Quality Control Inspector Salary in Minnesota, USA

OverviewAbout Cretex Medical Cretex Medical is a leading contract manufacturer of precision components and assemblies for the medical device industry. Our customers view us as a trusted partner in the areas of injection molding, laser processing, metal stamping and device assembly. Learn more at www.cretexmedical.com.Quality Inspector Position Summary The Quality Inspector performs first piece, in-process inspections, and final inspections of components and assemblies per control/quality plans. The Quality Inspector will review and approve final release documentation. Performs incoming inspections per control/quality plans for received materials. This role will also complete appropriate quality records within company and GMP guidelines, policies and procedures. Shifts Available: 6th: 6:30am-7pm Mon-Wed, every other Sunday ResponsibilitiesQuality Inspector Duties and Responsibilities Inspection of injection molded parts relating to quality, appearance and performance Inspection of assemblies relating to quality, appearance and performance Inspection of received materials relating to quality, appearance and performance Inspection and audit of final product documentation prior to release Determine reasons for defects Read and understand quality control plans, blueprints and specifications Check parts dimensionally by using precision testing equipment, including Tool Scope, CMM, OGP and various other metrology tools and equipment Effective organizational, oral and written communication skills Read and comply with work instructions, set up sheets, and checklists Accurately records and reports hours worked Maintain an organized work area (5S) to include workstations, equipment, walkways, and locker areas Participate in the Operational Excellence Program Understand and comply with the Cretex professional competencies, company policies, and employee manual Adhere to all safety policies; includes wearing personal protective equipment when required Support and complies with the company's Quality System, ISO, and medical device requirements Complete all other work duties as assigned QualificationsQuality Inspector Requirements Basic knowledge of inspection equipment use and maintenance Read and comprehend customer supplied drawings and specifications Communicate inspection results with team members Manage multiple requirements and deadlines Quickly shift priorities in support of production inspection needs High school diploma or equivalent degree (GED) Experience with measuring instruments, methods and practices including hand tools and machine devices including CMM and Vision Systems Basic knowledge of Microsoft Office (Outlook, Word, Excel) Ability to read, comprehend, follow and document work instructions, standard operating procedures, and training documents Mechanical aptitude Dexterity and hand and eye coordination Attention to detail Strong problem-solving skills Ability to prioritize work and manage multiple tasks Quality Inspector Preferred Knowledge, Skills and Abilities Knowledge of ISO 9001/13485 Quality training/certifications

At Entegris we are committed to providing equal opportunity to all employees and applicants. Our policy is to recruit, hire, train, and reward employees for their individual abilities, achievements and experience without regard to race, color, religion, sexual orientation, age, national origin, disability, marital or military status.Chaska, MN Full timePosted Yesterday REQ-5598 Job Title:Quality Inspector (2nd shift)Job Description:Summary: As a 2nd shift Quality Inspector you are an essential part of helping Entegris be part of the Future of Innovation! The Quality Inspector you will be responsible for: performing a wide variety of inspections, checks and tests for quality control for the manufacturing of products. You will need to be familiar with running tests and comparing the results to a known standard to ensure strict customer requirements. Schedule: Sunday - Thursday 2pm – 10pm Primary Responsibilities and Duties: Approve incoming materials, in process production, and finished products by confirming specifications; conducting visual and measurement tests; rejecting unacceptable materials; creating quality notification for non-conformances. Communicate discrepancies to production supervisor and help determine next steps. Documents inspection results by completing reports and logs; inputting data into quality database. Conducting process audits. Performing Capability studies. Keeps measurement equipment operating by following operating instructions and calling for repairs as needed. Maintains safe and healthy work environment by following standards and procedures; complying with legal regulations. Understands and applies statistical process control techniques, including basic chart interpretation and capability analysis Qualifications (Education, Training, Experience, Knowledge, Skills, Physical Requirements): Previous quality/inspector roles in a manufacturing environment preferred Experience navigating SAP and Quality systems preferred Good oral and written communication skills, proficient with excel, technical training in blueprint reading, good values, willingness to learn, thorough, detailed orientated, open to feedback. Skilled using a variety of measurement equipment including calipers, pin gage set, height gage, test indicator, micrometer, pitch micrometer, dial indicator, surface plate, optical comparator, smart scope, and coordinate measuring machine (CMM) At Entegris, we want you to be part of our culture, which values your unique talents, skills, and experiences. We believe what we do is as important as how we do it.People at our company bring their true selves to work, and are appreciated not only for what they do, but for who they are. This plus the technical complexity of our products and solutions means you can be sure your work is both challenging and changing the world for the better.PI239636544

