Quality control technician jobs in Lancaster, PA - 141 jobs

Job Description Inspects company products at various stages of manufacture and monitors compliance to the company's quality standards. Documents quality findings in designated software programs and maintains quality data in order to provide quality metric reporting for supplier and manufacturing scorecards. ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. Perform inspection and testing on parts received from external suppliers, in-line inspections in the manufacturing area, and outgoing inspections for product shipments. Follow Control Plans/Quality Inspection Plans to determine process/product conformance. Review non-conforming materials from value streams and document applicable information concerning the non-conformance on CAREL documentation. Assist with processing of products returned to CAREL on return material authorizations. Familiarity with and ability to utilize various types of measuring and test equipment such as calipers, micrometers, etc. Works with Assembly Operators and Manufacturing Engineers to affirm process controls are being adequately followed. Generate inspection records, product statuses, and summarize data. Be fluent in computer software programs such as MS Word and Excel. Familiarity with industrial manufacturing processes, including wave soldering, surface mount applications and mechanical type assembly. Performs inspection on products (cables, circuit cards, assemblies, systems, etc.) manufactured for compliance to CAREL and customer drawings. Performs first piece inspections and audits as required. Verifies all required documentation. Works with other Quality associates in the disposition of non-conforming material and in identification of defect trends in manufacturing processes. Completes documentation of defects through data entry into company software platforms. Submits products to source and/or customer inspectors as required. Assists in keeping the quality department compliant to ISO9001. Reviews and reads drawings, specifications, and other technical documents to understand quality requirements of manufactured products. QUALIFICATIONS/REQUIREMENTS · High School education with 3 years technical experience working in a manufacturing environment. · Previous experience reading drawings, specifications and other technical documentation. LANGUAGE SKILLS · Good verbal and written skills. MATHEMATICAL SKILLS · Basic Math skills. · Some statistics a plus. PHYSICAL DEMANDS · Regularly sit or stand, reach, bend and move about. · Must be able to lift up to 30lbs. WORK ENVIRONMENT · Work environments include, but are not limited to Carel's labs and manufacturing facilities, regional, national or international office, car, or airline flights · While performing the duties of this job, the employee is regularly required to stand or sit for long periods of time · The employee is occasionally required to walk, reach with hands and arms; stoop, kneel, or crouch. · 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. Monday - Friday 3pm-11:30pm

DHL Supply Chain is Hiring!At DHL, you will play a part in one of the world's most essential industries. There has never been a better time to join DHL Supply Chain. In a global business like ours, the opportunities are endless. So, join us. Work with us. Grow with us. The core responsibilities of this role include: Quality Position:Quality Tech I Shift:2ndshift Mon-Fri 3:00 PM- 11:00PM Pay: $19.95 Additional Incentives:All full-time employees are eligible to qualify for monthly performance and safety incentive bonuses! In addition to the general job description below, the ideal candidate will also possess the following skills and/or experience: Quality checks, excel, auditing Be part of the world's largest logistics company!DHL Supply Chain hasbeen certified as a Great Place to Work in the US and Canada! Our excellent benefits packages includes: * Affordable medical, dental, and vision coverage available beginning on your 30thday * PTO program for all associates, including paid holidays and vacation * 401(k) with generous company match * Tuition reimbursement program * Excellent training and career advancement opportunities Grow your skills. Shape your world. Role Purpose: Provide leadership, training, support and disciplines for establishment, maintenance, alignment and continual improvement of the QA System. Responsible for day-to-day Quality Assurance activities to ensure compliance with governmental regulations, customer requirements, quality assurance policies and procedures and accommodating requests for support. Leads QA team. Assigns QA team work schedules, directs team, trains associates in required QA processes and monitor's associates' compliance and progress. Key Accountabilities: * Monitor and report level of QMS implementation, compliance and effectiveness through audit activities, observation, review of quality metrics and customer feedback. * Facilitate QA training for new and existing associates. * Review documents and instruction prepared by members of the work group for accuracy and legibility. * Work with Quality Assurance, Ops Performance and Process Improvement teams to progress Quality initiatives. Incorporate QA, OP and PIM tools and methodologies, as appropriate, in performance of tasks. * Recommends appropriate methods for supporting the site operations' requirements for quality assurance compliance. * Lead/support coordination of QA license, permit and registration activities and provide direction for compliance with FDA, DEA, ATF, State and other similar regulatory requirements. * Perform daily quality assurance activities as required or directed by management. * Lead and facilitate development of QMS documentation. Required Education and Experience: * High School Diploma or Equivalent * Forklift operator certificate or satisfactory completion of a forklift-training program within the first 30 days of employment * Associate degree or equivalent in related field of study, preferred Our Organization is an equal opportunity employer. #LI-Onsite #LI-DNI ","title

Job Purpose Assist with implementing and supporting company standards to ensure quality specifications for packaging, raw ingredients, and finished products are met and food safety of manufactured products is upheld. Monitor and sample quality control plans and process control procedures to ensure production of finished product is to standard. Essential Functions Perform daily QA walk-throughs; verify GMPs are followed in the facility and set example by practicing correct GMP procedures at all times Monitor plant operations to ensure sanitary operational procedures are followed according to GMPs Perform pre-operational inspections, monitoring for food safety and quality Initiate and complete the hold process for non-conforming product, raw materials, and other materials as required; follow up and complete disposition when determined Verify batch formulas and product labels ensuring activities are complete and meet specifications Monitor and verify CCPs/preventive controls as required Perform equipment calibration as assigned Perform basic analytical testing Perform environmental swabbing for bacteria and pathogens; prepare, document, and send swabs to third- party lab as required Perform environmental and finished product testing for allergens Collect finished product samples Collect and record temperature readings Identify and report food safety issues and assist in conducting investigations into food safety issues, foreign material findings, and customer complaints Review production records for completion and compliance with good documentation practices Execute and maintain the document and photo retention process Serve as a resource to production employees for product quality, food safety, and regulatory issues Attend shift change meetings to ensure information and any issues are communicated across shifts Support food safety program, quality standards, and legality of manufactured products Perform other job-related duties as assigned Qualifications (Education, Experience, Competencies) Associate's/Bachelor's degree or equivalent work experience Basic knowledge of general food safety programs and policies including government regulations HACCP and PCQI certified or willing to become certified Basic analytical testing knowledge Basic ability to use instruments/equipment vital to completing duties (e.g., scales, thermometers, metal detectors, calculators, gauges, calipers, rulers, ovens) Ability to read and understand plant SOPs, work instructions, GMPs, and safety instructions Operational knowledge of computers and Microsoft Office applications Basic problem-solving ability Ability to work independently and as part of a team Ability to organize, manage multiple priorities, and maintain high attention to detail in a fast-paced environment Ability to work varied shifts as required California, Illinois, Massachusetts, Minnesota, Washington and New York Residents Only: The hourly range for this role is $19.02 to $22.00 per hour. Pay is based upon several factors including but not limited to local labor markets, education, work experience, certifications, etc. Rise Baking Company complies with all minimum wage laws as applicable. In addition to your hourly wages, Rise Baking Company offers benefits such as, a comprehensive benefits package, quarterly bonus eligibility, incentive and recognition programs and 401k contributions (all benefits are subject to eligibility requirements). At Rise Baking Company, our people are our finest ingredient. MON123 RISE123

