Assembly Operator jobs at West Pharmaceutical Services - 104 jobs

At West, we're a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West's indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future? There's no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families. We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts. Job Summary In this role, you will be responsible for the production of components that meet or exceed pre-determined specifications. Responsible for inspection, packaging, labeling, and completion of documentation necessary to provide quality, production, and traceability records in accordance with Quality Systems ISO 9001/ ISO 13485. Essential Duties and Responsibilities * Ensures the quality of the parts produced by inspecting parts visually. Ensures all relevant documentation is recorded and signed off in real time. * Always maintains accuracy of batch documentation and ensures that it is filled in and is right the first time. * Completes measurements, as required by the work instructions, reviews measurement results, and alerts appropriate personnel of any deviations from the customer specifications or part print. * Packages the parts according to customer specifications and indicates the status of the part (accept/reject) according to proper procedures and specifications. * Places the finished product in the correct location. * Understands and safely operates all equipment. * Reports and/or corrects unsafe working conditions. * Performs secondary operations as necessary to meet customer specifications. * Performs general cleaning of machines and ancillary equipment. * Verifies the labels for correct part and lot numbers. * Maintains proper levels of packaging supplies at each machine. * Maintains work areas in a clean and orderly manner by practicing good housekeeping. * Defines machine status on OEE System to determine machine downtime and run time. * Compliance with all site Environmental, Health and Safety requirements, training, and regulations. * Compliance with all local site company polices, procedures, and corporate policies. * Supports and contributes to Lean Sigma programs and activities towards the delivery of the set target. * Acts in accordance with the company's guiding principles and adherence to the corporate Code of Conduct. * Performs additional duties at the request of the direct supervisor. * Maintains methods/procedures and all supporting documentation to meet the requirements of Quality Systems ISO 13485:2016. #LI-Onsite #LI-JS1 Education * A High School Diploma or GED is required. Work Experience * Previous production work experience would be an advantage. * Knowledge of Good Manufacturing Practices (GMP) requirements would be an advantage. Preferred Knowledge, Skills and Abilities * Must have good verbal reasoning, numerate ability, and mechanical aptitude skills. * Must have good communication skills, both written and oral. * Must have good organizational skills. * Must be able to work in a team environment. * Basic knowledge and understanding of a computer. * Must be willing to work in a controlled environment, which involves the wearing of a gown, cap, and relevant personal protective equipment. Travel Requirements 5%: Up to 13 business days per year Physical Requirements Medium-Exerting up to 50lb/22kg of force occasionally and/or up to 20lbs/9kg of force frequently, and/or up to 10lbs/4kgs of force constantly to move objects. West is an equal opportunity employer and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, or disability status. If you have a special need that requires accommodation in order to apply to West, please send an email to Apply.Accommodation@westpharma.com. Where permitted by law, an offer of employment with West Pharmaceutical Services, or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of background screening and/or a pre-employment drug screening.

**At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world.** Job Description: **At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world.** This is a temporary position for an Assembly Operator III working directly with fiber optics. This position is responsible for optical connector assembly, termination of various configurations of fiber optic cable assemblies, and testing of these cable assemblies. This individual may assist in process development and resolution of problems encountered in the process of bringing new optical products from concept to market. The individual is a self-starter and has the ability to work well under schedule pressures and ability to balance workload as priorities change. Candidates will have a strong work ethic with a desire to continually learn & with a concentrated focus on serving the Customer. The ideal candidate works well in teams, has the desire to learn, possesses strong hand-eye coordination, and maintains the attention to detail needed to make quality products for our customers. Every team member is responsible for maintaining housekeeping and organization of the work area, following safety guidelines and all TE Connectivity's policies and procedures. **Shifts Available:** **1st:** Mon-Fri, 7am-3:30pm **2nd:** Mon-Fri, 3pm-11:30pm _(10% Shift Differential)_ **Weekend:** Fri-Sun, start on 6/13 - 7AM-7:30PM _(22% Shift differential)_ **Job Requirements** - Polish and test fiber optic cables - Assemble and package fiber optic connector components - Terminate single and multi-fiber cables - Operate fiber router & complete over-molding process (as needed) - Support prototype product builds, test product builds, pre-release NPI builds (as needed) - Measure components using calipers, gages, or other measuring devices - Complete necessary operational paperwork required to maintain the traceability of product - May troubleshoot and perform minor repairs to equipment - Understand cleaning methods and contamination assessment for optical assembly - Perform EFG & IPC (workmanship) checks on both single & multi-fiber termini - Mechanical Aptitude to safely & efficiently operate equipment (E-Stop/Soft Stop) and identify issues - Assist in the estimation process step durations - Suggest process changes to improve overall manufacturing efficiencies - Communicate within a team atmosphere to ensure clarity of purpose & Customer satisfaction - After training period of 30 days, works with limited supervision to provide timely and quality products - Inspect own work and products using quality standards, work instructions and prints - Accountability - takes responsibility for his/her own work. Respects confidential information and concerns shared by others. - Available to work overtime to support production goals as needed - Ability to work in a clean room environment wearing all required clean room gowning garments and PPE (gowns, shoe booties, hair nets, nitrile gloves, safety glasses, safety shoes) **What your background should look like** - High School diploma or GED preferred - Minimum 1 year manufacturing experience required with knowledge and understanding of manufacturing principles such as Safety, Quality, Delivery, Inventory, and Productivity. - Minimum 1 year experience in a fiber optic manufacturing environment preferred - SAP Manufacturing & ISO 9001 experience is preferred. - Proficient Hand-Eye Dexterity & Motor Skills for intricate/delicate work - Working knowledge of hand tools and blueprint reading preferred - Must be able to work with small parts in a clean room environment, using a microscope - Available to work overtime to support production goals as needed. - Must have good time management skills to work on numerous projects (sometimes simultaneously) - Attention to Detail (following bill of material, job routers, and understanding drawings/prints) - Team Oriented - will work effectively and cohesively with other employees to achieve required objectives and goals. - Credibility - takes responsibility for his/her own work. Respects confidential information and concerns shared by others. - A safe and quality conscious attitude and follow safety and quality requirements - Must be able to move materials weighing up to 50 pounds - Must be able to remain in stationary position 75% of the time - Must be able to operate machinery - Must be able to move between work zones - Must be proficient and able to understand written instructions in English language **Competencies** Values: Integrity, Accountability, Inclusion, Innovation, Teamwork **ABOUT TE CONNECTIVITY** TE Connectivity plc (NYSE: TEL) is a global industrial technology leader creating a safer, sustainable, productive, and connected future. As a trusted innovation partner, our broad range of connectivity and sensor solutions enable the distribution of power, signal and data to advance next-generation transportation, energy networks, automated factories, data centers enabling artificial intelligence, and more. Our more than 90,000 employees, including 10,000 engineers, work alongside customers in approximately 130 countries. In a world that is racing ahead, TE ensures that EVERY CONNECTION COUNTS. Learn more at ********** and on LinkedIn (************************************************** ,Facebook (***************************************** ,WeChat, (http://**********.cn/chn-zh/policies-agreements/wechat.html) Instagram andX (formerly Twitter). (*********************************** **COMPENSATION** - Competitive base salary commensurate with experience: $20.91/HR (subject to change dependent on physical location) - Posted salary ranges are made in good faith. TE Connectivity reserves the right to adjust ranges depending on the experience/qualification of the selected candidate as well as internal and external equity. - Total Compensation = Base Salary + Incentive(s) + Benefits **BENEFITS** - A comprehensive benefits package including health insurance, 401(k), disability, life insurance, employee stock purchase plan, paid time off and voluntary benefits. **EOE, Including Disability/Vets** **IMPORTANT NOTICE REGARDING RECRUITMENT FRAUD** TE Connectivity has become aware of fraudulent recruitment activities being conducted by individuals or organizations falsely claiming to represent TE Connectivity. Please be advised that TE Connectivity **never requests payment or fees** from job applicants at any stage of the recruitment process. All legitimate job openings are posted exclusively on our official careers website at te.com/careers, and all email communications from our recruitment team will come **only from actual email addresses ending ************ . If you receive any suspicious communications, we strongly advise you not to engage or provide any personal information, and to report the incident to your local authorities. **Job Locations:** Arden, North Carolina 28704 United States Arden, North Carolina 28730 United States Posting City: Arden Job Country: United States Travel Required: None Requisition ID: 145077 Workplace Type: Onsite External Careers Page: Manufacturing TE Connectivity and its subsidiaries, affiliates, and operating units (collectively, the "Company") is committed to providing a work environment that prohibits discrimination on the basis of age, color, disability, ethnicity, marital status, national origin, race, religion, gender, gender identity, sexual orientation, protected veteran status, disability or any other characteristics protected by applicable law or regulation.

