. Treat all employees with trust, respect, and professionalism. Speak up and hold others accountable for high integrity by providing constructive feedback. Take accountability for individual and team mistakes and participate in related corrective actions. Ensure patient safety by understanding you and your team's impact on product quality. Excel within a diverse and high performing team. Remain open to new ideas and perspectives, communicate across shifts as required, and comply with site process to create a safe work environment. Demonstrate a passion to perform by meeting personal and departmental goals. Self-driven and self-accountable, performs required tasks, and progresses on qualifications within reasonable timelines. Demonstrate innovation abilities by identifying and speaking up about viable options for improvements and exploring and creating a path for implementation. High School Diploma or equivalent. Must pass a drug test. Must speak, write, and read English. Must be a team player. Must have excellent attention to detail. Prior Sterile Compounding and Pharmaceutical Industry experience. Prior experience operating manufacturing equipment/machinery. Knowledge of FDA guidelines, cGMP, and GDP. Willingness to participate in training and gain other certifications as needed. Knowledge of basic arithmetic and chemistry calculations. Ability to work in a fast-paced environment with dynamic priorities and demands. Excellent written and verbal communication skills. Desire to expand knowledge and grow with the company. Leadership ability.