Do you have an eye for attention to detail and an impeccable desire to enforce and maintain high standards of Quality? Then look no further and join the Quality Team at Advanced Cooling Technologies, Inc. (ACT) - nominated as a "Best Places to Work" in PA in 2023, York location. The Quality Team ACT is looking for team members who are passionate about creativity and innovation and looking to make a difference every day. We are committed to developing world class Quality Assurance programs, processes, and people that support the ACT mission and family of brands, including Tekgard Environmental Control Units. We have an immediate opening for a Quality Inspection in our York location. Company Overview Advanced Cooling Technologies, Inc. (ACT), with locations in York and headquartered in Lancaster, PA, is a leading manufacturer of innovative thermal management products for diverse applications, serving a broad spectrum of industries including commercial satellites, military vehicles, medical devices, primary calibration equipment, and HVAC systems. We are dedicated to fostering creativity, innovation, and making a tangible difference every day. Our commitment extends to our customers, employees, and community, with core values centered on Innovation, Teamwork, and Customer Care-key drivers of our continuous growth and success. At ACT, our skilled and dedicated staff is our most valuable resource. ACT offers a robust benefits package including low-cost medical, dental, vision, company-paid life and disability insurance, paid time off, a 401k with company match, and a profit-sharing bonus plan. Enjoy a work-life balance at our York location supported by a 4-day work week (4/10 schedule), generous PTO, and 8 paid holidays. Position Summary This position is for a Quality Inspector at our facility located in York, PA. As a Quality Inspector, you will play a hands-on role within the organization and interface with both Operations and Product Development teams while performing incoming inspection of materials and components and performing in-process and final inspections of products for commercial and/or government customers. Key Duties and Responsibilities * Inspect incoming materials * Perform in-process inspections and/or final inspections on manufactured product * Ensure all materials and product meet Quality standards as per policy and ISO9001/AS9100 procedures * Identify and segregate non-conformances and write non-conformance reports * Support Supplier Quality initiatives ACT 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 protected veteran, status as a qualified individual with a disability, or any other trait protected by law. Requirements * High School Diploma or GED * Ability to read and interpret blueprints and shop drawings * Ability to use basic inspection tools such as micrometers, calipers, height gages, etc. * Basic computer skills (Outlook, Word, Excel). * Basic math skills * Strong verbal and written communication skills Additional Qualifications (preferred): * Authorized to work in the US. US Citizen, Permanent Resident, or Protected Individual (as defined by 8 U.S.C. § 1324b(a)(3)) preferred due to ITAR responsibilities. * Prior experience with ERP systems

Quality Technician | The Shyft Group (FVS) | Landisville, PA Regular Employee | Hourly Non-Exempt | $0.00 - 0.00 What you'll do: The Quality Technician position is responsible for ensuring that the product meets customer's requirements (both internal and external) at each stage of its manufacturing process, carrying out relevant testing and where necessary take corrective action to rectify non-conformance issues. Report quality issues data, ensuring the Quality Management System is adhered to at all stages. * Promote the expectation that team members will consider the impact of their work/actions on others and make deliberate decisions to act in ways which prevent rework or constraints on the process. * The Quality Technician is a coach, cheerleader, and player on the team * Facilitate creation of systems and processes which enhance the team's ability to meet customer expectations (identification of standards, creating of buy/sell agreements, audit processes, etc.) * Act as mediator when needed to clarify customer expectations or interpret standards * Perform Pre-Delivery Inspections of completed vehicles * Perform data entry, analysis, and sharing/explanation of same * Generate reports * Perform audits of new and existing processes * Document writing, control, and management * Facilitate/Participate in Root Cause Analysis, Design Failure Mode and Effects Analysis, Production Failure Mode and Effects Analysis, Practical Problem Solving, etc. • Initiate non-conforming material documents for supplier quality issues * Assist in the execution of activities which promote continuous improvement and protect customers * Conduct training, information sharing and orientation sessions * Lead by example regarding safety and acting in the best interests of the team * Provide coverage for other technicians as needed * Any other duties as assigned by the Quality Manager What you need to be successful: * High School Diplomas or GED required (Associates degree and/or CQT certification preferred) * Minimum 2-3 years related Quality Manufacturing experience * Knowledge of/ability to acquire a thorough understanding of customer expectations and regulatory requirements * Excellent attendance * Positive attitude * Strong interpersonal skills * Ability to read relevant measuring equipment * Provide appropriate feedback and documentation of any defects * Strong and consistent attention to detail * Self-motivated with the ability to stay on task * Team oriented Able to: * Read and understand Engineering documents such as part prints, assembly drawings * Work overtime on short notice Be willing to: * Learn and rotate within all quality areas * Improve self / area / company (including pursuing additional training, if needed) * Develop a working knowledge of company's systems (example: AS/400, Sparcon) Why The Shyft Group? Our people are our greatest asset, and your success is our success! That's why we provide comprehensive benefits that support your health, financial security, and work-life balance-so you can thrive both personally and professionally. * Health & Wellness: Medical, Dental, Vision, HSA/FSA, Wellness Plan * Financial Security: 401(k) with match, Disability, Life Insurance * Work/Life & Growth: Educational Reimbursement, EAP, Dependent Care. At The Shyft Group, we don't just offer benefits-we invest in your well-being. Join us and experience the difference! Who we are: The Shyft Group is the North American leader in specialty vehicles, including last-mile delivery vans, work trucks, and motorhome chassis. Our 10 brands- Utilimaster, Blue Arc, Royal Truck Body, DuraMag, Magnum, Strobes-R-Us, Spartan RV Chassis, Red Diamond, Builtmore and Independent Truck Upfitters-are powered by 3,000+ team members across the U.S. and Canada. Backed by 50 years of innovation and a supportive, entrepreneurial culture, we're leading the way in electrification and proudly ranked among Fortune's 100 Fastest Growing Companies. Equal Employment Opportunity (EEO) The Shyft Group 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, genetic information, status as a protected veteran or status as a qualified Individual with a Disability, or any other characteristic protected by applicable federal, state or local law. If you have a disability and would like to request an accommodation in order to apply, please email us at *************************. The Shyft Group is an E-Verify Employer Shyft uses E-Verify, which is an online system operated by the U.S. Department of Homeland Security in partnership with the Social Security Administration to verify employment eligibility and validate social security numbers. Through participation in the E-Verify program, information entered on Form I-9 will be provided and compared to information available at both of these agencies. See posters for more details. E-Verify Notice U.S. Right to Work Notice.