Electric Machinery Company LLC, a division of WEG Electric Corp. Minneapolis, MNPosition: Inspector Quality Testing | Tester - 1st shift Team: Quality TeamPrimary Objective of Position: An Inspector Quality Testing | Tester provides validated product performance data by performing test setup, operation, troubleshooting, calibration and reporting.Major Areas of Accountability: Set up, connect, test and adjust test items such as motors, generators, control equipment and specifically designed power apparatus to meet IEEE, API, NEMA and other product specifications. Read information pertaining to apparatus to be tested, such as production order, engineering data sheets, process specifications, test specifications, and drawings. Prepare data sheets, test plans and reports electronically to meet internal and external customer requirements. Use auxiliary testing apparatus such as pony brakes, generators, voltmeters, ammeters, dynamometers, driving motors, tachometers, meggers and high-pot equipment. Check machines for common defects before setup and, if found, reports to supervisor for proper disposition. Connect test unit through necessary meters, generators, shunts, instrument transformers, resistors, reactors or other apparatus as required. Collect, record and analyze data for comparison to specification. Mechanical setup, test and dynamic balance of components. Performs electrical in-process verification of compliance to specifications. Calibrates and maintains electrical test equipment including development of electronic databases, standards, work instructions and procedures. Lift and move materials using forklift, pallet jack, overhead crane or jib crane. Demonstrates a commitment to Continuous Improvement by identifying opportunities in day to day work. Performs to ISO 9001 Quality Standards and abides to OSHA and EPA regulations. Other duties as assigned. Knowledge/ Skills/Abilities: High School Diploma or equivalent required; advanced certificate/degree in related field desired. Ability to work with minimal supervision and is self-motivated. Must be able to work with a team and independently. Good oral and written communications skills. Ability to effectively partner and communicate with external and internal customers at all levels of the organization. Physical Requirements: Routinely lifts and moves objects up to 20 lbs. Occasionally lifts and moves objects up to 50 lbs. Occasionally ascends/descends ladders and stairs. Occasionally works at heights or on platforms. Occasionally positions self in various works spaces, including low, tight or confined spaces. Routinely remains in a stationary position, often standing or sitting for prolonged periods of time. Occasionally uses repetitive motions including the wrists, hands or fingers to operate machinery or tools. Occasionally operates machinery and power tools. Routinely moves from one work station to another to accomplish tasks. Job Type Monday � Friday, 7:00 a.m. � 3:30 p.m. Full-time (Union) Skills Matrix: The Tester position is part of the Quality Team skills Matrix. This position works as a team member utilizing and performing to the Quality Team skills matrix, which outlines the comprehensive skills in the Quality Team. Pay Types Voluntary weekday and weekend overtime. Saturday is paid at time and a half, Sundays are paid at double time!Benefits Medical, Dental & Vision Insurance eligible your 1st day on the job 401K with Match 1st month following hire Quarterly Bonus Program payout potential Company paid Holidays (12) Paid Time Off (PTO) accrued Paid Birthday (use anytime throughout the year) Company paid Short & Long Term Disability Company paid Life Insurance $6,000 annual Tuition Reimbursement program Company provided tools Company provided uniforms (laundered) Company reimbursement for Safety Shoes & Safety Glasses Secure, onsite free parking

