Quality control analyst jobs in Rhode Island

Neurotech Pharmaceuticals, Inc. is a private biotech company located in Cumberland, RI and Needham, MA, within the realm of Greater Boston's vast biotechnology landscape. Since our inception more than 20 years ago, our focus has been on developing and commercializing transformative therapies for chronic eye diseases. The core platform technology, Encapsulated Cell Therapy (ECT), is a first-in-class drug delivery platform designed to slow the progression of chronic eye diseases. Neurotech's first commercial product, ENCELTOTM (revakinagene taroretcel-lwey), is approved in the United States for the treatment of adults with idiopathic Macular Telangiectasia Type 2 (MacTel). Encapsulated cell-based gene therapy is designed to provide long-term, sustained delivery of therapeutic proteins for the treatment of chronic eye diseases.

Do you want to make a positive difference in the lives of people that are challenged with mental illness and substance use disorders? Do you want to join a high-performing team of dedicated professionals who work effectively together, have fun, and share the joy of truly making the word a better place? Through the dedication and commitment of our staff, Thrive's clients receive the highest quality of care available, incorporating proven, effective treatment for substance use and mental health disorders. The ideal candidate will be results-driven, team-and detail-oriented professional who is comfortable working on multiple tasks in a deadline-oriented environment. Responsibilities: Meet with clients to data enter client registration information and conduct client orientation prior to the initial assessment. Obtain all necessary documents for enrollment as a Thrive Organization client and prepare clinical record. Review assessments, treatment plans, and discharges for completeness, conduct EHR audits as assigned, and maintain computerized client database. Process all requests and inquires for client information and release information in accordance with all federal and state laws as well as Organization policies, standards and procedures. Stay current on rules and regulations related to privacy, security, and recordkeeping practices. Respond to questions regarding confidentiality and release of information. Prepare records subpoenaed in accordance with Organization protocols. Process transcribed reports from the vendor in accordance with the Department's Standards and Procedures. Retrieve client records for appointments and audit per Organization procedure. Maintain sign-out system of records and re-file client records as necessary. Accurately file or scan client information in accordance with established systems. Identify duplicate records and merge when identified according to procedure with 100% accuracy. Refile client records as necessary and in accordance with established systems. Assist in review and audit procedures conducted by the HI/QI Department. Assist in the completion of various department projects. Review e-mail account daily for new messages. Requirements: High school graduate with one year secretarial/office certification program Two years' experience in a computerized medical or behavioral health office environment Benefits: Thrive Behavioral Health provides a friendly/family working environment, whose values include Dignity, Respect, Teamwork and Professional Support and Development. Thrive offers generous benefits after 30 days, PTO, paid holidays, your birthday off, and a 401k plan. ****************** No Phone Calls EEO/VET/LGBTQ+ Employer

Job Description Senior Scientist, Analytical Chemistry & Quality Control Salary: $100,000-$130,000 FLSA Status: Exempt We are on the search for a Senior Scientist to join our team at Pharmaron's manufacturing site in Coventry, RI. In this position, the Senior Scientist, Analytical will support process chemistry and manufacturing activities through analytical method development, optimization, validation, and transfer in compliance with all applicable guidelines. Primary Responsibilities: Develop, optimize and validate analytical methods that are GMP friendly based on quality-by-design and document formal protocols and reports. Participate in method transfer activities, including writing protocols and reports. Perform stability testing and data trending, as required. Review and Approval of Scientific Reports and SOPs. Manage analytical projects, coordinate analytical activities and ensure the project timelines are met. Implementing new analytical techniques and strategies to expand departmental capabilities. Solving multiple complex scientific problems. Ensuring adherence to GMP. Presenting and communicating clearly and effectively with clients. Experience and Education: PhD in Chemistry with 2 years of experience or MSc/BS in Chemistry or related field with 6 years of experience with the following instrumentation: HPLC, GC, NMR, FTIR, UV. Excellent communication skills, both verbal and written. Effective in managing multiple competing activities and delivering to timelines. Ability to work in a cross-functional environment. Working knowledge of cGLP/cGMP and applicable FDA, EMA, and ICH guidance preferred. High level of awareness of innovative technologies and ability to adapt to in-house needs. Why Pharmaron? Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process. With over 21,000 employees and operations in the U.S., U.K., and China, Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China. Collaborative Culture: You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. Our core cultural values are "Employees Number One" and "Clients Centered," setting Pharmaron apart from other organizations. Benefits: As part of our commitment to your well-being, we offer a comprehensive benefits package, including: Medical, Dental & Vision Insurance with significant employer contributions. Employer-funded Health Reimbursement Account. Healthcare & Dependent Care Flexible Spending Accounts. 100% Employer-paid Employee Life and AD&D Insurance. Short- and Long-Term Disability Insurance. 401(k) plan with generous employer match. Access to an Employee Assistance Program. Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today! As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences. #ED-L1

