Quality Assurance Salary in Connecticut, USA

They key responsibilities of the Quality Systems Supervisor are: Quality Systems Oversight:Develop, implement, and maintain quality management systems to ensure compliance with industry standards and regulatory requirements.Monitor and evaluate the effectiveness of quality systems through audits, inspections, and performance metrics.Lead efforts to continuously improve quality processes, procedures, and documentation.Quality Assurance Leadership:Provide leadership and guidance to the quality assurance team, ensuring adherence to quality standards and objectives.Coordinate training programs to ensure staff competency in quality management systems and processes.Collaborate with cross-functional teams to resolve quality-related issues and implement corrective actions.Audit/Regulatory Compliance:Stay abreast of relevant industry regulations, standards, and best practices to ensure compliance.Lead efforts to obtain and maintain relevant ISO certifications and accreditations.Serve as the primary point of contact for regulatory agencies during audits and inspections.Supplier Quality Management:Develop and maintain relationships with key suppliers to ensure the quality of incoming materials and components.Establish supplier quality requirements and conduct supplier audits as necessary.Work closely with suppliers to address quality issues and drive continuous improvement.MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.The successful Quality Systems Manager will have the following:Bachelor's Degree 5+ years of Professional Experience in Manufacturing Environment Knowledge of ISO Standards ISO 9001, 13485, and AS9100Hands-on Inspection experience highly preferred Ability to communicate effectively with Customers and Suppliers If interested, please apply using the link below. Qualified applicants will be contacted within 24/48 hours of submittal.

Beacon Hill Life Sciences is actively recruiting for a Senior Manager of GCP Quality Assurance to work a contract assignment, part-time hours. Hours: Part-time, approximately 20 hours per weekDuration of assignment: 6 months with possibility of extensionFully remote is possible, preference is hybrid (Location: Cambridge, MA)Pay Rate is based on experience with range being $100 - $125/hourSummary: The Sr Manager, GCP Quality Assurance coordinates GCP Compliance activities with Clinical Operations, Regulatory Affairs, Clinical Supply & Logistics, Sample Management and Pharmacovigilance as well as varied vendors supporting Clinical Studies.This is a high visibility role and will be directly involved in development and continuous improvement of GCP Quality and overall Quality Management Systems. This individual will be responsible for coordinating with key stakeholders to develop/implement processes and systems governing GCP activities. Will be Subject Matter Expert in GCP Compliance with respect to planning, execution, and close-out Clinical Studies.Responsibilities include: Oversight of ongoing compliance of Clinical Studies. Act as GCP QA Program Lead while working with internal customers to ensure overall compliance from risk-based principles. Work with internal and external GCP customers and develop and execute strategic plans to identify, mitigate, monitor and report study risks and Quality Tolerance Limits on a per study basis. Assist in resolving compliance issues at clinical sites, clinical vendors, and laboratories and provide assessment of the impact of any deficiencies. Escalate issues through the Quality Organization as needed.GCP Vendor Audits and Oversight. Support the GCP Vendor Audit Schedule including CRO, Central and Specialty Laboratories, IxRS/IRT/Randomization liaising with QA Vendor Auditing. Coordinate with Study Team members to ensure vendor audits are appropriately scoped and that third-party auditors are provided all the documentation and insights required for successful audit execution. Review and approve submitted audit reports. Ensure audits were performed to internal standards. Ensure proposed CAPAs are adequate and executed properly.Clinical Investigator Site Audits. Manage the Clinical Investigator (CI) Site Audit program for assigned studies. Coordinate with Study Team members to determine CI sites to be audited per study via risk-based criteria. Coordinate with Study Team members and third-party auditors to ensure CI site audits are appropriately scoped and audit planned. Review and approve submitted audit reports. Ensure audits were performed to internal standards. Ensure proposed CAPAs are adequate and track to closure. Determine if CI Site audit observations may represent study-wide or program-wide risks and ensure Impact/Risk Assessments and Study-wide/Program-wide CAPAs are adequate.Quality Management System. Coordinate with Program Leads, Biostatistics, Data Management, Medical Affairs, Pharmacovigilance to develop/implement Phase appropriate procedures to ensure consistency and quality with respect to Clinical Trial support activities. Perform internal audits of processes and functional areas to ensure compliance with GCP, internal SOPs and other applicable regulations. Coordinate with Senior Management, Functional Area Leads, and third-party vendors, to plan and execute resolution to compliance gaps identified during mock