Quality control analyst jobs in New Britain, CT

The Senior Quality Control Technician role in our Bloomfield, CT facility drives improvement in the reliability of CO2 Laser products. The incumbent will be engaging directly with a cross functional team on a wide variety of products to ensure our product and processes meet the dynamic laser manufacturing requirements. Working with a quality mindset team, this role will provide hands on support for the incoming goods, in-process, and final inspection of laser systems to ensure we meet Coherent Quality Standards. Primary Duties & Responsibilities Inspection manufactured laser systems: Detail oriented inspection of electronic and mechanical assemblies Utilize common inspection methods to evaluate critical design requirements Develop inspection test plans with a cross functional team Assist in problem solving activities to support identified nonconformities Evaluation and verification of purchased components Define and execute incoming material test plans for qualification activities Document and present inspection results to key stakeholders Verification of vendor supplied documentation including first article inspections and material certifications Support of Quality Systems: Document detailed findings to be used for Continuous Improvement Initiatives Accomplish root cause analysis and provide corrective actions with follow-up Ensure practices align with best practices, procedures and inspection techniques Perform internal product and business system audits Reliability system maintenance: Utilize computers for automated data collection and control of instruments Collaborate with the Quality organization regarding calibration of test instruments Monitor and troubleshoot long term unmanned tests with engineering support Assist in developing new methods and protocols for component level testing and measurement Complete calibration of monitoring and measuring equipment support Education & Experience High School diploma A minimum of 4 years of related experience or combination of education and relevant experience Proficient in the use of automated and manual measuring devices and test equipment Excellent verbal and written skills in the English language required Skills Preferred experience with layout inspections and sound Geometric Dimensioning and Tolerancing knowledge Preferred experience automating inspection test method is preferred Knowledge of centralizing data for analysis Experience of test and measurement of electronic and/or optical systems Continuous improvement mindset - improves products and processes Well organized and knowledgeable of 6S methodology Demonstrated problem-solving abilities combined with hands-on experience Knowledge of electronic component manufacturing Self-motivated to thoroughly document data and test results Working Conditions Manufacturing working environment. Some areas under cleanroom protocol. Minimal to no expected travel Support of seconds shift operations required This is an on-site position in our Bloomfield, CT facility. Shift will be Monday to Friday 11am to 7:30pm Physical Requirements Must be able to move around manufacturing floor Must be able to lift a maximum of 30 pounds Safety Requirements All employees are required to follow the site EHS procedures and Coherent Corp. Corporate EHS standards. Quality and Environmental Responsibilities Depending on location, this position may be responsible for the execution and maintenance of the ISO 9000, 9001, 14001 and/or other applicable standards that may apply to the relevant roles and responsibilities within the Quality Management System and Environmental Management System. Culture Commitment Ensure adherence to company's values (ICARE) in all aspects of your position at Coherent Corp.: Integrity - Create an Environment of Trust Collaboration - Innovate Through the Sharing of Ideas Accountability - Own the Process and the Outcome Respect - Recognize the Value in Everyone Enthusiasm - Find a Sense of Purpose in Work Coherent Corp. is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law. If you need assistance or an accommodation due to a disability, you may contact us at [email protected].About Us Coherent is a global leader in lasers, engineered materials and networking components. We are a vertically integrated manufacturing company that develops innovative products for diversified applications in the industrial, optical communications, military, life sciences, semiconductor equipment, and consumer markets. Coherent provides a comprehensive career development platform within an environment that challenges employees to perform at their best, while rewarding excellence and hard-work through a competitive compensation program. It's an exciting opportunity to work for a company that offers stability, longevity and growth. Come Join Us! Note to recruiters and employment agencies: We will not pay for unsolicited resumes from recruiters and employment agencies unless we have a signed agreement and have required assistance, in writing, for a specific opening.

IS IN MIDDLETOWN,CT Who is Habasit? Habasit is the global leader in the manufacturing of lightweight conveyor belting. Our slogan “Solutions in Motion” defines us; we are a provider of world class power-transmission and conveying solutions. At Habasit, we understand that a global leader is only as good as the people who represent it, and we are always searching for the right people to keep us in motion. We are looking for ambitious individuals, leaders, and students who are ready to help move us forward. If you have a can-do attitude and want to join a world-class organization, read on and apply today! We offer an attractive place to work and personal development in an empowering work culture. You will benefit from the expertise and opportunities of a solid global group of companies and the reputation of its products. Things you should know about Habasit's opportunities: Competitive Salary Excellent health insurance benefits which includes a bundled medical + dental package 401(k) program with up to 6% company match (at 100%) Tuition reimbursement (with Manager approval) Gym membership reimbursement Employee Assistance program Referral bonus OVERVIEW OF POSITION: Support R&D production trials and testing R ESPONSIBILITIES OF THIS POSITION - DEPARTMENT: Support of R&D production trials, which includes preparation trial documentation, attendance, and sample collection, labeling, and storage. Preparation of test samples from R&D production trials, which includes slitting and joining for tensile testing and wear and tear fatigue testing. Lab testing, which includes melt flow, tensile strength, wear and tear, coefficient of friction, abrasion, dimensional measurements … etc. Maintenance and upkeep of lab equipment, accessories, and supplies. Analysis and reporting of data and results collected from lab testing. Maintaining R&D inventory of production prototypes and shipping out of customer prepared samples for evaluation and field testing. COMPETENCIES/SPECIFIC EXPERIENCE OR TRAINING PREFERRED: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements/preferences 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 - College degree. Required - Read, Write and Comprehend English. Preferred - R&D laboratory experience including polymer products testing, mixing of rubber or plastic materials. Preferred - Mechanical or chemical technician background. Preferred - Thorough understanding of MRP. Preferred - Microsoft Office, including Word, Excel, PowerPoint.

