Manufacturing associate jobs in Brookhaven, NY

North Atlantic Industries is a leading provider of embedded electronic solutions, specializing in rugged embedded computing, power supplies and motion simulation and measurement technologies. Our products and services are used by the military, aerospace, and industrial markets, helping to advance technology and protect the free world. NAI was proud to be recognized as a Top Workplace on Long Island by Newsday! Our culture is very collaborative. We have team building events, company picnics, special event day and employee game room. Please visit our website at ******************** to see more about what makes us a unique place to work. Summary: The Production Operator works in an electronics manufacturing environment assembling printed circuit boards (PCBs). This role involves using computers and equipment to perform daily production tasks. Following instructions and maintaining attention to detail are essential to ensuring the quality of the products. Keeping the workspace clean and organized is a key part of maintaining high production standards. The Production Operator will be trained to operate various machines, including Pick and Place, Automated Optical Inspection (AOI), Selective Soldering equipment, and hand assembly. Flexibility is important, as the operator frequently moves between tasks and functional areas. Teamwork, punctuality, and communication are critical to the success of this role. Requirements * Organize and label products to ensure proper tracking during production. * Apply gels and adhesives to components as part of the assembly process. * Prepare electronic components for assembly into PCBs. * Use basic hand tools for mechanical assembly tasks. * Utilize machines to assemble printed circuit boards. Qualifications and Education Requirements: * High School Diploma or equivalent. Language Skills: * Fluent in English (reading, writing, and speaking). * Strong oral and written communication skills. Other Skills and Abilities: * Experience working in a team environment. * Ability to lift 40 pounds. * Ability to work on your feet. * Familiarity with basic hand tools. * Effective communication skills, both written and verbal. * Computer literate a plus * Ability to learn new skills (Certified Training will be provided). * Conscientious regarding quality, time management, teamwork, and safety. * Flexibility to train and move between functional areas. North Atlantic Industries offer comprehensive and competitive packages including: * Medical, Dental, and Vision Insurance * Company-provided Life and AD&D Insurance * Voluntary Supplemental Life Insurance * Long-term Disability Insurance * Flexible Spending Accounts (FSA) * Employee Assistance Program (EAP) * Tax-deferred 401K with company matching contributions. * Vacation, holidays, sick * Employee tuition reimbursement * Business casual dress environment * Schedule: M-F 1st Shift 7AM-3:30PM North Atlantic Industries (NAI) is proud to be an Equal Opportunity Employer and is committed to providing equal employment opportunity for all persons in all facets of employment. All qualified applicants will receive consideration for employment without regard to any legally protected status. If you are an individual with a disability or a disabled veteran and require a reasonable accommodation in applying for any posted position, please contact Human Resources at ************ or by email at ***********. As a federal government contractor, in accordance with applicable laws, regulations, and Executive Orders, North Atlantic Industries (NAI) is required to develop annual Affirmative Action Plans for Protected Veterans and Individuals with Disabilities. Any employees or applicants who wish to review the Affirmative Action Plan for Protected Veterans and Individuals with Disabilities can contact us by sending an email to *********** or by calling ************. Salary Description $18-$23 per hour

Job Description LNK International, Inc. is one of the nation's largest manufacturers of solid and liquid dose, over the counter (OTC) pharmaceuticals. For over 40 years, we have built a reputation for delivering the highest quality products, outstanding service and product innovation. What sets LNK apart? We believe it is our employees. From our lab chemists who consistently test every batch of product, our production workers who take genuine pride in their work, to our customer service reps who are dedicated to serving your business. There is a commitment to quality in every department at LNK. Our full time employees enjoy competitive benefits including: 401(k) with generous employer match Health Insurance Dental Insurance Paid holidays Paid vacation Responsibilities Opportunities exist for an operator to join the liquid manufacturing team. A liquid manufacturing operator is responsible for following all standard operating procedures while operating liquid manufacturing equipment. Able to master basic operations of each machine including starting and stopping and basic set up. Monitor operations of machinery. Communicate with management on machinery Record data as required by SOP's Maintain a clean and organized work environment following all GMP's. Adhere to all safety standards. Qualifications Must be able to lift 50 lbs. Strong work ethic, Honesty & integrity, Teamwork, Safety and reliability are the LNK Core Values and a requirement for all positions. The above statements are intended to describe the general nature and level of work being performed by the personnel assigned to do this job. They are not intended to be an exclusive list of all responsibilities, duties and skills required. The salary listed is a good faith determination of potential base compensation that may be offered to a successful applicant for this position at the time of this job advertisement and may be modified in the future. When determining a team member's base salary and/or rate, several factors may be considered as permitted by law. LNK provides equal employment opportunities to all applicants and prohibits discrimination of any type on the basis of actual or perceived race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth and pregnancy-related conditions), gender identity or expression (including transgender status), sexual orientation, marital status, military service and veteran status, physical or mental disability, genetic information or any other characteristic protected by applicable federal, state or local laws. Job Posted by ApplicantPro

Principal Responsibilities Solve technical problems supporting production. Troubleshoot problem, identify and fix root cause to eliminate re-occurring issues affecting daily production. Implement continuous improvement ideas that support the management goals outlined yearly. Creating, updating, training on Standard Operating Procedures Manage technical projects to completion. This may include machine rebuilds, corrective actions, new product launches, machine repairs, lean activities, designing tooling, etc. Knowledge, Skills & Abilities Problem solving Communicate effectively Work well on teams. Computer skills (Microsoft Suite, Email, etc.) Understanding lean manufacturing principles Machine shop skills Bearing technology Grinding theory

