Quality control analyst jobs in Westerly, RI - 122 jobs

About Us We are a leading regenerative medicine company in the advanced and acute wound care space and are always looking for exceptional talent. Join a company where you will have an opportunity to grow professionally and personally and give strength to others by Empowering Healing. Our advanced wound care products are specially developed for the successful treatment of chronic and acute wounds. Our comprehensive portfolio of skin substitutes and other regenerative medicine products empower our patients with life-changing solutions. Our strength is giving others strength. Learn more about Careers at Organogenesis What You Will Achieve: The QC Analyst III is responsible for the performance and reporting of analytical testing in support of product production and release, as well as developmental assays, as required. The QC Analyst III helps provide delivery of compliant laboratory systems and data in support of Organogenesis products, and in accordance with appropriate regulatory, corporate and scientific guidelines. In addition, the QC Analyst III will also provide input in support of method validation, cleaning validation, process validation, and characterization activities. In this position, the QC Analyst III will also interact with external entities including contractors and suppliers. How You Will Achieve It: * Perform chemical analysis and ELISA assays for raw materials, intermediates, and finished product testing. * Demonstrate knowledge in analytical test methods to support in-process, raw materials, and routine final product test samples. * Prepare and send out samples for testing, when necessary. * Perform visual inspection of finished product. * Generate trend reports, as they relate to Quality testing. * Author and revise SOPs. * Identify and implement issues and opportunities for improvements. * Participate extensively in high-level quality systems programs (CAPA, etc.). * Interact with Manufacturing and other departments to ensure support of processes and product testing. Job Requirements What You Need to Achieve It: * BS in a relevant scientific discipline (i.e., Chemistry, Biology, Biochemistry * 5+ years of experience in a cGMP Quality Control Department in a FDA-regulated industry. * In-depth knowledge of compendial (USP, EP) test methods, and relevant ICH and FDA guidelines * Technical and Scientific Proficiency * Proven technical proficiency and demonstrated skills in quality technology practices. * Demonstrates understanding of relatively complex data with proficiency to problem solve. * Data Analysis Requirements * Proficient in the use and application of quality tools, databases, and process skills. * Regulatory Requirements * Advanced knowledge of relevant Quality System and SOP procedures. Advanced knowledge of industry regulations and standards such as FDA, USP, and/or ISO, with an ability to interpret and apply quality and Regulatory standards. * Advanced understanding of corporate documentation standards (SOP) and the interrelationship of SOPs and the functional areas. * Ability to work independently on complex assignments and exercise sound judgment under minimal supervision. * Ability to analyze non-conformance issues, recommend corrective action, and ensure compliance with company and Regulatory requirements. * Ability to act independently and determine methods and strategies for addressing and documenting issues during product testing. * Demonstrated strong leadership and communication skills. * Ability to establish strong working relationships and work collaboratively in a team environment. * Background in handling OOS, retest, and stability testing. * Quality Control new hires are required to undergo a visual acuity screening test and periodic re-testing during employment. The results of this testing are neither a condition for employment nor of continued employment and are utilized solely for purposes of qualifying individuals for performance of certain visual tests/assays requiring minimum visual standards. What can we offer you? * 401k -- generous employer match with immediate vesting and financial planning resources * Comprehensive Medical, Dental and Vision coverage options effective on day one of employment * Flexible Spending Account (medical expenses or dependent care expenses) or Health Savings Account * Company paid insurances including Short Term, Long Term and Life insurances as well as voluntary options * Paid maternity leave and parental leave for all new parents * Adoption benefits * Education Assistance Policy - $5,000 per year for all employees * Wellness Program including free trainings on mental health, mindfulness, stress reduction, on-site flu shots and more * Employee Assistance Program * Generous paid time off including vacation, floating holidays, sick days, and company holidays * Free parking including an electric charging station (Canton and La Jolla) * Discounts at BJs Wholesale, Dell, Sullivan Tire, and Sprint The anticipated annualized base salary is $81,000-$97,000 and reflects current market data for similarly-sized life science companies and internal equity. Organogenesis is a multi-state employer, and this salary range may not reflect positions that work in other states. Base salary is part of our total rewards package which also includes the opportunity for merit-based increases, eligibility for our 401(k) plan with competitive company match, medical, dental, vision, education assistance, life and disability insurances and leaves provided in line with your work state and federal law. Our time-off policy includes paid vacation days, paid company holidays, and paid sick time. Total compensation, including base salary to be offered, will depend on elements unique to each candidate, including candidate experience, skills, education, and other factors permitted by law. We are an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to age, sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, genetic information or any other characteristic protected by law. Physical Required Job Type Full-time Location Organogenesis Rhode Island - Smithfield, RI US (Primary) Education Bachelor's Degree Career Level Individual Contributor Travel