Challenge Yourself and Impact the Future! MacDermid Alpha Electronic Solutions, a business of Element Solutions Inc (NYSE: ESI), is renowned worldwide for it's commitment to revolutionizing the electronics industry. With a legacy spanning over a centrury, we have continually set new benchmarks for excellence, reliability and sustainability in electronic materials. Our Expertise: Wafer Level Solutions - Revolutionizing wafer fabrication processes for enhanced efficiency and performance Semiconductor Assembly Solutions - Driving innovation in semiconductor assembly processes for unparalelled reliability Circuitry Solutions - Tailored solutions to meet the dynamic demands of modern circuitry Circuit Board Assembly Solutions - Elevating circuit board assembly processes for optimal performance Film & Smart Surface Solutions - Transforming electronics with cutting-edge materials and technologies for enhanced functionality and reliability Across diverse sectors including automotive, consumer electronics, mobile devices, telecom, data storage, and infrastructure, MacDermid Alpha Electronic Solutions has earned the trust of manufacturers worldwide. Our comprehensive rance of high quality solutions and technical services covers the entire electronics supply chain, empowering businesses to thrive in today's competitive landscape. We strive to embody the five 'Elements of our Culture'- our '5C's'; Challenge, Commit, Collaborate, Choose, and Care. These core values are the foundation of our organization which our employees embrace in their interactions with customers, colleagues and other stakeholders, to drive financial performance and create a rewarding work environment. Who are we looking for? This role is responsible for performing laboratory procedures for testing in process and finished products from manufacturing, raw material samples prior to use in manufacturing, and customer plating solutions. The preferred candidate will be able to step into a dynamic work environment and will be a true team player who can flex and enjoys working in a number of different areas and with various instruments. What will you be doing? * Follows written analytical procedures and methods for testing of in-process, finished and customer product samples including Plating tests, Volumetric and Gravimetric analysis, Instrumental analysis, etc. * Collects and enters data into WinLIMS data management system to review and validate results of sample data. Performs calculations associated for the test results. * Communicates status of testing samples to Production Supervisors and Chemical Operators. * Submits results for approval to the Laboratory Supervisor/Manager. * Validates established methods. * Troubleshoots and makes recommendations concerning product quality. * Stores hazardous materials in the proper locations and dispose of hazardous waste properly. * Schedule and maintain instrument calibration database. * Works with Quality Assurance personnel to investigate any product quality issues. * Uses and promotes the Six Sigma methodology and emphasized on 5-S. * Attend required HSE training including Hazardous Waste Management, emergency response, and Hazard Communication, and demonstrate an acceptable level of understanding of topics. * Operate equipment and follow procedures in accordance with IATF16949, ISO 14001, and OHSAS 18001 standards * Follows all safety procedures including general site safety rules and Chemical Hygiene Plan. * Coordinates with MSA team to adhere to requirements for MSA studies including Gage R&R, Accuracy, Linearity, Bias as well as matching and correlation studies * Ability to work with mathematical concepts such as probability and statistical inference, fractions, percentages, ratios, and proportions to practical situations Who are You? * Bachelor's Degree in chemistry or related field and at least 2 years of strong laboratory experience * Proficient in bench chemistry,manual titrations and extractions, with working knowlege of gravimetric assays, pH measurement and UV-Vis spectrophometry. * Highly preferred - previous experience in one or more of the following: ICP-OES, ICP-MS, HPLC/IC * Candidate should have a solid undestanding of analytical accuracy and precison, demonstrate strong data analysis skills and attention to detail, and show willingness to learn new techniques. We understand that not all candidates may meet the requirements listed above. If you believe you have the knowledge and experience necessary to excel in this role, we encourage you to apply. We are Offering... Challenge Yourself and Impact the Future - You will be part of a highly collaborative culture that promotes continuous improvement through cross-functional partnerships to achieve our mission. We do this through a strong and unified culture and transparent management which has empowered us to create high performing global teams that achieve superior solutions for our customers. As part of the MAES Team, you will have ... * Opportunities for career growth, competitive compensation (competitive base salary and performance related bonus plan) and benefits packages (health, dental, and vision insurance, Wellness Program, PTO/Holidays, as well as a 401(k)-retirement plan with a company match). * Innovated work environment where you will be a part of a dynamic and collaborative team. * Perks and Incentives such as paid parental leave, tuition reimbursement, and opportunities for professional development. The typical base salary range for this position is between $69,561.00 and $104,341.00 Equal Opportunity Employer All qualified applications will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, pregnancy, genetic information, disability, status as a protected veteran, or any other protected category applicable under federal, state and local laws. Nearest Major Market: New Haven Nearest Secondary Market: Hartford

About ALK ALK is a forward-thinking allergy company with a long tradition of allergy innovation. ALK is devoted to improving quality of life for people with allergies by developing pharmaceutical products that target the actual cause of allergy. ALK is the world leader in allergy vaccination (immunotherapy) - a unique treatment that induces a protective immune response which reduces and potentially halts the allergic reaction. Since 1923, we have been working to improve the quality of life for allergy patients by developing products that target the cause of allergy. With over 2,200 employees, and with subsidiaries, production facilities and distributors worldwide, we are in a unique position to further the advancement of allergy treatments. The company is publicly traded on NASDAQ OMX Copenhagen (OMX: ALKB) with global headquarters in Horsholm, Denmark and US Offices in Round Rock, TX, Bedminster, NJ, Port Washington, NY, Post Falls, ID, Luther, OK, Oklahoma City, OK, Plainville, CT and Mississauga, Canada. We are currently looking for a Full-Time Quality Control Chemist to join team in our Plainville, CT . The QC Chemist will be working alongside the QC and Product Supply teams. The ideal candidate will be comfortable working in a fast-paced environment, can manage multiple site-specific projects at one time and feel comfortable taking the lead when necessary. Primary Responsibilities: The primary responsibilities for this position include: Test raw materials and finished product samples per USP/compendial methods and in-house procedures Perform tests for stability and complaints Tests performed will include UV Assay, FTIR, Solution Chemistry (pH, Conductivity, TOC). Calibration, maintenance and operation of lab instrumentation, including balance, pH meter, UV/vis spectrophotometer, FTIR, TOC, and microplate readers Standard and sample solution preparation Write and revise QC Chemistry SOP's and reports Documentation of laboratory work using laboratory worksheets/notebooks; documentation must be detailed, accurate and meet cGMP requirements Filing, data entry, and ordering (entering lab results in Excel, organization and filing of MSDS and CoAs, ordering of lab materials as needed) Perform routine laboratory maintenance tasks including organization and cleaning of work areas, checking for expired reagents and standards, disposal of product samples, chemicals and hazardous waste Perform batch record review and in-process QC releases Perform peer review of notebooks and forms as necessary Author and assist in execution of validation testing as required Support aseptic processes as needed Other duties may be assigned Skills and Experience: Competences required to fulfil the area of responsibilities and work assignments:

First shift 445am-3pm Monday - Friday with some Saturdays through the year Summary: The Quality Control Technician is primarily responsible for quality assurance of all products through administration of HACCP, GMP's, Sanitation, Pest Management and other programs that ensure regulatory compliance and education of staff. The position supports the Quality, Food Safety and SQF initiatives outlined in the Quality Manual and SQF Program. Essential Job Functions : Ensures specifications are met by measuring, recording, analyzing data and working with equipment and production personnel to improve results. Perform and document daily pre-op inspections and related checks. Assist Production Supervisor with daily line set up. Calibrate scales, thermometers, and water meters daily. Prepare all the necessary paperwork needed to complete documentation of all products and processes. Test, analyze, record, and control all product and component weights as well as sensory evaluations according to specified time intervals. Record and document all HACCP related processes. Report problems or deficiencies in quality or related processes to QA Manager and Shift Supervisor. Maintain USDA, HACCP, GMP guidelines on the production floor. Interact with USDA Inspectors. Work with Production Supervisors and personnel to maintain quality /customer standards. Pre-operations testing to ensure production is authorized to start. Ensure sufficient supply of items such as gloves, hairnets/beard nets, hearing protection, aprons, hand and shoe sanitizing stations, soap, and paper towel stations. Monitor all freezer and cooler temperatures. Monitor the temperature of the meet during cooking and cooling. Monitor the pasta hydration. Ensure all metal detection/X-ray devices are operating properly. Interact with outside technicians for scale and metal detection calibrations. Take product samples at scheduled times. May participate as member of Safety Committee. Participate in Allergen and Pest Management Program. Provide support for other positions when needed. Check and record sanitizer concentrations. Verify ingredients, lots, and quantities in production batches. Other duties as assigned. Job Requirements: High School diploma or equivalent. English, Bilingual preferred. 1-2 years of Production Line Experience within the food industry a plus. Product knowledge: Acquire and maintain full knowledge of USDA and FDA codes, rules, and regulations. Proficiency in follow-up; ability to meet deadlines. Team player, positive can-do attitude. Ability to assess situations and make independent decisions to achieve success. Ability to bend, sit and stand. Ability to perform multiple complex tasks concurrently. Ability to communicate both verbally and in writing. Ability to see and walk for inspections of plant sites. Ability to hear. Ability to lift at least 25 lbs.

About the Organization IMIA,LLC is the only national marine surface preparation painting contractor servicing every U.S. Port with a mobile full time workforce that ensures that a quality product is delivered on time every time. IMIA, LLC has the equipment, seasoned deckplate supervision and mechanics, as well as rigorous corporate safety and quality programs and financial strength to support our customer's preservation needs in a truly superior and comprehensive fashion. IMIA, LLC offers a comprehensive benefit package to eligible employees. Eligible employees may enroll in: • Health • Dental • Vision • Life • LTD • Accident • Critical Illness • 401k Employees and their household members are also eligible to participate in the company's Employee Assistance Program. Per Diem OR Dislocation Allowance may be provided to eligible employees to reimburse some or all of the cost an employee might be reasonably expected to incur for lodging, meals, and incidental expenses while traveling out of town for work. EOE Statement IMIA, LLC is an equal opportunity employer and provides equal employment opportunities (EEO) to all employees regardless of race, color, religion, gender, gender identity or expression, national origin, sexual orientation, age, sex, disability status, marital status, status as a covered veteran, genetics, or any other protected groups under state, federal or local Equal Opportunity Laws. This policy applies to all terms and conditions of employment including but not limited to hiring, placement, promotion, termination, layoff, recall, transfer, leave of absence, compensation, and training. Description JOB TITLE: Quality Control Inspector JOB CODE: Quality Control REPORTS TO: Quality Assurance Manager. Direct on-site project direction and daily scheduling provided through continuous communication with the applicable IMIA Project Manager and/or Supervisor. PAY RANGE: $32.00/hour- $42.00/hour based on experience Summary of position: Responsible for monitoring quality control/assurance requirements of all preservation preformed onboard commercial and US Navy vessel in accordance with established Navy regulations and industry standards or specific contractual requirements as defined in the Scope of Work. Collaborate with customer QA personnel on necessary aspects of the job. Essential Job Requirements: Produce/create electronic/handwritten Quality Assurance documentation as Objective Quality Evidence for work performed throughout the preservation process. Develop and Maintain Test and Inspection Plan (TIP) for all assigned jobs. Monitor and document all required readings with regard to, but not limited to, metal anchor tooth (profile), paint wet/dry film thickness (DFT), steel temperatures and all required environmental readings using appropriate equipment to include: micrometer, dry film thickness gauge, infrared thermometer, psychomotor. Ensure all assigned equipment is maintained in good working order with within all calibration certification intervals. All of the above requirements shall be completed in a safe and efficient manner so as not to cause injury to self or others. Required Education: High School diploma or equivalent Required Certification: NACE Inspector and/or SSPC NBPI required. Required Experience: Formal or informal on-the-job training in the marine industry; familiarity with Navy and Society for Protective Coatings standards. Required Skills: Must possess knowledge of Maritime paintings standards with particular emphasis in US Navy ship preservation criterion. Word processing, spreadsheet, email, and database computer skills required. Must be able to accomplish mathematical calculations associated with preservation readings and documentation; must be able to discern and carry out complex written, oral, or diagramed instructions. Must be able to take direction; interact professionally, knowledgeably and cooperatively with supervisors and co-workers and customer representatives. Physical Requirements: Must be physically capable of working an 8-10 hour day requires average use of computer, some physical dexterity, and agility within confined and restricted spaces & tanks. Reasonable Accommodations may be made to enable qualified individuals with disabilities to perform essential job functions. Supervisory Responsibilities: None Working Conditions: Regularly stand for long periods of time; work on scaffolds and ladders; work on top of machinery; work in confined spaces. Regularly exposed to extreme temperatures, high noise levels, toxic or caustic chemicals, fumes, airborne particles, outdoor weather conditions, dusty conditions, wet and/or humid conditions, hazardous machinery, precarious places, close proximity to other employees. Overtime or shift work involved. Travel often required. Must follow strict safety procedures. Location Connecticut Salary Range DOE Exempt/Non-Exempt Non-Exempt This position is currently accepting applications.