Employment Type: Contract Business Unit: ARI QC Bioanalytics Duration: 2+ years (with likely extensions) Notes: Only qualified candidates, please. Targeting candidates with 4-6 years of industry/ non academia experience and some Capillary electrophoresis experience 3 Key Consulting is hiring a Quality Control Senior Associate for a consulting engagement with our direct client, a leading global biopharmaceutical company. Job Description: Quality Control Separation Sciences lab is searching is for an team member to support testing for routine, in-process, and stability samples. This person will be responsible for working in the Quality Control laboratory, using GMPs and GDPs to execute analytical testing. The ideal candidate enjoys tackling challenges and excels at time management with attention to detail. Responsibilities will include, but are not limited to: Performing analytical testing for CE (capillary electrophoresis, SDS-PAGE, polysorbate extraction and other general chemistry testing. Interacting cross-functionally with a wide variety of people and teams; Troubleshoot, solve problems and communicate with stakeholders. Participate in initiatives and projects that may be departmental or organizational in scope. Evaluate lab practices for compliance and operational excellence on a continuous basis. Basic Qualifications: 4-6 years of experience in capillary electrophoresis and/or quality control setting Bachelors Degree in any science field Demonstrated experience in investigations and QC processes Self-motivated, strong organizational skills and ability to manage multiple tasks at one time with minimal supervision Strong communication skills (both written and oral), facilitation and presentation skills Understanding and application of principles, concepts, theories and standards of GMP QC analytical laboratories, preferably with GMP experience Understanding of biopharmaceuticals process and related unit operations Strong analytical skills with the ability to collect, organize, analyze, and disseminate significant amounts of information with attention to detail and accuracy Independent, self-motivated, organized, able to multi-task in time-sensitive environments. Top Must-Have Skill Sets: Capillary Electrophorese and/or Empower experience preferred Teamwork and collaborative mind set Must have Quality Control lab experience and understanding of GMP expectations HPLC and UPLC experience Day to Day Responsibilities: Routine and non-routine testing Maintain training maintain laboratory workspace Review documents Red Flags: R&D experience only Frequent job changes Interview process: Video conference call (webex) with manager and/or potential team member Second interview with team if required (webex) We invite qualified candidates to send your resume to **************************. If you decide that you're not interested in pursuing this particular position, please feel free to take a look at the other positions on our website ******************************* You are also welcome to share this opportunity with anyone you think might be interested in applying for this role. Regards, 3KC Talent Acquisition Team

+ Highly trainable and eager to learn new technologies and processes. **Must Have Skill Sets:** + Demonstrated ability to work independently and deliver right first-time results + Focus on data integrity and cGMP practices + Experience with analytical laboratory testing with the ability to plan and perform routine tasks with efficiency and accuracy. **Day to Day Responsibilities:** + Execute routine work orders and interact routinely with end customers and vendors, ensuring reliable QC equipment support in a fast-paced environment. + Own change controls for new and/or replacing of QC equipment. + Manage the procurement of new QC equipment. Work autonomously to lead cross-functional stakeholders to identify end-user requirements, establish validation requirements and Change Control strategy. + Supports inspection readiness activities across Quality Control, and site audits and inspections. + Monitor and trouble shoot analytical benchtop equipment. + Lead projects and project planning responsibilities to ensure on time implementation of analytical instruments. Responsible to implement projects on time and on budget. + Complete all assigned tasks on time, in collaboration with key stakeholders. + Provide oversight of vendor PMs. + Create new assets and PM scheduling in Maximo. + Obtain end user requirement and vendor quotes for lifecycle replacement of equipment. **Basic Qualifications:** + High school/GED + 2 years work experience OR + Associates and 6 months work experience OR + Bachelors **About US Tech Solutions:** _US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit_ _************************ _._ _"US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran"_

WHY WORK AT SILK TITLE CO. Silk Title Co. is a privately owned, fast-growing company which handles billions of dollars a year in real estate transactions for some of the nation's top fin-tech institutions. Our motto, Service at Scale, combines our technology, proprietary processes, and talented team to deliver title insurance, search, and settlement services across the nation. We recently completed the expansion of our office in Warwick, RI into a brand-new modern workspace and dedicated employee flex space and training room. We plan to bring on new hires as we continue our growth . Stuffy cover letters and fancy sounding resumes are not our thing. We want people with focused energy, solid work ethic and curious minds capable of absorbing everything we can teach about our business. Our employees are what make our company exceptional; we are a diverse team of problem solvers, QA experts, and business process gurus. We all depend on each other which is why everyone brings their A game each day. We work hard but also know how to incorporate some fun through team building challenges, staff meetings and an abundance of swag. Our workplace exemplifies our core values of quality, communication, experience, transparency, and respect. Other benefits include: Positive work environment where individual and team contributions are recognized and rewarded. Brand New Modern Workspace Dedicated Employee Flex Space and Training Room Tech focused environment Health Benefits Paid time off Employee Assistance Program 401k Pay range: $17-$21/hr., eligible for overtime. Business hours are 9am until 10pm THE POSITION: Recording/ Quality Control Specialist We are currently looking for top talent to fill our role of Recording/ Quality Control Specialist. The Recording/ Quality Control Specialist works as part of a team to ensure that all closing conditions, as laid out by the lender or their investor, are met after signing and that all transactions are disbursed timely as scheduled. ESSENTIAL RESPONSIBILITIES OF THE RECORDING/ QUALITY CONTROL SPECIALIST INCLUDE BUT ARE NOT LIMITED TO: Responsible for the daily workflow within the department and may include Reviewing, processing, or servicing of loan documentation Ensuring that all work has been completed and departmental deadlines have been met Responsible to understand and comply with bank policies and federal, state, and other governmental rules and regulations for multiple banks in multiple states Open packages, confirm contents, and distribute work based on what packages have arrived Responsible for quality control review of received packages Communicate and resolve any discrepancies on required documents Scan packages into Resware, confirm documents have been uploaded, and organize file per department standards Prepare and box original package for FedEx delivery to final destination Collaborate with the Funding department to ensure timely funding of completed packages Manage the Post-Closing inbox, ensuring to communicate with clients in a timely manner via telephone or email Review reporting and follow-up on files pending funding to ensure needed documents and corrections have been resolved Resolve any problems, issues or questions, both verbally and in writing, to ensure customer satisfaction and to maintain productive relationships with other bank departments. Participates in other duties as assigned. **The Recording Specialist must live within a commutable distance to the Warwick, RI office.**