**At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world.** Job Description: **At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world.** This opening is for a highly skilled Assembly Operator IV working directly with fiber optics. This person will be a key member of our team and will be responsible for optical connector and cable assembly, termination of various configurations of fiber optic cable assemblies, test station set up for various cable assemblies, and advanced testing of cable assemblies. This individual will assist in process development and resolution of problems encountered in the process of bringing new optical products from concept to market. The position will also provide continuous improvement suggestions for the simplification of new products to reduce costs and increase overall manufacturing efficiency. The individual is to be a self-starter and have the ability to work well under schedule pressures and be able to balance workload as priorities change. Candidates need to have a strong work ethic with a desire to continually learn & with a concentrated focus on serving the Customer. The ideal candidate works well in teams, has the desire to learn, possesses strong hand-eye coordination, and maintains the attention to detail needed to make quality products for our customers. Every team member is responsible for maintaining housekeeping and organization of the work area, following safety guidelines and all TE Connectivity's policies and procedures. **Shifts Available:** **1st:** Mon-Fri, 7am-3:30pm **2nd:** Mon-Fri, 3pm-11:30pm _(10% Shift Differential)_ **Weekend:** Fri-Sun, start on 6/13 - 7AM-7:30PM _(22% Shift differential)_ **Job Requirements** - Polish and test fiber optic cables - Assemble and package fiber optic connector components - Operate fiber router & coating equipment (as needed) - Complete over-molding processes (as needed) - Support prototype product builds, test product builds, pre-release NPI builds (as needed) - Measure components using calipers, gages, or other measuring devices. - Complete necessary operational paperwork required to maintain the traceability of product. - Troubleshoot and perform minor repairs to equipment - Understand and demonstrate cleaning methods and contamination assessment for optical assembly - Termination of various standard fiber optic termini as well new termini designs - Perform IL & RL testing of various configurations of cable assemblies. - Perform EFG & IPC (workmanship) checks on both single & multi-fiber termini - Safely & efficiently operate equipment (E-Stop/Soft Stop) and identify issues - Assist in the estimation process step durations. - Assist in setting-up new manufacturing processes. - Suggest process changes to improve overall manufacturing efficiencies - Communicate within a team atmosphere to ensure clarity of purpose & Customer satisfaction - After training period of 30 days, works with minimal supervision and is proficient in providing timely and accurate products according to skills matrix - Use of Fiber Optic & Electronic Test Equipment: Optical Power Meters, IL/RL Test, Oscilloscope, DMM (Digital Multi Meter), Variable Power Supplies, Variable Attenuators, Optical & RF Switch - Train new and existing team members on products, process, and procedures. - Inspect own work and products using quality standards, work instructions and prints. - Accountability - takes responsibility for his/her own work. Respects confidential information and concerns shared by others. - Available to work overtime to support production goals (as needed) - Ability to work in a clean room environment wearing all required clean room gowning garments and PPE (gowns, shoe booties, hair nets, nitrile gloves, safety glasses, safety shoes) **What your background should look like** - High School diploma or GED preferred - Minimum 2 years manufacturing experience required with knowledge and understanding of manufacturing principles such as Safety, Quality, Delivery, Inventory, and Productivity. - Minimum 1 year experience in a fiber optic manufacturing environment required - SAP Manufacturing & ISO 9001 experience is preferred. - Proficient Hand-Eye Dexterity & Motor Skills for intricate/delicate work - Working knowledge of hand tools and blueprint reading preferred - Must be able to work with small parts in a clean room environment, using a microscope - Available to work overtime to support production goals as needed. - Must have good time management skills to work on numerous projects (sometimes simultaneously) - Attention to Detail (following bill of material, job routers, and understanding drawings/prints) - Team Oriented - will work effectively and cohesively with other employees to achieve required objectives and goals. - Credibility - takes responsibility for his/her own work. Respects confidential information and concerns shared by others. - A safe and quality conscious attitude and follow safety and quality requirements - Experience using electronic testing equipment such as Oscilloscope, DMM (Digital Multi Meter), Variable Power Supplies preferred - Excel skills to record, organize, & analyze data is preferred - Some post high school technical courses are preferred - Familiarity of AutoCAD or similar program is preferred - Must be able to move materials weighing up to 50 pounds - Must be able to remain in stationary position 75% of the time - Must be able to operate machinery - Must be able to move between work zones - Must be proficient and able to understand written instructions in English language **Competencies** Values: Integrity, Accountability, Inclusion, Innovation, Teamwork **ABOUT TE CONNECTIVITY** TE Connectivity plc (NYSE: TEL) is a global industrial technology leader creating a safer, sustainable, productive, and connected future. As a trusted innovation partner, our broad range of connectivity and sensor solutions enable the distribution of power, signal and data to advance next-generation transportation, energy networks, automated factories, data centers enabling artificial intelligence, and more. Our more than 90,000 employees, including 10,000 engineers, work alongside customers in approximately 130 countries. In a world that is racing ahead, TE ensures that EVERY CONNECTION COUNTS. Learn more at ********** and on LinkedIn (************************************************** ,Facebook (***************************************** ,WeChat, (http://**********.cn/chn-zh/policies-agreements/wechat.html) Instagram andX (formerly Twitter). (*********************************** **COMPENSATION** - Competitive base salary commensurate with experience: $24.28/HR (subject to change dependent on physical location) - Posted salary ranges are made in good faith. TE Connectivity reserves the right to adjust ranges depending on the experience/qualification of the selected candidate as well as internal and external equity. - Total Compensation = Base Salary + Incentive(s) + Benefits **BENEFITS** - A comprehensive benefits package including health insurance, 401(k), disability, life insurance, employee stock purchase plan, paid time off and voluntary benefits. **EOE, Including Disability/Vets** **IMPORTANT NOTICE REGARDING RECRUITMENT FRAUD** TE Connectivity has become aware of fraudulent recruitment activities being conducted by individuals or organizations falsely claiming to represent TE Connectivity. Please be advised that TE Connectivity **never requests payment or fees** from job applicants at any stage of the recruitment process. All legitimate job openings are posted exclusively on our official careers website at te.com/careers, and all email communications from our recruitment team will come **only from actual email addresses ending ************ . If you receive any suspicious communications, we strongly advise you not to engage or provide any personal information, and to report the incident to your local authorities. **Job Locations:** Arden, North Carolina 28704 United States Fairview, North Carolina 28730 United States Posting City: Arden Job Country: United States Travel Required: None Requisition ID: 145073 Workplace Type: Onsite External Careers Page: Manufacturing TE Connectivity and its subsidiaries, affiliates, and operating units (collectively, the "Company") is committed to providing a work environment that prohibits discrimination on the basis of age, color, disability, ethnicity, marital status, national origin, race, religion, gender, gender identity, sexual orientation, protected veteran status, disability or any other characteristics protected by applicable law or regulation.