Defibtech is seeking a QC Inspector responsible for maintaining quality standards by in-process production, performing final quality assurance, and recording quality results. This role is based on site at our manufacturing site in Branford, CT. Core Responsibilities: Performs final quality assurance inspection of Automated External Defibrillators, Automated Resuscitation Machines, batteries, and other such duties as may be appropriate for this position. Approves materials through each stage of production by confirming specifications; conducting visual, mechanical, measurement and/or functional tests; rejecting and returning unacceptable materials. Documents inspection results by completing Device History Reports and logs; inputting data into appropriate quality system database. Monitors all inspection and testing equipment to ensure proper working order and current, valid calibration. Demonstrates Defibtech's values on the job by focusing actions on Integrity, Passion, Ownership, and Innovation. Promotes and participates in continuous improvement. Actively supports compliance of Company operations to all applicable laws, regulations and standards, good business practices and company documented procedures (including but not limited to FDA, Quality Systems Regulations, safety regulations, and applicable statutes). Qualifications / Requirements: Highschool diploma or GED or equivalent. Previous experience supporting manufacturing is preferred. Previous experience with quality control review and inspection or a related field, highly preferred. Demonstrated proficiency with computers, MS Office, and ability to learn new programs quickly. Ability to meet deadlines while being detail oriented Demonstrated reliability and strong work ethic. Availability and willingness to work overtime as needed. Ability to adapt quickly to changes in work assignments based on customer needs. Positive, friendly attitude and ability to work together with a team Desire to learn new skills in a fast-paced environment Work Environment and Physical Demands: Work is based in a light manufacturing setting. Light work that includes moving objects up to 20 lbs; frequent walking/standing up to 6 hours per day. Frequent moving between sitting, standing, and walking. Frequent pushing/pulling and continuous use of hands for fine manipulation. Performing visual inspection at a seated inspection bench/station Compensation and Benefits: Defibtech offers competitive salaries and a comprehensive benefits package including core health benefits, company-paid disability, and a company matching 401k plan. Defibtech promotes a challenging, collaborative, and friendly culture that is centered around our values: Passion, Innovation, Integrity, and Ownership. Defibtech is supportive of work balance, providing company gatherings to add fun and generous paid time off and flexibility for employees to manage time and responsibilities. Defibtech is committed to empowering and supporting our employees in their philanthropic efforts through donation programs and time off for volunteerism. Defibtech is committed to a diverse workplace and is an Equal Opportunity/Affirmative Action employer and E-Verify Company. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, pregnancy, sexual orientation, gender identity, national origin, age, protected veteran status, or disability status. The above description of core responsibilities and qualifications are intended to describe the general nature and level of the work being performed, but they are not an exhaustive list of all the required responsibilities and skills of this position. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. Defibtech endeavors to make ***************** accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please contact Human Resources at ************. This contact information is for accommodation requests only and should not be used to inquire about the status of applications.

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description • Working with some supervision, applies established knowledge of laboratory techniques such as HPLC, dissolution, UV/VIS spectrophotometry, moisture by KF, and others to perform product stability testing. • Candidate will be responsible for understanding and performing routine analytical testing for stability samples, evaluating and documenting results in a timely manner. Understands and follows all SOPs and written test procedures. • Performs testing within established standard test times and maintains quality and productivity at acceptable levels as communicated by the supervisor. Candidate will execute troubleshooting of instrumentation and will be expected to maintain laboratory equipment in good working condition. • Candidate will perform laboratory investigation steps with appropriate approvals and with some guidance from supervisor. Keeps supervisor fully informed of all results and project status on a daily basis and reports critical information in a timely manner. Qualifications • Qualifications: Essential Skills- 1-3 years of experience in a related laboratory, HPLC, Dissolution, UV/VIS spectrometry, moisture by KF. Strong understanding of GMP concepts and requirements is desired. • Empower (CDAS) experience is desirable Additional Information For more information, please contact, Sneha Shrivastava **********

Job DescriptionDescription: 12:00 pm-8:30 pm, Mon-Friday SCA Pharmaceuticals is a dynamic rapidly growing company consisting of passionate individuals who believe in our mission of providing high quality medications that are critical in saving and sustaining human life. SCA Pharma is an FDA 503B outsourcing facility providing customized medications for hospitals and healthcare facilities across the United States. We do this through unyielding quality, safety and integrity, our commitment to accountability and ownership, teamwork and creating better solutions by simplifying the complex. Summary: The Microbiology Analyst I will be responsible for supporting the Microbiology Department with data processing/entry in addition to performing Environmental Microbiological testing and/or Filtration Testing in addition to daily housekeeping of the laboratory. Essential functions: May include a combination of the following: · Assisting with and performing membrane filtration for sterility testing · Performing environmental monitoring, including Viable Surface, Viable Air, and Particulate Testing · Performing endotoxin testing · Maintain daily logs. · Maintain and file proper documentation. · Perform sample plate enumeration. · Perform media fill reads. · Assist with maintaining laboratory inventory. · Assist with maintaining laboratory equipment. · Perform laboratory cleaning. · Perform biohazard bin removal. · Ensure GMP compliance in all activities performed. · Perform other additional job-related duties as required. Requirements: Required Qualifications & Experience: Bachelor's degree (in life sciences) Laboratory experience preferred Desired Knowledge, Skills, and Abilities: Strong knowledge of MS Office Suite (Word, Excel, Outlook) Ability to achieve and maintain gowning qualification and wear all required Personal Protective Equipment Ability to communicate and work with team members in an effective manner. Ability to work independently on scientific projects. Scientific technical writing ability including authoring and revising SOPs or technical reports. SCA Pharma is an equal opportunity employer (Minorities/Females/Disabled/Veterans). We recruit, employ, train, compensate, and promote without regard to race, religion, creed, color, national origin, age, gender, sexual orientation, marital status, disability, veteran status, or any other basis protected by applicable federal, state, or local law.