inspections.Candidate Requirements:Bachelor's degree in the Life Sciences with 7+ years in pharmaceutical or biotech drug development. Advanced degree preferred.Minimum 3 years of experience in Clinical QA. Experience in auditing both Vendors and Clinical Investigator Sites a plus. Experience helping with phase 3 registrational study preferred. Demonstrated experience working with clinical trial teams.Extensive experience with Global Clinical trial conduct, knowledge and understanding of ICH E6 (R2) GCP Guideline, FDA Regulations and EU Requirements.Ability to evaluate and reorganize priorities quickly in a dynamic matrixed setting.Excellent interpersonal skills, personal integrity, professional manner and ability to gain respect and develop good working relationship with cross functional personnel at all levels.Experience helping with phase 3 registrational study preferred.Must be organized and ability to multi-task with multitude of different pieces.Beacon Hill is an Equal Opportunity Employer that values the strength diversity brings to the workplace. Individuals with Disabilities and Protected Veterans are encouraged to apply.If you would like to complete our voluntary self-identification form, please click here or copy and paste the following link into an open window in your browser: https://jobs.beaconhillstaffing.com/eeoc/Completion of this form is voluntary and will not affect your opportunity for employment, or the terms or conditions of your employment. This form will be used for reporting purposes only and will be kept separate from all other records. Company Profile:Founded by industry leaders to set a new standard in search, career placement and flexible staffing, we deliver coordinated staffing solutions with unparalleled service, a commitment to project completion and success and a passion for innovation, creativity and continuous improvement.Our niche brands offer a complete suite of staffing services to emerging growth companies and the Fortune 500 across market sectors, career specialties/disciplines and industries. Over time, office locations, specialty practice areas and service offerings will be added to address ever changing constituent needs.Learn more about Beacon Hill Staffing Group and our specialty divisions, Beacon Hill Associates, Beacon Hill Financial, Beacon Hill HR, Beacon Hill Legal, Beacon Hill Life Sciences and Beacon Hill Technologies by visiting www.beaconhillstaffing.com . We look forward to working with you!Beacon Hill. Employing the Future™

They key responsibilities of the Quality Systems Supervisor are:Quality Systems Oversight:Develop, implement, and maintain quality management systems to ensure compliance with industry standards and regulatory requirements.Monitor and evaluate the effectiveness of quality systems through audits, inspections, and performance metrics.Lead efforts to continuously improve quality processes, procedures, and documentation.Quality Assurance Leadership:Provide leadership and guidance to the quality assurance team, ensuring adherence to quality standards and objectives.Coordinate training programs to ensure staff competency in quality management systems and processes.Collaborate with cross-functional teams to resolve quality-related issues and implement corrective actions.Audit/Regulatory Compliance:Stay abreast of relevant industry regulations, standards, and best practices to ensure compliance.Lead efforts to obtain and maintain relevant ISO certifications and accreditations.Serve as the primary point of contact for regulatory agencies during audits and inspections.Supplier Quality Management:Develop and maintain relationships with key suppliers to ensure the quality of incoming materials and components.Establish supplier quality requirements and conduct supplier audits as necessary.Work closely with suppliers to address quality issues and drive continuous improvement.MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.The successful Quality Systems Supervisor will have the following:Bachelor's Degree5+ years of Professional Experience in Manufacturing EnvironmentKnowledge of ISO Standards ISO 9001, 13485, and AS9100Hands-on Inspection experience highly preferredAbility to communicate effectively with Customers and Suppliers

Job ID: 496083Ash Grove Cement, a CRH company, provides portland and masonry cements to help build the foundation and infrastructure for the world around us. We ship millions of tons of cement from our plants and network of terminals located across North America. When you work for Ash Grove, you are connecting to something bigger. Join our team and help Ash Grove build America.Position: Quality Control Technician Shift: 12-hour rotating swing shift 7:00 a.m. -7:00 p.m. ET and 7:00 p.m.