JOB TITLE: Quality Control Inspector JOB CODE: Quality Control REPORTS TO: Quality Assurance Manager. Direct on-site project direction and daily scheduling provided through continuous communication with the applicable IMIA Project Manager and/or Supervisor. PAY RANGE: $32.00/hour- $42.00/hour based on experience Summary of position: Responsible for monitoring quality control/assurance requirements of all preservation preformed onboard commercial and US Navy vessel in accordance with established Navy regulations and industry standards or specific contractual requirements as defined in the Scope of Work. Collaborate with customer QA personnel on necessary aspects of the job. Essential Job Requirements: Produce/create electronic/handwritten Quality Assurance documentation as Objective Quality Evidence for work performed throughout the preservation process. Develop and Maintain Test and Inspection Plan (TIP) for all assigned jobs. Monitor and document all required readings with regard to, but not limited to, metal anchor tooth (profile), paint wet/dry film thickness (DFT), steel temperatures and all required environmental readings using appropriate equipment to include: micrometer, dry film thickness gauge, infrared thermometer, psychomotor. Ensure all assigned equipment is maintained in good working order with within all calibration certification intervals. All of the above requirements shall be completed in a safe and efficient manner so as not to cause injury to self or others. Required Education: High School diploma or equivalent Required Certification: NACE Inspector and/or SSPC NBPI required. Required Experience: Formal or informal on-the-job training in the marine industry; familiarity with Navy and Society for Protective Coatings standards. Required Skills: Must possess knowledge of Maritime paintings standards with particular emphasis in US Navy ship preservation criterion. Word processing, spreadsheet, email, and database computer skills required. Must be able to accomplish mathematical calculations associated with preservation readings and documentation; must be able to discern and carry out complex written, oral, or diagramed instructions. Must be able to take direction; interact professionally, knowledgeably and cooperatively with supervisors and co-workers and customer representatives. Physical Requirements: Must be physically capable of working an 8-10 hour day requires average use of computer, some physical dexterity, and agility within confined and restricted spaces & tanks. Reasonable Accommodations may be made to enable qualified individuals with disabilities to perform essential job functions. Supervisory Responsibilities: None Working Conditions: Regularly stand for long periods of time; work on scaffolds and ladders; work on top of machinery; work in confined spaces. Regularly exposed to extreme temperatures, high noise levels, toxic or caustic chemicals, fumes, airborne particles, outdoor weather conditions, dusty conditions, wet and/or humid conditions, hazardous machinery, precarious places, close proximity to other employees. Overtime or shift work involved. Travel often required. Must follow strict safety procedures.

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 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. 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

A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Job Description Job Summary- • Working with some supervision, applies established knowledge of laboratory techniques such as HPLC, dissolution, moisture by KF, and others to perform product stability testing. • Candidate will be responsible for understanding and performing routine analytical testing for stability samples, evaluating and documenting results in a timely manner. • Understands and follows all SOPs and written test procedures. • Performs testing within established standard test times and maintains quality and productivity at acceptable levels as communicated by the supervisor. • Candidate will execute troubleshooting of instrumentation and will be expected to maintain laboratory equipment in good working condition. • Candidate will perform laboratory investigation steps with appropriate approvals and with some guidance from supervisor. • Keeps supervisor fully informed of all results and project status on a daily basis and reports critical information in a timely manner. Qualifications • A minimum of BS degree in Science related field • MS in science related field preferred. • 1-3 years of experience in SOP Additional Information