NOTICE: The posting for local applicants only - is not for those applying for a global assignment and/or for employees working outside of Cipla's U.S. Subsidiaries or Affiliates. Job Title Manufacturing Operator II Organization Name InvaGen Pharmaceuticals, Inc. Location Central Islip, NY Employment Type Full Time Salary Range (Base/salary) $21.00 - $24.00/hr Benefits In addition to a fulfilling career and competitive salary, the Company offers a comprehensive benefits package to include a 401(k) savings plan and matching, health insurance - medical/dental/vision, health savings account (HSA), flexible spending account (FSA), paid time off (PTO) - vacation/sick/flex time, paid holidays, short-term disability (STD), long-term disability (LTD), parental leave, paid family leave, employee discounts, and other benefits. Work Hours/ Shift/ Remote 1st Shift 7:00 am -3:30 pm Responsibilities/ Accountabilities Must be willing to work in a pharmaceutical setting. Must be able to know how to operate pharmaceutical production machinery independently and thoroughly complete required documentation (legible writing, accurate reporting, maintain and file, etc.) Execute procedures for manufacturing processes in accordance with batch manufacturing record (BMR) and Standard Operating Procedures (SOP) requirements. Perform machine changeovers, cleaning and set up as per SOPs. Ensure the proper area & equipment cleanliness and setup in stipulated time. Prepare a room and equipment for line clearance, replace room filters, Ensure verification and calibration of balance/scale and check pressure differential for the rooms. Ensure line clearance before initiating manufacturing activities in each area. Receive/transfer material from/to dispensing/manufacturing storage and check dispensed materials/final mix blend/compressed tablets and labeling as per BMR. Wear appropriate personal protective equipment (PPE) as stated in the SOP/BMR before initiating the process. Able to operate applicable equipment independently as per area of operation. Ensure adherence to quality standards during all stages of the manufacturing process. Complete manufacturing documents on time, ensuring accuracy and completeness. Responsible for training on all relevant SOPs and always maintain compliance with related SOPs and current Good Manufacturing Practices (cGMP) in the manufacturing process. Perform duties through the proper, safe use of equipment, according to Health & Safety procedures and Equipment Manuals. Flexible to work extended hours, to achieve manufacturing schedule when needed. Maintain discipline and comply with company policies and procedures. Perform entire duties as communicated time to time by department management/designee. Participate in safety related programs and or safety teams as needed. Enforce and follow safety regulations and ensure the working area is clean. Adhere to CIPLA's Safety, Health, and Environmental policies. Must be able to work under general supervision and able to work independently and in a team environment. Must be able to exercise appropriate professional judgment on matters of significance. Other duties assigned by Manufacturing Management. Education Qualifications/Experience High School Diploma (or educational equivalent (i.e. GED) Minimum three years of direct work experience in pharmaceutical manufacturing. Preference will be given to candidates with experience in generic pharmaceutical manufacturing. Skills/ Competencies Must have legible handwriting, and the ability to perform accurate documentation. Understanding of granulation, compression, coating, and encapsulation machines. Capable of conducting troubleshooting, investigations and root cause identification and analysis. Able to prioritize, plan and work under tight schedules and deadlines. Technical writing skills and application of relevant scientific principles and practices (preferred). Must communicate clearly and concisely, both orally and in written. English proficiency required. Physical Requirements Should not have any restriction to work with powder containing active pharmaceutical ingredients. This position requires the ability to do heavy lifting / bending frequently. Long periods of standing up/walking during the working hours; ability to ascend/descend ladders; and able to lift to 35 pounds. Must be able to move pallets/equipment weighing about 200 - 300 kgs using suitable moving equipment like pallet jacks. About Cipla Cipla is a leading global pharmaceutical company, dedicated to high-quality, branded, and generic medicines. We are trusted by healthcare professionals and patients across geographies. Over the last eight decades, we have strengthened our leadership in India's pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world. Driven by the purpose ‘Caring for Life', Cipla's focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world. In the last 85 + years, Cipla has emerged as one of the most respected pharmaceutical names in India as well as across more than 100 countries. Cipla is a fast-growing pharmaceutical company with a continued focus on the expanse of our strong legacy. Over the last five years, Cipla has significantly expanded its portfolio and presence in the U.S. with both a generic and brand division. InvaGen Pharmaceuticals, Inc. InvaGen Pharmaceuticals is a Cipla subsidiary engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on a range of therapeutic areas, including cardiovascular, anti-infective, CNS, anti-inflammatory, anti-diabetic, and anti-depressants. The company was founded in 2003 and is based in Central Islip and Hauppauge, New York. In October 2020, InvaGen established its project site in Fall River, Massachusetts to support the launch of Cipla's respiratory business in the United States. Equal Opportunity Employer Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Cipla, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require reasonable accommodation to make your application or interview experience a great one, please contact the recruiter. About the Salary/ Pay Range: The salary range mentioned above is an anticipated base salary range for this position. Exact salary depends on several factors such as experience, skills, education, and budget. Salary range may vary based on geographic location. In addition to base salary, this position may be eligible for benefits and participation in a bonus program based on performance and company results.

Job Description Qualifications: Education and/or Work Experience Requirements: At least (3) years experience in a production environment Experience with metal fabrication processes such as die forming, roll forming, welding strongly desired Press operation and setup strongly desired Experience with basic measuring equipment such as calipers or micrometers Experience reading and interpreting job instructions and blueprints Experience in a smaller production environment Experience with closely related seal products a plus Responsibilities: Perform specific metal fabrication operations as specified by supervisor. Read and interpret process sheets/work instructions to perform assigned tasks. Set up and operate both die forming and roll forming equipment. Measure work piece dimensions to ensure accuracy to blueprint. Work with manufacturing engineers and other production operators to resolve production issues.