At Sheffield Pharmaceuticals, the home of the original Sheffield Toothpaste, we offer exclusive, quality, branded products to promote wellness and relief to our customers. Our wellness and first aid products include a variety of creams and ointments, nasal products, and toothpaste all made in the USA since 1850. We are currently seeking a junior level quality focused QC Chemist with analytical or quality control laboratory experience in a Manufacturing environment. EDUCATION/EXPERIENCE: Bachelors degree in chemistry or related field. Minimum of one-year experience in analytical or quality control laboratory preferred. DUTIES: Under direction from the Laboratory Supervisor, performs quality control analysis on raw materials, in-process samples, finished/filled products, process validation/evaluation, and stability testing Routine, repetitive checking and testing of production product, including visual and sample inspections of parts used, weights, and measures Inspects production equipment for various Q.C. aspects Maintains proper documentation for Filling department quality control Assists in experiments relative to the discovery and development of new products Makes pilot batches of experimental products Creates processing batch sheets and batch records (PBR's), and checks artwork, crimp codes, log sheets, & shipping requirements Prepare artwork ingredient list General electronic and hard copy file, records, documents and database maintenance Maintain cleanliness and appearance of department, and assist in the disposal of hazardous (laboratory) waste Assist in laboratory instrument qualification and/or calibration Act as subject matter expert for laboratory instrumentation or analytical techniques Maintain proper liaison with all departments to contribute to the team philosophy Responsible for following all safety regulations and complying with S.O.P.'s, DEP, EPA, OSHA, FDA, and cGMP's while performing duties Sheffield Pharmaceuticals is an Equal Employment Opportunity employer. We provide equal opportunity to employees and applicants for employment without regard to race, creed, color, religion, sex, age, national origin, physical or mental disability, sexual orientation, marital or familial status, genetic information, protected veteran status, or other basis protected by law.'

Job Purpose for Inspector: Maintains quality standards by approving incoming materials, in-process production, and finished products and recording quality results. Duties of Bench Inspector: * Approves in-process and finished products by confirming specifications; conducting visual and measurement tests. * Working from purchase orders, special process certifications, operation sheets, blueprints, and other specifications, ensures that all parts and materials are in full compliance. * Performs complex dimensional layout inspection to operation sheet/blueprint. * Completes Inspection Method Sheets and verifies special process certifications to part specifications. * Performs 1st piece/FAI. Has proven knowledge of Inspection Xpert/Net-Inspect a plus. Aerospace Bench Inspector Skills/Qualifications: * Layout experience is a plus * 0-8 years experience as an inspector in Aerospace or similar industry * Analyzing manufacturing methods and procedures * GD&T skills are highly emphasized * Solid verbal and interpersonal skills, analytical and shop math skills, as well as working knowledge of Microsoft Excel It is the policy of this company to extend equal employment opportunities to all qualified employees without regard to race, color, religion, creed, marital status, learning disability, sexual orientation, national origin, sex, age, history of mental illness, mental retardation or physical, unless such disability prevents performance of the work involved. This policy applies to all phases of employment including, but not limited to, recruitment, hiring, placement, upgrading and promotion, transfer, layoff and recall, termination, selection for company sponsored training programs, rates of pay and other forms of compensation, use of facilities, and participation in all company sponsored activities.

Enjet Aero machines and fabricates complex jet engine parts, components and assemblies for leading OEMs in the commercial, defense and general aviation sectors. Our goal is to be regarded as an irreplaceable resource by our customers. The only way for a company to meet such a goal is to consistently meet production deadlines and expectations. Position Description: Quality Inspector will perform in-process and 1st article inspections, evaluate part to print specifications and understand the inspection methods used for inspection and support the manufacturing process and personnel, while adhering to the Quality Policy, AS 9100 requirements. Position reports to the Quality Manager and takes daily direction from the Inspection Supervisor. You will receive a 20% night shift premium. Essential Responsibilities: Strong blueprint and Geometric Dimensioning & Tolerance (GD&T) comprehension Able to use inspection tools, such as micrometer, indicators, comparator, etc Detailed to complete all paperwork, as required, including inspection reports Able to make mold casts to check ID dimensions Ability to identify dimensional and visual defects Able to understand and implement customer specifications and requirements Accuracy and attention to detail is highly important Experienced with completing 1st article inspections, in-process inspections and final inspections Knowledge of aerospace specifications and requirements preferred. Perform other duties as required Qualifications: Proficient at reading blueprints Knowledge of dimensional symbols Ability to identify visual defects Ability to read micrometers, calipers and comparator Knowledge of measuring equipment Ability to work together for team effort Team oriented Organized and detail oriented Adherence to document control requirements Knowledge of various inspection reports General computer knowledge Ability to work without supervision Benefits: Enjet offers a comprehensive benefits package to full-time employees including paid time off, health insurance, dental insurance, vision insurance, paid holidays, a 401K retirement plan, disability insurance, and more. As an EOE/AA employer, Enjet Aero will not discriminate in its employment practices due to an applicant's race, color, religious creed, national origin, ancestry, sex, age, veteran status, marital status or physical challenges.

Job Title: Inspector Quality Control- 1st Article Inspector Department: MPA Warehouse Reports To: Quality Control Manager FLSA Status: Hourly Non-Exempt In- Direct Position Date: 11/17/25 Work Hours: 7:00AM - 3:30PM SUMMARY Responsible for performing detailed inspections on New GG8 spare parts and Customer owner tooling using overhaul manuals, standard practice manuals and WGPW established procedures. Strong-dimensional skills, drawing interpretation are required and previous experience in the aerospace industry is a strong plus. ESSENTIAL DUTIES AND RESPONSIBILITIES The position includes but is not limited to the following essential duties and responsibilities. Maintains a safe and clean work area and adheres to all housekeeping requirements. Follows all safety procedures and rules and properly wears all safety protective equipment as required. Able to read and understand Pratt & Whitney engine manuals, blue prints, service bulletins, illustrated parts catalogs, standard practice, and spare parts bulletins. Able to understand GD&T and drawing interpretation. Able to process quality transactions in ERP system, including non-conformities. Able to use basic shop measuring equipment including Micrometers, Vernier and Dial Calipers, Plunge and Test Indicators, Dial Bore Gages, Snap Gages, profilometer, and PI-Tapes. Working knowledge of a Window's based computer system. Works overtime as required. Conducts oneself in a business-like manner and in the spirit of teamwork. Receiving Inspection: Visual and dimensional inspection of various gas generators using MPA overhaul manuals and WGPW technical data. May be required to work at other WGPW locations or departments due to fluctuating workloads. Able to approve AS9102 First Article Inspection, including certification package and Supplier/Vendor inspection reports. 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. Experience with job audits, including internal ISO9001 audits. Ability to calculate figures such as ratios, area, circumference, and volume. Ability to apply the basic concepts of algebra, geometry, trigonometry, and shop math as they relate to inspection or trouble shooting. EDUCATION and/or EXPERIENCE Equivalent to high school plus additional broad specialized training in the Quality Control field or technical school, military training and one to three years related experience; or equivalent combination of education and experience. PHYSICAL & ENVIRONMENTAL DEMANDS While performing the duties of this job, the employee is regularly required to sit, stand, and use hands to handle parts. The employee must occasionally lift and move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus. While performing the duties of this job, the employee may occasionally work with chemicals while receiving consumable materials in for use on parts within the shop. Possible use of alcohol and/or acetone for light cleanings of oils or dirt as parts are prepared for inspection. WGPW Industrial Turbine Services is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, disability, genetic information, pregnancy, citizenship, marital status, sex/gender, sexual preference/ orientation, gender identity, age, veteran status, national origin, or any other status protected by law or regulation.