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

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

Ready to be pushed beyond what you think you're capable of? At Coinbase, our mission is to increase economic freedom in the world. It's a massive, ambitious opportunity that demands the best of us, every day, as we build the emerging onchain platform - and with it, the future global financial system. To achieve our mission, we're seeking a very specific candidate. We want someone who is passionate about our mission and who believes in the power of crypto and blockchain technology to update the financial system. We want someone who is eager to leave their mark on the world, who relishes the pressure and privilege of working with high caliber colleagues, and who actively seeks feedback to keep leveling up. We want someone who will run towards, not away from, solving the company's hardest problems. Our ******************************** is intense and isn't for everyone. But if you want to build the future alongside others who excel in their disciplines and expect the same from you, there's no better place to be. While many roles at Coinbase are remote-first, we are not remote-only. In-person participation is required throughout the year. Team and company-wide offsites are held multiple times annually to foster collaboration, connection, and alignment. Attendance is expected and fully supported. Coinbase stores more digital currency than any company in the world, making us a top tier target on the internet. Security is core to our mission and has been a key competitive differentiator for us as we scale worldwide. Essential to scaling is building and running a security compliance program that reflects how we protect the data and assets in our care, to open the doors with customers, regulators, auditors, and other external stakeholders. Coinbase is looking for an Analyst, Tech Controls to support the second line of defense technology compliance initiatives. This role will play a critical part in assisting with the design, implementation, and monitoring of a technology control framework. The Analyst will work closely with cross-functional teams to ensure excellence in control ownership and contribute to the maturity of the Technology Risk and Controls program. *What you'll be doing (ie. job duties):* * Lead IT process and gap assessments against industry standards and technology regulatory requirements to evaluate control design and operating effectiveness * Design, review and validate processes and configurations across technology systems, including cloud environments, operating systems, databases, and network infrastructure, to ensure alignment with established standards, compliance requirements, and best practices * Assist in maintaining and providing oversight over the technology controls inventory to mitigate technology risks and meet regulatory requirements, technology policies, and frameworks * Collaborate with stakeholder teams including Security, Engineering, Technology Governance, IT, and Operational Risk to support technology requirements and ensure control ownership * Developing technology requirements for new products, updating existing controls, and providing subject matter expertise to product teams * Support Security Compliance, Information Security, Platform, and Engineering stakeholders in identifying and executing on continuous control monitoring opportunities * Provide guidance and leverage technical expertise to determine effectiveness of change management processes, i.e. unit testing, CI/CD, etc. * Define, draft and communicate identified issues and technology process improvement opportunities and assist in developing creative solutions to mitigate risks and address regulatory challenges * Provide reporting to stakeholders and management on progress, escalations, and control initiatives * Drive the creation of procedural documentation, including training materials that support first line of defense risk management, in the form of runbooks and narratives * Validate remediation efforts for identified gaps and issues to ensure resolution effectively aligns with regulatory requirements, industry standards, and internal policies * Drive creation of clear and concise technical documentation for control monitoring *What we look for in you (ie. job requirements):* * Minimum of 2+ years of experience in Security Engineering, Technology Compliance, IT audit, or equivalent roles * Strong knowledge and hands-on experience in technology frameworks such as COBIT, NIST, ISO 27001 * Hands on experience in security engineering, implementing security frameworks, or designing and managing technical controls * Proven technical understanding and operation within cloud technologies, AWS preferred * Strong understanding of control monitoring processes * Excellent oral and written communication skills * Ability to effectively and autonomously accomplish outcomes across cross-functional teams in ambiguous situations with limited supervision * Ability to multitask, prioritize work, and meet deadlines in a fast paced environment * Ability to communicate with technical and non-technical stakeholders to align on shared outcomes *Nice to haves:* * BA or BS in a technical field or equivalent experience * Cloud certifications such as AWS Certified Security Specialty, or equivalent certifications * Security certifications e.g. CISA, CISSP, COBIT or other relevant certifications * Technical understanding of fintech services and/or crypto space Position ID: P60079 \#LI-Remote *Pay Transparency Notice:* Depending on your work location, the target annual salary for this position can range as detailed below. Full time offers from Coinbase also include bonus eligibility + equity eligibility**+ benefits (including medical, dental, vision and 401(k)). Pay Range: $135,320-$159,200 USD Please be advised that each candidate may submit a maximum of four applications within any 30-day period. We encourage you to carefully evaluate how your skills and interests align with Coinbase's roles before applying. Commitment to Equal Opportunity Coinbase is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, sex, gender expression or identity, sexual orientation or any other basis protected by applicable law. Coinbase will also consider for employment qualified applicants with criminal histories in a manner consistent with applicable federal, state and local law. For US applicants, you may view the *********************************************** in certain locations, as required by law. Coinbase is also committed to providing reasonable accommodations to individuals with disabilities. If you need a reasonable accommodation because of a disability for any part of the employment process, please contact us at accommodations*********************************** *Global Data Privacy Notice for Job Candidates and Applicants* Depending on your location, the General Data Protection Regulation (GDPR) and California Consumer Privacy Act (CCPA) may regulate the way we manage the data of job applicants. Our full notice outlining how data will be processed as part of the application procedure for applicable locations is available ********************************************************** By submitting your application, you are agreeing to our use and processing of your data as required. *AI Disclosure* For select roles, Coinbase is piloting an AI tool based on machine learning technologies to conduct initial screening interviews to qualified applicants. The tool simulates realistic interview scenarios and engages in dynamic conversation. A human recruiter will review your interview responses, provided in the form of a voice recording and/or transcript, to assess them against the qualifications and characteristics outlined in the job description. For select roles, Coinbase is also piloting an AI interview intelligence platform to transcribe and summarize interview notes, allowing our interviewers to fully focus on you as the candidate. *The above pilots are for testing purposes and Coinbase will not use AI to make decisions impacting employment*. To request a reasonable accommodation due to disability, please contact accommodations[at]coinbase.com