- 7:00 a.m. ETAt Ash Grove Cement, people are our first priority. We offer a complete benefits package to include: Health Insurance Dental Insurance Vision Insurance 401k with company match and profit-sharing Paid Time Off, Paid Holidays, Paid Sick Time Tuition Reimbursement Employee Assistance Program Disability Pay Life Insurance Growth Opportunities and more! Summary:Under general supervision and accordance to established policies and procedures, assures and maintains the quality of all process samples, including but not limited to the collection of production samples, performance of production control tests and cement silo analysis, and accurate record keeping and documentation of all test results.What you'll be contributing: Promote and follow all plant safety guidelines. Observe all applicable safety policies and regulations. Complies with the plant sampling schedule of process samples, as determined by the Quality Control Manager. Collects representative raw mill product and kiln feed samples and conducts appropriate tests to ensure proper control and maintenance raw kiln feed chemistry according to quality targets. Performs formulation and raw mill feeder adjustments as needed to maintain quality targets. Collects representative clinker samples and conducts appropriate tests to ensure and maintain proper clinker chemistry according to quality targets. Collects representative finish mill samples, as well as conducts appropriate tests and finish mill feeder adjustments to ensure and maintain proper cement chemistry according to quality targets. Analyzes coal samples for fineness and moisture. Collects representative bag house dust samples and conducts appropriate tests at interval decided by the Quality Control Manager. Analyzes bottom stage samples for loss on ignition and oxide analysis and determines percent calcination of sample. Maintains accurate records in designated log books and locations for all testing performed and adjustments made. Checks grinding aid and masonry additive flow rates at intervals set by the Quality Control Manager. Reports problems observed in the plant and ensures all samplers are working properly. Works routinely with Control Room Operators and shift supervisors. Indirectly reports to shift supervisors on off-shifts. Communicates test results to production personnel and issues process and production change orders. Assists in maintaining lab reagents and supplies. Performs additional non-routine testing for process control and research when necessary. Responsible for housekeeping and clean-up of immediate work areas and sample areas or in other areas in conjunction with assigned duties. Responsible for documentation associated with job duties. As required assists in major plant repair projects. Additional duties as assigned by supervisor. To succeed in this position, you will need: High school graduation or equivalent is required Ability to read, write and understand warning labels, instructions, signs, etc. Willingness to learn, training will be provided Knowledge of and ability to comply with ASTM standards and testing procedures. Ability to analyze and interpret data, and make accurate corrections based on the data analyzed. Knowledge of basic math including addition, subtraction, multiplication and division. Must successfully complete on-the-job training provided by designated supervision or otherwise qualified individuals. Ability to accurately use all laboratory equipment used in performing various tests such as balances, burets, flasks, jet sieves, x-ray fluorescence, manometer, and other related equipment. Ability to use personal computer for record-keeping calculations. Must be familiar with spreadsheet and word processing software. Ability to stand for long periods of time, walk over rough and uneven surfaces and climb stairs. What to expect in a cement environment: Work to be performed in a shop environment as well as outdoor exposure throughout the plant. Mild exposure to cement dust, heat, cold, and noise requires compliance with specified safety guidelines and procedures. Exposure to high elevations of up to 250 feet in height. Exposure to all weather conditions. Normal operation of mobile equipment may result in jarring and vibratory exposure.What's next for you? We provide stability and advancement opportunities across North America. Use our tuition reimbursement program to help you meet your career goals.This job description in no way states or implies that these are the only duties to be performed by the employee occupying this position. The employee will be required to follow all job instructions of his/her supervisor and to perform other work assignments related to plant operations that are not inconsistent with the current labor contract, past practices, or safety policies. What CRH Offers You Highly competitive base pay Comprehensive medical, dental and disability benefits programs Group retirement savings program Health and wellness programs A culture that values opportunity for growth, development, and internal promotion About CRH CRH has a long and proud heritage. We are a collection of hundreds of family businesses, regional companies and large enterprises that together form the CRH family. CRH operates in a decentralized, diversified structure that allows you to work in a small company environment while having the career opportunities of large international organization.If you're up for a rewarding challenge, we invite you to take the first step and apply today! Once you click apply now, you will be brought to our official employment application. Please complete your online profile and it will be sent to the hiring manager. Our system allows you to view and track your status 24 hours a day. Thank you for your interest!Ash Grove Cement, a CRH company, is an Affirmative Action and Equal Opportunity Employer.EOE/Vet/Disability--If you want to know more, please click on this link .