Job Description Innodyne Systems is seeking a dedicated, experienced individual who is interested in becoming part of our team. This position provides an excellent opportunity to play a key role in a fast-growing aerospace service company. Our FAA/EASA certified repair facility services a wide range of aircraft electronic and airframe components used in business and regional aircraft. We are seeking dedicated aviation professional who is interested in pursuing a rewarding, long-term career. Essential Job Functions: Assesses condition of received damaged or worn airframe components and enters findings into repair database. Researches technical data in support of repairs including maintenance manuals, engineering drawings and other sources. Performs inspections of completed airframe work. Performs FAA/EASA Return to Service documentation. Provides technical information to engineers for development of repairs outside of approved data scope when required. Documents inspection/repair actions per company and FAA requirements. Performs other duties as assigned. Requirements: Minimum of 4 years experience with civilian airframe maintenance required. Must have an in-depth knowledge of FAR Part 145, Part 43 and other regulations applicable to repair station operations. Must be skilled in researching and interpreting maintenance data and repair related prints/drawings. Must be skilled in the use of inspection tooling related to the responsibilities described herein. Intermediate level computer skills including use of MS Outlook (or other e-mail application), MS Word, MS Excel required. High level written composition skills for correspondence, documentation, and technical instructions. Good interpersonal skills and ability to work in a team. FAA Airframe license required. Current certification at Level II Fluorescent Penetrant Inspection a plus.

Our QC Inspector supports Mativ's Sustainable & Adhesive Solutions Function. This individual will perform inspections and tests throughout the manufacturing process to ensure compliance with specifications under the supervision of Quality Engineering. The shift schedule is 6pm-6am. responsibilities: * Performs all auditing and testing of in-process, and finished goods to include Retain, Coat Weight, Cure and any additional testing as required by the Product Requirement Sheet, (PRS) or Tech 11. * Record and enter test results into the Scapa ERP System * Perform all manufacturing audits prior to production and at required intervals. * Maintain and organize product master files. * Coordinate shop floor QC testing based on daily and weekly production schedule. * Issue non-conformance report for any tested material that is out of specification. * Perform visual inspections of materials being coated and slit/converted and immediately inform coating/converting operators of any defects. * Interfaces with Quality Assurance and Production scheduling in the preparation and reviewing of slitting specifications. * Evaluates product quality based on product specifications and makes appropriate usage decisions. * Responsible for setting up test equipment. * Maintaining inventory of QC lab MRO items * Responsible for maintaining all related files and documents according to Good Documentation Practice, (GDP). * Assists in training new QA Inspectors and manufacturing personnel. * Participates as a team member in continuous improvement events. * Maintain QC test equipment and calibration status. * Assists quality engineers and quality technicians with gage R&R, and other validation activities. * Follows safety rules and keeps the work area in a clean and orderly manner. * Complies with company attendance policies. * Issue Supplier Complaints in the ICS, (Internal Complaint System), for nonconforming raw material. qualifications: Required * Minimum of 2 years' experience in Q. A. or Q. C. manufacturing environment. * High School diploma required, bachelor's degree highly preferred. * Familiar with basic measurements, test equipment and basic math skills. * Medical device industry experience preferred. * Ability to communicate and work within a team environment. * Fluency in English both verbal and written Preferred * 2 years' experience in Quality Assurance or Quality Control. * 2 years' experience in medical device or industrial manufacturing. * Associate degree in chemistry, physical sciences, or tech field. Relevant job experience may be considered in place of a 2-year degree. * Able to collaborate and work well with others. Position Demands Conditions are that of a manufacturing environment: * Air Temperatures can range from cold to hot. * The atmosphere may contain dust, fumes, and odors. * May include mechanical, electrical, chemical, explosive and radiation hazards. Employees are required to wear Personal Protective Equipment (PPE) including: * Safety shoes (steel toe or composite toe) * Safety Glasses * Bump Caps * Protective Gloves, when performing certain tasks * Hearing Protection, when required. * Other personal protective equipment as required for certain tasks. While performing the duties of this job the employee must meet the physical demands: * Be able to lift a minimum of 50 pounds. * Be able to work 12-hour shifts. * Perform repetitive tasks. * Routinely stand, sit, hear, walk, and talk. * Reach, climb, bend, kneel, crouch, twist, and balance, sometimes in awkward or tight spaces. * Have good close vision, depth perception, and the ability to focus. WHAT WE OFFER At Mativ, our benefits reflect how much we value and care for each other. We know that employees and their families have unique needs, so our comprehensive benefits offer flexibility, quality, and affordability. Here are just a few of the ways we support your well-being and that of your loved ones: * Medical, dental and vision insurance * Consumer-Driven Health Plan (CDHP) * Preferred Provider Organization (PPO) * Exclusive Provider Organization (EPO) * Company-paid basic life insurance and Additional voluntary life coverage * Paid vacation and competitive personal time off * 401(k) savings plan with company match * Employee assistance programs - available 24/7 to you and your family * Wellness and Work Life Support - career development and educational assistance ABOUT MATIV Mativ Holdings, Inc. is a global leader in specialty materials headquartered in Alpharetta, Georgia. The company connects, protects, and purifies the world every day through a wide range of critical components and engineered solutions that solve our customers' most complex challenges. We manufacture on three continents and generate sales in nearly 100 countries through our family of business-to-business and consumer product brands. The company's two segments, Filtration & Advanced Materials and Sustainable & Adhesive Solutions, target premium applications across diversified and growing end-markets, from filtration to healthcare to sustainable packaging and more. Our broad portfolio of technologies combines polymers, fibers, and resins to optimize the performance of our customers' products across multiple stages of the value chain. Our leading positions are a testament to our best-in-class global manufacturing, supply chain, and materials science capabilities. We drive innovation and enhance performance, finding potential in the impossible. Mativ and its subsidiaries are Equal Opportunity Employers. Qualified applicants will be considered without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Quality Control Inspector- 2nd Shift 3 pm-1:30 am M-Thursday (Training is days) Dion Label Printing is an Inovar Packaging Group company, is proud to be one of North America's premier flexographic and digital printing companies, dedicated to the success of our employees and customers. We invest in the latest equipment and technology, continually seeking the best strategies and solutions to deliver cutting-edge, top-quality products. Our culture is customer-driven, team-oriented, and built on win-win partnerships. Why Join Us? Competitive pay and a bonus program Comprehensive benefits package, including medical, dental, vision, life insurance, short/long-term disability 401(k) Retirement Plan with generous company match Paid Time Off (PTO) Cash incentive program at your 90-day mark Tuition Assistance Growth opportunities within a rapidly expanding company Job Summary We are seeking a Quality Control Inspector to ensure our printed labels meet the highest industry standards. This role is responsible for inspecting labels and ensuring our final products meet customer specifications. The ideal candidate is detail-oriented and passionate about maintaining exceptional product standards. This is a production-based position, and applicants must be willing to operate machinery and be comfortable working in a production environment. Key Responsibilities & Essential Functions Product Inspection Conduct visual and strobe camera inspections for in-process products, and finished labels to ensure company and customer specifications including verifying color accuracy, registration, die-cut alignment, and barcode readability. Product Handling & Labeling Perform the finishing process by ensuring products are properly rolled, stacked, marked, and labeled with roll and core labels. Manage sample saving to support quality tracking and compliance. Documenting & Reporting Complete all required quality records, inspection forms, and digital logs accurately and on time. Continuous Improvement & Training Assist in identifying and improving quality control procedures and best practices. Train team members on inspection standards, and process improvements to enhance overall quality and efficiency. Qualifications High school diploma or equivalent; technical or quality-related certifications are a plus. Strong attention to detail with solid problem-solving skills. Previous experience with light equipment operation or inspection tools is highly preferred. Ability to read and interpret order specifications, drawings, and quality standards. Experience using measuring tools such as rulers. Coachable, punctual, and reliable with a strong willingness to learn. Ability to stand for extended periods and work in a production environment with exposure to noise and machinery. Good communication skills and ability to work collaboratively. Ability to lift and carry materials as needed to support production and quality processes. Join Our Team! If you are passionate about quality and want to contribute to a growing company, we'd love to hear from you. Apply today and become a part of Inovar Packaging Group!