Job Title: Chemist - Stability Testing - Quality Control FLSA Classification: Full-Time Work Hours: 8 AM - 5 PM (May vary based on business needs) Salary: $75,000 - $105,000 (DOE) Benefits: Bi-Weekly Pay, Paid Time Off, Health Insurance Benefits start on day 1 (Medical, Dental, Vision), Disability Insurance, Shift Differential, Overtime, 401K Match, company sponsored events, career advancement, training, etc. Cipla is seeking a Stability QC Chemist who will provide support to the Quality Control Department in drug quality assessments under the influence of environmental factors. The general duties and responsibilities of the job include but are not limited to the following: Conduct routine testing or other analysis in a specific group or department setting. Conduct advanced testing and/or critical testing, as required. Operate specialized equipment or conduct specialized skill testing Working knowledge of raw materials testing and release Working knowledge of instruments such as Karl Fisher, HPLC, GC, Particle size, ICP Lead investigation activities. Ensure compliance to all data integrity and cGMP practices, procedures, and expect Ensure compliance with all good documentation practices. Other duties and responsibilities as assigned by the Head of the Department or Section Head Education and Experience Bachelor's degree (BS or BA), physical sciences preferred Proficiently speak English as a first or second language Have at least 3 years' experience with formulations stability testing. Proficiently communicate and understand (read and write) scientific work in English Have excellent organization, learning and teaching skills required to work in teams Ability to understand and analyze complex data sets. Working knowledge of Microsoft Office programs and other scientific based software. Experience in Inhalation products (MDI) is a plus Must be authorized to work permanently in the United States Must be able to work on-site Working conditions This role works in a cGMP laboratory or manufacturing environment, where personal protective equipment is required, which may include uniforms, lab coats, safety glasses, respiratory protective equipment, hearing protection, etc. Work with or around solvents, powders, or other materials commonly found in a pharmaceutical laboratory or manufacturing facility is required. Physical requirements Work standing or walking unassisted for 75% or greater of an 8-hour period. Unassisted lifting up-to10 kg, may be required. Able to wear appropriate personal protective equipment at all times, when required. Sitting at a desk and/or working at a computer or other "screen" 75% or greater of an 8-hour period. GLOBAL COMPANY Cipla is a leading global pharmaceutical company, dedicated to high-quality, branded and generic medicines. We are trusted by healthcare professionals and patients across geographies. Over the last eight decades, we have strengthened our leadership in India's pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world. Cipla employs handpicked professionals not just for their knowledge and experience but for their zeal to make a difference to the world of healthcare. The company believes that our biggest assets are the employees, who lead us to prosperity and growth in the future. Driven by the vision, none shall be denied, Cipla's focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world. GLOBAL COMPANY Cipla is a leading global pharmaceutical company, dedicated to high-quality, branded and generic medicines. We are trusted by healthcare professionals and patients across geographies. Over the last eight decades, we have strengthened our leadership in India's pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world. Cipla employs handpicked professionals not just for their knowledge and experience but for their zeal to make a difference to the world of healthcare. The company believes that our biggest assets are the employees, who lead us to prosperity and growth in the future. Driven by the vision, none shall be denied, Cipla's focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world. CIPLA Fall River (INVAGEN PHARMACEUTICALS, INC.) About InvaGen Pharmaceuticals, a Cipla subsidiary InvaGen Pharmaceuticals, Inc. is engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on metered dose inhaler (MDI). The company was founded in 2003 and is based in Central Islip and Hauppauge, New York. As of February 18, 2016, InvaGen Pharmaceuticals, Inc. operates as a subsidiary of Cipla (EU) Limited. Scope: The scope (content and statements) of this is designed to describe the general nature and level of work as well as provide a basic understanding of the role, responsibilities, and expectations of the person assigned to perform the job. This job description is not designed to provide an exact or exhaustive list of all job duties, tasks, skills, and qualifications. The intent is to give a general scope of the knowledge, skills, and abilities needed to satisfactorily perform the essential functions of the position and provide basic performance expectations. The scope of the job may be modified with respect to the department, group, and on an individual assigned basis to a sometimes-specific testing group. Consideration of education, relevant training, and experience or a combination of all three may also result in further modification of the role.