Job Description Natural Organics Inc. is a privately held company in Melville, NY proudly doing business for over 50 years. NaturesPlus is the flagship brand of Natural Organics, a family-driven dietary supplement manufacturer that has been trusted by generations of loyal consumers. Our unique fusion of nature and science has led to the development of formulations including multivitamins, shake powders and specialty products tailored to the needs of men, women and children...all designed to enable our customers to live their best lives. We are currently seeking entry level workers for our Amityville NY facility to assist in the manufacture and packaging of nutraceuticals such as vitamins and energy supplements. We offer Full-time, Day Shift positions in various departments including but not limited to Product-Compression, Product-Encapsulation, and Product-Coating. Some lifting up to 50 lbs. Candidate must be a highly motivated self-starter with checkable references. Benefits: Competitive salary, Medical, Dental, Life Insurance, Aflac, Short- and Long-Term Disability, 401(k) with company match, Generous paid time off days and holidays, Opportunities for professional development and growth, Discounted vitamins and supplements. Job Posted by ApplicantPro

Production Associate I- Farmingdale NY- onsite ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. Production Associate I- Farmingdale NY- onsite We are currently seeking a Production Associate I to join our diverse and dynamic team. As a Production Associate I at ICON, you will play a key role in supporting the production processes by managing day-to-day tasks that ensure the efficient and timely delivery of high-quality products. You will work closely with production teams and other departments to maintain standards, troubleshoot issues, and contribute to continuous improvement initiatives. What You Will Be Doing: * Assisting in the coordination of production activities, including tracking workflow, managing inventory, and ensuring that production schedules are met. * Collaborating with production and quality teams to identify and resolve any issues that may arise during the production process. * Maintaining accurate records of production activities, including data entry, report generation, and documentation of any deviations or issues. * Ensuring compliance with safety and quality standards, performing routine checks, and following established protocols. * Supporting continuous improvement efforts by providing feedback, participating in team meetings, and suggesting ways to enhance production efficiency. Your Profile: * High school diploma or equivalent. Some experience in a production, manufacturing, or related environment is preferred. * Basic understanding of production processes and quality control principles. * Strong attention to detail, with good organizational and time management skills. * Ability to work collaboratively in a team environment, with good communication and problem-solving skills. * Proactive and eager to learn, with a commitment to supporting production goals and contributing to the success of the team. Hourly Rate range: Up to $20.50 hour Actual compensation will be determined based on factors such as geographic location, work experience, education/training, and skill level. You may be eligible for a bonus, stock compensation and commissions in some cases depending on your role and performance. Visit our careers site to read more about the benefits ICON offers. #LI-FL1 What ICON can offer you: Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: * Various annual leave entitlements * A range of health insurance offerings to suit you and your family's needs. * Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. * Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being. * Life assurance * Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles. Salary range: $35,208.00-$44,010.00 Bonus, Com, Stock, Benefits & Disclaimer verbiage: Actual compensation will be determined based on factors such as geographic location, work experience, education/training, and skill level. You may be eligible for a bonus, stock compensation and commissions in some cases depending on your role and performance. Are you a current ICON Employee? Please click here to apply

NOTICE: The posting for local applicants only - is not for those applying for a global assignment and/or for employees working outside of Cipla's U.S. Subsidiaries or Affiliates Job Title Manufacturing Operator I Organization Name InvaGen Pharmaceuticals, Inc. Location Central Islip, NY Shift / Hours 1st Shift 7:00am-3:30pm Employment Type Full Time Salary Range (Base/salary) $ 18.25-20.75 /hr Benefits In addition to a fulfilling career and competitive salary, the Company offers a comprehensive benefits package to include a 401(k) savings plan and matching, health insurance - medical/dental/vision, health savings account (HSA), flexible spending account (FSA), paid time off (PTO) - vacation/sick/flex time, paid holidays, short-term disability (STD), long-term disability (LTD), parental leave, paid family leave, employee discounts, and other benefits. Responsibilities/ Accountabilities * Must be willing to work in a pharmaceutical manufacturing setting. * Must be able to know how to operate pharmaceutical production machinery independently. * Execute procedures for manufacturing processes in accordance with batch manufacturing record (BMR) and Standard Operating Procedures (SOP) requirements. * Perform machine changeovers, cleaning and set up as per SOPs. Ensure the proper area & equipment cleanliness and setup in stipulated time. * Prepare a room and equipment for line clearance, replace room filters, Ensure verification and calibration of balance/scale and check pressure differential for the rooms. * Ensure line clearance before initiating manufacturing activities in each area. * Receive/transfer material from/to dispensing/manufacturing storage and check dispensed materials/final mix blend/compressed tablets and labeling as per BMR. * Wear appropriate personal protective equipment (PPE) as stated in the SOP/BMR before initiating the process. * Able to operate applicable equipment independently as per area of operation. * Ensure adherence to quality standards during all stages of the manufacturing process. * Complete manufacturing documents on time, ensuring accuracy and completeness. * Responsible for training on all relevant SOPs and always maintain compliance with related SOPs and current Good Manufacturing Practices (cGMP) in the manufacturing process. * Perform duties through the proper, safe use of equipment, according to Health & Safety procedures and Equipment Manuals. * Flexible to work extended hours, to achieve manufacturing schedule when needed. * Maintain discipline and comply with company policies and procedures. * Perform entire duties as communicated time to time by department management/designee. * Participate in safety related programs and or safety teams as needed. * Enforce and follow safety regulations and ensure the working area is clean. * Adhere to CIPLA's Safety, Health, and Environmental policies. * Must be able to work under general supervision and able to work independently and in a team environment. * Must be able to exercise appropriate professional judgment on matters of significance. * Other duties assigned as required by Manufacturing Management. Education Qualifications * High School Diploma (or equivalent experience) Experience * Zero (0) to three (3) years of direct work experience in pharmaceutical manufacturing. Preference will be given to candidates with experience in generic pharmaceutical manufacturing. Skills/ Competencies * Understanding of granulation, compression, coating, and encapsulation machines. * Capable of conducting troubleshooting, investigations and root cause identification and analysis. * Able to prioritize, plan and work under tight schedules and deadlines. * Must possess strong documentation and technical writing skills and be able to apply relevant scientific principles and practices. * Must communicate clearly and concisely across levels, both orally and in written. * Strong command over written and verbal English is required. Physical Requirements * Should not have any restriction to work with powder containing active pharmaceutical ingredients. * This position requires the ability to do heavy lifting / bending frequently. * Long periods of standing up/walking during the working hours; ability to ascend/descend ladders; and able to lift to 35 pounds. * Must be able to move pallets/equipment weighing about 200 - 300 kgs using suitable moving equipment like pallet jacks. About Cipla Cipla is a leading global pharmaceutical company, dedicated to high-quality, branded, and generic medicines. We are trusted by healthcare professionals and patients across geographies. Over the last eight decades, we have strengthened our leadership in India's pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world. Driven by the purpose 'Caring for Life', Cipla's focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world. In the last 85 + years, Cipla has emerged as one of the most respected pharmaceutical names in India as well as across more than 100 countries. Cipla is a fast-growing pharmaceutical company with a continued focus on the expanse of our strong legacy. Over the last five years, Cipla has significantly expanded its portfolio and presence in the U.S. with both a generic and brand division. InvaGen Pharmaceuticals, Inc. InvaGen Pharmaceuticals is a Cipla subsidiary engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on a range of therapeutic areas, including cardiovascular, anti-infective, CNS, anti-inflammatory, anti-diabetic, and anti-depressants. The company was founded in 2003 and is based in Central Islip and Hauppauge, New York. In October 2020, InvaGen established its project site in Fall River, Massachusetts to support the launch of Cipla's respiratory business in the United States. Equal Opportunity Employer Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Cipla, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require reasonable accommodation to make your application or interview experience a great one, please contact the recruiter. About the Salary/ Pay Range: The salary range mentioned above is an anticipated base salary range for this position. Exact salary depends on several factors such as experience, skills, education, and budget. Salary range may vary based on geographic location. In addition to base salary, this position may be eligible for benefits and participation in a bonus program based on performance and company results.