OverviewAbout rms Companyrms Company provides contract manufacturing of high-quality, tight-tolerance medical implants, components and sub-assemblies using cutting-edge technology. rms is part of the Cretex Medical family of companies. Learn more at www.rmsmachining.com and www.cretexmedical.com.Quality Engineer I Position SummaryThe Quality Engineer I will provide comprehensive quality assurance support for manufacturing operations. This role is crucial in defining, implementing, and enhancing quality-related practices, ensuring inclusivity and diversity are integral parts of the process. The incumbent will offer technical guidance, support measurement methodologies, and foster an environment that embraces inclusivity.ResponsibilitiesQuality Engineer I Essential Job Functions Offer quality engineering support for manufacturing and project management, ensuring inclusivity and diversity are considered in all processes. Develop inspection requirements, facilitate PFMEAs, resolve discrepant material issues, and create and maintain quality documents, such as control plans and inspection plans, with a focus on inclusivity. Analyze data to identify improvement opportunities, incorporating diverse perspectives into decision-making processes. Act as the quality interface for a production team in addressing customer complaints, utilizing failure analysis, developing corrective and preventative actions, and conducting trend analysis with an inclusive approach. Support internal and external audit activities, ensuring inclusivity and diversity are considered in all quality-related processes. Lead and participate in company projects, providing quality recommendations that promote inclusivity and diversity. Support validation activities of processes, equipment, and metrology, with a commitment to inclusivity and diversity. Create protocols and analyze data, considering diverse perspectives and ensuring inclusivity. Support Quality Inspectors to ensure inspection plans align with relevant customer requirements, emphasizing inclusivity. Support and comply with the company Quality System, ISO standards, and medical device requirements, ensuring inclusivity and diversity are integrated into all quality-related procedures. Collaborate with other business segments, including sales/marketing, customer service, engineering, quality, and finance, fostering an inclusive environment. Understand customer needs and the core business markets served, ensuring inclusivity and diversity are considered in all interactions. Ensure business systems are implemented, maintained, and functioning properly, with a commitment to inclusivity and diversity. Participate in required company meetings, fostering an inclusive environment where diverse perspectives are valued. Maintain an organized work area (5S) with inclusivity and diversity in mind. Participate in the Operational Excellence Program with a focus on inclusivity and diversity. Complete all other work duties as assigned, ensuring inclusivity and diversity are prioritized. Ability to work in a manufacturing environment, promoting inclusivity and diversity among colleagues.QualificationsQuality Engineer I Qualifications Bachelor's Degree in Mechanical, Industrial, or another Engineering Science, with a commitment to promoting inclusivity and diversity in the workplace. Knowledge of quality systems, regulatory requirements, and industry standards, with a focus on inclusivity and diversity. Intermediate knowledge of blueprint reading and GD&T, with an understanding of how inclusivity and diversity can be integrated into technical processes. Ability to analyze data and ensure data integrity, incorporating diverse perspectives into data interpretation. Ability to operate a variety of inspection equipment, ensuring inclusivity and diversity are considered in equipment usage. Ability to consistently achieve short and long-term business results, with a commitment to promoting inclusivity and diversity. Proficiency in Microsoft Office (Outlook, Word, Excel, PowerPoint, Publisher), with an understanding of how technology can promote inclusivity and diversity. Clear and effective verbal and written communication skills, promoting inclusivity and diversity in all communications. Attention to detail and organizational skills, with a commitment to inclusivity and diversity in all tasks. Ability to work in a fast-paced team environment, fostering inclusivity and diversity among team members. Ability to prioritize and multitask, ensuring inclusivity and diversity are prioritized in workload management.rms Company Benefits As a Cretex Medical company, rms offers a full benefit package to its employees. Benefits include medical, dental, vision and life insurance options. rms also offers a 401(k) retirement plan with employer match, profit sharing, short- term and long-term disability insurance, paid time off, holiday pay, and an onsite medical clinic.rms Company also offers company specific benefits, such as: Onsite Clinic Paid Parental Leave Monthly Social Events Annual Employee Appreciation Week Volunteer Opportunities Training and Development Opportunities Tuition Reimbursement Wellness ProgramApplicants will receive consideration for employment regardless of their race, color, creed, religion, national origin, sex, sexual orientation, disability, age, veteran status, marital status, family status, status with regard to public assistance, or any other protected status as required by law.Our company uses E-Verify to confirm the employment and eligibility of all newly hired employees. To learn more about E-Verify, including your rights and responsibilities, please visit www.dhs.gov/E-Verify.Cretex Companies use cutting oils, solvents, and other chemicals in the manufacturing process. Testing is conducted on a periodic basis to ensure that all chemicals are kept well below the OSHA permissible exposure levels.