Located in Bristol, Rhode Island for 50 years, Tri-Mack is a leading manufacturer of high-temperature thermoplastic components for the aerospace-defense, semiconductor, energy and medical industries. Our broad capabilities include collaborative engineering, tool making, injection molding, thermoplastic composite processing, multi-axis CNC machining, bonding and assembly, testing and quality control - all within a modern, environmentally controlled 60,000 sq. ft. facility. Our culture is based on values that promote respect, teamwork and accountability and we are committed to meeting customer requirements through our ISO 9001/AS9100 quality management system. PLEASE NOTE - Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time Position: Quality Control Technician / Inspector Summary: This position is responsible for inspecting and documenting incoming material and finished parts, and performing detailed 1st piece inspections as well as final inspections. It requires good working knowledge of standard measurement tools such as micrometer, calipers, height gages, and optical comparator. The position also requires completing documentation, use of our CMM system to verify parts and familiarity with blueprint reading related to highly-engineered parts and assemblies. Responsibilities & Accountabilities: Perform first piece inspection, in process and final inspection; Perform receiving inspection, validate quality of purchased and manufactured materials, parts and components as per set acceptance criteria, determining conformance to prints and specifications. Provide assistance in the performance of any other quality functions as defined in the Quality Manual, such as gauge calibration, inventory, and nonconforming parts assessment. Pursue opportunities to develop new skills both within the department and across departmental lines, beginning in CNC and learning other operations and processes as part of your onboarding and ongoing development. Investigate product quality issues and determine root cause and corrective actions Assist Lead Quality Technician in pre-inspection and screening; Ensure Production employees understand drawings and parts measurement. Perform process capability studies and periodic SPC data input. Maintain organized quality records and correspondence. Assist with both internal and external audits. Work with Engineering and Production to address any product issues. Record all measurements and findings in the appropriate documentation (Visual Manufacturing, Excel, customer files, etc.) Maintain safe operations by adhering to safety procedures and regulations. Conduct yourself in an ethical and professional manner, show respect for your fellow workers and all company and personal property, and follow Tri-Mack values - Respect, Teamwork, Integrity, Accountability, and Durability. Show up to work on time and adhere to the schedule agreed upon by you and your supervisor. Get along with your co-workers, and support others as needed. Adhere to all AS9100 requirements as per work instructions and your team leader and manager. All other duties as assigned. Education, Skills & Experience: High School diploma required. Some college-level coursework preferred. 2+ years working in a Quality Control position in a manufacturing environment. Experience with manual micrometers, calipers and optical comparators. Vision system inspection experience a plus. Demonstrated written and oral communication skills Ability to analyze and prioritize information. Must be able to work independently. Use of computers and Microsoft Word, Excel and Outlook. Our Benefits: We offer competitive salaries and generous benefits, including: 40 hour week - Monday-Friday, overtime available Generous Medical, Life, Dental and Vision Insurance programs Paid Time Off, Paid Holidays, Sick & Safe Leave 401(k) with Company Match Tuition Reimbursement If you are looking for an innovative, values-driven company where you can put your quality-focused aptitude and expertise to work, grow your career and take on ever-bigger challenges, you may just have found the place! We know our continued success is dependent upon our employees, which is why we are always on the lookout for reliable, knowledgeable and dynamic individuals with past success in a collaborative team setting, working with clear objectives and direction. *Tri-Mack Plastics provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status or genetic information. Tri-Mack is a drug-free work environment. Pre-employment drug screening (excludes THC) and background checks are required.

Tremco Construction Products Group brings together Tremco CPG Inc.'s Commercial Sealants & Waterproofing and Roofing & Building Maintenance divisions; Tremco Barrier Solutions Inc.; Dryvit, Nudura, and Willseal brands; Prebuck LLC; Weatherproofing Technologies, Inc.; Weatherproofing Technologies Canada and PureAir Control Services, Inc. Altogether, Tremco CPG companies operate 21 manufacturing facilities, 6 distribution sites, and 3 R&D/ R&D/technology sites, and employ more than 2,700 people across North America. GENERAL PURPOSE OF THE JOB: Performs visual and physical inspection, sampling, testing, and control of parts, products, and raw materials to conform to established specifications, applicable standards, and the ISO 9001 Quality System. ESSENTIAL DUTIES AND RESPONSIBILITIES: Follows the established quality control procedures to ensure all products are manufactured in compliance with IMS, customer specifications, ISO9001:2015, and ISO14000-2015. Conducts the inspection and testing of raw materials and products, both in process and finished. Performs color quality control and corrections by interpreting results obtained using appropriate measurements. Inspects, calibrates, and supervises the use of various instrumentation for testing. Performs data analysis and provides feedback and improvement suggestions to plant personnel, production management, QC Supervisor, and Quality Assurance Manager on all issues concerning quality. Maintains Quality Control documents and daily reporting of information. Assists in complaint investigations by performing tests to detect or duplicate issues observed in the field. Assists in troubleshooting machine functions and production issues as they arise. Maintains a clean and organized work area. Performs other duties as assigned. EDUCATION REQUIREMENT: High school diploma or general education degree (GED). EXPERIENCE REQUIREMENT: A minimum of 1-2 years of experience in a quality control role within a manufacturing environment with oversight of both raw materials and finished goods. OTHER SKILLS, ABILITIES, AND QUALIFICATIONS: Microsoft Office Suite. Previous experience using enterprise software such as SPA is preferred. PHYSICAL DEMANDS: Incumbent must be able to stand, walk, sit, use hands, reach, climb, balance, kneel, talk, hear, and lift up to 50 lbs. BENEFITS AND COMPENSATION: The hourly rate for applicants in this position generally ranges between $19.57 and $23.00. This range is an estimate, based on potential employee qualifications, operations, needs, and other considerations permitted by law. The Company offers a variety of benefits to its employees, including but not limited to health insurance, paid holidays, paid time off, 401(k) Savings and Trust & Plan with company match, Company Pension Plan, Performance-Based Bonus/Commission, and continuing education. All qualified applicants will receive consideration for employment without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