Join Our Team as a Production Operator - 2nd Shift (3:30 pm - 11:30 pm) At Rea Magnet Wire, we don't just produce magnet wire - we are POWERING WHAT'S NEXT. If you're experienced in operating safely, quality production, and driving process improvements, we want you on our team! ⚡️ Ready to take the next step? New Start Pay: $24.00/hour $25.00/hour at 90 days $26.00/hour at 1 year Main Responsibilities: Set Up and Operate Taping Machines Follow Specification for Insulation Wire Inspect Finished Products and Testing Maintain Work Area Clean Comply with PPE and Safety Requirements Ability to train and support new employees by sharing job knowledge, demonstrating correct procedures, and reinforcing safety and quality standards until they achieve full qualification. Set up and operate taping machines to insulate aluminum and copper wire based on order specifications for insulation type, width, thickness of layers, and footage. Additional Responsibilities: Inspect product diameter Set tape overlap and registration Monitor product packaging Tag and identify finished products Utilize material handling equipment Operate welding and swaging devices Perform safety inspections Maintain material supply Record production data We are an Equal Employment Opportunity/Affirmative Action/Vet/Disability Employer Job Type: Full-time Pay: $24.00 - $26.00 per hour Benefits: 401(k) 401(k) matching Dental Insurance Employee assistance program Employee discount Flexible spending account Health insurance Health savings account Life insurance Paid time off Referral program Tuition reimbursement Vision insurance Schedule: Monday through Friday 2nd Shift (3:30 pm to 11:30 pm) 8-Hour Shift Overtime Weekends as needed Position Specifications Minimum Qualifications: High school diploma or GED required. At least 2 years of recent manufacturing experience. At least 2 years of recent Machine Operator experience. Knowledge of safety, distribution, and manufacturing best practices. High level of mechanical aptitude and hands-on experience with basic hand tools and measuring devices, verified through work history and references. Preferred Qualifications: Preference for candidates demonstrating recent, consistent work history. Preference for candidates with a strong work ethic, reliability, and a demonstrated commitment to professional growth in a manufacturing setting. Forklift certification is preferred. Physical Demands and Work Environment: The physical demands and work environment characteristics 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. Physical Demands: Frequently uses hoist to push/pull reels weighing up to 3,200lbs Frequent standing, walking and bending Frequent use of arms below shoulder height; minimal use of arms above shoulder height Frequent reading and interpreting test data and visually inspecting wire Frequent lifting up to 25lbs Work Environment: Work performed in a plant manufacturing environment. Slippery floors due to steel plates. Incumbent will occasionally be exposed to Cold Temperatures 80 degrees. The environment is well lit; the noise level is often minimal but incumbent may be exposed to higher than 85 decibels Work Location: In person

Are you looking for a new challenge? Passionate about innovation? Want to work for a global company that values integrity, teamwork, and loyalty? At LATICRETE International, we aim to be the leading construction brand trusted globally for high-performance tile and stone installation systems and building finishing solutions. We've been in business for over 65 years, family-owned for three generations, and can be found in over 100 countries. The Hartford Business Journal even named us one of Connecticut's top family-owned companies in 2017! We don't just make innovative, industry-leading products. Our purpose is to improve the built world and the lives of those who build it. We strive to connect with, engage with and improve the lives of our employees, our customers, our partners, and the global communities in which we operate. We are seeking passionate and ambitious employees who want to make a difference not just within our organization, but within their communities, our industry, and the world. If that sounds like you, then what are you waiting for? Join the family and expand your horizons! Just some of our benefits: Medical Dental Vision 401k Tuition reimbursement 13 paid holidays, that includes 1 week of paid plant shutdown between the Christmas and New Year's Day holidays Paid vacation and sick time Flexible spending Life Insurance, AD&D and Supplemental Insurance ESSENTIAL DUTIES AND RESPONSIBILITIES Additional duties and responsibilities may be assigned, as necessary. 1. Machine Operation and Order Fulfillment (55%): Prepare Materials Needed for Order. Senior Production Associate is focused on 5 to 8 pieces of equipment to ensure fulfillment of the following duties: Review Order and list of materials and utilize RF Gun to locate and pick the materials. Review order and weigh materials based on order needs - input information into machine that will prepare the batch. Start up machinery, review production schedule, load bags into machine and work with batcher to determine when to run the machine. Ensure safety protocols are always followed. 2. Housekeeping (10%): Ensure proper housekeeping and maintenance of worksite - Sweeping, vacuuming, removing packing materials/debris and equipment cleaning. 3. Staging and Shift Handoff (5%): Prepare materials for next shift to ensure smooth transition and handoff with minimal downtime. 4. Quality Control (10%): Ensure team is utilizing raw materials that are not expired and follow correct formulas. Collect samples for the QC team and based on results, adjust batch as needed. Ensure final product is meeting quality specifications. 5. Equipment & Materials (10%): Communicate with Leadership and maintenance any equipment and materials needs, shortages, failures, required repairs, forklift inspection results etc. 6. Leadership, Mentorship & Training (10%): Assists with training new team members on equipment and areas in the plant. Able to assist Supervisor with workload balancing and provide direction to team in absence of the leader. Floor level escalation for team questions. REQUIRED SKILLS & 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 may be made to enable individuals with disabilities to perform the essential functions . Able to utilize math to perform basic weights for formulas. Able to read and interpret directions and order details. Able to communicate both in writing and verbally. Proficient in 5-8 pieces of plant equipment or equivalent work experience. 4+ Years Plant experience. Education and Experience: High School Diploma or equivalent. Physical Requirements: Must pass pre-employment physical. Lift: Must be able to lift and/or carry a minimum of 60 pounds. Push/Pull: Must be able to push/pull 55 pounds. Stand: Must be able to stand 80% - 85% of the day. Sitting: Must be able to sit 5% of the day. Twisting/Bending: Must be able to twist/bend 20% of the day. Squatting, Climbing and/or Crawling: Must be able to squat/climb/crawl 10% of the day. #LI-DS1