Job Title: Chemist - Stability Testing - Quality Control FLSA Classification: Full-Time Work Hours: 8 AM - 5 PM (May vary based on business needs) Salary: $75,000 - $105,000 (DOE) Benefits: Bi-Weekly Pay, Paid Time Off, Health Insurance Benefits start on day 1 (Medical, Dental, Vision), Disability Insurance, Shift Differential, Overtime, 401K Match, company sponsored events, career advancement, training, etc. Cipla is seeking a Stability QC Chemist who will provide support to the Quality Control Department in drug quality assessments under the influence of environmental factors. The general duties and responsibilities of the job include but are not limited to the following: * Conduct routine testing or other analysis in a specific group or department setting. * Conduct advanced testing and/or critical testing, as required. * Operate specialized equipment or conduct specialized skill testing * Working knowledge of raw materials testing and release * Working knowledge of instruments such as Karl Fisher, HPLC, GC, Particle size, ICP * Lead investigation activities. * Ensure compliance to all data integrity and cGMP practices, procedures, and expect * Ensure compliance with all good documentation practices. * Other duties and responsibilities as assigned by the Head of the Department or Section Head Education and Experience * Bachelor's degree (BS or BA), physical sciences preferred * Proficiently speak English as a first or second language * Have at least 3 years' experience with formulations stability testing. * Proficiently communicate and understand (read and write) scientific work in English * Have excellent organization, learning and teaching skills required to work in teams * Ability to understand and analyze complex data sets. * Working knowledge of Microsoft Office programs and other scientific based software. * Experience in Inhalation products (MDI) is a plus * Must be authorized to work permanently in the United States * Must be able to work on-site Working conditions This role works in a cGMP laboratory or manufacturing environment, where personal protective equipment is required, which may include uniforms, lab coats, safety glasses, respiratory protective equipment, hearing protection, etc. Work with or around solvents, powders, or other materials commonly found in a pharmaceutical laboratory or manufacturing facility is required. Physical requirements * Work standing or walking unassisted for 75% or greater of an 8-hour period. Unassisted lifting up-to10 kg, may be required. * Able to wear appropriate personal protective equipment at all times, when required. * Sitting at a desk and/or working at a computer or other "screen" 75% or greater of an 8-hour period. GLOBAL COMPANY Cipla is a leading global pharmaceutical company, dedicated to high-quality, branded and generic medicines. We are trusted by healthcare professionals and patients across geographies. Over the last eight decades, we have strengthened our leadership in India's pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world. Cipla employs handpicked professionals not just for their knowledge and experience but for their zeal to make a difference to the world of healthcare. The company believes that our biggest assets are the employees, who lead us to prosperity and growth in the future. Driven by the vision, none shall be denied, Cipla's focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world. GLOBAL COMPANY Cipla is a leading global pharmaceutical company, dedicated to high-quality, branded and generic medicines. We are trusted by healthcare professionals and patients across geographies. Over the last eight decades, we have strengthened our leadership in India's pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world. Cipla employs handpicked professionals not just for their knowledge and experience but for their zeal to make a difference to the world of healthcare. The company believes that our biggest assets are the employees, who lead us to prosperity and growth in the future. Driven by the vision, none shall be denied, Cipla's focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world. CIPLA Fall River (INVAGEN PHARMACEUTICALS, INC.) About InvaGen Pharmaceuticals, a Cipla subsidiary InvaGen Pharmaceuticals, Inc. is engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on metered dose inhaler (MDI). The company was founded in 2003 and is based in Central Islip and Hauppauge, New York. As of February 18, 2016, InvaGen Pharmaceuticals, Inc. operates as a subsidiary of Cipla (EU) Limited. Scope: The scope (content and statements) of this is designed to describe the general nature and level of work as well as provide a basic understanding of the role, responsibilities, and expectations of the person assigned to perform the job. This job description is not designed to provide an exact or exhaustive list of all job duties, tasks, skills, and qualifications. The intent is to give a general scope of the knowledge, skills, and abilities needed to satisfactorily perform the essential functions of the position and provide basic performance expectations. The scope of the job may be modified with respect to the department, group, and on an individual assigned basis to a sometimes-specific testing group. Consideration of education, relevant training, and experience or a combination of all three may also result in further modification of the role.