This field based position is an integral part of our commitment to the quality and service we provide for our customers and to their equipment. The work is varied from day to day and is ideally suited to a self-motivated individual who can work independently. A successful inspector will have excellent communications skills and the ability to work with clients and customers in a professional manor with high integrity.The position has minimum qualifications of a high school diploma and work experience with boilers and pressure vessels or nuclear reactors. The required work experience can be reduced if you have an engineering degree.Our entry level inspectors start with 12 weeks of intensive training to gain the necessary experience and qualifications required to perform inspection during construction, repairs or operation of in-service equipment. Training is provided annually for all of our inspectors, which is developed and supported by our technical industry experts.Qualifications :Required:High school diploma and technical working knowledge of commercial equipment.Experience operating, maintaining or inspecting boilers, pressure vessels and machinery.Basic algebra skillsBasic computer knowledge.Must be an effective communicator in both written and verbal forms.Meet the required experience and qualifications to obtain the National Board of Boiler and Pressure Vessel Inspectors commission.Preferred:National Board of Boiler & Pressure Vessel Inspectors Commission.Technical College Graduate.Engineering degree (BSME, BSEE or BSChE).Physical Requirements:This position requires a person to routinely move about at a site facility. As such, candidates for this position must be able to perform the below physical requirements:• Ability to crawl through 11" X 15" openings into confined spaces. Enter and function in very tight confined spaces.• Ability to climb vertical ladders and several stories of stairs.• Ability to climb and function at heights of at least 30 feet, and up to eight(8) to ten (10) stories.• Ability to perform bending, stretching and twisting motions.• Ability to withstand temperature variations. Temperature variations could be as much as 70 degrees.• Ability to walk 3-5 miles.• Ability to stand for long periods of time and able to remain in a stationary position 50% of the time.• Ability to lift own body weight while hanging or entering a confined space with associated safety equipment• Ability to lift equipment up to 50 lbs.• Visual acuity of 20/20 (natural or corrected) and identify colors.• Ability to hear (corrected) the sounds of equipment operation.

Volt is immediately hiring for Warehouse Production Worker in Maplewood, MN As an Warehouse Production Worker you will: Job Roles and Responsibilities: Follow generally defined procedures and use fixed or variable measuring instruments (visual, gauge) to inspect parts, products and/or processes and ensure conformance with standards. Check for irregularities and defects and record findings. May also be responsible for monitoring automated packaging equipment. This is a Full-time, Contract position. The ideal Warehouse Production Worker Candidate will have: The ability to follow simple verbal or written instructions. Detail orientation, good manual dexterity skills, and good hand/eye coordination are required. Basic data entry skills and computer proficiency is preferred. Inspection/quality control experience. Schedule: Monday - Friday 6am -2:30pm, Occasional weekends Location: Maplewood, MN Pay Rate: $16-17/hr. *Pay range offered to a successful candidate will be based on several factors, including the candidate's education, work experience, work location, specific job duties, certifications, etc. Qualified candidates should APPLY NOW for immediate consideration! Please hit APPLY to provide the required information, and we will be in touch as soon as possible. Benefits: Volt offers benefits (based on eligibility) that include the following: health, dental, vision, term life, short term disability, AD&D, 401(k), Sick time, and other types of paid leaves (as required by law), Employee Assistance Program (EAP). Volt is an Equal Opportunity Employer and prohibits any kind of unlawful discrimination and harassment. Volt is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment on the basis of race, color, religion or belief, national origin, citizenship, social or ethnic origin, sex, age, physical or mental disability, veteran status, marital status, domestic partner status, sexual orientation, or any other status protected by the statutes, rules, and regulations in the locations where it operates. If you are an individual with a disability and need a reasonable accommodation to assist with your job search or application for employment, please click here or call (866) -898-0005. Please indicate the specifics of the assistance needed. Volt does not discriminate against applicants based on citizenship status, immigration status, or national origin, in accordance with 8 U.S.C. § 1324b. The company will consider for employment qualified applicants with arrest and conviction records in a manner that complies with the San Francisco Fair Chance Ordinance, the Los Angeles Fair Chance Initiative for Hiring Ordinance, and other applicable laws.Job ID : 424864