Open Scientific provides contract staffing and direct hire recruitment services for the scientific, engineering, laboratory and manufacturing sectors. Job Description Shift: Both 1st and 2nd shifts are available (Monday through Friday) 1st shift start time: 5:00am / 2nd shift start time: 2:00pm Job Responsibilities: Operate various production machines Assure that the machines are running properly Perform quality checks to confirm finished products are properly sealed Qualifications: Prior warehouse or manufacturing experience preferred Experience working with pharmaceutical or food manufacturing a plus Must be able to lift 60lbs This is a physical, active position that requires standing, bending, lifting, carrying, kneeling, etc Ability to work in a refrigerated environment Additional Information All your information will be kept confidential according to EEO guidelines.

Job Description iRocket is developing reusable, fully autonomous small launch vehicles to deliver more frequent, lower-cost access to space. We work across propulsion, structures, integration, and test domains, building toward an era of responsive launch systems. The Role: We are seeking a Manufacturing Technician to support the fabrication, assembly, and integration of structural and mechanical subassemblies for our rocket hardware. You'll work closely with manufacturing and quality engineers to build reliable flight hardware in line with strict aerospace standards. Manufacture and assemble flight hardware using methods such as drilling, fastening, bonding, and other mechanical processes Use precision calibrated tools (e.g. torque wrenches, micrometers, calipers) Read and interpret technical drawings, blueprints, and work instructions Follow procedures, specifications, and test instructions to ensure hardware is built to design requirements Collaborate with manufacturing engineers and quality personnel to develop, refine, and document work instructions Ensure production tasks are completed on schedule, safely, and to the required quality Perform other related duties as needed to support efficient operations Requirements High school diploma, GED, or equivalent work experience Strong communication and collaboration skills Ability to interact effectively (verbal and written) with engineering, production, and quality teams Experience in New Product Introduction (NPI) or development environments Precision drilling experience (tolerance ~ ±0.001 in) Experience in aerospace, aviation, military, medical device, or other high-reliability industries Ability to read and interpret advanced technical drawings, manuals, and reports Proficient use of precision measuring instruments Experience working in cleanroom or controlled environments Familiarity with forklifts, cranes, or heavy equipment Benefits Health Care Plan (Medical, Dental & Vision) Retirement Plan (401k, IRA) Life Insurance (Basic, Voluntary & AD&D) Paid Time Off (Vacation, Sick & Public Holidays) Family Leave (Maternity, Paternity) Short Term & Long Term Disability Wellness Resources

Job Description Burrow Global is seeking two experienced Process Production Operator for a chemical manufacturing company located in Stratford, CT. The Process Production Operator is responsible for fulfilling customer orders ensuring that packaging of chemical products, including but not limited to Milling, blending, and packaging to meet the customer specifications in a safe and efficient manner. Candidates must have the ability to identify, troubleshoot production and quality problems as they arise. Candidates note: No Per diem or relocation is available on this position. You must live within driving distance of Stratford, CT. Required Education / Experience: High School diploma or GED equivalent. Process Technology certification is desired. With 1 or more years' of experience manufacturing and packaging of chemical products in the petrochemical industry Required Qualifications: Ability to work a rotating shift schedule. Willingness to adjust schedule and or work additional hours in response to departmental needs Knowledge of the production operation processes Knowledge of Process Safety Management Knowledge of safety procedures in the handling of all hazardous materials Experience with forklift operation Possess a “hands-on” work ethic Self-directed individual who performs high quality work without close supervision, yet takes orders as directed Takes ownership of responsibilities following on-the-job training Successfully complete “Miller Packer” orientation program Responsibilities: Complete production records completely as required Performs all task in a safe manner and complies with all safety rules and policies including those for PPE use Preform s equipment clean out as required Package and Transport finished product & container to proper location Communicate processing problems and equipment malfunctions to Lead Operator or Production Supervisor. Collection of required QC samples as required Perform duties as a confined space attendant/rescuer as required Maintain dust collector units and package material for recycling Package antioxidant material as scheduled Maintain the central vacuum system Other duties as assigned Packages materials to fulfill customer orders, ensuring that packaging and weights meet the customer's specifications Sweep, vacuum, and cleans up the plant area as required Actively involved with the Responsible Care Management System Contain and clean up small (< 5 gallons) spills of hazardous materials Maintain good housekeeping and materials management to prevent raw materials from collecting into storm water Actively involved with Safety Management Systems Participate in CPR/AED/First Aid certification training Perform assigned confined space entry and rescue duties Set an example in safety-related activities, including but not limited to, wearing appropriate PPE, following safe work practices, and compliance with all applicable rules and regulations Report all undesired events such as near miss, anomalies, personal injury, and process safety hazards Responsible for performing activities and participating with the OSHA Process Safety Management System.