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

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

Chemist - Rubber Injection MoldingPortland, CT | Direct Hire | $70K-$100K DOE Be the chemistry behind the product! Our client is seeking a Chemist with rubber injection molding experience to support materials, processes, and production in a leading manufacturing environment. You'll Do: Test and validate rubber compounds, raw materials, and bonding processes Support injection molding operations with lab testing & troubleshooting Perform wet chemistry and instrumental analysis (spectroscopy, chromatography, titration) Lead safety initiatives for chemical handling Partner with engineering, QA, and production on product improvements You Bring: Bachelor's in Chemistry, Chemical Engineering, or Polymer Science 3-5+ years' experience in a manufacturing lab or R&D setting Hands-on knowledge of rubber chemistry & injection molding Familiarity with QA standards, OSHA/EPA regulations Strong lab instrumentation & data analysis skills Apply today and shape what's next! A.R. Mazzotta is an equal opportunity employer. It is the policy of A.R. Mazzotta to employ, recruit, hire, train and promote individuals without regard to race, color, religious creed, sex, national origin, age, marital status, present or past history of mental disability, intellectual disability, learning disability, or physical disability, religion, political affiliation or belief, pregnancy, ancestry, veteran status, sexual orientation, gender identity or expression or any other status protected by federal, state, or local laws.

Job DescriptionChemist - Rubber Injection MoldingPortland, CT | Direct Hire | $70K-$100K DOE Be the chemistry behind the product! Our client is seeking a Chemist with rubber injection molding experience to support materials, processes, and production in a leading manufacturing environment. You'll Do: Test and validate rubber compounds, raw materials, and bonding processes Support injection molding operations with lab testing & troubleshooting Perform wet chemistry and instrumental analysis (spectroscopy, chromatography, titration) Lead safety initiatives for chemical handling Partner with engineering, QA, and production on product improvements You Bring: Bachelor's in Chemistry, Chemical Engineering, or Polymer Science 3-5+ years' experience in a manufacturing lab or R&D setting Hands-on knowledge of rubber chemistry & injection molding Familiarity with QA standards, OSHA/EPA regulations Strong lab instrumentation & data analysis skills Apply today and shape what's next! A.R. Mazzotta is an equal opportunity employer. It is the policy of A.R. Mazzotta to employ, recruit, hire, train and promote individuals without regard to race, color, religious creed, sex, national origin, age, marital status, present or past history of mental disability, intellectual disability, learning disability, or physical disability, religion, political affiliation or belief, pregnancy, ancestry, veteran status, sexual orientation, gender identity or expression or any other status protected by federal, state, or local laws.