QC Lab Technician - Lebanon, PA Hours are 7:00am - 3:00pm Monday thru Friday. The employee is expected to be proficient in the duties of the Quality Control Technician position as they appear below. It is also expected that the employee will have read and understand all Brentwood Industries policies and procedures for their intended position Employees may perform other related duties as required to meet the ongoing needs of the organization. Essential Responsibilities: Ensure the safe operation of all equipment during their shift. Know the location of all safety stops. Obtain probed regrind samples from appropriate departments and insure traceability. Know the proper technique of cleaning the lab mil and essential housekeeping duties. Produce a quality lab mil sample from regrind samples and provide these samples for inspection by a qualified quality control lab technician. Communicate all probing and sample preparation in a timely and concise manner. Test roll samples for proper gauge and determine pass/fail results based on pre-determined standards. Report excessively high or low gauge results to the lab lead and/or lab supervisor and also to calender operators. Prepare documentation for testing of roll stock samples. Complete testing of roll stock samples. Cut leaf strips from roll samples and press them into bars for testing. Prepare bars for testing including sanding flash. Conduct impact tests on roll samples and determine pass/fail results based on pre-determined standards. Perform specific gravity on specimens obtained from roll samples collected from the calender lines. Communicate results of all testing in a timely and concise manner. Set up and conduct the following ASTM tests with assistance: ASTM D790 Flexural testing ASTM D882 Tensile testing ASTM D792 Specific gravity testing ASTM D5420 Impact resistance testing ASTM D4226 Impact resistance testing ASTM D648 Heat Deflection Shrinkage/Stretch testing Essential Skills: EDUCATION and/or EXPERIENCE: High school diploma or equivalent preferred. LANGUAGE SKILLS: The ability to read, write (print legibly), speak and understand the English language at the high school level is required. The ability to communicate with other members of the Quality Control and Production departments and understand instructions, either verbal or written, is essential. MATHEMATICAL SKILLS: The ability to add, subtract, multiply, divide and calculate the average of numbers to the fourth decimal place is required. The ability to read digital micrometers and digital calipers as well as various other dial gauges and measuring devices is essential in order to perform the required duties listed above. REASONING ABILITY: The ability to ascertain the pass/fail status of a roll based on standards set forth in instructions whether verbal or written is imperative. The ability to grasp the concept that the end of a roll sample is the core of the next roll and determine the ramifications of that concept as they effect the status of the roll that follows is required. OTHER: By the completion of the 65 day trial period, the individual must possess or have developed most of the skills necessary to complete each duty satisfactorily. The employee must have developed a working knowledge of the Quality Control department and its function within the company. The employee must begin developing a working knowledge of all quality control software used in the lab. Brentwood offers professional growth potential, a pleasant work environment, and an excellent wage and benefits package including 401k w/employer match. Brentwood Industries, Inc., provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, or genetics. At Brentwood, we have a passion for both our products and our people. Our goal as an employer is to help you excel as an individual and as part of a team by providing you with satisfying, motivating, and stimulating work experience. The varied nature of the environment at Brentwood allows you to work alongside industry professionals on a wide range of projects, contributing your knowledge and strengths to develop innovative, market-driven solutions. Please note: We are not working with external recruiters at this time and are not accepting unsolicited resumes.

Job Description Quality Technician Day Shift: work 2 days, off 2 days, work 3 days, off 3 days (6am to 6pm) Pay: $22.50/hr. with increase opportunities after 120 days Requirements: 1-2 years of experience with quality experience; preferably within the printing, food, or regulated industry with knowledge of GMP's (21CFR 110/111/210/211) Proficiency in Microsoft Office suite is essential Excellent communication skills, both verbal and written Excellent time management skills Attention to detail is essential Ability to work rotating shift 2-2-3-3; including weekends when scheduled Prior experience in the food environment is beneficial Ability to walk, stand, sit, stoop, bend, twist and lift up to 50 pounds. Job Functions: Responsible for monitoring and identifying critical control points (CCP) within the processes. Responsible for monitoring processes and product food safety and quality throughout the manufacturing process. Responsible for the correct documentation and filing of all relevant record logs and Documentation. Ensures the correct recipe guidelines for products are met during processing. Ensures employees are following all Food Safety and worker safety practices. Ensures and educates employees on quality expectations. Collect product samples for the Quality lab. Perform inspections on in-process printing to ensure quality and accuracy of the print according to customer specifications. Identifying non-conformances and ensuring they are corrected “real time” when feasible. Working directly with Operations on the presses, slitter, lamination, etc. to identify areas for continuous improvement. Ensuring paperwork is accurate and filled out in a timely manner on the production lines. The above duties and responsibilities are representative of the nature and level of work assigned and are not necessarily all-inclusive. Benefits: Medical, dental, vision, and prescription drug coverage 401(k) plan with generous company match Bonus program Paid vacation and personal days Paid holidays Company-paid life and AD&D insurance Company paid short-term disability coverage Employee Assistance Program (EAP)