Electric Machinery Company LLC, a division of WEG Electric Corp. Minneapolis, MN Position: Quality Manager Department: Quality Department Primary Objective: The Quality Manager is responsible to provide day to day leadership, direction, and planning for all Quality Control and Quality Assurance areas within the Company. This will include direct responsibility for quality reporting, analysis, certifications, and compliance as it relates to product and process quality. Major Areas of Accountability: Communicates Company�s vision, mission and strategic direction at a level that allows every employee to understand they are a part of something bigger than themselves and that their role is strategically important to the organization. Leads, guides, directs, and evaluates work of direct reports, including meeting budget goals and accountability measures that are aligned with the mission statement. Sets the vision and strategy for the quality group. Partners with WEM�s management and executive teams; ensures all Products and processes adhere to multiple certification aspects noted by Electric Machinery (EM), including ISO, Nuclear, and other independent agencies or customers. Ensures compliance with applicable company policies, procedures, and processes regarding production methods, quality and safety. Defines and implements solutions to continuously improve business process, eliminating safety risks, cutting production costs and continuously defining and improving quality of products and processes. Responsible for accomplishment of short- and long-term goals and objectives, for Quality departments, including test, as established jointly with business leaders and executive team. Manages efforts and results of Quality and Test area supervisors, Quality technicians / inspectors, testers and directly assigned support personnel. Interacts with all levels and functions within the organization to promote a total quality environment. Maintains communication with customers and suppliers to ensure EM�s quality and customer service priorities are being maintained. Provides coaching, development, and day to day support for production, production support, and next tier leadership personnel. Prepares operating budgets and ensures responsible functions are conducted according to budget guidelines. Works closely and harmoniously with Operations and Engineering support departments, as well as, other functional and support groups inside and outside of WEM. Understands and works within the guidelines of current labor agreement. Other duties may be assigned by President to meet business needs. Knowledge / Skills / Abilities: Minimum of 5 years direct supervisory experience in a manufacturing environment. BS degree required, preferably an engineering, or technical related field. Demonstrated knowledge of manufacturing processes, and quality assurance techniques. Experience with Quality procedures and documentation with emphasis on the development and improvement of Quality processes. Excellent leadership, organizational, and decision-making skills. Excellent communication skills, both written and verbal. Strong critical thinking, negotiation, and planning skills. Ability to prioritize workload and shift work activities to meet business, and business segment goals. Ability to advise and contribute on activities to maximize profit, protect and grow the Company. Ability to work well within a team, as well as independently in a fast-paced environment. Ability to teach and work with all levels of production and support personnel. Demonstrated knowledge and experience using SAP strongly preferred. Demonstrated problem-solving skills. Experience with process improvements and lean manufacturing implementation in a factory setting. Proven ability to interact effectively across all levels of the organization required. Proven customer interaction and management skills are essential. Proven self-starting, results-oriented, flexible, team-player skills required. Proficiency in Microsoft: Word, Excel, PowerPoint, and Outlook. Must be able to travel worldwide on short notice. Physical Requirements: Work is performed in both an office and manufacturing environment. Requires the ability to routinely move throughout the office and manufacturing facility to perform work. Requires the ability to routinely lift up to 25 pounds. Requires the ability to ascend and descend stairs daily to reach all areas in the manufacturing facility.