Tremco Construction Products Group (CPG), part of RPM International Inc., unites industry-leading building envelope solutions manufacturers, service providers, and trusted brands-including Tremco, Nudura, Dryvit, Willseal, Weatherproofing Technologies, Inc., and Weatherproofing Technologies Canada-to deliver comprehensive, integrated building systems. With operations spanning North America, Europe, Asia-Pacific, India, and Latin America, Tremco CPG has a global presence supported by regional businesses and distributors who understand local market needs for commercial, industrial, and residential construction and restoration projects. GENERAL PURPOSE OF THE JOB: Performs visual and physical inspection, sampling, testing, and control of parts, products, and raw materials to conform to established specifications, applicable standards, and the ISO 9001 Quality System. ESSENTIAL DUTIES AND RESPONSIBILITIES: Follows the established quality control procedures to ensure all products are manufactured in compliance with IMS, customer specifications, ISO9001:2015, and ISO14000-2015. Conducts the inspection and testing of raw materials and products, both in process and finished. Performs color quality control and corrections by interpreting results obtained using appropriate measurements. Inspects, calibrates, and supervises the use of various instrumentation for testing. Performs data analysis and provides feedback and improvement suggestions to plant personnel, production management, QC Supervisor, and Quality Assurance Manager on all issues concerning quality. Maintains Quality Control documents and daily reporting of information. Assists in complaint investigations by performing tests to detect or duplicate issues observed in the field. Assists in troubleshooting machine functions and production issues as they arise. Maintains a clean and organized work area. Performs other duties as assigned. EDUCATION REQUIREMENT: High school diploma or general education degree (GED). EXPERIENCE REQUIREMENT: A minimum of 1-2 years of experience in a quality control role within a manufacturing environment with oversight of both raw materials and finished goods. OTHER SKILLS, ABILITIES, AND QUALIFICATIONS: Microsoft Office Suite. Previous experience using enterprise software such as SPA is preferred. PHYSICAL DEMANDS: Incumbent must be able to stand, walk, sit, use hands, reach, climb, balance, kneel, talk, hear, and lift up to 50 lbs. BENEFITS AND COMPENSATION: The hourly rate for applicants in this position generally ranges between $19.57 and $23.00. This range is an estimate, based on potential employee qualifications, operations, needs, and other considerations permitted by law. The Company offers a variety of benefits to its employees, including but not limited to health insurance, paid holidays, paid time off, 401(k) Savings and Trust & Plan with company match, Company Pension Plan, Performance-Based Bonus/Commission, and continuing education. All qualified applicants will receive consideration for employment without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

Do you look forward to a new challenge each day in a fast paced ever changing environment?Are you good at organizing information and are interested in working in a manufacturing environment? Do you enjoy using your skills and learning new ones and helping a team reach its goals? If you said yes, then our Quality Control Technician role at The Town Dock might be right for you! The Quality Control Technician is responsible for completing precise raw whole squid and prepared calamari product quality assessments, data entry, daily plant inspections, and equipment sanitation and calibration accuracy checks. Additional responsibilities include, but are not limited to, reporting quality and policy deviations, operating a fryer for calamari taste tests, and providing real-time feedback to the Operations team during in-line quality checks and boat unloading. Specific day-to-day activities depend on boat arrivals and catch volumes (hails). Responsibilities for this position include (but are not limited to): Complete daily pre-Operational (pre-op) sanitation plant inspections, environmental swabbing, and paperwork for the interior and exterior of the plant, communicate corrective actions to the Operations team leadership immediately, and verify the assigned corrective actions were done in the agreed-upon timeframe Complete cooler checks and associated paperwork twice per day and report any deviations immediately Sample and grade raw whole squid during processing and boat unloading against specifications, such as external quality, internal quality, appearance, aroma, texture, count per pound, weight, length, width, and others as needed Upload photographs of raw whole squid samples, enter all quality data to assigned computer location, and report results to assigned individuals the same day as the evaluation Conduct daily calibration accuracy checks for equipment such as thermometers and scales and report any deviations immediately Perform quality control assessments of prepared calamari products against specifications, such as appearance, aroma, texture, taste, count per pound, net weight, glaze percent, size, and defects Upload photographs of prepared calamari samples, enter all quality data to assigned computer location, and report results to assigned individuals the same day as the evaluation Check in-line samples and rework against specifications and report status to Operations immediately Fulfill sales samples requests by picking orders, packing them appropriately for the product and outside temperature, and arranging shipping and pick-up as needed Clean and sanitize work stations to standard regularly Perform other job-related duties as assigned. Requirements Ideal candidate will have: Associates degree in a science curriculum or work equivalent Prior experience in a quality control role, food industry experience preferred. Self-starter with organized and detailed work habits and excellent time management skills Driven to work collaboratively with a preventative mindset. Attention to detail. Ability to perform repetitive tasks Ability to be seafood HACCP certified Available to work a set 5-day schedule in Narragansett with opportunity for rotating on-call overtime as needed Ability to travel to New Bedford for a set rotating on-call summer schedule as needed Proficient math skills Proficient computer skills including MS Office, especially Excel Physical abilities: climb ladders to inspect equipment, lift 30 lbs., and stand for long periods of time in cool temperatures and wet manufacturing environments Flexibility in planning to accommodate the quick changes in seafood production Good communication skills (verbal and written) in English required, Spanish a plus A strong belief and commitment to continuous learning and improvement, positive attitude, teamwork, accountability and ethical behavior. Salary Description $20-$23/hour