Job Description About Us At Tate we are passionate about everything we do. As an independent brand operating within Kingspan Group, a global plc group of companies, Tate has been recognized worldwide as an industry leader in the development and manufacture of data center infrastructure solutions and commercial office raised access floors, for over 60 years. With revenues of over $600m and growing, Tate plays a pivotal role in offering expertise in cutting edge design engineering to craft solutions, by working collaboratively with clients as a trusted partner. Tate continues to grow and expand, operating multiple manufacturing and commercial sites across the US, Europe, the Middle East, Asia, and Australia. We are excited about our fresh, dynamic, and inclusive team of experts working on new innovations and forward-thinking designs, as we remain a market leading player within our industry. We continue to invest heavily in the best available manufacturing tools and equipment needed to adhere to Tate's world class standards and in keeping with our Planet Passionate sustainability strategy, our focus is on having minimal climate impact. We are excited to potentially welcome you as part of our team as we continue to grow on a worldwide scale. About the Role The Quality Technician 1 is responsible for quality inspection for all products to ensure they conform to all applicable company and quality standards. This position will test products after, in process, and in final stages to ensure quality levels are met. Note: This position is for 3rd Shift. Hours for this role are Sunday-Thursday 10pm-630am What You'll Do · Ensures all test equipment is properly maintained and calibrated · Performs routine & job specific load performance tests to ensure compliance with published specs. · Performs incoming inspections on products received from vendor. · Has a working knowledge of all equipment and machinery within the facility. · Performs daily in process quality audits on products on production floor. · Performs testing needed for qualifications of new or revised products. · Maintains updated certified testing reports on standard products. · Assists with continuous improvement of product and manufacturing processes to improve quality, reduce costs, and ensure product quality objectives are met. · As assigned by supervisor, visits job sites to identify problems and recommends solutions. · Maintains good housekeeping and follow established safety procedures. · Performs other duties as assigned or directed by Team Leader/Supervisor. · Follows all policies, procedures, and work instructions including Employee Handbook, Standard Operating Procedures (SOPs), Manufacturing Operating Procedures (MOPs), Job Safety Analysis (JSAs), and Safety Manual. · Maintains awareness of individual contribution to and impact of the quality, safety, environmental, and product compliance policies and activities; reports all quality issues, unsafe acts, and unsafe conditions to the proper personnel. Additional Expectations Remain compliant with the Code of Conduct and Policies which includes the Kingspan Group Compliance Policy. Ensure that all duties related to product compliance are adhered to in accordance with the Product Compliance Policy, Laws, Regulations, and market demands. Responsible for all tasks to achieve compliance goals and demands of the Compliance Management System. Must raise concerns related to the Compliance Management System to their supervisor, manager, or any member of the Leadership Team, or through the confidential whistle blower service. What You'll Bring High school diploma or GED; or equivalent experience. Must be able to lift up to 50 lbs. unassisted. Must be able to stand, walk, bend, stoop or crouch for at least an 8-hour shift. Must be computer literate, including proficiency with Microsoft Office Products. Ability to use various tools and measuring instruments such as calipers, micrometers, tape measures, dial indicators, feeler gauges, etc. and verify all test equipment is in calibration and maintained in good working order. Strong shop-floor orientation. Knowledge of aluminum cutting and milling operation is a plus. Must be able to work in a fast-paced working environment with accuracy and integrity. Strong written and verbal communication skills. Detail-oriented. Three (3) plus years manufacturing experience. What You'll Get Pay range: $22.45 USD to $26.57 USD per hour. Career Scope and Advancement: As we grow, new positions and career opportunities arise, offering accelerated paths for the right candidates, locally and globally. World of Wellness Philosophy: We empower you to take charge of your health and well-being. You'll have access to a wide range of medical, dental, and vision benefits, along with personalized guidance from a “Health Advocate.” We also offer other supplemental options, including 401k, legal, disability, and theft insurance, to ensure your financial wellness. Corporate Social Responsibility: Through Planet Passionate we are determined to reduce our manufacturing carbon (CO2e) emissions to as close to zero as technically possible, together with halving carbon intensity in our primary supply chain. We are very involved in our community, and you will have ample opportunities to support us in creating a better world. Skills Development: Given the dynamic pace of our business and a strong collaborative environment, your new role will be diverse and multifaceted - allowing you to be more versatile and develop a broader skill set. Mentorship and development: At Tate, we don't believe in hierarchy, we work together as one team for one common goal. You will have access and exposure to our senior leaders and experts for learning in your role, and additionally mentorship for the future. Culture: We have a great team culture, highly collaborative, supportive, and social. Together we innovate, collaborate, take ownership, and strive for excellence. Tate Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to legally protected characteristics. We are committed to providing reasonable accommodations to qualified individuals with disabilities. Employment may be contingent upon completion of post-offer requirements in accordance with applicable law. Stay connected with us on LinkedIn for insights into life at Tate. Join us in our mission to make a difference through exceptional solutions.

The SQT position is responsible for managing all the needed steps to obtain customer satisfaction in regards to purchased parts. Position will include series monitoring, containment monitoring, part audits, part problem analysis, production support, review of parts during pre-series to ensure quality and generation levels. Essential Duties and Responsibilities:• Solve manufacturing issues via monitoring and analysis of the quality problems, ensuring that the contingency and definitive measures are implemented assuring process stability and preventing these issues in the future. • Audit the product at the OEM manufacturing line, making sure that it is specification compliant and the manufacturing process and quality can be granted. • Evaluate and authorize manufacturing processes and packaging related to the CKD logistic process, according to the corporate guidelines. • Apply methods like DOE, 6 Sigma, CEP (Closed-Ended Problems), etc. to analyze the root causes of complaints. • Coordinate with the SQE's the follow-up of projects to achieve the quality requirements and the stability of the processes. • Define action plans to implement the needed improvements, based on the results. • Influence continuous improvement of our product through audits and series monitoring• Recommend technical product improvements evaluating risks and potential chances to avoid quality manufacturing issues by comparing similar parts in the assembly line. • Issue KPM complaints and review supplier 8D responses to close open quality topics• Support production with part related quality topics Required Qualifications:• 2+ years manufacturing experience• BS Engineering or Quality related or equivalent experience• Strong understanding of quality systems and processes. • Knowledge of inspection techniques and statistical methods (i. e. DOE, 6 Sigma, CEP, Fishbone, etc. ) Preferred Qualifications:• Experience at a Tier 1 Supplier or OEM as a Supplier Quality Engineer• International experience• BS/MS Engineering• Familiar with manufacturing processes associated with electronics, plastics, textiles, and metals• Knowledge of OEM Systems. • Technical Knowledge of OEM specifications/drawings. • German and Spanish languages. Environmental Requirements:• Job may require employee to move objects up to fifty (50) lbs• Regularly stands, bends, lifts and moves intermittently during shifts of 8+ hours