**Country:** United States of America ** Onsite **U.S. Citizen, U.S. Person, or Immigration Status Requirements:** U.S. citizenship is required, as only U.S. citizens are authorized to access certain necessary systems. **Security Clearance:** None/Not Required At Raytheon, the foundation of everything we do is rooted in our values and a higher calling - to help our nation and allies defend freedoms and deter aggression. We bring the strength of more than 100 years of experience and renowned engineering expertise to meet the needs of today's mission and stay ahead of tomorrow's threat. Our team solves tough, meaningful problems that create a safer, more secure world. Operations Supply Chain (OSC) within Raytheon supporting Land & Air Defense System (LADS) Strategic Business Unit has an immediate opening for a Principal Specialist, Program Controls Financial Analyst to join our team supporting inter organization contracts. As a member of the OSC Finance team, the successful candidate will be able to train a group of financial analysts responsible for the daily business and financial activities for programs within the Inter organization transfer (IOT) function. You will be responsible for cost/schedule control and analysis, Earned Value Management Systems (EVMS), Forecasting, Estimate-at-Completion (EAC), Latest Revised Estimates (LRE), variance analysis, data reviewing and reporting, partnering with the Program Manager and CAMs, and providing financial leadership in the successful execution of various production contracts. You will drive the operations finance process, monitor program health and compliance, and partner with other functional team members to improve program financial metrics. In addition, this position is responsible for actively identifying risks that affect cost and/or schedule and providing proactive analysis of all financial aspects of the responsible programs. Performance of additional ad-hoc analysis will be required as well as support of 5 Year and AOP forecasting. The ideal candidate would be able to work in a challenging fast paced team environment, have a strong earned value analysis skillset, be a success-minded team member who possesses strong self-initiative and multi-tasking skills, be able to provide analytical support while under critical deadlines and be involved in process improvement initiatives. Additionally, the ability to effectively communicate analysis and results with RMD East IOT customer is important to this role. **What You Will Do** + You will be responsible for supporting the financial performance and execution of programs in the LADS IOT portfolio. This role requires a business partner approach to independent work effort under the direction of finance management. + You will be responsible for implementing, reporting, and maintaining financial data within SAP APEX and other standard company tools. You should be able to problem-solve given sufficient input and create methods to analyze data and identify potential issues. + Implementation and maintenance of Earned Value Management ensuring compliance and accurate reporting. + Establish and maintain program logs (MR, UB, BCRs, etc.) + Develop and support Bi-Annual Estimate-at-Completion (EAC) and Monthly Latest Revised Estimate (LRE) + Prepare and lead program financial forecasts, monitor actual costs, and explain variances to plans and forecasts. + Financial point of contact for Program Management and be able to provide financial guidance to Program Operations Managers and non-finance organizations including Engineering, Supply Chain, and Operations. **Qualifications You Must Have** + **Typically requires:** A University Degree or equivalent experience and minimum 5 years prior relevant experience, _or_ An Advanced Degree in a related field and minimum 3 years experience + Experience in using SAP Business Systems APEX EV & PRISM EV. + Program Controls experience with data analysis, reporting and/or process improvement. + Experience with Accounting/Financial information systems and Earned Value (EV) tools. + Experience with Microsoft Excel (i.e., pivot tables, advanced formulas), Word and/or PowerPoint. **Qualifications We Prefer** + Previous experience using SAP, APEX, APEX EV, Business Warehouse, and Program Management Excellence (PMX) preferred. + Demonstrated analytical and problem-solving skills. + Ability to work in a highly collaborative team setting. + Must be detail oriented . + Self-starter and takes ownership of assignments . + Willing and able to learn new systems/tools and processes. + Excellent oral and written communication skills, including demonstrated ability to communicate clearly and concisely across functional teams and with immediate management. **What We Offer** + Our values drive our actions, behaviors, and performance with a vision for a safer, more connected world. At RTX we value: Trust, Respect, Accountability, Collaboration, and Innovation. **Learn More & Apply Now!** + Please consider the following role type definition as you apply for this role. Onsite: Employees who are working in Onsite roles will work primarily onsite. This includes all production and maintenance employees, as they are essential to the development of our products. **_As part of our commitment to maintaining a secure hiring process, candidates may be asked to attend select steps of the interview process in-person at one of our office locations, regardless of whether the role is designated as on-site, hybrid or remote._** The salary range for this role is 82,000 USD - 164,000 USD. The salary range provided is a good faith estimate representative of all experience levels. RTX considers several factors when extending an offer, including but not limited to, the role, function and associated responsibilities, a candidate's work experience, location, education/training, and key skills. Hired applicants may be eligible for benefits, including but not limited to, medical, dental, vision, life insurance, short-term disability, long-term disability, 401(k) match, flexible spending accounts, flexible work schedules, employee assistance program, Employee Scholar Program, parental leave, paid time off, and holidays. Specific benefits are dependent upon the specific business unit as well as whether or not the position is covered by a collective-bargaining agreement. Hired applicants may be eligible for annual short-term and/or long-term incentive compensation programs depending on the level of the position and whether or not it is covered by a collective-bargaining agreement. Payments under these annual programs are not guaranteed and are dependent upon a variety of factors including, but not limited to, individual performance, business unit performance, and/or the company's performance. This role is a U.S.-based role. If the successful candidate resides in a U.S. territory, the appropriate pay structure and benefits will apply. RTX anticipates the application window closing approximately 40 days from the date the notice was posted. However, factors such as candidate flow and business necessity may require RTX to shorten or extend the application window. _RTX is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability or veteran status, or any other applicable state or federal protected class. RTX provides affirmative action in employment for qualified Individuals with a Disability and Protected Veterans in compliance with Section 503 of the Rehabilitation Act and the Vietnam Era Veterans' Readjustment Assistance Act._ **Privacy Policy and Terms:** Click on this link (******************************************************** to read the Policy and Terms Raytheon Technologies is An Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status, age or any other federally protected class.