**At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world.** Job Description: **At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world.** This opening is for an Assembly Operator III working directly with fiber optics. This position is responsible for optical connector assembly, termination of various configurations of fiber optic cable assemblies, and testing of these cable assemblies. This individual may assist in process development and resolution of problems encountered in the process of bringing new optical products from concept to market. The individual is a self-starter and has the ability to work well under schedule pressures and ability to balance workload as priorities change. Candidates will have a strong work ethic with a desire to continually learn & with a concentrated focus on serving the Customer. The ideal candidate works well in teams, has the desire to learn, possesses strong hand-eye coordination, and maintains the attention to detail needed to make quality products for our customers. Every team member is responsible for maintaining housekeeping and organization of the work area, following safety guidelines and all TE Connectivity's policies and procedures. **Shifts Available:** **1st:** Mon-Fri, 7am-3:30pm **2nd:** Mon-Fri, 3pm-11:30pm _(10% Shift Differential)_ **Weekend:** Fri-Sun, start on 6/13 - 7AM-7:30PM _(22% Shift differential)_ **Job Requirements** - Polish and test fiber optic cables - Assemble and package fiber optic connector components - Terminate single and multi-fiber cables - Operate fiber router & complete over-molding process (as needed) - Support prototype product builds, test product builds, pre-release NPI builds (as needed) - Measure components using calipers, gages, or other measuring devices - Complete necessary operational paperwork required to maintain the traceability of product - May troubleshoot and perform minor repairs to equipment - Understand cleaning methods and contamination assessment for optical assembly - Perform EFG & IPC (workmanship) checks on both single & multi-fiber termini - Mechanical Aptitude to safely & efficiently operate equipment (E-Stop/Soft Stop) and identify issues - Assist in the estimation process step durations - Suggest process changes to improve overall manufacturing efficiencies - Communicate within a team atmosphere to ensure clarity of purpose & Customer satisfaction - After training period of 30 days, works with limited supervision to provide timely and quality products - Inspect own work and products using quality standards, work instructions and prints - Accountability - takes responsibility for his/her own work. Respects confidential information and concerns shared by others. - Available to work overtime to support production goals as needed - Ability to work in a clean room environment wearing all required clean room gowning garments and PPE (gowns, shoe booties, hair nets, nitrile gloves, safety glasses, safety shoes) **What your background should look like** - High School diploma or GED preferred - Minimum 1 year manufacturing experience required with knowledge and understanding of manufacturing principles such as Safety, Quality, Delivery, Inventory, and Productivity. - Minimum 1 year experience in a fiber optic manufacturing environment preferred - SAP Manufacturing & ISO 9001 experience is preferred. - Proficient Hand-Eye Dexterity & Motor Skills for intricate/delicate work - Working knowledge of hand tools and blueprint reading preferred - Must be able to work with small parts in a clean room environment, using a microscope - Available to work overtime to support production goals as needed. - Must have good time management skills to work on numerous projects (sometimes simultaneously) - Attention to Detail (following bill of material, job routers, and understanding drawings/prints) - Team Oriented - will work effectively and cohesively with other employees to achieve required objectives and goals. - Credibility - takes responsibility for his/her own work. Respects confidential information and concerns shared by others. - A safe and quality conscious attitude and follow safety and quality requirements - Must be able to move materials weighing up to 50 pounds - Must be able to remain in stationary position 75% of the time - Must be able to operate machinery - Must be able to move between work zones - Must be proficient and able to understand written instructions in English language **Competencies** Values: Integrity, Accountability, Inclusion, Innovation, Teamwork **ABOUT TE CONNECTIVITY** TE Connectivity plc (NYSE: TEL) is a global industrial technology leader creating a safer, sustainable, productive, and connected future. As a trusted innovation partner, our broad range of connectivity and sensor solutions enable the distribution of power, signal and data to advance next-generation transportation, energy networks, automated factories, data centers enabling artificial intelligence, and more. Our more than 90,000 employees, including 10,000 engineers, work alongside customers in approximately 130 countries. In a world that is racing ahead, TE ensures that EVERY CONNECTION COUNTS. Learn more at ********** and on LinkedIn (************************************************** ,Facebook (***************************************** ,WeChat, (http://**********.cn/chn-zh/policies-agreements/wechat.html) Instagram andX (formerly Twitter). (*********************************** **COMPENSATION** - Competitive base salary commensurate with experience: $20.91/HR (subject to change dependent on physical location) - Posted salary ranges are made in good faith. TE Connectivity reserves the right to adjust ranges depending on the experience/qualification of the selected candidate as well as internal and external equity. - Total Compensation = Base Salary + Incentive(s) + Benefits **BENEFITS** - A comprehensive benefits package including health insurance, 401(k), disability, life insurance, employee stock purchase plan, paid time off and voluntary benefits. **EOE, Including Disability/Vets** **IMPORTANT NOTICE REGARDING RECRUITMENT FRAUD** TE Connectivity has become aware of fraudulent recruitment activities being conducted by individuals or organizations falsely claiming to represent TE Connectivity. Please be advised that TE Connectivity **never requests payment or fees** from job applicants at any stage of the recruitment process. All legitimate job openings are posted exclusively on our official careers website at te.com/careers, and all email communications from our recruitment team will come **only from actual email addresses ending ************ . If you receive any suspicious communications, we strongly advise you not to engage or provide any personal information, and to report the incident to your local authorities. **Job Locations:** Arden, North Carolina 28704 United States Fairview, North Carolina 28730 United States Posting City: Arden Job Country: United States Travel Required: None Requisition ID: 145071 Workplace Type: Onsite External Careers Page: Manufacturing TE Connectivity and its subsidiaries, affiliates, and operating units (collectively, the "Company") is committed to providing a work environment that prohibits discrimination on the basis of age, color, disability, ethnicity, marital status, national origin, race, religion, gender, gender identity, sexual orientation, protected veteran status, disability or any other characteristics protected by applicable law or regulation.

ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. Operates and performs changeovers on the lines/equipment within required timelines and demonstrates the ability to consistently meet safety, quality and efficiency goals. Follows work instructions, standards and SOP's for equipment set up and changeover. Identifies and resolves issues during set up and changeover. Prepares work area at beginning of shift and cleans up work area at end of shift and/or at end of production run to ensure area is ready for next job. Cleans or sanitizes all food contact surfaces between changes of product. Ensures availability of all required materials and supplies, using the appropriate lift trucks, hand jacks and other equipment once certifications are achieved. Operates equipment, including troubleshooting and making adjustments in accordance with established work standards. Cleans and assembles equipment according to standard operating procedures. Conducts quality checks at regular intervals; inspects ingredients and finished product to ensure product is processed according to specifications. Truthfully and legibly completes required paperwork, written and electric reports. (i.e. Excel, Word, PCDA, Oracle, etc.). Reduces downtime by assuring tasks are performed promptly, safely and efficiently. Performs operator scheduled maintenance checklist. Diagnoses and performs minor machine maintenance and makes any needed adjustments. Works closely with maintenance when escalation to maintenance is needed for a mechanical issue. Submits daily report of duties performed and production quantities produced. Identifies and submits suggestions to improve efficiencies, quality and safety. Actively participates in root cause analysis and other plant continuous improvement initiatives. Recommends and assists with implementing continuous improvement ideas. Complies with safety requirements, GMP requirements, and SOP's/WI's for work area. Packaging Area: Conducts quality checks at regular intervals; inspects filled containers and finished product to ensure product is packaged according to specifications. Assists coworkers set up machine and stacks, marks, packs, and transports finished product. Processing Area: Examines product for identity and any impurities. Weighs out ingredients as listed using scales with printers and mixes ingredients, using appropriate mixing method, carefully and thoroughly. Follows batch instructions on BPR or deviation to meet desired specification via use of reactors, blenders, mixers, fitzmill, metal detector, sifter, roller compactor, rotary press, oscillating granulator, tote tumbler, lift truck, hand jack and other equipment. Notifies supervisor, lead or R&D of any concerns with instructions on BPR or deviation. Records all item and lot number information on production ticket. Documents and updates mix tickets and log book, ensuring that all information is written truthfully and legibly. Enters all information into computer system for tracking and accountability purposes, ensuring that all information is correct. Lifts and places raw materials into appropriate tote or tank equipment or mixers via automatic or manual lifting. Properly labels bulk containers, mixes etc. Keeps Quality Control and Research & Development departments informed, to ensure correct amounts of raw materials are used and to recommend improvements to existing products. SAFETY RESPONSIBILITY STATEMENT Supports a culture of safe production and exhibits safe work practices. Actively participates in the safety program by engaging in safety activities. Effectively provides and accepts constructive peer-to-peer feedback on safety performance. Adheres to policies, procedures, SOP's, safe work practices, and safety policies and procedures. Reports ALL workplace incidents to supervisor immediately. Communicates concerns to supervisor, reports hazards, and provides input on prevention. Properly uses, wears, and stores Personal Protective Equipment when required. Participates on safety teams and/or completes safety-related activities as part of regular job responsibilities. QUALIFICATIONS To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations will be made to enable individuals with disabilities to perform the essential functions. EDUCATION and/or EXPERIENCE High school diploma or general education degree (GED) and six (6) months of related experience and/or training or equivalent combination of education and experience. Prior experience operating blending/processing and/or packaging machines/equipment preferred. Experience in a manufacturing environment, preferably food or pharmaceuticals, preferred. PERFORMANCE ABILITY Certification as a Machine Operator in one (1) to three (3) Packaging and/or Processing areas (any combination). Processing areas: (1) Encapsulation; (2) Roller Compactor; (3) Tablet Coating; (4) Tablet Press; (5) Wet and/or Dry Blending (considered certification in one area). Fitzmill is not included. Packaging areas: (1) Cloud; (2) Simplex Oil and/or HPC (considered certification in one area); (3) Monoblock Oil (4) Powder and/or Mateer (considered certification in one area); (5) Tea; (6) Vitamin line 4/8 head filler; (7) All other Vitamin lines (not 4/8 head filler). Proven ability through certification to operate various Packaging and Processing equipment according to set standards; set up, run and adjust machines; conduct timely quality checks; perform minor machine maintenance; accurately complete paperwork; and perform sanitation and changeover of equipment. Solid knowledge of machine capabilities, manufacturing process, and ability to troubleshoot. Demonstrated ability to consistently meet quality, safety and efficiency goals. Good problem-solving skills required. Good time management skills; ability to prioritize and calmly handle multiple tasks simultaneously in a fast-paced environment; demonstrate a strong sense of urgency; and flexibility to change tasks frequently and work in different work centers as business needs require. Strong teamwork skills; ability to work and communicate effectively with others; strong attention to detail skills; and demonstrated high quality of work. Consistently follows all company policies and procedures, including all safety policies and procedures. Ability to work in Packaging and Processing at both the 391 and 395 manufacturing facilities in Bloomingdale. LANGUAGE SKILLS Ability to communicate professionally and effectively both verbally and in writing. Ability to read and comprehend instructions, correspondence, and memos such as safety rules, operating and maintenance instructions, and procedure manuals (S.O.P.). Ability to accurately complete sanitation/production paperwork. MATHEMATICAL SKILLS Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals to understand weights and measures and to use digital and balancing scales. Ability to compute rate, ratio, and percent. REASONING ABILITY Ability to apply commonsense understanding to carry out instructions furnished in written, oral, or diagram form. Good problem solving ability. OTHER SKILLS AND ABILITIES Basic understanding of mechanical principles; ability to troubleshoot and adjust machines. Ability to operate hand operated electronic lifting equipment (Interthor). Basic computer and data entry skills required. Ability to work a flexible schedule, including weekends to support the business. 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. While performing the duties of this job, the employee is regularly required to talk and hear; stand and walk; ascend and descend stairs and ladders; use hands to finger, handle, and feel; crouch or half kneel, and reach with hands and arms. Critical demands of the position include moving pallets, moving pallet jacks, lifting and loading product, and changing over and cleaning equipment. Packaging: The employee must regularly lift, move (in some cases drag items), slide, raise and/or place: Up to 20 lbs. from 5 inches to 47 inches and then returning to 5 inches Up to 20 lbs. at 30 inches, turn 90 degrees and place at 30 inches Ascend and descend stairs carrying 30 lbs. Up to 55 lbs. from floor onto side, move up to 10 ft. and then return to original position Push and pull of force up to 35 lbs. at 54 inch height Push and pull of force up to 65 lbs. at 36 inch height Reach up to 78 inches Processing: The employee must regularly lift, move (in some cases drag items), slide, raise and/or place: Up to 20 lbs. to 30 inches, turn at a 90 degree angle and place at 30 inches. Ascend and descend steps carrying up to 35 lbs. Up to 50 lbs. to waist height. Up to 55 lbs. from floor onto side, move 10 ft. and then return to original position. Push and pull up to 65 lb. force at 36 inch height Reach up to 78 inches WORK ENVIRONMENT The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee regularly works near moving mechanical parts. The employee is frequently exposed to herbal aromas, dust, and/or airborne particles, some classified as allergens or irritants. This position works in all areas of NOW's manufacturing facilities with direct exposure to ingredients (powders and liquids), mixes (powders and liquids), equipment, and packaging. The noise level in the work environment is usually moderately loud, and in some areas where louder hearing protection is required. 2025 BENEFITS AT A GLANCE