The Quality Technician plays a critical role in ensuring product integrity and compliance with regulatory and company standards. This position is responsible for performing detailed inspections, testing, and documentation to support food safety, customer satisfaction, and continuous improvement initiatives. The ideal candidate is detail-oriented, proactive, and passionate about maintaining high-quality standards in a fast-paced, regulated environment. Essential functions * Performs CCP verifications * Completes COA's needed for each day's shipments * Performs quality checks and enters data into database. * Enters data into supplier sites (United/Ingridion etc.) * Observe and perform pre operation inspections * Assists in customer complaints and investigations * Calibrates lab equipment and instruments per schedule * Handle customer sampling requests as per customer schedule * Handle sales sample shipments to support new business efforts. * Places all non-conforming products on hold and notifies team and management * Understands product flow and production equipment. * Identifies areas to reduce waste, rework, and other inefficiencies with a focus on continuous process improvement * Maintains overall cleanliness and housekeeping of the lab. * Conducts inventory of supplies and re-stocks the lab. * Trains production team members to perform analytical tests and data entry of results * Performs accurate microbiology testing using approved methods. * Performs and interprets microbiological tests, generates, and maintains accurate/legible/understandable lab data. * Initiates product hold process when product contamination is noted and completes re-sampling/retesting process * Follows SOP's/work instructions for all testing methods to ensure accurate, repeatable results * Reviews SOPs/Policy for accuracy, compliance and effectiveness as per schedule * Conducts internal GMP Audits * Participates in internal audits with audit team, corrective actions and follow up. * Monitors data and production schedule changes to ensure testing is conducted to meet all food safety and quality program testing requirements such as environmental monitoring and equipment hygiene testing, etc. * Contributes to ensuring lab SOPs/procedures are documented, accurate and up-to-date to industry and customer standard testing methods * Properly maintains lab equipment such as pH meters, scales, Refractometers, PLC * Performs other relate duties as assigned Supervisory responsibilities * None Knowledge, Skills and Abilities * Effectively communicates information in one-on-one and small group situations * Ability to follow and implement written or oral instructions. * Ability to problem solve with limited information. * Ability to analyze a situation and investigate root cause. * Critical thinking skills * Basic knowledge of Microsoft Office, an ERP system such as SAP * Ability to read, write and interpret documents in English such as safety rules, operating and maintenance instructions and procedure manuals. * Ability to work with mathematical concepts such as probability and statistical inference, and fundamentals of plane and solid geometry and trigonometry. Ability to apply concepts such as fractions, percentages, ratios, and proportions to practical situations. * Ability to apply common sense understanding to carry out detailed but uninvolved written or oral instructions. Ability to deal with problems involving a few concrete variables in standardized situations. Required education and experience: * High school diploma or GED * Minimum 6 months of quality assurance experience * Ability to obtain HACCP certification (company-sponsored) Preferred education and experience: * AAS or Bachelor's degree in Food Science or related field * Experience in regulated environments (food, pharma) * Familiarity with HACCP, BRC, ISO 9001, FDA, FSIS, USDA standards * Certifications in HACCP, BRC, or ISO 9001 Work environment and physical demands * While performing the duties of this job, the employee is regularly required to stand, walk, sit, use hands, reach with hands and arms, climb or balance, stoop, kneel, crouch, or crawl, and talk/hear, and taste/smell. * The employee must regularly lift and/or move up to 50 pounds. * Specific vision abilities required by this job include close vision, distance vision, peripheral vision, depth perception, ability to see color, and ability to adjust focus. * While performing the duties of this job, the employee is regularly exposed to wet or humid conditions (non-weather), work near moving mechanical parts, work in high, precarious places, fumes or airborne particle, toxic or caustic chemicals, outdoor weather conditions, extreme cold (non-weather), extreme heat (non-weather), risk of electrical shock, vibration, and allergens. * The noise level in the work environment is usually very loud. Benefits include: * Direct deposit paid weekly. * Quarterly performance bonus opportunities! * Affordable health, vision, and dental insurance plans - Eligible 1st day of the month following 30 days of employment. * Free health savings account with employer match. * Fidelity 401(k) with competitive employer match - fully vested from date of hire. * 3 weeks paid time off plus sick time (pro-rated based on start date). * 9 paid company holidays and 3 paid personal holidays. * Boot allowance twice per year. * Protective equipment and company swag provided. * Free life insurance up to $150,000. * Free employer-paid short-term and long-term disability coverages. * Employee Assistance Programs. * And more! Travel required * The home office for this role is indicated at the top of this . Travel to other Ingredients Plus locations may be required as business needs arise. Affirmative Action/EEO statement We are an equal opportunity employer. We do not discriminate on the basis of race, color, creed, religion, gender, sexual orientation, gender identity, age, national origin, disability, veteran status or any other category protected under federal, state, or local law. All employment is decided on the basis of qualifications, merit, and business need. Other duties Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.

Inspection of in-process, finished, and third-party products using a coordinate measuring machine, hand measurement tools, and other test procedures. Maintain forms and documents as required by ISO Certification. Assist in conducting internal audits of internal processes and calibration of gages used within facility. Implement and assist in corrective actions. Assist in implementing Quality Systems to ensure continuous production of safe and reliable products consistent with established standards and requirements. Essential Duties and Responsibilities include the following. ( Other duties may be assigned .) Perform inspections of incoming supplies as well as finished product to ensure all products are within stated specifications. Maintain quality systems documentation. Implement the Corrective/Preventive Action (CAR) and Complaint on Material (COM) systems and maintain databases. Assist quality engineers with initiating and coordinating the materials disposition, root cause determination, and corrective/preventative action. Maintain and manage calibration of inspection tools and equipment. 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. Required Education and/or Experience Should have a High School Diploma or General Education Degree (GED); six to twelve months manufacturing related experience and/or training; or equivalent combination of education and experience. Other Useful Skills and Abilities Skills to communicate appropriately with departments such as outside vendors, truck drivers, Engineering, Quality, Shipping, Labeling, and other internal customers Capabilities to add, subtract, multiply, and divide in all units of measure using whole numbers, common fractions, and decimals. Occasionally this position is required to convert one unit of measure to another through basic math skills. Able to demonstrate basic computer skills using programs such as Word, Excel, and MAPICS Strong organizational skills are a must 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 stand: walk; use hands to finger, handle, or feel; reach with hands and arms and talk or hear. The employee must regularly lift and /or move up to 50 pounds, and occasionally lift and/or move up to 100 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision and ability to adjust focus. 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 is frequently exposed to moving mechanical parts. The employee is occasionally exposed to high, precarious places; fumes or airborne particles; toxic or caustic chemicals and risk of electrical shock. The noise level in the work environment is usually moderate.