Job ID: 496083Ash Grove Cement, a CRH company, provides portland and masonry cements to help build the foundation and infrastructure for the world around us. We ship millions of tons of cement from our plants and network of terminals located across North America. When you work for Ash Grove, you are connecting to something bigger. Join our team and help Ash Grove build America.Position: Quality Control Technician Shift: 12-hour rotating swing shift 7:00 a.m. -7:00 p.m. ET and 7:00 p.m.- 7:00 a.m. ETAt Ash Grove Cement, people are our first priority. We offer a complete benefits package to include: Health Insurance Dental Insurance Vision Insurance 401k with company match and profit-sharing Paid Time Off, Paid Holidays, Paid Sick Time Tuition Reimbursement Employee Assistance Program Disability Pay Life Insurance Growth Opportunities and more! Summary:Under general supervision and accordance to established policies and procedures, assures and maintains the quality of all process samples, including but not limited to the collection of production samples, performance of production control tests and cement silo analysis, and accurate record keeping and documentation of all test results.What you'll be contributing: Promote and follow all plant safety guidelines. Observe all applicable safety policies and regulations. Complies with the plant sampling schedule of process samples, as determined by the Quality Control Manager. Collects representative raw mill product and kiln feed samples and conducts appropriate tests to ensure proper control and maintenance raw kiln feed chemistry according to quality targets. Performs formulation and raw mill feeder adjustments as needed to maintain quality targets. Collects representative clinker samples and conducts appropriate tests to ensure and maintain proper clinker chemistry according to quality targets. Collects representative finish mill samples, as well as conducts appropriate tests and finish mill feeder adjustments to ensure and maintain proper cement chemistry according to quality targets. Analyzes coal samples for fineness and moisture. Collects representative bag house dust samples and conducts appropriate tests at interval decided by the Quality Control Manager. Analyzes bottom stage samples for loss on ignition and oxide analysis and determines percent calcination of sample. Maintains accurate records in designated log books and locations for all testing performed and adjustments made. Checks grinding aid and masonry additive flow rates at intervals set by the Quality Control Manager. Reports problems observed in the plant and ensures all samplers are working properly. Works routinely with Control Room Operators and shift supervisors. Indirectly reports to shift supervisors on off-shifts. Communicates test results to production personnel and issues process and production change orders. Assists in maintaining lab reagents and supplies. Performs additional non-routine testing for process control and research when necessary. Responsible for housekeeping and clean-up of immediate work areas and sample areas or in other areas in conjunction with assigned duties. Responsible for documentation associated with job duties. As required assists in major plant repair projects. Additional duties as assigned by supervisor. To succeed in this position, you will need: High school graduation or equivalent is required Ability to read, write and understand warning labels, instructions, signs, etc. Willingness to learn, training will be provided Knowledge of and ability to comply with ASTM standards and testing procedures. Ability to analyze and interpret data, and make accurate corrections based on the data analyzed. Knowledge of basic math including addition, subtraction, multiplication and division. Must successfully complete on-the-job training provided by designated supervision or otherwise qualified individuals. Ability to accurately use all laboratory equipment used in performing various tests such as balances, burets, flasks, jet sieves, x-ray fluorescence, manometer, and other related equipment. Ability to use personal computer for record-keeping calculations. Must be familiar with spreadsheet and word processing software. Ability to stand for long periods of time, walk over rough and uneven surfaces and climb stairs. What to expect in a cement environment: Work to be performed in a shop environment as well as outdoor exposure throughout the plant. Mild exposure to cement dust, heat, cold, and noise requires compliance with specified safety guidelines and procedures. Exposure to high elevations of up to 250 feet in height. Exposure to all weather conditions. Normal operation of mobile equipment may result in jarring and vibratory