States considered: Michigan Role Description Packaging Operator Zoetis, the global leader in animal health, is looking for an engaged and driven individual to join our packaging team. Zoetis has been leading animal health since its inception in 2012 and we pride ourselves on providing all manner of quality solutions for our customer's animal health needs. A Packaging Operator is an entry level position that performs general pharmaceutical production related tasks and responsibilities in a lean manufacturing environment. This includes inspection and packaging of products, as well as material handling and setup of packaging lines with “right first time” accuracy and efficiency. This postion requires high attention to detail with regard to ensuring a quality product is provided to our customers and ensuring production related documents are complete and correct according to Standard Operating Procedures (SOPs) and current Good Manufacturing Practices (cGMPs). This position also requires the use of Microsoft applications and good organizational skills in order to maintain an orderly work environment. All activities are conducted within a safety-minded culture that strives for continuous improvement. This position is an ideal first step for those seeking to enter the pharmaceutical production industry. If you have an engaged work ethic and enjoy the challenge of maximizing quality and efficiency as part of a high performance team, this may be a great opportunity for you! Required skills, education, and experience: · High school diploma or general education degree (GED) · Basic math, English communication skills, legible penmanship, and reading comprehension · Ability to follow detailed instructions · Basic use of Microsoft applications and general computer skills · Effective interpersonal communication and a positive outlook · Candidates cannot be allergic to Cephalosporin/Penicillin Preferred candidate qualifications: · Basic mechanical skills and experience in the use of various hand tools · Experience in a Lean Production and/or manufacturing environment · Knowledge of cGMPs and production practices · Reliable transportation and good attendance/time management skills Physical and Time requirements: · Routine lifting of 20-50 lbs. · Prolonged periods of sitting and standing · Flexible hours and overtime may be required · Manual dexterity and ability to keep up with pace of production standards · Work Environment: Colleague could be exposed to airborne particles, including cephalosporin. Must work near moving mechanical parts. Eye protection and other personal protective equipment are required. · 3rd Shift: 9:45pm - 6:15am Full time RegularColleague Any unsolicited resumes sent to Zoetis from a third party, such as an Agency recruiter, including unsolicited resumes sent to a Zoetis mailing address, fax machine or email address, directly to Zoetis employees, or to Zoetis resume database will be considered Zoetis property. Zoetis will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume. Zoetis will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor but does not have the appropriate approvals to be engaged on a search. Zoetis is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status or any other protected classification. Disabled individuals are given an equal opportunity to use our online application system. We offer reasonable accommodations as an alternative if requested by an individual with a disability. Please contact Zoetis Colleague Services at ********************************** to request an accommodation. Zoetis also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must possess or obtain authorization to work in the US for Zoetis. Zoetis retains sole and exclusive discretion to pursue sponsorship for the acquisition or maintenance of nonimmigrant status and employment eligibility, considering factors such as availability of qualified US workers. Individuals requiring sponsorship must disclose this fact. Please note that Zoetis seeks information related to job applications from candidates for jobs in the U.S. solely via the following: (1) our company website at ********************** site, or (2) via email to/from addresses using only the Zoetis domain of “@zoetis.com”. In addition, Zoetis does not use Google Hangout for any recruitment related activities. Any solicitation or request for information related to job applications with Zoetis via any other means and/or utilizing email addresses with any other domain should be disregarded. In addition, Zoetis will never ask candidates to make any type of personal financial investment related to gaining employment with Zoetis.

Trifecta Medical currently has an opening for an assembler to join our Team in Plainfield, Indiana. This is a full-time position. Assembler Responsibilities: · Receiving work order jobs for work to be performed. · Develop a method and process to assemble multiple components to product · Set up and adjust machines used for assembly purposes · Examining work orders to determine estimated processing times We offer competitive pay, health benefits, vision, dental, 401(k) and paid vacation. Skills/Qualifications: Manufacturing Quality, Controls and Instrumentation, Equipment Maintenance, Manufacturing Experience, Mechanical Inspection Tools, Decision Making, Tooling, Safety Management, Problem Solving, Judgment, Job Knowledge Must be able to stand for long periods, lift 50 pounds and work in a fast-paced warehouse environment. Pay: $21.00 per hour Benefits: 401(k) Dental insurance Health insurance Paid time off Vision insurance Schedule: 8-hour shift Monday to Friday Job Type: Full-time Work Location: In person - Plainfield, IN Company DescriptionManufacturer of custom sterilization cases and trays for orthopedic surgeries.Company DescriptionManufacturer of custom sterilization cases and trays for orthopedic surgeries.

Join a Purpose-Driven Team as a Medical Device Assembler at Rose Medical! At Rose Medical, we believe that behind every life-changing device is a dedicated and talented team member striving for excellence. We are guided by a strong commitment to ethical decision-making, service to others, and creating a positive impact. If you're dependable, eager to learn, and ready to contribute to meaningful work, we want you on our team! Now Hiring for 2nd Shift Assemblers - $1,000 Hiring Bonus Bonus contingent upon meeting attendance expectations. Available Schedules: 2nd Shift: Monday - Thursday, 3 PM to 1 AM | Starting pay: $21.00/hr Optional Overtime: Fridays Why Join Rose Medical? Quarterly Bonuses: Celebrate your contributions with generous bonuses Paid Time Off (PTO): Accrue 3 weeks per year starting on your first day Paid Holidays: 8 paid holidays annually from day one Parental Leave: 2 weeks of paid leave for the birth, adoption, or fostering of a child Benefits After 30 Days: Medical, dental, and vision coverage 401(k) with 4% company match Disability and life insurance options Career Growth: We believe that as the company grows, so do our people. We invest in your personal and professional development so you can thrive. What You'll Do Work with Purpose: Assemble, inspect, and package medical devices that impact lives Quality-First Mindset: Follow FDA Good Manufacturing Practices (GMPs) and Quality System Procedures (QSPs) to meet the highest product standards Collaborate as One Rose: Rotate between stations, meet production goals, and support your teammates Always Improving: Contribute ideas for innovation, efficiency, and continuous improvement Stay Organized: Maintain documentation and a clean, safe work environment What You Bring High school diploma or GED Experience in assembly or medical device manufacturing is a plus Leadership experience is a bonus Strong attention to detail and excellent hand-eye coordination A commitment to high-quality work and a positive, ethical work environment Our Values in Action Integrity: Honesty and transparency in every decision Stewardship: Responsible use of resources for the good of our team and community Growth: Opportunities to develop personally and professionally Innovation & Productivity: Empowering ideas and results Diversity: Valuing the unique experiences and perspectives of every team member Be Part of Something Bigger. Apply today and join a company where your work truly matters! Please note: Due to the holiday season, interview scheduling will begin after the New Year. Applications will continue to be reviewed during this time.