US Tech Solutions is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit our website ********************************** are constantly on the lookout for professionals to fulfill the staffing needs of our clients, and we currently have a job opening that may interest you Title: Quality Control Microbiologist Duration: 12 Months Location: Myerstown, PA 17067 Job Description: Microbiology Team working in a fast paced environment, supporting manufacturing and packaging of OTC Drug and Nutritional products, across multiple shifts, by performing all aspects of Microbiological testing. POSITION SUMMARY This position is in the Quality Assurance department and the incumbent will be expected to continuously learn Quality Assurance systems, manufacturing, and effectively engage in relationships with peers in the laboratories, Manufacturing/Production and personnel in other departments as needed. Once the incumbent is assigned specific products on which to perform the quality assurance tests, or provide development or troubleshooting, the incumbent will have considerable impact on results from his/her work. Material can be rejected and manufacturing procedures can be altered significantly either in schedule changes or in process itself. Perform analysis on raw materials, intermediates, purified water systems, environmental monitoring and finished products, following prescribed procedures to provide the information base leading to raw material/intermediates/product disposition. Assist in troubleshooting and problem solving as directed, within the Microbiology area; focus is on Microbiological testing. Position Duties & Responsibilities Perform standard qualitative and quantitative analysis on: purchased raw materials, in-process products, pure drug substances and finished pharmaceutical preparations employing standard procedures, in accordance with approved testing procedures of BAYER, the National Formulary (NF) and the United States Pharmacopoeia (USP). Utilize standard "bench" microbiological aseptic technique Maintain records of all analysis information of assigned products on data sheets for permanent file and proper entry of information on laboratory forms. Evaluate all data obtained from analysis; if discrepancy or deviation occurs, consult with Supervisor and recommend additional testing if necessary. Adhere to the pertinent aspects of Corporate and plant safety programs and adhering to GMP's, ISO standards or other regulations. Assist in investigating non-compliance investigations. Assist with troubleshooting analytical methodology and instrumentation malfunctions. Perform special assignments as directed by supervisor. Assist in validation of manufacturing and production lines and equipment pertinent to microbiology (e.g. equipment and room cleaning validation). Prepare microbiological testing media/diluents. Perform testing of water samples from Purified (Reverse Osmosis) Water, USP systems. Perform microbiological environmental monitoring in production areas and in the Microbiology Laboratory. Qualifications Requirements/Preferences Education Requirement(s): Bachelor's degree in Chemistry, Biology, Pharmacy, or related 4 year science degree required. Skill & Competency Requirements: At least 1 year of lab experience is required: Assigned within the Microbiology area and/or previous experience in microbiology processes is preferred. Knowledge, practical application, and understanding of microbiology are necessary to perform the functions of this position. Good documentation practices Ability to work collaboratively in a team-based environment is required. Good working knowledge of personal computer skills are required; Working knowledge of aseptic techniques, environment monitoring methods, Gram staining and microbiological test methods is required. Competencies required: analytical problem solving, work within established policies and procedures, effective written and interpretive communication skills, and organization and planning skills. Preferences: A working knowledge of statistics, data processing and good manufacturing practices is desirable. A thorough understanding of National Formulary (NF); United States Pharmacopoeia (USP); and European Pharmacopoeia (EP) testing procedures, as well as, US Pharmaceutical Industry Good Manufacturing Practices (GMP's), quality control methods and procedures preferred. Thanks & Regards, Mayank Gupta ( Lead Pharma Technical Recruiter) Additional Information All your information will be kept confidential according to EEO guidelines.

TAIT partners with artists, brands, IP holders and place makers to bring culture-defining, never-before-seen experiences to life. With a legacy of innovation spanning over 45 years, TAIT has grown from pioneering in rock 'n' roll concert staging to setting the global standard for extraordinary live events and experiences through cutting-edge technology, precision engineering, and creative design. TAIT's 20 global offices have developed iconic productions and experiences in over 30 countries, all seven continents, and even outer space for renowned performers, theme parks, exhibits, and venues across the globe, including partnerships with Taylor Swift, Cirque Du Soleil, Royal Opera House, Nike, NASA, Bloomberg, Google, Beyoncé, and The Olympics Position Purpose The Production Technician will assist with all manufacturing, assembly, and fabrication on TAIT products and projects in a group setting with minimal guidance from the group lead. This position will require the Production Technician to be highly functional in multiple disciplines and help support the fabrication team to deliver a finished product to TAIT's standards of quality. This position also provides access to continued growth within the department based on skillset and training. Essential Responsibilities - Adhere to and implement proper fabrication and assembly techniques. - Maintain accurate dimensional tolerances set forth on drawings. - Produce a quality product while focusing on TAIT brand quality and standards. - Clean and maintain workspace area, facility tools, and equipment. - Ability to read, understand, and follow blueprints, internal drawings, and SOP's. - Adhere to all company safety policies and procedures. - Attend meetings, seminars, and training sessions as required. - Perform assigned duties according to the policies and expectations prescribed by the company. Minimum Qualifications - High School Diploma or GED. - One (1) year of instructional/professional training. - Skill set focused in general fabrication, carpentry, complex mechanical assembly and/or TAIT experience preferred. - Ability to identify materials and hardware. - Ability to read, understand, and follow blueprints and internal drawings. - Knowledge in rigging equipment and practices (WLL, COG, & LAF) - Advanced knowledge and experience using precision measuring instruments and general manufacturing tools (wood, plastic, metal). - Effective oral and written communication skills. - Ability to use (proficient in) TAIT business systems (Epicor, Slack, and Box). - Capacity to work independently, and as a member of a small team. - Ability to handle changing priorities in a fast-paced environment. - Flexibility with work schedule. Normal work schedule is forty hours per week; however operational demands may necessitate other schedules to meet business needs. Working Conditions 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. The employee is required to frequently walk, bend, climb, push, pull, twist, squat, stoop, and kneel each day. Specific requirements are: - Must be able to stand for extended periods of time - Must be able to lift or move 50 lbs. - Must be able to carry 50 lbs. - Must be able to pull or push 50 lbs. - Must be able to reach overhead - Must be able to work in small, sometimes awkward spaces and positions. \#LI-JH1 TAIT is an equal opportunity employer fully committed to diversity and inclusion in the workplace. 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 or any other protected characteristic as outlined by international, national, state, or local laws.

Inspects company products at various stages of manufacture and monitors compliance to the company's quality standards. Documents quality findings in designated software programs and maintains quality data in order to provide quality metric reporting for supplier and manufacturing scorecards. ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. Perform inspection and testing on parts received from external suppliers, in-line inspections in the manufacturing area, and outgoing inspections for product shipments. Follow Control Plans/Quality Inspection Plans to determine process/product conformance. Review non-conforming materials from value streams and document applicable information concerning the non-conformance on CAREL documentation. Assist with processing of products returned to CAREL on return material authorizations. Familiarity with and ability to utilize various types of measuring and test equipment such as calipers, micrometers, etc. Works with Assembly Operators and Manufacturing Engineers to affirm process controls are being adequately followed. Generate inspection records, product statuses, and summarize data. Be fluent in computer software programs such as MS Word and Excel. Familiarity with industrial manufacturing processes, including wave soldering, surface mount applications and mechanical type assembly. Performs inspection on products (cables, circuit cards, assemblies, systems, etc.) manufactured for compliance to CAREL and customer drawings. Performs first piece inspections and audits as required. Verifies all required documentation. Works with other Quality associates in the disposition of non-conforming material and in identification of defect trends in manufacturing processes. Completes documentation of defects through data entry into company software platforms. Submits products to source and/or customer inspectors as required. Assists in keeping the quality department compliant to ISO9001. Reviews and reads drawings, specifications, and other technical documents to understand quality requirements of manufactured products. QUALIFICATIONS/REQUIREMENTS · High School education with 3 years technical experience working in a manufacturing environment. · Previous experience reading drawings, specifications and other technical documentation. LANGUAGE SKILLS · Good verbal and written skills. MATHEMATICAL SKILLS · Basic Math skills. · Some statistics a plus. PHYSICAL DEMANDS · Regularly sit or stand, reach, bend and move about. · Must be able to lift up to 30lbs. WORK ENVIRONMENT · Work environments include, but are not limited to Carel's labs and manufacturing facilities, regional, national or international office, car, or airline flights · While performing the duties of this job, the employee is regularly required to stand or sit for long periods of time · The employee is occasionally required to walk, reach with hands and arms; stoop, kneel, or crouch. · 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. Monday - Friday 3pm-11:30pm