OverviewAbout rms Companyrms Company provides contract manufacturing of high-quality, tight-tolerance medical implants, components and sub-assemblies using cutting-edge technology. rms is part of the Cretex Medical family of companies. Learn more at www.rmsmachining.com and www.cretexmedical.com.Quality Floor Inspector Position SummaryThe Quality Inspector I is responsible for conducting basic dimensional and visual inspections across various manufacturing processes using a range of methods and equipment. This role involves interpreting and accurately documenting inspection results, identifying and isolating non-conforming products, and adhering to company and Good Manufacturing Practices (GMP) guidelines. Additionally, the Quality Inspector I supports the company's Quality System, ISO standards, and medical device requirements while collaborating with different business segments and maintaining a proactive approach to customer needs and market understanding. The Quality Floor Inspector position will be working on the production floor. 1st Shift: Monday - Friday 6:00am to 2:30pm or 7:00am to 3:30pm ResponsibilitiesQuality Inspector Responsibilities: Conduct inspections on received materials, components, and assemblies for quality, appearance, and performance. Interpret and accurately document inspection results. Identify and isolate non-conforming products. Utilize various inspection measurement tools and equipment, including micrometers, calipers, gauges, profilometers, optical comparators, microscopes, and precision testing equipment like Tool Scope, CMM, and Vision systems. Support and comply with the company's Quality System, ISO standards, and medical device requirements. Follow work instructions and standard work procedures. Collaborate with other business segments such as sales/marketing, customer service, engineering, quality, and finance. Understand customer needs and target business markets. Ensure proper implementation and maintenance of business systems. Participate in company meetings and maintain an organized work area (5S). Contribute to the Operational Excellence Program. Perform other assigned duties as required. Ability to work in a manufacturing environment.QualificationsMinimum Requirements, Education & Experience (incl. KSA's and certifications) Basic knowledge of inspection equipment use and maintenance. Ability to work from customer-supplied drawings and specifications. Effective communication of inspection results with team members. Flexibility to prioritize production inspection needs. Ability to manage multiple requirements and deadlines. Mechanical aptitude. Dexterity and hand-eye coordination. Proficiency in using a microscope and hand tools. Willingness to cross-train in other production areas. Proficiency in Microsoft Office applications (Outlook, Word, Excel, PowerPoint, Publisher). Clear and effective verbal and written communication skills. Attention to detail and organizational skills. Ability to work in a fast-paced team environment. Prioritization and multitasking abilities.Desirable Requirements/Qualifications: 1 year of experience in a manufacturing environment. Familiarity with measuring instruments, methods, and practices, including hand tools and machine devices like CMM and Vision Systems. Knowledge of ISO 9001/13485 standards. Quality training or certifications.rms Company Benefits As a Cretex Medical company, rms offers a full benefit package to its employees. Benefits include medical, dental, vision and life insurance options. rms also offers a 401(k) retirement plan with employer match, profit sharing, short- term and long-term disability insurance, paid time off, holiday pay, and an onsite medical clinic.rms Company also offers company specific benefits, such as: Onsite Clinic Paid Parental Leave Monthly Social Events Annual Employee Appreciation Week Volunteer Opportunities Training and Development Opportunities Tuition Reimbursement Wellness ProgramApplicants will receive consideration for employment regardless of their race, color, creed, religion, national origin, sex, sexual orientation, disability, age, veteran status, marital status, family status, status with regard to public assistance, or any other protected status as required by law.Our company uses E-Verify to confirm the employment and eligibility of all newly hired employees. To learn more about E-Verify, including your rights and responsibilities, please visit www.dhs.gov/E-Verify.Cretex Companies use cutting oils, solvents, and other chemicals in the manufacturing process. Testing is conducted on a periodic basis to ensure that all chemicals are kept well below the OSHA permissible exposure levels.