North Atlantic Industries is a leading provider of embedded electronic solutions, specializing in rugged embedded computing, power supplies and motion simulation and measurement technologies. Our products and services are used by the military, aerospace, and industrial markets, helping to advance technology and protect the free world. NAI was proud to be recognized as a Top Workplace on Long Island by Newsday! Our culture is very collaborative. We have team building events, company picnics, special event day and employee game room. Please visit our website at ******************** to see more about what makes us a unique place to work. Summary: The Production Operator works in an electronics manufacturing environment assembling printed circuit boards (PCBs). This role involves using computers and equipment to perform daily production tasks. Following instructions and maintaining attention to detail are essential to ensuring the quality of the products. Keeping the workspace clean and organized is a key part of maintaining high production standards. The Production Operator will be trained to operate various machines, including Pick and Place, Automated Optical Inspection (AOI), Selective Soldering equipment, and hand assembly. Flexibility is important, as the operator frequently moves between tasks and functional areas. Teamwork, punctuality, and communication are critical to the success of this role. Requirements * Organize and label products to ensure proper tracking during production. * Apply gels and adhesives to components as part of the assembly process. * Prepare electronic components for assembly into PCBs. * Use basic hand tools for mechanical assembly tasks. * Utilize machines to assemble printed circuit boards. Qualifications and Education Requirements: * High School Diploma or equivalent. Language Skills: * Fluent in English (reading, writing, and speaking). * Strong oral and written communication skills. Other Skills and Abilities: * Experience working in a team environment. * Ability to lift 40 pounds. * Ability to work on your feet. * Familiarity with basic hand tools. * Effective communication skills, both written and verbal. * Computer literate a plus * Ability to learn new skills (Certified Training will be provided). * Conscientious regarding quality, time management, teamwork, and safety. * Flexibility to train and move between functional areas. North Atlantic Industries offer comprehensive and competitive packages including: * Medical, Dental, and Vision Insurance * Company-provided Life and AD&D Insurance * Voluntary Supplemental Life Insurance * Long-term Disability Insurance * Flexible Spending Accounts (FSA) * Employee Assistance Program (EAP) * Tax-deferred 401K with company matching contributions. * Vacation, holidays, sick * Employee tuition reimbursement * Business casual dress environment * Schedule: M-F 2nd Shift 3PM-11:30PM North Atlantic Industries (NAI) is proud to be an Equal Opportunity Employer and is committed to providing equal employment opportunity for all persons in all facets of employment. All qualified applicants will receive consideration for employment without regard to any legally protected status. If you are an individual with a disability or a disabled veteran and require a reasonable accommodation in applying for any posted position, please contact Human Resources at ************ or by email at ***********. As a federal government contractor, in accordance with applicable laws, regulations, and Executive Orders, North Atlantic Industries (NAI) is required to develop annual Affirmative Action Plans for Protected Veterans and Individuals with Disabilities. Any employees or applicants who wish to review the Affirmative Action Plan for Protected Veterans and Individuals with Disabilities can contact us by sending an email to *********** or by calling ************. Salary Description $18-$23 per hour +Night Differential

NOTICE: The posting for local applicants only - is not for those applying for a global assignment and/or for employees working outside of Cipla's U.S. Subsidiaries or Affiliates Job Title Manufacturing Operator I Organization Name InvaGen Pharmaceuticals, Inc. Location Central Islip, NY Shift / Hours 1st Shift 7:00am-3:30pm Employment Type Full Time Salary Range (Base/salary) $ 18.25-20.75 /hr Benefits In addition to a fulfilling career and competitive salary, the Company offers a comprehensive benefits package to include a 401(k) savings plan and matching, health insurance - medical/dental/vision, health savings account (HSA), flexible spending account (FSA), paid time off (PTO) - vacation/sick/flex time, paid holidays, short-term disability (STD), long-term disability (LTD), parental leave, paid family leave, employee discounts, and other benefits. Responsibilities/ Accountabilities Must be willing to work in a pharmaceutical manufacturing setting. Must be able to know how to operate pharmaceutical production machinery independently. Execute procedures for manufacturing processes in accordance with batch manufacturing record (BMR) and Standard Operating Procedures (SOP) requirements. Perform machine changeovers, cleaning and set up as per SOPs. Ensure the proper area & equipment cleanliness and setup in stipulated time. Prepare a room and equipment for line clearance, replace room filters, Ensure verification and calibration of balance/scale and check pressure differential for the rooms. Ensure line clearance before initiating manufacturing activities in each area. Receive/transfer material from/to dispensing/manufacturing storage and check dispensed materials/final mix blend/compressed tablets and labeling as per BMR. Wear appropriate personal protective equipment (PPE) as stated in the SOP/BMR before initiating the process. Able to operate applicable equipment independently as per area of operation. Ensure adherence to quality standards during all stages of the manufacturing process. Complete manufacturing documents on time, ensuring accuracy and completeness. Responsible for training on all relevant SOPs and always maintain compliance with related SOPs and current Good Manufacturing Practices (cGMP) in the manufacturing process. Perform duties through the proper, safe use of equipment, according to Health & Safety procedures and Equipment Manuals. Flexible to work extended hours, to achieve manufacturing schedule when needed. Maintain discipline and comply with company policies and procedures. Perform entire duties as communicated time to time by department management/designee. Participate in safety related programs and or safety teams as needed. Enforce and follow safety regulations and ensure the working area is clean. Adhere to CIPLA's Safety, Health, and Environmental policies. Must be able to work under general supervision and able to work independently and in a team environment. Must be able to exercise appropriate professional judgment on matters of significance. Other duties assigned as required by Manufacturing Management. Education Qualifications High School Diploma (or equivalent experience) Experience Zero (0) to three (3) years of direct work experience in pharmaceutical manufacturing. Preference will be given to candidates with experience in generic pharmaceutical manufacturing. Skills/ Competencies Understanding of granulation, compression, coating, and encapsulation machines. Capable of conducting troubleshooting, investigations and root cause identification and analysis. Able to prioritize, plan and work under tight schedules and deadlines. Must possess strong documentation and technical writing skills and be able to apply relevant scientific principles and practices. Must communicate clearly and concisely across levels, both orally and in written. Strong command over written and verbal English is required. Physical Requirements Should not have any restriction to work with powder containing active pharmaceutical ingredients. This position requires the ability to do heavy lifting / bending frequently. Long periods of standing up/walking during the working hours; ability to ascend/descend ladders; and able to lift to 35 pounds. Must be able to move pallets/equipment weighing about 200 - 300 kgs using suitable moving equipment like pallet jacks. About Cipla Cipla is a leading global pharmaceutical company, dedicated to high-quality, branded, and generic medicines. We are trusted by healthcare professionals and patients across geographies. Over the last eight decades, we have strengthened our leadership in India's pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world. Driven by the purpose ‘Caring for Life', Cipla's focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world. In the last 85 + years, Cipla has emerged as one of the most respected pharmaceutical names in India as well as across more than 100 countries. Cipla is a fast-growing pharmaceutical company with a continued focus on the expanse of our strong legacy. Over the last five years, Cipla has significantly expanded its portfolio and presence in the U.S. with both a generic and brand division. InvaGen Pharmaceuticals, Inc. InvaGen Pharmaceuticals is a Cipla subsidiary engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on a range of therapeutic areas, including cardiovascular, anti-infective, CNS, anti-inflammatory, anti-diabetic, and anti-depressants. The company was founded in 2003 and is based in Central Islip and Hauppauge, New York. In October 2020, InvaGen established its project site in Fall River, Massachusetts to support the launch of Cipla's respiratory business in the United States. Equal Opportunity Employer Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Cipla, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require reasonable accommodation to make your application or interview experience a great one, please contact the recruiter. About the Salary/ Pay Range: The salary range mentioned above is an anticipated base salary range for this position. Exact salary depends on several factors such as experience, skills, education, and budget. Salary range may vary based on geographic location. In addition to base salary, this position may be eligible for benefits and participation in a bonus program based on performance and company results.