exposure. What's next for you? We provide stability and advancement opportunities across North America. Use our tuition reimbursement program to help you meet your career goals. This job description in no way states or implies that these are the only duties to be performed by the employee occupying this position. The employee will be required to follow all job instructions of his/her supervisor and to perform other work assignments related to plant operations that are not inconsistent with the current labor contract, past practices, or safety policies. What CRH Offers You Highly competitive base pay Comprehensive medical, dental and disability benefits programs Group retirement savings program Health and wellness programs A culture that values opportunity for growth, development, and internal promotion About CRHCRH has a long and proud heritage. We are a collection of hundreds of family businesses, regional companies and large enterprises that together form the CRH family. CRH operates in a decentralized, diversified structure that allows you to work in a small company environment while having the career opportunities of large international organization.If you're up for a rewarding challenge, we invite you to take the first step and apply today! Once you click apply now, you will be brought to our official employment application. Please complete your online profile and it will be sent to the hiring manager. Our system allows you to view and track your status 24 hours a day. Thank you for your interest! Ash Grove Cement, a CRH company, is an Affirmative Action and Equal Opportunity Employer.EOE/Vet/Disability--If you want to know more, please click on this link. Date: Apr 15, 2024 Nearest Major Market: Lake City Job Segment: Testing, Maintenance, Technician, Technology, Manufacturing

Overview The symplr Quality Assurance Specialist performs a critical role in auditing all phases of provider enrollment on behalf of medical providers with commercial and/or government payers. Duties & Responsibilities Audit data entry, CAQH, follow up logs/calls, enrollment applications, link letters and spreadsheets for accuracy and completeness based on internally documented standards and payer standards. Provide feedback to our enrollment team managers in a courteous and confidential manner. Maintain necessary logs, lists, records, and current documentation required for internal audits. Provide routine follow up and status confirmation of audits pending corrections. During auditing, identify and record trends to contribute to process improvement efforts in both quality and efficiency. Maintain relationships with payer representatives and clients as required. Respond to all external/internal inquiries in a timely manner. Participate in team meetings and process improvement initiatives to continuously improve work product quality and efficiency. Performs other duties as assigned. Skills Required Highly self-motivated, preferably with some expertise with payer enrollment process for all levels of licensure including but not limited to MD/DO, NP, PhD, PT, OT, LCSW, OD, DDS, DPM, etc. across all specialties including medical, dental, vision, behavioral health, and physical health. Success-driven and results-oriented, with the ability to implement and manage cross-functional projects Proficiency with credentialing systems and learns new systems/processes quickly Familiarity using payer websites including but not limited to CAQH, Pecos, NPI/NPPES, Availity, Navinet, CMS I&A Ability to interact effectively with a variety of people (such as physicians, medical staff offices and Health plans) Provides highest level of customer service for both internal and external customers Strong written and verbal communication skills, along with strong presentation and client interaction skills Ability to prioritize tasks and projects. Accurate discernment on when to act independently and when to ask for guidance and/or assistance Consistently demonstrates flexibility, a customer-focus, terrific organizational skills and a passion for details Qualifications Required: Every organization has a culture, whether they mean to or not, so why not be intentional about it?Together, if we shape our intentions, actions, and interactions around a common, purposeful culture, we are able to quickly achieve more, attract others who help realize our goals, and thrive in our professional relationships. Associate degree or an equivalent combination of education and/or experience in healthcare 3+ years of Payor Enrollment Experience. Preferred experience in managed care, provider credentialing, patient financial services or provider relations Prior data management/data integrity experience preferred MinUSD $22.00/Hr. MaxUSD $25.00/Hr.