We are looking for an Associate Scientist, Quality Control. This position is an on-site role requiring a five (5) days per week, Monday-Friday, at our Minneapolis production facility in New Hope, MN, which is a cGMP production manufacturing facility for our product lines.Job duties: Develop and validate analytical methods for the quantification and qualification of drug substances, excipients, and finished products. Review and interpret laboratory data, ensuring accuracy and consistency in test results through the use of statistical quality control techniques. Investigate out-of-specification (OOS) results and implement corrective actions to prevent recurrence, documenting all findings and procedures. Maintain and calibrate analytical instruments and laboratory equipment to ensure precise and accurate testing capabilities. Prepare detailed reports and documentation that summarize test results, methodologies, and any deviations from standard procedures. Collaborate with research and development (R&D) teams to support the development of new products and the improvement of existing formulations. Manage the disposal of hazardous materials and chemicals in accordance with environmental and safety regulations, ensuring a safe laboratory environment. Perform analytical testing on raw materials, in-process samples, and finished products to ensure compliance with quality standards and regulatory requirements. Authors Change Controls and performs/updates documents, as required, (i.e., specifications in accordance with test method changes, component changes, qualification of alternate sourced drug substances) Analyzes and interprets test results Operates general analytical instruments during raw material, IP and FP testing such as: High Pressure Liquid Chromatography (HPLC) Ultra Performance Liquid Chromatography (UPLC) Gas Chromatography (GC) Ultra Violet visible spectroscopy (UV/Vis) automatic titration Infra-Red Spectroscopy (IR) Thin Layer Chromatography (TLC) dissolution apparatus (Distek) Creates and uses custom fields in Empower software while operating HPLC/UPLC and GC instruments Collaborates closely with R&D for analytical method transfer studies and other analytical method related issues. Assists/performs identification and troubleshooting of problems with instrumentation, analytical anomalies, and laboratory investigations. Authors Residual Solvent, Elemental Impurity and Nitrosamine risk assessments Authors or updates SOPs, as needed Meets project deadlines and performance standards, as assigned Complies with all company policies and procedures, including safety rules and regulations Performs other related duties and responsibilities, on occasion, as assigned Minimum qualifications: B.S. degree in Chemistry, or other related fields. 5 plus years job related experience in developing and validating analytical methods within the pharmaceutical or similar cGMP environment. Ability to maintain accurate records. Ability to apply existing work methods to different situations and solves problems ranging from recurring/routine to complex situations. About us:At Padagis our focus is on health care products that improve people's lives. We are a market-leading generic prescription pharmaceutical company that specializes in "extended topical" medications, like creams, foams, mousses, gels, liquids and inhalable products. It's a great time to join our team because we have a high growth trajectory with now more than 1,300 employees across six locations in the United States and Israel. We've already established a successful track record of launching first-to-file and first-to-market generic pharmaceutical products that have helped to make prescription products more affordable for patients and reduce costs for the healthcare system. Our team members work in a dynamic environment where opportunity is built on a foundation of honesty and transparency. Please consider joining our team where great things are happening and you can make a difference.What's Next:At Padagis a real recruiter AND the hiring manager will review your application, not just a bot. This means we pay special attention to each application submitted for the position. While it could take a couple of days for us to get back with you, please know that we appreciate you applying for the open position and ask that you monitor your email for updates.

ESSENTIAL FUNCTIONS To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Reasonable Accommodations may be made to enable qualified individuals with disabilities to perform the essential functions. Essential Functions: Conduct inspections at First Article, In-Process, and Incoming per inspection plans. Identify nonconforming material and initiate nonconforming reports per established procedures. Communicate effectively with management, operators, and Engineers about quality related concerns. Utilize inspection tools such as calipers, micrometers, micro-vu scope, scales, fixtures, gages, and microscopes to measure or inspect parts for compliance, CMM. Read and interpret blueprints and specifications Provide input on inspection methods related to continuous improvement initiatives related to the job. Assist quality, engineering and production personnel with investigations of part defects or any quality related issues. Complete accurate and legible reports on the in-process inspection plans. Organize work and storage areas for efficient workflow. Other duties may be assigned. POSITION QUALIFICATIONS High School Diploma or Associates DegreeExperience/abilities:2+ years of experience inspecting high precision mechanical components. •Broad experience using inspection tools such as calipers, micrometers, micro-vu scope, scales, fixtures, gages, and microscopes to measure or inspect parts for compliance. •Ability to read and interpret Engineering blueprints and specifications •Broad knowledge manufacturing processes necessary for mechanical components (stamping, forging, casting, machining, etc.) and electrical/electronic components •Experience with automotive PPAP processes is a plus •Ability to review and interpret First Article and In-Process inspection results •Strong quantitative, analytical, and problem-solving skills. •Strong verbal and written communication skills •Fluency in English mandatory