Employment Type: Contract Business Unit: Quality Control, Bio-Analytics, and Raw Materials Testing Duration: 3 years with likely conversion to FTE. Notes: Shift: Tuesday - Friday 7AM to 5PM, 10 hour shift schedule. 3 Key Consulting is hiring an Associate Quality Control for a consulting engagement with our direct client, a leading global biopharmaceutical company. Job Description: Under minimal supervision, this position will be responsible for activities including microbiology & analytical testing, sample and data management and equipment and instrumentation operation and maintenance in a highly dynamic, team environment. This position will be responsible for one or more of the following activities: Perform sample collection and sample handling to support GMP operations and Environmental/Water monitoring. Perform testing and possible data review for compendia, non-compendia methods, and routine laboratory procedures. Generate complete, accurate, and concise laboratory documentation using electronic systems and laboratory notebooks. Operate and maintain specialized laboratory equipment and instrumentation. Participate in laboratory investigations and audits as necessary. Perform general laboratory housekeeping activities. Maintain training compliance and proficiency. At all times, comply with safety guidelines, cGMPs/CFRs and other applicable regulatory requirements Basic Qualifications: Science related background, lab experience. Why is the Position Open? Staff Augmentation Top Must-Have Skill Sets: Lab experience, good documentation practices, experience working with passing/failing sample results. This is an entry level position, however, they must have proven experience in Quality control. Any science degree is considered Day to Day Responsibilities: Environmental sampling/Incubation, utilities sampling/testing, Manufacturing sample collections, entering into clean room areas with QC equipment and ensuring all SOPs are being followed. Employee Value Proposition: The person in this role will work with the microbiology team. This team interacts in manufacturing and QC. Red Flags: Multiple jobs within a short period of time, issues working within a team. Interview process: Phone screening followed by in-person interview. 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

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.

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.**

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