JOIN THE TEAM! Under the supervision of our Operations Director, you will be trained to ensure all company standards are met and maintained at each individual location. We are looking for responsible individuals that: Will be reviewing daily store status reports Documenting and tracking store readiness per the given guidelines. Observing locations using video monitoring systems to ensure and report the given sales process are being followed. The individual must stay up-to date on all current sales promotions and processes. Requirements: High school diploma or general education degree (GED), required Ability to use video monitoring equipment Ability to interpret a variety of instructions furnished in written, oral or schedule form Ability to work on the internet, Spreadsheet, Presentation and Word Processing software Strong written and verbal communication skills Must have the ability to complete required applicable forms in English, which requires the ability to read and write in English. Ability to work well with others in fast paced, dynamic environment. Ability to be respectful, approachable and team oriented while building strong working relationships and a positive work environment. .

The Quality Control Technician will assist the Quality Control Supervisor with the implementation and monitoring of the Quality Management System (QMS). They will also be responsible for inspecting and auditing the manufacturing lines for proper product specification, product quality, and packaging quality. RESPONSIBILITIES AND DUTIES: The Quality Control Technician will: Assure the Edesia is adhering to all relevant international, state and local food manufacturing regulations and help to maintain BRC certification Monitor sanitation, safety regulations and procedures, GMPs and HACCP, FSMA and BRC Standards. Ensure and educate employees on food safety, BRC and quality standards; provide real time feedback to production line workers to make necessary corrections Perform on-line production floor checks at a minimum of every 2 hours throughout duration of shift. Sample and inspect finished product for safety, quality and organoleptic to assure compliance to customer specifications Check label and packaging for correct code dates, product size, clarity, product, and customer Conduct bench analysis for nutrient and physical parameters Prepare necessary laboratory titrations Record inspection and testing data such as weights, temperatures, package integrity checks, water activity, chloride, and vitamin C Perform ATP swabbing of surfaces and equipment Perform the daily Quality Pre-Operational line clearance inspections and documents the inspection Communicate issues and important information to the appropriate person immediately Peer review to confirm that all the documentation is recorded correctly (including sanitation paperwork and operation quality check paperwork) Collect and manage all finished product samples for micro testing, retains, sample library, and other analytical testing or customer requirements Check and record cooler temperature, once per shift Perform CCP verification checks Prepare and perform stability testing and analysis of finished products Identify and isolate finished product that does not meet standards Conduct GMP inspections throughout the facility and communicate findings to supervisor and staff Receive, sample, inspect and test bulk oil deliveries Maintain inventory of lab supplies, and order as needed Solve quality issues on the production floor when they arise Other QA tasks and production-support tasks as assigned

The QC inspector is responsible for ensuring that all products meet quality standards. This includes inspecting raw materials used in the production process, conducting tests on finished products and performing audits to identify potential areas of improvement. The QC inspector must be knowledgeable of the relevant safety regulations and have excellent attention to detail and problem-solving skills. Essential Functions Responsible for individual Inspection activities Undergo training when necessary Adhere to policies and procedures related to specific customer requirements Ability to understand specific directions and follow guidelines that are common throughout the department Ability to maintain a constant focus on quality and accuracy Ability to work with minimal supervision Specific competencies include but are not limited to following the Gowning, Personal Hygiene Procedures, and all other QC Inspection Work Instructions and SOPs including formatting Excel if required, Use of inspection equipment (Bench Linc, Vision Systems, Tensile Tester, Pin Gages, Ring Gages, Calipers, rulers, and Customer supplied fixtures) Perform Visual Inspection (using Tappi Chart) and Feel Testing. Operating the Annealing Ovens Obey all safety rules, use caution in work activities, and continuously practice safe behaviors Immediately report unsafe conditions/behaviors and work-related injuries to site supervision Qualifications Preferred High school diploma or equivalent 1 year of Product Operator experience necessary Experience within the department must be gained within 90 days for use of specific measuring equipment, displaying an understanding of the job requirements and any devices required to complete inspection/test activities Understand Quality Management System (QMS) requirements Training on the specific equipment must be fully completed within 90 days of hire Equivalent combination of education and experience is preferred An Affirmative Action / Equal Opportunity Employer Proterial Cable America, Inc. provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, genetic information, disability, or veteran status. As a Federal Contractor, we encourage priority referral of protected veterans under VEVRAA.