**Why Us?** At Par Health, we believe great healthcare is built on getting the essentials right. We're looking for passionate, talented individuals who share our commitment to improving lives. With 4,000+ team members worldwide, we lead with pride and purpose-prioritizing quality and safety while fostering a culture of continuous improvement, accountability, and teamwork. Elevating the Essentials isn't just our tagline, it's the higher standard we live by every day. ** Summary** The Janitor will perform general cleaning activities associated with the upkeep of all manufacturing, maintenance, office, and locker room areas at the site. The Janitor will also be cross trained to cover other production positions as needed and will be paid the appropriate rate for the position assigned. **Job Description** **TYPICAL RESPONSIBILITIES / DUTIES:** + Engage fully in the site's EHS, quality and Performance Excellence programs + Maintain the qualification and skills required to perform the Packager role within the Spray Dryer unit and to be able to assist the packaging operation in the granulation unit by performing duties of the Dryer Operator role when assigned. + Perform housekeeping duties on a daily basis as assigned by the supervisor + Lock and secure the general plant after normal business hours + Load special waste material into the special waste dumpster as required + Operate forklift trucks and other machinery, as required, in a safe manner, ensuring that daily checks are completed and documented + Assist other operators on site, as directed by the supervisor / management, to complete assigned tasks as a team + Other duties as assigned **QUALIFICATIONS (Education, Experience, Special Skills):** + High School Diploma + Must have good oral and written communication skills + Must be able to meet the physical demands of the position with or without accommodation. **Job classifications:** New hires generally start at the Janitor position and bid on other jobs as they become available. Positions and shift assignments will be determined following the employee's start date and will be awarded by seniority. + Janitor - $23.47 + Packager - $26.60 + Prestager - $27.81 + Mix Operator - $29.99 + Material Handler - $30.26 + Dryer Operator - $30.26 **Shifts:** Schedule to be determined, shifts vary based on position available on employee's start date and will be awarded by seniority per the collective bargaining agreement. + **Continuous work week schedule:** Three days on, Three days off - 6 am to 6 pm or 6 pm to 6 am + **5 Day Work Week:** 8-hour shifts - filling 1st, 2nd, & 3rd shifts **Resume: Please submit your up-to-date resume in a word document or a PDF. Resumes in other formats including jng, gif, picture or txt files may not be compatible with the applicant tracking system and will not be considered.** **EEO Statement:** We comply with all applicable federal, state, and local laws prohibiting discrimination and harassment, and provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, veteran status, or genetic information, or any other classification protected by federal, state or local law. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Why Us? At Par Health, we believe great healthcare is built on getting the essentials right. We're looking for passionate, talented individuals who share our commitment to improving lives. With 4,000+ team members worldwide, we lead with pride and purpose-prioritizing quality and safety while fostering a culture of continuous improvement, accountability, and teamwork. Elevating the Essentials isn't just our tagline, it's the higher standard we live by every day. Summary The Janitor will perform general cleaning activities associated with the upkeep of all manufacturing, maintenance, office, and locker room areas at the site. The Janitor will also be cross trained to cover other production positions as needed and will be paid the appropriate rate for the position assigned. Job Description TYPICAL RESPONSIBILITIES / DUTIES: Engage fully in the site's EHS, quality and Performance Excellence programs Maintain the qualification and skills required to perform the Packager role within the Spray Dryer unit and to be able to assist the packaging operation in the granulation unit by performing duties of the Dryer Operator role when assigned. Perform housekeeping duties on a daily basis as assigned by the supervisor Lock and secure the general plant after normal business hours Load special waste material into the special waste dumpster as required Operate forklift trucks and other machinery, as required, in a safe manner, ensuring that daily checks are completed and documented Assist other operators on site, as directed by the supervisor / management, to complete assigned tasks as a team Other duties as assigned QUALIFICATIONS (Education, Experience, Special Skills): High School Diploma Must have good oral and written communication skills Must be able to meet the physical demands of the position with or without accommodation. Job classifications: New hires generally start at the Janitor position and bid on other jobs as they become available. Positions and shift assignments will be determined following the employee's start date and will be awarded by seniority. Janitor - $23.47 Packager - $26.60 Prestager - $27.81 Mix Operator - $29.99 Material Handler - $30.26 Dryer Operator - $30.26 Shifts: Schedule to be determined, shifts vary based on position available on employee's start date and will be awarded by seniority per the collective bargaining agreement. Continuous work week schedule: Three days on, Three days off - 6 am to 6 pm or 6 pm to 6 am 5 Day Work Week: 8-hour shifts - filling 1st, 2nd, & 3rd shifts Resume: Please submit your up-to-date resume in a word document or a PDF. Resumes in other formats including jng, gif, picture or txt files may not be compatible with the applicant tracking system and will not be considered. EEO Statement: We comply with all applicable federal, state, and local laws prohibiting discrimination and harassment, and provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, veteran status, or genetic information, or any other classification protected by federal, state or local law. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

Why Us? At Par Health, we believe great healthcare is built on getting the essentials right. We're looking for passionate, talented individuals who share our commitment to improving lives. With 4,000+ team members worldwide, we lead with pride and purpose-prioritizing quality and safety while fostering a culture of continuous improvement, accountability, and teamwork. Elevating the Essentials isn't just our tagline, it's the higher standard we live by every day. Summary Handles and inspects components and filled product in accordance with Current Good Manufacturing Practices, Operating Procedures and Safety Regulations Documents and communicates functions and duties necessary to complete the manufacture of products produced in the Sterile Filling Department. Job Description About Endo International plc At Par Health, we believe great healthcare is built on getting the essentials right. We're looking for passionate, talented individuals who share our commitment to improving lives. With 4,000+ team members worldwide, we lead with pride and purpose-prioritizing quality and safety while fostering a culture of continuous improvement, accountability, and teamwork. Elevating the Essentials isn't just our tagline, it's the higher standard we live by every day. POSITION SUMMARY: Handles and inspects components and filled product in accordance with Current Good Manufacturing Practices, Operating Procedures and Safety Regulations Documents and communicates functions and duties necessary to complete finishing activities for products processed in the Inspection and Packaging Department. Union job at Rochester, MI. ROLE AND RESPONSIBILITIES: Operational Performs all tasks as outlined in Batch Cards, SOPs and Job Aids Effectively demonstrates the ability to perform on automated lines Inspects finished product as required. Requires attention to detail Configures and counts product into trays and cases. Requires lifting weights of up to 35 lbs. Operates equipment as defined within the labor grade Maintains a smooth flow of production and monitors equipment as assigned Basic knowledge of manufacturing equipment, such as interaction with HMI panels and safe interaction with automated machinery Issues Communicates to PMO or Supervisor in a timely manner any equipment or process deviations Documentation Documents in a timely manner all tasks requiring written or electronic records as specified in GMP regulations Compliance Performs all functions in accordance with cGMPs, Corporate regulations, SOPs, and all other relevant regulations and standards Effectively demonstrates and understands the SOPs and job aids pertinent to each task performed Other Performs other duties as assigned by supervision Critical thinking is imperative while executing manufacturing standard operating procedures. Critical thinking includes observation, analysis, interference, communication and problem-solving Working individually and as part of a team. Therefore, the ability to work collaboratively and positively within a team is important for this role Being methodical to effectively and accurately work when completing steps of a task or following instructions given to you by your supervisor or SOP REQUIRED QUALIFICATIONS: Education & Experience High school Diploma or GED from recognized institution or organization Successful completion of certified in house qualification programs PHYSICAL REQUIREMENTS: Required to reach with hands and arms and frequently required to use hands to finger, handle or feel. Occasionally lift and/or move up to 50 pounds Specific vision abilities required by this job include close vision Frequently exposed to moving mechanical parts Frequently exposed to toxic or caustic chemicals The noise level is moderate Work environment is a production/manufacturing environment ADDITIONAL INFORMATION: Under contract agreement between Par Pharmaceutical and USW Local 176 Shift premium where eligible The above is intended to describe the general nature and level of work being performed by employees assigned to this role. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. EEO Statement: We comply with all applicable federal, state, and local laws prohibiting discrimination and harassment, and provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, veteran status, or genetic information, or any other classification protected by federal, state or local law. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

As a growing organization and leading manufacturer of atmosphere and vacuum heat-treating systems, Ipsen is continually hiring talented, motivated individuals to join our team across the United States. We offer competitive wages, excellent benefits package and generous paid time off. Job Description We are seeking full time, first shift, temp to hire assembly mechanics. Position is 6:30am to 3pm with some overtime and involves reading blueprints to assemble mechanical components. Use of hand tools, power tools and some metal work is involved. Qualifications Must be able to work 6:30am to 3pm Mon-Fri with some overtime, stand/walk for up to 8 hours per day, lift up to 50 lbs. Read blueprints, have good math skills and some mechanical experience/assembly background. Additional Information Wages depend on experience. Please reply with resume and desired hourly rate. "All your information will be kept confidential according to EEO guidelines".