Job Summary:Perform Metallurgical Services functions through chemical analysis of heat samples, hot billet inspection and inventory control, and managing billet hot charging. Maintain and operate spectrometer, Leco analyzer, and related equipment to examine the chemical composition of heats from melting and casting. Disposition non conforming heats as needed. Maintain and operate the slag analyzer and related equipment for determination of slag composition in melting. Inspect hot billets at the caster for surface and dimensional conformity to orders. Coordinate hot charging of heats with the mill. Assess product grade change samples to maintain traceability during rolling. Record, verify and submit test and inspection results to supervisor.Primary Duties and Responsibilities:Prepare and perform chemistry tests for samples taken from EAF, ladle, and billets. Verify and discuss test results to Melter and check against product specifications.Work with the Melter to disposition non conforming heats or portions of heats. Inspect hot billets as they are cast for dimensions and quality and report results to the supervisor. Notify the operators of any non conformance.Maintain and operate pad grinder, cutoff saw, ARL spectrometer, Leco C/S analysis unit, slag analyzer and weigh scales.Calibrate equipment per schedule.Enter test results and sample information into personal computer.Coordinate hot charging of billets during rolling.Check heat samples for radiation.Assess grade change samples from the mill and alert supervisor of any discrepancies.Additional Responsibilities:Actively participate and support 5S initiatives in the work area.The above statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of personnel so classified.Requirements:Must be willing and able to work a rotating shift1-2 years experience in a quality role preferredHigh school diploma or GEDBasic Computer SkillsPrior experience operating/maintaining spectrograph and other related lab testing equipment.Knowledge of physical and chemical metallurgy test procedures and recording routines.

Aegis is partnering with a company who is looking for a Quality inspector to come join their team!Pay Rate:$22 - $29/hr DOE!!Shift Diff:15% shift differential for any off shiftPTO: 2 WeeksTechnical:ERP System ExperienceExperience with any ERP Will SufficeIdeally Someone with at Least 2 Years experience and good tenure3 Big Things This Person Must Have Skillset / EXP Wise on Day One:GD&T / Blueprint ReadingGood TenureCan Operate Machining EquipmentVision System / CMM ExperienceAttention to Detail.QUALIFICATIONS:EducationHigh school diploma, GED, or equivalent directly transferrable work experience (Manufacturing or Engineering discipline preferred).ExperienceMinimum of 0-2 years' experience in a regulated manufacturing environment.