Neurotech Pharmaceuticals, Inc. is a private biotech company located in Cumberland, RI and Needham, MA, within the realm of Greater Boston's vast biotechnology landscape. Since our inception more than 20 years ago, our focus has been on developing and commercializing transformative therapies for chronic eye diseases. The core platform technology, Encapsulated Cell Therapy (ECT), is a first-in-class drug delivery platform designed to slow the progression of chronic eye diseases. Neurotech's first commercial product, ENCELTO TM (revakinagene taroretcel-lwey), is approved in the United States for the treatment of adults with idiopathic Macular Telangiectasia Type 2 (MacTel). Encapsulated cell-based gene therapy is designed to provide long-term, sustained delivery of therapeutic proteins for the treatment of chronic eye diseases. The QC Scientist Technical Services (QCTS) is responsible for the planning, coordination, and technical oversight of Neurotech's QCTS group. This role will lead the scheduling and execution of activities supporting both Quality Control Analytical operations and cross-functional initiatives with Commercialization Sciences. The incumbent will ensure the consistent availability, integrity, and traceability of all reference standards, assay controls, reagents, and other critical testing materials. This role combines technical leadership and hands-on scientific support to enable method development, method transfer, and continuous improvement initiatives across the QC and R&D interface. Job Requirements Oversee daily scheduling, prioritization, and execution of QCTS activities supporting QC Analytical operations. Lead the creation, qualification, and maintenance of reference standards, assay controls, and test reagents in compliance with GMP requirements. Ensure appropriate documentation, lifecycle management, and traceability of all QCTS materials. Collaborate closely with the QC Analytical, Commercial Sciences, and Process Development teams to support method development, method optimization, and transfer activities. Support new product development and characterization testing through technical expertise and resource management. Author, review, and approve technical documents including SOPs, protocols, reports, and investigations. Serve as a subject matter expert (SME) for analytical reagents, control systems, and reference material management. Train and mentor QCTS staff to ensure consistent performance, technical competency, and adherence to cGMP and GDP practices. Partner with Quality Assurance to ensure inspection readiness and continuous improvement of laboratory systems. Drive operational excellence by identifying and implementing process improvements in material management, documentation, and testing workflows. Education & Experience Bachelor's or Master's degree in Biology, Biochemistry, Biotechnology, or related scientific discipline. 6-10 years of progressive laboratory experience within Quality Control or Analytical Development, preferably in a biologics, cell therapy, or gene therapy environment. Demonstrated expertise in bioassay execution, analytical reagent management, and method lifecycle support. Proven leadership experience, with the ability to coordinate multidisciplinary teams and projects. Strong understanding of GMP, GLP, and data integrity requirements. Excellent technical writing, organizational, and communication skills. Experience with method development, transfer, and validation activities highly desirable. Prior supervisory or team lead experience preferred. Knowledge, Skills & Abilities Technical and Analytical Rigor Leadership and Team Development Problem Solving and Decision Making Cross-functional Collaboration cGMP Compliance and Documentation Excellence

Senior Scientist, Analytical Chemistry & Quality Control Salary: $100,000-$130,000 FLSA Status: Exempt We are on the search for a Senior Scientist to join our team at Pharmaron's manufacturing site in Coventry, RI. In this position, the Senior Scientist, Analytical will support process chemistry and manufacturing activities through analytical method development, optimization, validation, and transfer in compliance with all applicable guidelines. Primary Responsibilities: Develop, optimize and validate analytical methods that are GMP friendly based on quality-by-design and document formal protocols and reports. Participate in method transfer activities, including writing protocols and reports. Perform stability testing and data trending, as required. Review and Approval of Scientific Reports and SOPs. Manage analytical projects, coordinate analytical activities and ensure the project timelines are met. Implementing new analytical techniques and strategies to expand departmental capabilities. Solving multiple complex scientific problems. Ensuring adherence to GMP. Presenting and communicating clearly and effectively with clients. Experience and Education: PhD in Chemistry with 2 years of experience or MSc/BS in Chemistry or related field with 6 years of experience with the following instrumentation: HPLC, GC, NMR, FTIR, UV. Excellent communication skills, both verbal and written. Effective in managing multiple competing activities and delivering to timelines. Ability to work in a cross-functional environment. Working knowledge of cGLP/cGMP and applicable FDA, EMA, and ICH guidance preferred. High level of awareness of innovative technologies and ability to adapt to in-house needs. Why Pharmaron? Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process. With over 21,000 employees and operations in the U.S., U.K., and China, Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China. Collaborative Culture: You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. Our core cultural values are "Employees Number One" and "Clients Centered," setting Pharmaron apart from other organizations. Benefits: As part of our commitment to your well-being, we offer a comprehensive benefits package, including: Medical, Dental & Vision Insurance with significant employer contributions. Employer-funded Health Reimbursement Account. Healthcare & Dependent Care Flexible Spending Accounts. 100% Employer-paid Employee Life and AD&D Insurance. Short- and Long-Term Disability Insurance. 401(k) plan with generous employer match. Access to an Employee Assistance Program. Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today! As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences. #ED-L1