The Senior Quality Control Technician role in our Bloomfield, CT facility drives improvement in the reliability of CO2 Laser products. The incumbent will be engaging directly with a cross functional team on a wide variety of products to ensure our product and processes meet the dynamic laser manufacturing requirements. Working with a quality mindset team, this role will provide hands on support for the incoming goods, in-process, and final inspection of laser systems to ensure we meet Coherent Quality Standards. Primary Duties & Responsibilities Inspection manufactured laser systems: Detail oriented inspection of electronic and mechanical assemblies Utilize common inspection methods to evaluate critical design requirements Develop inspection test plans with a cross functional team Assist in problem solving activities to support identified nonconformities Evaluation and verification of purchased components Define and execute incoming material test plans for qualification activities Document and present inspection results to key stakeholders Verification of vendor supplied documentation including first article inspections and material certifications Support of Quality Systems: Document detailed findings to be used for Continuous Improvement Initiatives Accomplish root cause analysis and provide corrective actions with follow-up Ensure practices align with best practices, procedures and inspection techniques Perform internal product and business system audits Reliability system maintenance: Utilize computers for automated data collection and control of instruments Collaborate with the Quality organization regarding calibration of test instruments Monitor and troubleshoot long term unmanned tests with engineering support Assist in developing new methods and protocols for component level testing and measurement Complete calibration of monitoring and measuring equipment support Education & Experience High School diploma A minimum of 4 years of related experience or combination of education and relevant experience Proficient in the use of automated and manual measuring devices and test equipment Excellent verbal and written skills in the English language required Skills Preferred experience with layout inspections and sound Geometric Dimensioning and Tolerancing knowledge Preferred experience automating inspection test method is preferred Knowledge of centralizing data for analysis Experience of test and measurement of electronic and/or optical systems Continuous improvement mindset - improves products and processes Well organized and knowledgeable of 6S methodology Demonstrated problem-solving abilities combined with hands-on experience Knowledge of electronic component manufacturing Self-motivated to thoroughly document data and test results Working Conditions Manufacturing working environment. Some areas under cleanroom protocol. Minimal to no expected travel Support of seconds shift operations required This is an on-site position in our Bloomfield, CT facility. Shift will be Monday to Friday 11am to 7:30pm Physical Requirements Must be able to move around manufacturing floor Must be able to lift a maximum of 30 pounds Safety Requirements All employees are required to follow the site EHS procedures and Coherent Corp. Corporate EHS standards. Quality and Environmental Responsibilities Depending on location, this position may be responsible for the execution and maintenance of the ISO 9000, 9001, 14001 and/or other applicable standards that may apply to the relevant roles and responsibilities within the Quality Management System and Environmental Management System. Culture Commitment Ensure adherence to company's values (ICARE) in all aspects of your position at Coherent Corp.: Integrity - Create an Environment of Trust Collaboration - Innovate Through the Sharing of Ideas Accountability - Own the Process and the Outcome Respect - Recognize the Value in Everyone Enthusiasm - Find a Sense of Purpose in Work Coherent Corp. is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law. If you need assistance or an accommodation due to a disability, you may contact us at ****************************** .