This is what you will do: The Development Scientist I position is a technical position responsible for development and optimization of release and stability methods including physicochemical methods pertaining to Imaged Capillary Electrophoresis (icIEF) as well as traditional Gel/Capillary Electrophoresis (CE-SDS, CIEF, CZE, IEF and SDS-PAGE) as well as support for chromatography charge separation (IEX) for clinical and commercial biotherapeutics. This position will also support other analytical method development related to characterization and investigation efforts, as well as conduct testing for Alexion's biotherapeutic products when required. Participation in method validation and transfer or troubleshooting of methods to internal and external laboratories may be required. In addition, this position is expected to interact regularly with scientific staff in other Research & Development groups as well as Manufacturing, Quality Assurance and Quality Control groups.You will be responsible for: Development, optimization, and phase-appropriate qualification of custom capillary electrophoresis methods to evaluate key quality attributes for therapeutic proteins (charge heterogeneity, primary structure, PTMs, size variant, etc.)Organizing activities of self and others as well as supervise operation, maintenance and troubleshooting of analytical instrumentation (e.g., Revvity LabChip, Protein Simple iCE3 and MauriCE)Supporting application of new innovative technologies to improve throughput and enhance capability of cGMP testingAuthoring SOPs, study plans, protocols, and method development reports. Draft reports for regulatory filingWorking with various Research and Development teams to support transfer of analytical test methods for development and clinical support.Collaborating with Analytical Technical Transfer Services (ATTS) to develop and execute validation protocols, provide support during and post method transfer (e.g. on-site training and troubleshooting as needed)Maintaining knowledge of current scientific principles and theories. Train other lab personnel as assigned in areas of expertise and participate in cross-functional process development teamsSeeking out and evaluate new instruments, methods, techniques, and technology platforms to enhance analytical operationsYou will need to have:Ph.D. degree or master's degree with equivalent level of experience, in Chemistry, Biochemistry, Chemical Engineering or related discipline.Analytical method development experience in protein/peptide analysis by gel/capillary electrophoresis in pharmaceutical or biotechnology company is a plus.Scientific and practical knowledge of protein characterization for protein therapeutics including monoclonal antibodies and glycoproteins.Experience with assay development, optimization, qualification, and validation for protein therapeutics is a significant plus.Ability to take initiative in problem solving and consistently bring independent, scientific approach to method development.Knowledge of cGMP and quality guidelines is desired.Ability to travel up to 20% to support on-site training and troubleshooting.The duties of this role are conducted in a lab environment. As is typical of a lab-based role, employees must be able, with or without an accommodation to: lift/carry 15/30 pounds unassisted/assisted; work comfortably in a controlled environment with and around biological, infectious, and hazardous materials; gown/degown PPE; use a computer; engage in communications via phone, video, and electronic messaging; engage in problem solving and non-linear thought, analysis, and dialogue; collaborate with others; maintain general availability during standard business hours.We would prefer for you to have:Experience with assay development, optimization, qualification, and validation for protein therapeutics.Excellent people skills and a strong ability to communicate effectively.Knowledge of cGMP and quality guidelines (e.g., ICH Q2 and ICH Q14)High level of proficiency in MS Office software including Word, Excel, Outlook, Visio, and PowerPointThe ability to accurately and independently contribute and oversee the generation of procedures, protocols and reports pertaining to test methods.The ability to manage and lead projects independently, drive CE method development strategies, improve quality and efficiency of workflows, provide scientific guidance to team members, and train and oversee some day-to-day responsibilities of junior scientists.Ability to lead and participate in cross-functional development teams representing Analytical Development and Quality Control.Experience with authoring and reviewing CMC sections for regulatory, technical reports, department specific protocols and reports and generating operating procedures is a significant plus.Expectation of working in the office 4 days a week statement: When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working give us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of four days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world. AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.

SUMMARY: Management Business Solutions is seeking a Quality Control Supervisor for its client in Danbury, CT. The role involves overseeing quality inspections, coordinating testing procedures, and implementing continuous improvement initiatives to enhance product quality and efficiency.RESPONSIBILITIES:Coordinate routine quality inspections and testing to ensure product compliance.Analyze data to identify improvement areas and implement necessary actions.Collaborate with cross-functional teams to resolve quality issues and drive improvements.Manage QC documentation and participate in audits to ensure compliance.Stay updated on industry trends and regulations to ensure continuous improvement.QUALIFICATIONS:Bachelor's degree in Chemistry, Biology, Pharmacy or any relevant scientific field.5+ years of experience in quality control or related roles within the pharmaceutical or biotech industry. OR Master's degree with at least 3 years' experience, or equivalent combination of experience and training.Experience in pharmaceutical or laboratory settings is preferred.Proficient in Microsoft Office tools.Excellent interpersonal and organizational abilities.Demonstrated supervisory experience.MANAGEMENT BUSINESS SOLUTIONS IS AN EQUAL-OPPORTUNITY EMPLOYER