Job DescriptionDescription: Do you have an eye for attention to detail and an impeccable desire to enforce and maintain high standards of Quality? Then look no further and join the Quality Team at Advanced Cooling Technologies, Inc. (ACT) - nominated as a “Best Places to Work” in PA in 2023, York location. The Quality Team ACT is looking for team members who are passionate about creativity and innovation and looking to make a difference every day. We are committed to developing world class Quality Assurance programs, processes, and people that support the ACT mission and family of brands, including Tekgard Environmental Control Units. We have an immediate opening for a Quality Inspection in our York location. Company Overview Advanced Cooling Technologies, Inc. (ACT), with locations in York and headquartered in Lancaster, PA, is a leading manufacturer of innovative thermal management products for diverse applications, serving a broad spectrum of industries including commercial satellites, military vehicles, medical devices, primary calibration equipment, and HVAC systems. We are dedicated to fostering creativity, innovation, and making a tangible difference every day. Our commitment extends to our customers, employees, and community, with core values centered on Innovation, Teamwork, and Customer Care-key drivers of our continuous growth and success. At ACT, our skilled and dedicated staff is our most valuable resource. ACT offers a robust benefits package including low-cost medical, dental, vision, company-paid life and disability insurance, paid time off, a 401k with company match, and a profit-sharing bonus plan. Enjoy a work-life balance at our York location supported by a 4-day work week (4/10 schedule), generous PTO, and 8 paid holidays. Position Summary This position is for a Quality Inspector at our facility located in York, PA. As a Quality Inspector, you will play a hands-on role within the organization and interface with both Operations and Product Development teams while performing incoming inspection of materials and components and performing in-process and final inspections of products for commercial and/or government customers. Key Duties and Responsibilities Inspect incoming materials Perform in-process inspections and/or final inspections on manufactured product Ensure all materials and product meet Quality standards as per policy and ISO9001/AS9100 procedures Identify and segregate non-conformances and write non-conformance reports Support Supplier Quality initiatives ACT 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 protected veteran, status as a qualified individual with a disability, or any other trait protected by law. Requirements: High School Diploma or GED Ability to read and interpret blueprints and shop drawings Ability to use basic inspection tools such as micrometers, calipers, height gages, etc. Basic computer skills (Outlook, Word, Excel). Basic math skills Strong verbal and written communication skills Additional Qualifications (preferred): Authorized to work in the US. US Citizen, Permanent Resident, or Protected Individual (as defined by 8 U.S.C. § 1324b(a)(3)) preferred due to ITAR responsibilities. Prior experience with ERP systems

Quality Technician Day Shift: work 2 days, off 2 days, work 3 days, off 3 days (6am to 6pm) Pay: $22.50/hr. with increase opportunities after 120 days Requirements: 1-2 years of experience with quality experience; preferably within the printing, food, or regulated industry with knowledge of GMP's (21CFR 110/111/210/211) Proficiency in Microsoft Office suite is essential Excellent communication skills, both verbal and written Excellent time management skills Attention to detail is essential Ability to work rotating shift 2-2-3-3; including weekends when scheduled Prior experience in the food environment is beneficial Ability to walk, stand, sit, stoop, bend, twist and lift up to 50 pounds. Job Functions: Responsible for monitoring and identifying critical control points (CCP) within the processes. Responsible for monitoring processes and product food safety and quality throughout the manufacturing process. Responsible for the correct documentation and filing of all relevant record logs and Documentation. Ensures the correct recipe guidelines for products are met during processing. Ensures employees are following all Food Safety and worker safety practices. Ensures and educates employees on quality expectations. Collect product samples for the Quality lab. Perform inspections on in-process printing to ensure quality and accuracy of the print according to customer specifications. Identifying non-conformances and ensuring they are corrected “real time” when feasible. Working directly with Operations on the presses, slitter, lamination, etc. to identify areas for continuous improvement. Ensuring paperwork is accurate and filled out in a timely manner on the production lines. The above duties and responsibilities are representative of the nature and level of work assigned and are not necessarily all-inclusive. Benefits: Medical, dental, vision, and prescription drug coverage 401(k) plan with generous company match Bonus program Paid vacation and personal days Paid holidays Company-paid life and AD&D insurance Company paid short-term disability coverage Employee Assistance Program (EAP)