Employment Type: Contract Business Unit: Quality Control, Bio-Analytics, and Raw Materials Testing Duration: 2 years with likely extension or conversion to FTE Notes: 100% onsite 3 Key Consulting is hiring an Associate Quality Control for a consulting engagement with our direct client, a leading global biopharmaceutical company. Job Description: Experience with LIMS would be a great preference - analytical data reporting system Compendia experience is a plus but not required Lab experience is a must (pro or academia) Overview: Quality Control is searching is for an analyst to support routine testing of Raw Materials. This person will be responsible for working in the Quality analytical laboratory, using GMPs and GDPs to execute analytical testing. The ideal candidate enjoys tackling challenges and excels at time management with attention to detail. Responsibilities will include, but are not limited to: Performing analytical testing for general chemistry (pH, osmolality, appearance, etc.), Interacting cross-functionally with a wide variety of people and teams; Troubleshoot, solve problems and communicate with stakeholders. Participate in initiatives and projects that may be departmental or organizational in scope. Evaluate lab practices for compliance and operational excellence on a continuous basis. What we are looking for: Experience with analytical laboratory testing with the ability to plan and perform routine tasks with efficiency and accuracy. Demonstrated ability to work independently and deliver right first time results Excellent communication skills (written and verbal) Must have focus on data integrity Qualified to work in the U.S. without employer sponsorship Commitment of a 40-hour work week in West Greenwich, RI Experience: Bachelor's degree OR Associate's degree and 1-2 years of Quality or Analytical Laboratory experience Preferred Qualifications: 1-3 years of experience in GMP analytical laboratory Experience with bench chemistry Experience with Compendial testing Self-motivated, strong organizational skills and ability to manage multiple tasks at one time with minimal supervision Strong communication skills (both written and oral), facilitation and presentation skills Understanding and application of principles, concepts, theories and standards of GMP QC analytical laboratories. Understanding of biopharmaceuticals process and related unit operations Strong analytical skills with the ability to collect, organize, analyze, and disseminate significant amounts of information with attention to detail and accuracy Independent, self-motivated, organized, able to multi-task in time-sensitive environments. Demonstrated experience in investigations and QC processes Why is the Position Open? Staff augmentation. Top Must-Have Skill Sets: Strong Analytical Skills Must have lab experience - (pro or academia) Bachelor's degree/Associates or Highschool degree with 1-3 years of experience in GMP analytical laboratory Understanding and application of principles, concepts, theories and standards of GMP QC analytical laboratories. Interpersonal Skills: Can Do Attitude - Ideal Candidate will have a positive attitude and be willing to participate in lean initiatives on site. Day to Day Responsibilities: Daily responsibilities will be focused on executing analytical testing of raw materials in a GMP laboratory. Basic Qualifications: Quality control lab experience and use of HPLC/UPLC equipment is preferred Red Flags: Candidates with no prior lab experience Interview process: Phone screening of possible candidates. Possible second phone screen and/or in-person interview for those who pass the initial phone screening. We invite qualified candidates to send your resume to *****************************. If you decide that you're not interested in pursuing this position, please feel free to look at the other positions on our website ******************************* You are welcome to also share this opportunity with anyone you think might be interested in applying for this role. Regards, 3KC Talent Acquisition Team

Job Description Located in Bristol, Rhode Island for 50 years, Tri-Mack is a leading manufacturer of high-temperature thermoplastic components for the aerospace-defense, semiconductor, energy and medical industries. Our broad capabilities include collaborative engineering, tool making, injection molding, thermoplastic composite processing, multi-axis CNC machining, bonding and assembly, testing and quality control - all within a modern, environmentally controlled 60,000 sq. ft. facility. Our culture is based on values that promote respect, teamwork and accountability and we are committed to meeting customer requirements through our ISO 9001/AS9100 quality management system. PLEASE NOTE - Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time Position: Quality Control Technician / Inspector (2nd Shift) Summary: This position is responsible for inspecting and documenting incoming material and finished parts, and performing detailed 1st piece inspections as well as final inspections. It requires good working knowledge of standard measurement tools such as micrometer, calipers, height gages, and optical comparator. The position also requires completing documentation, use of our CMM system to verify parts and familiarity with blueprint reading related to highly-engineered parts and assemblies. Responsibilities & Accountabilities: Perform first piece inspection, in process and final inspection; Perform receiving inspection, validate quality of purchased and manufactured materials, parts and components as per set acceptance criteria, determining conformance to prints and specifications. Provide assistance in the performance of any other quality functions as defined in the Quality Manual, such as gauge calibration, inventory, and nonconforming parts assessment. Pursue opportunities to develop new skills both within the department and across departmental lines, beginning in CNC and learning other operations and processes as part of your onboarding and ongoing development. Investigate product quality issues and determine root cause and corrective actions Assist Lead Quality Technician in pre-inspection and screening; Ensure Production employees understand drawings and parts measurement. Perform process capability studies and periodic SPC data input. Maintain organized quality records and correspondence. Assist with both internal and external audits. Work with Engineering and Production to address any product issues. Record all measurements and findings in the appropriate documentation (Visual Manufacturing, Excel, customer files, etc.) Maintain safe operations by adhering to safety procedures and regulations. Conduct yourself in an ethical and professional manner, show respect for your fellow workers and all company and personal property, and follow Tri-Mack values - Respect, Teamwork, Integrity, Accountability, and Durability. Show up to work on time and adhere to the schedule agreed upon by you and your supervisor. Get along with your co-workers, and support others as needed. Adhere to all AS9100 requirements as per work instructions and your team leader and manager. All other duties as assigned. Education, Skills & Experience: High School diploma required. Some college-level coursework preferred. 2+ years working in a Quality Control position in a manufacturing environment. Experience with manual micrometers, calipers and optical comparators. Vision system inspection experience a plus. Demonstrated written and oral communication skills Ability to analyze and prioritize information. Must be able to work independently. Use of computers and Microsoft Word, Excel and Outlook. Our Benefits: We offer competitive salaries and generous benefits, including: 40 hour week - Monday-Thursday, overtime available $3.00/hr 2nd Shift differential Generous Medical, Life, Dental and Vision Insurance programs Paid Time Off, Paid Holidays, Sick & Safe Leave 401(k) with Company Match Tuition Reimbursement If you are looking for an innovative, values-driven company where you can put your quality-focused aptitude and expertise to work, grow your career and take on ever-bigger challenges, you may just have found the place! We know our continued success is dependent upon our employees, which is why we are always on the lookout for reliable, knowledgeable and dynamic individuals with past success in a collaborative team setting, working with clear objectives and direction. *Tri-Mack Plastics provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status or genetic information. Tri-Mack is a drug-free work environment. Pre-employment drug screening (excludes THC) and background checks are required. Powered by JazzHR eRqbujAxQm