As a growing organization and leading manufacturer of atmosphere and vacuum heat-treating systems, Ipsen is continually hiring talented, motivated individuals to join our team across the United States. We offer competitive wages, excellent benefits package and generous paid time off. Job Description We are seeking full time, first shift, temp to hire assembly mechanics. Position is 6:30am to 3pm with some overtime and involves reading blueprints to assemble mechanical components. Use of hand tools, power tools and some metal work is involved. Qualifications Must be able to work 6:30am to 3pm Mon-Fri with some overtime, stand/walk for up to 8 hours per day, lift up to 50 lbs. Read blueprints, have good math skills and some mechanical experience/assembly background. Additional Information Wages depend on experience. Please reply with resume and desired hourly rate. "All your information will be kept confidential according to EEO guidelines".

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of. Lonza Tampa is seeking a Packaging Operator to support the implementation of new packaging and labeling processes. This role ensures our products meet the highest standards and positively impact lives worldwide. This role requires availability for the 3:00pm - 11:30pm shift. What you will get: An agile career and dynamic working culture. An inclusive and ethical workplace. Compensation programs that recognize high performance. Medical, dental, and vision insurance. Opportunities for growth and development. Supportive team environment. Access to global career opportunities. Key Responsibilities: Complete manual packaging tasks by following batch record instructions. Operate and set up automated packaging equipment. Ensure accurate material movement and maintain chain of custody. Report issues to QA or supervisors to prevent deviations. Support equipment qualification with the Equipment Specialist. Stay current on SOPs and GMP documentation. Participate in safety meetings and uphold safety standards. Key Requirements: High school diploma or GED. Experience in a pharmaceutical GMP environment preferred. Skilled in cleaning and sanitizing packaging rooms. Ability to build professional and respectful relationships. Understanding of regulatory compliance. Willingness to take on additional duties as needed. Strong attention to detail and safety. Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference. Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

Corium Innovations is seeking a Pharmaceutical Machine Operator for 2nd shift who will set up, operate, and troubleshoot extrusion and web equipment to meet product quality specifications. This position also maintains accurate production documentation, following cGMP and company policies. Your most Innovative career move is here! At Corium Innovations, we've led the way in innovating drug delivery technologies for millions of patients whose GI systems just can't tolerate pills, who can't remember to take their meds as directed, or who have needle-phobia. This is only the beginning! There's so much more to deliver, and we need YOU to do it! Our Purpose is to create, develop and manufacture innovative healthcare products for partners that deliver superior value to patients. Our Goal is to be the best-in-class specialty CDMO through the use of innovative technologies and superior execution. Our Company Values are core to our positive and people-centric culture which inspires all of us to come to work every day on behalf of our people, our partners, our customers, and our patients. Through our four core values, we put people first and create opportunities to make each day better than the last. Celebrate Individuals: We're looking for talent who will celebrate the uniqueness of each of our team members by encouraging everyone to bring their authentic self to work. Successful Together: We believe we're better together, so we prioritize teamwork as we work to achieve our shared vision knowing each one of us has an important role to play. Embrace Innovation: We embrace new challenges and opportunities while encouraging creative thinking and innovative solutions to best meet the needs of our people and our partners. Pride in Ownership: We take pride in owning our progress and successes, feeling empowered to pursue our growth to reach our full potential. And we hope you will too! Responsibilities: Maintain a working knowledge of Good Manufacturing Practices. Operation, troubleshooting and basic maintenance of production equipment. Accurately complete all required batch record, equipment cleaning, and equipment logbook documentation. Ensure production crew is on task and focused on safety, quality, and productivity. Perform digital inventory material transactions. Communicate with Crew Leaders, Shift Leaders, Maintenance, and Engineering personnel regarding process and equipment related issues. Clean equipment and manufacturing facility per cGMP procedures. Qualifications: High school diploma or GED. Minimum of 1 year of experience in a manufacturing environment preferred Proven mechanical aptitude and troubleshooting skills. Ability to follow written instructions and procedures. Ability to follow press diagrams and read part prints. Ability to effectively communicate quality issues effectively to supervision. Ability to accurately complete documentation. Strong team player. Strong interpersonal and communication skills. Ability to work 2pm-10pm Monday-Friday. Benefits: Highly competitive benefits program including medical, dental, vision, flexible spending accounts, life insurance, disability insurance, and employee assistance program. 401(k) retirement savings account with a company match and immediate vesting. 12 paid holidays. Competitive paid vacation plan plus ~1 additional week of paid time off for our annual holiday shutdown. $2.00/hour 2 nd shift premium.

Why Us? We want the best and brightest people to help us achieve our mission to develop and deliver life-enhancing products through focused execution. Our nearly 3,000 global team members understand the important role we play in delivering healthcare and are dedicated to supporting each other as we work to bring the best treatments forward. Our shared values of Integrity & Quality, Innovation, Drive, Collaboration and Empathy guide our team and enable us to deliver upon our vision of helping everyone we serve live their best life. Summary In accordance with Current Good Manufacturing Practices, Standard Operating Procedures (written and/or oral) instructions and Safety Regulations are responsible for the continuity of complex operations required to maintain production. Job Description Key Accountabilities - key outcomes/deliverables, the major responsibilities, and % of time Accountability Responsibilities % of Time Operational Sets-up, checks, adjusts and runs production equipment as required by product and size change over. This requires the PMO to bend, lift, use both hands and have correct 20/20 vision Communicates effectively and on a timely basis to fill and seal operators Coordinates with Area Supervisors to ensure an efficient filling operation Communicates with Supervisor in a proactive manner with respect to line operating conditions, product quality status, and potential improvements Cleans lubricates, starts, stops and services equipment necessary to promote and maintain a smooth & efficient flow of production When necessary, performs required environmental and personnel monitoring sampling and recording Determines and verifies that correct and adequate labels, materials and supplies have been provided to meet production schedules Maintains a continuous supply of materials to production lines Notifies Area Supervisor of processes or equipment not in a state of regulatory compliance when discovered 70% Documentation Documents all line clearance forms and other documentation forms necessary for the processing of each batch Records downtime, production output and other manufacturing documents as assigned 10% Compliance Maintains eligibility for core qualification 10% Testing Integrity tests sterilizing filters 10% Other Performs other duties as assigned by Area Supervisor Continuous Total 100% Qualifications Education & Experience Minimal acceptable level of education, work experience and certifications required for the job High School Diploma, GED or equivalent Successful completion of in-house training programs (includes Upgrader Exam) Knowledge Proficiency in a body of information required for the job e.g. knowledge of FDA regulations, GMP/GLP/GCP, Lean Manufacturing, Six-Sigma, etc. Arithmetic Aptitude preferred Pressure and Temperature Aptitude preferred Skills & Abilities Often referred to as “competencies”, leadership attributes, skills, abilities or behaviors that may be enterprise, functional or job specific e.g. coaching, negotiation, calibration, technical writing etc. Mechanical Aptitude preferred Hand Tools and Measuring Instruments Aptitude preferred Physical Requirements Physical & mental requirements e.g. lift 40 pounds, walk across plant/warehouse, business travel (% of time), driving as part of work responsibilities, etc. Required to reach with hands and arms and frequently required to use hands to finger, handle or feel Occasionally lift and/or move up to 50 pounds Specific vision abilities required by this job include close vision Frequently exposed to moving mechanical parts Frequently exposed to toxic or caustic chemicals The noise level is moderate Work environment is a production/manufacturing environment EEO Statement: We firmly believe in the principles of equal employment opportunity and strive to create an atmosphere where all employees, regardless of their race, color, creed, religion, sex, gender identity or expression, sexual orientation, national origin, genetics, disability (including pregnancy), age, or military or veteran status, feel valued, respected, and empowered. Our commitment to EEO extends to every aspect of employment, including recruitment, hiring, training, promotions, compensation, benefits, transfers, terminations, and all other employment practices. We are dedicated to ensuring that all employment decisions are based on qualifications, skills, and merit.