US Tech Solutions is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit our website ********************************** are constantly on the lookout for professionals to fulfill the staffing needs of our clients, and we currently have a job opening that may interest you Job Description Title: Quality control chemist- 2nd shift Duration: 12 Months Location: Myerstown, PA 17067 Description: The Raw Material testing team is responsible for Quality Control testing of APIs and excipients used in the manufacture of pharmaceutical and nutritional products. This is a fast-paced, energetic team that works together across two shifts to meet aggressive throughput times to support a lean manufacturing operation. Position Summary: In this position, the incumbent will be expected to draw upon previous analytical experience, as well as continuously learn Quality Control systems and effectively engage in relationships with peers in the laboratories, Manufacturing/Production, and personnel in other departments as needed. The incumbent will perform analysis on raw materials following prescribed procedures to provide the information base leading to material disposition, as well as assist in troubleshooting and problem solving as directed. Once the incumbent is assigned specific materials on which to perform the quality control tests, or provide development or troubleshooting, the incumbent will have considerable impact on results from his/her work. Material can be rejected and manufacturing procedures can be altered significantly either in schedule changes or in process itself. Position Duties & Responsibilities : Perform standard qualitative and quantitative analysis: • Utilize standard analytical chemistry techniques: wet analytical methods, HPLC, UV, GC, AA, polarimeter, FT-IR, NIR, RAMAN, etc.) to test raw materials in accordance with approved testing procedures, including those from company, the National Formulary (NF), the United States Pharmacopoeia (USP), the European Pharmacopoeia (EP), and the FDA. • Properly document and maintain records of all analysis information of assigned materials on data sheets and laboratory notebooks for permanent file. • Evaluate all data obtained from analysis; if discrepancy or deviation occurs, consult with Supervisor and recommend additional testing if necessary. • Communicate to supervision in a timely manner all non-compliance situations, and assist in investigations. • Assist with troubleshooting analytical methodology and instrumentation malfunctions. • Perform special assignments as directed by supervisor, for example, revise existing analytical testing monographs to comply with compendia changes or other specific needs. • Accurate, complete and timely fulfillment of the job responsibilities will, in part, ensure GMP compliance as outlined in various Bayer and U.S. government rules and regulations. Documentation Review: • Review testing documentation performed by other analysts for compliance with BAYER, FDA, National Formulary (NF), United States Pharmacopoeia (USP), and European Pharmacopoeia (EP) procedures. Safety: • Adhere to the pertinent aspects of Corporate and plant safety programs and adhering to GMP's, ISO standards or other regulations. Qualifications Requirements/Preferences: • Bachelor's degree in Chemistry, Biology, Pharmacy, or related 4 year science degree required. Chemistry degree is preferred. • At least 1-3 years of experience in a GMP laboratory environment. Master's degree in a related field with 1 year of experience may be considered. • Knowledge, practical application, and understanding of analytical chemistry is required to perform the functions of this position. • Basic experience with Personal Computer (PC). • Demonstrated capability for communicating ideas, concepts, and work results effectively to colleagues and supervision. • Demonstrated ability to be self-motivated as well as to work collaboratively in a team-based environment is required. • Must demonstrate initiative and a willingness to learn. • Good working knowledge of advanced laboratory instrumentation and personal computer skills are required. • Good working knowledge of advanced laboratory instrumentation and computers are required; This is defined as strong troubleshooting skills for assigned area such as HPLC, GC, AA, UV, TOC, NIR and/or dissolution and low error rates with microbiology or chemistry techniques for defined area • A working knowledge of organic chemistry, statistics, data processing and good manufacturing practices is required • Demonstrated ability to clearly communicate technical information in writing required. • Demonstrated ability to manage key projects and display area of expertise; i.e. clear/consistent notebook skills and function as an independent worker. • Demonstrated ability to be self-motivated as well as to work collaboratively in a team-based environment is required. • Demonstrated ability to take initiative and display a willingness to learn required. • A thorough understanding of National Formulary (NF); United States Pharmacopeia (USP); and European Pharmacopeia (EP) testing procedures, as well as, US Pharmaceutical Industry Good Manufacturing Practices (GMP's), quality control methods and procedures is required. • Competencies required: analytical problem solving, alertness, work within established policies and procedures, commitment to task, decisiveness, effective written and interpretive communication skills, and organization and planning skills. • Enter here Travel Requirements: None Thanks & Regards, Mayank Gupta, (M. Pharmacy) (Lead Pharma Technical Recruiter) Additional Information All your information will be kept confidential according to EEO guidelines.

The Production Technician will assist with all manufacturing, assembly, and fabrication on TAIT products and projects in a group setting with minimal guidance from the group lead. This position will require the Production Technician to be highly functional in multiple disciplines and help support the fabrication team to deliver a finished product to TAIT's standards of quality. This position also provides access to continued growth within the department based on skillset and training. Essential Responsibilities Adhere to and implement proper fabrication and assembly techniques. Maintain accurate dimensional tolerances set forth on drawings. Produce a quality product while focusing on TAIT brand quality and standards. Clean and maintain workspace area, facility tools, and equipment. Ability to read, understand, and follow blueprints, internal drawings, and SOP's. Adhere to all company safety policies and procedures. Attend meetings, seminars, and training sessions as required. Perform assigned duties according to the policies and expectations prescribed by the company. Minimum Qualifications High School Diploma or GED. One (1) year of instructional/professional training. Skill set focused in general fabrication, carpentry, complex mechanical assembly and/or TAIT experience preferred. Ability to identify materials and hardware. Ability to read, understand, and follow blueprints and internal drawings. Knowledge in rigging equipment and practices (WLL, COG, & LAF) Advanced knowledge and experience using precision measuring instruments and general manufacturing tools (wood, plastic, metal). Effective oral and written communication skills. Ability to use (proficient in) TAIT business systems (Epicor, Slack, and Box). Capacity to work independently, and as a member of a small team. Ability to handle changing priorities in a fast-paced environment. Flexibility with work schedule. Normal work schedule is forty hours per week; however operational demands may necessitate other schedules to meet business needs. Working Conditions 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. The employee is required to frequently walk, bend, climb, push, pull, twist, squat, stoop, and kneel each day. Specific requirements are: Must be able to stand for extended periods of time Must be able to lift or move 50 lbs. Must be able to carry 50 lbs. Must be able to pull or push 50 lbs. Must be able to reach overhead Must be able to work in small, sometimes awkward spaces and positions. #LI-JH1

Inspects company products at various stages of manufacture and monitors compliance to the company's quality standards. Documents quality findings in designated software programs and maintains quality data in order to provide quality metric reporting for supplier and manufacturing scorecards. ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. Perform inspection and testing on parts received from external suppliers, in-line inspections in the manufacturing area, and outgoing inspections for product shipments. Follow Control Plans/Quality Inspection Plans to determine process/product conformance. Review non-conforming materials from value streams and document applicable information concerning the non-conformance on CAREL documentation. Assist with processing of products returned to CAREL on return material authorizations. Familiarity with and ability to utilize various types of measuring and test equipment such as calipers, micrometers, etc. Works with Assembly Operators and Manufacturing Engineers to affirm process controls are being adequately followed. Generate inspection records, product statuses, and summarize data. Be fluent in computer software programs such as MS Word and Excel. Familiarity with industrial manufacturing processes, including wave soldering, surface mount applications and mechanical type assembly. Performs inspection on products (cables, circuit cards, assemblies, systems, etc.) manufactured for compliance to CAREL and customer drawings. Performs first piece inspections and audits as required. Verifies all required documentation. Works with other Quality associates in the disposition of non-conforming material and in identification of defect trends in manufacturing processes. Completes documentation of defects through data entry into company software platforms. Submits products to source and/or customer inspectors as required. Assists in keeping the quality department compliant to ISO9001. Reviews and reads drawings, specifications, and other technical documents to understand quality requirements of manufactured products. QUALIFICATIONS/REQUIREMENTS · High School education with 3 years technical experience working in a manufacturing environment. · Previous experience reading drawings, specifications and other technical documentation. LANGUAGE SKILLS · Good verbal and written skills. MATHEMATICAL SKILLS · Basic Math skills. · Some statistics a plus. PHYSICAL DEMANDS · Regularly sit or stand, reach, bend and move about. · Must be able to lift up to 30lbs. WORK ENVIRONMENT · Work environments include, but are not limited to Carel's labs and manufacturing facilities, regional, national or international office, car, or airline flights · While performing the duties of this job, the employee is regularly required to stand or sit for long periods of time · The employee is occasionally required to walk, reach with hands and arms; stoop, kneel, or crouch. · 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 withdisabilities to perform the essential functions.