Challenge Yourself and Impact the Future! MacDermid Alpha Electronic Solutions, a business of Element Solutions Inc (NYSE: ESI), is renowned worldwide for it's commitment to revolutionizing the electronics industry. With a legacy spanning over a centrury, we have continually set new benchmarks for excellence, reliability and sustainability in electronic materials. Our Expertise: Wafer Level Solutions - Revolutionizing wafer fabrication processes for enhanced efficiency and performance Semiconductor Assembly Solutions - Driving innovation in semiconductor assembly processes for unparalelled reliability Circuitry Solutions - Tailored solutions to meet the dynamic demands of modern circuitry Circuit Board Assembly Solutions - Elevating circuit board assembly processes for optimal performance Film & Smart Surface Solutions - Transforming electronics with cutting-edge materials and technologies for enhanced functionality and reliability Across diverse sectors including automotive, consumer electronics, mobile devices, telecom, data storage, and infrastructure, MacDermid Alpha Electronic Solutions has earned the trust of manufacturers worldwide. Our comprehensive rance of high quality solutions and technical services covers the entire electronics supply chain, empowering businesses to thrive in today's competitive landscape. We strive to embody the five 'Elements of our Culture'- our '5C's'; Challenge, Commit, Collaborate, Choose, and Care. These core values are the foundation of our organization which our employees embrace in their interactions with customers, colleagues and other stakeholders, to drive financial performance and create a rewarding work environment. Who are we looking for? This role is responsible for performing laboratory procedures for testing in process and finished products from manufacturing, raw material samples prior to use in manufacturing, and customer plating solutions. The preferred candidate will be able to step into a dynamic work environment and will be a true team player who can flex and enjoys working in a number of different areas and with various instruments. What will you be doing? Follows written analytical procedures and methods for testing of in-process, finished and customer product samples including Plating tests, Volumetric and Gravimetric analysis, Instrumental analysis, etc. Collects and enters data into WinLIMS data management system to review and validate results of sample data. Performs calculations associated for the test results. Communicates status of testing samples to Production Supervisors and Chemical Operators. Submits results for approval to the Laboratory Supervisor/Manager. Validates established methods. Troubleshoots and makes recommendations concerning product quality. Stores hazardous materials in the proper locations and dispose of hazardous waste properly. Schedule and maintain instrument calibration database. Works with Quality Assurance personnel to investigate any product quality issues. Uses and promotes the Six Sigma methodology and emphasized on 5-S. Attend required HSE training including Hazardous Waste Management, emergency response, and Hazard Communication, and demonstrate an acceptable level of understanding of topics. Operate equipment and follow procedures in accordance with IATF16949, ISO 14001, and OHSAS 18001 standards Follows all safety procedures including general site safety rules and Chemical Hygiene Plan. Coordinates with MSA team to adhere to requirements for MSA studies including Gage R&R, Accuracy, Linearity, Bias as well as matching and correlation studies Ability to work with mathematical concepts such as probability and statistical inference, fractions, percentages, ratios, and proportions to practical situations Who are You? Bachelor's Degree in chemistry or related field and at least 2 years of strong laboratory experience Proficient in bench chemistry,manual titrations and extractions, with working knowlege of gravimetric assays, pH measurement and UV-Vis spectrophometry. Highly preferred - previous experience in one or more of the following: ICP-OES, ICP-MS, HPLC/IC Candidate should have a solid undestanding of analytical accuracy and precison, demonstrate strong data analysis skills and attention to detail, and show willingness to learn new techniques. We understand that not all candidates may meet the requirements listed above. If you believe you have the knowledge and experience necessary to excel in this role, we encourage you to apply. We are Offering... Challenge Yourself and Impact the Future - You will be part of a highly collaborative culture that promotes continuous improvement through cross-functional partnerships to achieve our mission. We do this through a strong and unified culture and transparent management which has empowered us to create high performing global teams that achieve superior solutions for our customers. As part of the MAES Team, you will have ... Opportunities for career growth, competitive compensation (competitive base salary and performance related bonus plan) and benefits packages (health, dental, and vision insurance, Wellness Program, PTO/Holidays, as well as a 401(k)-retirement plan with a company match). Innovated work environment where you will be a part of a dynamic and collaborative team. Perks and Incentives such as paid parental leave, tuition reimbursement, and opportunities for professional development. The typical base salary range for this position is between $69,561.00 and $104,341.00 Equal Opportunity Employer All qualified applications will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, pregnancy, genetic information, disability, status as a protected veteran, or any other protected category applicable under federal, state and local laws.

Job Description At Sheffield Pharmaceuticals, the home of the original Sheffield Toothpaste, we offer exclusive, quality, branded products to promote wellness and relief to our customers. Our wellness and first aid products include a variety of creams and ointments, nasal products, and toothpaste all made in the USA since 1850. We are currently seeking a junior level quality focused QC Chemist with analytical or quality control laboratory experience in a Manufacturing environment. EDUCATION/EXPERIENCE: Bachelors degree in chemistry or related field. Minimum of one-year experience in analytical or quality control laboratory preferred. DUTIES: Under direction from the Laboratory Supervisor, performs quality control analysis on raw materials, in-process samples, finished/filled products, process validation/evaluation, and stability testing Routine, repetitive checking and testing of production product, including visual and sample inspections of parts used, weights, and measures Inspects production equipment for various Q.C. aspects Maintains proper documentation for Filling department quality control Assists in experiments relative to the discovery and development of new products Makes pilot batches of experimental products Creates processing batch sheets and batch records (PBR's), and checks artwork, crimp codes, log sheets, & shipping requirements Prepare artwork ingredient list General electronic and hard copy file, records, documents and database maintenance Maintain cleanliness and appearance of department, and assist in the disposal of hazardous (laboratory) waste Assist in laboratory instrument qualification and/or calibration Act as subject matter expert for laboratory instrumentation or analytical techniques Maintain proper liaison with all departments to contribute to the team philosophy Responsible for following all safety regulations and complying with S.O.P.'s, DEP, EPA, OSHA, FDA, and cGMP's while performing duties Sheffield Pharmaceuticals is an Equal Employment Opportunity employer. We provide equal opportunity to employees and applicants for employment without regard to race, creed, color, religion, sex, age, national origin, physical or mental disability, sexual orientation, marital or familial status, genetic information, protected veteran status, or other basis protected by law.'