B Shift: Monday-Friday, 1pm-9pm What Assembly contributes to Cardinal Health Manufacturing is responsible for cost of production and maintenance activities including process improvement, supply chain management, quality assurance, employee safety and engagement, and environmental commitment. Performs a variety of tasks ranging from repetitive to non-repetitive production to put together component parts to make assemblies, sub-assemblies or completed units, using standard operating procedures. May conduct quality inspections on processing line in accordance with quality specifications. Job Summary The Associate II, Assembly plays a key role in the manufacturing process of Cardinal Health medical products. The Associate II, Assembly operates multiple machines at once and performs routine inspections of manufactured products in accordance with quality specifications. This job reports defects and works with the quality team to investigate and identify route causes. This job ensures that manufactured parts are captured in bins and prepared for transport. The Associate II, Assembly tasks are performed in accordance with applicable safety guidelines, as well as appropriate processing standards. Responsibilities Sets up and operates production equipment in accordance with current manufacturing practices and standard operating procedures. Measures and records data associated with operating and manufacturing equipment. Verifies outputs in the manufacturing process and ensures that quality and quantity standards are met. Inspects components for debris, and or any other potential quality defect and reports defects as needed to management and the quality team. Performs duties in compliance with all safety rules and regulations required by the Company, Local, and State and Federal provisions. Qualifications 1-2 years of experience preferred High school degree or GED preferred What is expected of you and others at this level Applies acquired knowledge and skills to complete standard tasks Readily learns and applies new information and methods to work in assigned area Maintains appropriate licenses, training and certifications Works on routine assignments that require some problem resolution Works within clearly defined standard operating procedures and/or scientific methods Adheres to all quality guidelines Works under moderate degree of supervision Work typically involves regular review of output by work lead or supervisor Refers complex unusual problems to supervisor Pay rate: $16.45 per hour (includes shift differential) Bonus eligible: No Benefits: Cardinal Health offers a wide variety of benefits and programs to support health and well-being. Medical, dental and vision coverage Paid time off plan Health savings account (HSA) 401k savings plan Access to wages before pay day with my FlexPay Flexible spending accounts (FSAs) Short- and long-term disability coverage Work-Life resources Paid parental leave Healthy lifestyle programs Application window anticipated to close: 02/06/2026 *if interested in opportunity, please submit application as soon as possible. Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply. Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law. To read and review this privacy notice click here

**B Shift:** Monday-Friday, 1pm-9pm **_What Assembly contributes to Cardinal Health_** Manufacturing is responsible for cost of production and maintenance activities including process improvement, supply chain management, quality assurance, employee safety and engagement, and environmental commitment. Performs a variety of tasks ranging from repetitive to non-repetitive production to put together component parts to make assemblies, sub-assemblies or completed units, using standard operating procedures. May conduct quality inspections on processing line in accordance with quality specifications. **_Job Summary_** The Associate II, Assembly plays a key role in the manufacturing process of Cardinal Health medical products. The Associate II, Assembly operates multiple machines at once and performs routine inspections of manufactured products in accordance with quality specifications. This job reports defects and works with the quality team to investigate and identify route causes. This job ensures that manufactured parts are captured in bins and prepared for transport. The Associate II, Assembly tasks are performed in accordance with applicable safety guidelines, as well as appropriate processing standards. **_Responsibilities_** + Sets up and operates production equipment in accordance with current manufacturing practices and standard operating procedures. + Measures and records data associated with operating and manufacturing equipment. + Verifies outputs in the manufacturing process and ensures that quality and quantity standards are met. + Inspects components for debris, and or any other potential quality defect and reports defects as needed to management and the quality team. + Performs duties in compliance with all safety rules and regulations required by the Company, Local, and State and Federal provisions. **_Qualifications_** + 1-2 years of experience preferred + High school degree or GED preferred **_What is expected of you and others at this level_** + Applies acquired knowledge and skills to complete standard tasks + Readily learns and applies new information and methods to work in assigned area + Maintains appropriate licenses, training and certifications + Works on routine assignments that require some problem resolution + Works within clearly defined standard operating procedures and/or scientific methods + Adheres to all quality guidelines + Works under moderate degree of supervision + Work typically involves regular review of output by work lead or supervisor + Refers complex unusual problems to supervisor **Pay rate:** $16.45 per hour (includes shift differential) **Bonus eligible:** No **Benefits:** Cardinal Health offers a wide variety of benefits and programs to support health and well-being. + Medical, dental and vision coverage + Paid time off plan + Health savings account (HSA) + 401k savings plan + Access to wages before pay day with my FlexPay + Flexible spending accounts (FSAs) + Short- and long-term disability coverage + Work-Life resources + Paid parental leave + Healthy lifestyle programs **Application window anticipated to close:** 02/06/2026 *if interested in opportunity, please submit application as soon as possible. _Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply._ _Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal_ _Opportunity/Affirmative_ _Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law._ _To read and review this privacy notice click_ here (***************************************************************************************************************************

B Shift: Monday-Friday, 1pm-9pm What Assembly contributes to Cardinal Health Manufacturing is responsible for cost of production and maintenance activities including process improvement, supply chain management, quality assurance, employee safety and engagement, and environmental commitment. Performs a variety of tasks ranging from repetitive to non-repetitive production to put together component parts to make assemblies, sub-assemblies or completed units, using standard operating procedures. May conduct quality inspections on processing line in accordance with quality specifications. Job Summary The Associate II, Assembly plays a key role in the manufacturing process of Cardinal Health medical products. The Associate II, Assembly operates multiple machines at once and performs routine inspections of manufactured products in accordance with quality specifications. This job reports defects and works with the quality team to investigate and identify route causes. This job ensures that manufactured parts are captured in bins and prepared for transport. The Associate II, Assembly tasks are performed in accordance with applicable safety guidelines, as well as appropriate processing standards. Responsibilities * Sets up and operates production equipment in accordance with current manufacturing practices and standard operating procedures. * Measures and records data associated with operating and manufacturing equipment. * Verifies outputs in the manufacturing process and ensures that quality and quantity standards are met. * Inspects components for debris, and or any other potential quality defect and reports defects as needed to management and the quality team. * Performs duties in compliance with all safety rules and regulations required by the Company, Local, and State and Federal provisions. Qualifications * 1-2 years of experience preferred * High school degree or GED preferred What is expected of you and others at this level * Applies acquired knowledge and skills to complete standard tasks * Readily learns and applies new information and methods to work in assigned area * Maintains appropriate licenses, training and certifications * Works on routine assignments that require some problem resolution * Works within clearly defined standard operating procedures and/or scientific methods * Adheres to all quality guidelines * Works under moderate degree of supervision * Work typically involves regular review of output by work lead or supervisor * Refers complex unusual problems to supervisor Pay rate: $16.45 per hour (includes shift differential) Bonus eligible: No Benefits: Cardinal Health offers a wide variety of benefits and programs to support health and well-being. * Medical, dental and vision coverage * Paid time off plan * Health savings account (HSA) * 401k savings plan * Access to wages before pay day with my FlexPay * Flexible spending accounts (FSAs) * Short- and long-term disability coverage * Work-Life resources * Paid parental leave * Healthy lifestyle programs Application window anticipated to close: 02/06/2026 *if interested in opportunity, please submit application as soon as possible. Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply. Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law.