NOTICE: The posting for local applicants only - is not for those applying for a global assignment and/or for employees working outside of Cipla's U.S. Subsidiaries or Affiliates Job Title Manufacturing Operator II Organization Name InvaGen Pharmaceuticals, Inc. Location Hauppauge, NY Employment Type Full Time Salary Range (Base/salary) $21.00 - $24.00/hr Benefits In addition to a fulfilling career and competitive salary, the Company offers a comprehensive benefits package to include a 401(k) savings plan and matching, health insurance - medical/dental/vision, health savings account (HSA), flexible spending account (FSA), paid time off (PTO) - vacation/sick/flex time, paid holidays, short-term disability (STD), long-term disability (LTD), parental leave, paid family leave, employee discounts, and other benefits. Work Hours/ Shift 2nd Shift / 3:00 pm -11:30 pm Responsibilities/ Accountabilities * Must be willing to work in a pharmaceutical setting. * Must be able to know how to operate pharmaceutical production machinery independently and thoroughly complete required documentation (legible writing, accurate reporting, maintain and file, etc.) * Execute procedures for manufacturing processes in accordance with batch manufacturing record (BMR) and Standard Operating Procedures (SOP) requirements. * Perform machine changeovers, cleaning and set up as per SOPs. Ensure the proper area & equipment cleanliness and setup in stipulated time. * Prepare a room and equipment for line clearance, replace room filters, Ensure verification and calibration of balance/scale and check pressure differential for the rooms. * Ensure line clearance before initiating manufacturing activities in each area. * Receive/transfer material from/to dispensing/manufacturing storage and check dispensed materials/final mix blend/compressed tablets and labeling as per BMR. * Wear appropriate personal protective equipment (PPE) as stated in the SOP/BMR before initiating the process. * Able to operate applicable equipment independently as per area of operation. * Ensure adherence to quality standards during all stages of the manufacturing process. * Complete manufacturing documents on time, ensuring accuracy and completeness. * Responsible for training on all relevant SOPs and always maintain compliance with related SOPs and current Good Manufacturing Practices (cGMP) in the manufacturing process. * Perform duties through the proper, safe use of equipment, according to Health & Safety procedures and Equipment Manuals. * Flexible to work extended hours, to achieve manufacturing schedule when needed. * Maintain discipline and comply with company policies and procedures. * Perform entire duties as communicated time to time by department management/designee. * Participate in safety related programs and or safety teams as needed. * Enforce and follow safety regulations and ensure the working area is clean. * Adhere to CIPLA's Safety, Health, and Environmental policies. * Must be able to work under general supervision and able to work independently and in a team environment. * Must be able to exercise appropriate professional judgment on matters of significance. * Other duties assigned by Manufacturing Management. Education Qualifications/Experience * High School Diploma (or educational equivalent (i.e. GED) * Minimum three years of direct work experience in pharmaceutical manufacturing. * Preference will be given to candidates with experience in generic pharmaceutical manufacturing. Skills/ Competencies * Must have legible handwriting, and the ability to perform accurate documentation. * Understanding of granulation, compression, coating, and encapsulation machines. * Capable of conducting troubleshooting, investigations and root cause identification and analysis. * Able to prioritize, plan and work under tight schedules and deadlines. * Technical writing skills and application of relevant scientific principles and practices (preferred). * Must communicate clearly and concisely, both orally and in written. * English proficiency required. Physical Requirements * Should not have any restriction to work with powder containing active pharmaceutical ingredients. * This position requires the ability to do heavy lifting / bending frequently. * Long periods of standing up/walking during the working hours; ability to ascend/descend ladders; and able to lift to 35 pounds. * Must be able to move pallets/equipment weighing about 200 - 300 kgs using suitable moving equipment like pallet jacks.