The QC inspector is responsible for ensuring that all products meet quality standards. This includes inspecting raw materials used in the production process, conducting tests on finished products and performing audits to identify potential areas of improvement. The QC inspector must be knowledgeable of the relevant safety regulations and have excellent attention to detail and problem-solving skills. Essential Functions * Responsible for individual Inspection activities * Undergo training when necessary * Adhere to policies and procedures related to specific customer requirements * Ability to understand specific directions and follow guidelines that are common throughout the department * Ability to maintain a constant focus on quality and accuracy * Ability to work with minimal supervision * Specific competencies include but are not limited to following the Gowning, Personal Hygiene Procedures, and all other QC Inspection Work Instructions and SOPs including formatting Excel if required, Use of inspection equipment (Bench Linc, Vision Systems, Tensile Tester, Pin Gages, Ring Gages, Calipers, rulers, and Customer supplied fixtures) Perform Visual Inspection (using Tappi Chart) and Feel Testing. Operating the Annealing Ovens * Obey all safety rules, use caution in work activities, and continuously practice safe behaviors * Immediately report unsafe conditions/behaviors and work-related injuries to site supervision Qualifications Preferred * High school diploma or equivalent * 1 year of Product Operator experience necessary * Experience within the department must be gained within 90 days for use of specific measuring equipment, displaying an understanding of the job requirements and any devices required to complete inspection/test activities * Understand Quality Management System (QMS) requirements * Training on the specific equipment must be fully completed within 90 days of hire * Equivalent combination of education and experience is preferred An Affirmative Action / Equal Opportunity Employer Proterial Cable America, Inc. provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, genetic information, disability, or veteran status. As a Federal Contractor, we encourage priority referral of protected veterans under VEVRAA.

Job Description Position: QC Scientist/Sr. Scientist (3rd shift, working hours: 11 pm- 7am), Quality Control & Analytical FLSA Status: Exempt We are on the search for a 3rd shift QC Scientist to join our QC team at Pharmaron's manufacturing site in Coventry, RI. In this position, the Scientist will support manufacturing and process chemistry activities through analytical method verification, optimization and sample testing in compliance with all applicable guidelines. Primary Responsibilities: Sample raw materials and conduct QC testing of raw materials, intermediates, API, IPC and cleaning verification samples following established procedures. Document and report results of all experiments in a timely-manner consistent with department practices and governing procedures, as applicable. Participate in method transfer or validation activities, including executing the protocols and preparing the reports. Review experimental data, notebooks, and instrument qualification protocols / reports. Write, revise, develop, and evaluate SOPs. Maintain good laboratory practices and GMP in compliance with safety and environmental requirements. Ability to work successfully in both a team/matrix environment as well as independently. Report lab event or deviation and participate in the investigation. Ensure high quality in QC and analytical work and accurately document all necessary and relevant information in a clear concise manner as per cGMPs. Provide training to other team members on instrument and testing method. Participate, support and facilitate site audits as directed and required. Perform other related assignments and duties as required and assigned. Experience and Education: BS in Chemistry with 3+ years of experience or MSc in Chemistry with 1+ year of experience. Have experience of using the following instrumentation: HPLC, GC, FTIR and KF. Ability to perform routine QC work independently or with less guidance. Excellent communication skills, both verbal and written. Effective in managing multiple competing activities and delivering to timelines. Ability to work in a cross-functional environment. Working knowledge of cGLP/cGMP and applicable FDA, EMA, and ICH guidance preferred. Why Pharmaron? Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process. With over 21,000 employees and operations in the U.S., U.K., and China, Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China. Collaborative Culture: You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. Our core cultural values are "Employees Number One" and "Clients Centered," setting Pharmaron apart from other organizations. Benefits: As part of our commitment to your well-being, we offer a comprehensive benefits package, including: Medical, Dental & Vision Insurance with significant employer contributions. Employer-funded Health Reimbursement Account. Healthcare & Dependent Care Flexible Spending Accounts. 100% Employer-paid Employee Life and AD&D Insurance. Short- and Long-Term Disability Insurance. 401(k) plan with generous employer match. Access to an Employee Assistance Program. Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today! As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences. #IL-14