Are you looking for a new challenge? Passionate about innovation? Want to work for a global company that values integrity, teamwork, and loyalty? At LATICRETE International, we aim to be the leading construction brand trusted globally for high-performance tile and stone installation systems and building finishing solutions. We've been in business for over 65 years, family-owned for three generations, and can be found in over 100 countries. The Hartford Business Journal even named us one of Connecticut's top family-owned companies in 2017! We don't just make innovative, industry-leading products. Our purpose is to improve the built world and the lives of those who build it. We strive to connect with, engage with and improve the lives of our employees, our customers, our partners, and the global communities in which we operate. We are seeking passionate and ambitious employees who want to make a difference not just within our organization, but within their communities, our industry, and the world. If that sounds like you, then what are you waiting for? Join the family and expand your horizons! Just some of our benefits: Medical Dental Vision 401k Tuition reimbursement 12 paid holidays in addition to paid vacation and sick time Flexible spending Life Insurance, AD&D and Supplemental Insurance ESSENTIAL DUTIES AND RESPONSIBILITIES Additional duties and responsibilities may be assigned, as necessary. 1. Machine Operation and Order Fulfillment (65%): Prepare materials needed for order. Ensure fulfillment of one/two areas below: Review Order and list of materials and utilize RF Gun to locate and pick the materials. Review order and weigh materials based on order needs - input information into machine that will prepare the batch. Start-up machinery, review production schedule, load bags into machine and work with batcher to determine when to run the machine. Ensure safety protocols are always followed. 2. Housekeeping (15%): Ensure proper housekeeping and maintenance of worksite - Sweeping, vacuuming, removing packing materials/debris and equipment cleaning. 3. Staging and Shift Handoff (5%): Prepare materials for next shift to ensure smooth transition and handoff with minimal downtime. 4. Quality Control (10%) Ensure team is utilizing raw materials that are not expired and follow correct formulas. Collect samples for the QC team and based on results, adjust batch as needed. Ensure final product is meeting quality specifications. 5. Equipment & Materials (5%) Communicate with Leadership and maintenance any equipment and materials needs, shortages, failures, required repairs, forklift inspection results etc. REQUIRED SKILLS & 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 may be made to enable individuals with disabilities to perform the essential functions . Able to utilize math to perform basic weights for formulas. Able to read and interpret directions and order details. Able to communicate both in writing and verbally. Education and Experience: High School Diploma or equivalent. Physical Requirements: Must pass pre-employment physical. Lift: Must be able to lift and/or carry a minimum of 60 pounds. Push/Pull: Must be able to push/pull 55 pounds. Stand: Must be able to stand 80% - 85% of the day. Sitting: Must be able to sit 5% of the day. Twisting/Bending: Must be able to twist/bend 20% of the day. Squatting, Climbing and/or Crawling: Must be able to squat/climb/crawl 10% of the day. #LI-DS1

Burrow Global is seeking two experienced Process Production Operator for a chemical manufacturing company located in Stratford, CT. The Process Production Operator is responsible for fulfilling customer orders ensuring that packaging of chemical products, including but not limited to Milling, blending, and packaging to meet the customer specifications in a safe and efficient manner. Candidates must have the ability to identify, troubleshoot production and quality problems as they arise. Candidates note: No Per diem or relocation is available on this position. You must live within driving distance of Stratford, CT. Required Education / Experience: High School diploma or GED equivalent. Process Technology certification is desired. With 1 or more years' of experience manufacturing and packaging of chemical products in the petrochemical industry Required Qualifications: Ability to work a rotating shift schedule. Willingness to adjust schedule and or work additional hours in response to departmental needs Knowledge of the production operation processes Knowledge of Process Safety Management Knowledge of safety procedures in the handling of all hazardous materials Experience with forklift operation Possess a “hands-on” work ethic Self-directed individual who performs high quality work without close supervision, yet takes orders as directed Takes ownership of responsibilities following on-the-job training Successfully complete “Miller Packer” orientation program Responsibilities: Complete production records completely as required Performs all task in a safe manner and complies with all safety rules and policies including those for PPE use Preform s equipment clean out as required Package and Transport finished product & container to proper location Communicate processing problems and equipment malfunctions to Lead Operator or Production Supervisor. Collection of required QC samples as required Perform duties as a confined space attendant/rescuer as required Maintain dust collector units and package material for recycling Package antioxidant material as scheduled Maintain the central vacuum system Other duties as assigned Packages materials to fulfill customer orders, ensuring that packaging and weights meet the customer's specifications Sweep, vacuum, and cleans up the plant area as required Actively involved with the Responsible Care Management System Contain and clean up small (< 5 gallons) spills of hazardous materials Maintain good housekeeping and materials management to prevent raw materials from collecting into storm water Actively involved with Safety Management Systems Participate in CPR/AED/First Aid certification training Perform assigned confined space entry and rescue duties Set an example in safety-related activities, including but not limited to, wearing appropriate PPE, following safe work practices, and compliance with all applicable rules and regulations Report all undesired events such as near miss, anomalies, personal injury, and process safety hazards Responsible for performing activities and participating with the OSHA Process Safety Management System.

Open Scientific provides contract staffing and direct hire recruitment services for the scientific, engineering, laboratory and manufacturing sectors. Job Description Job Title: Production Operator Location: Hicksville, NY Salary: Start rate: $10.00/hr. up to $12.50 within 90 days probation Shift: Both 1st and 2nd shifts are available (Monday through Friday) 1st shift start time: 5:00am / 2nd shift start time: 2:00pm Benefits - 30 day wait, 401K 4% match Job Responsibilities: This position requires for the Operator to change plastic rolls as needed and place them in the machine for wrapping product. The Operator will also walk to get the rolls that are being replaced when the previous rolls are empty. Operate various production machines Assure that the machines are running properly Perform quality checks to confirm finished products are properly sealed Qualifications: Prior warehouse or manufacturing experience preferred Experience working with pharmaceutical or food manufacturing a plus Must be able to lift 60lbs This is a physical, active position that requires standing, bending, lifting, carrying, kneeling, etc Ability to work in a refrigerated environment Additional Information All your information will be kept confidential according to EEO guidelines.