Quality control analyst jobs in Falmouth, MA

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

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.

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

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: QC Chemist II FLSA Classification: Full-Time, Exempt Professional Work Hours: General Shift: 8:30AM - 5:00PM (may vary based on business needs) Reports To: Quality Control Manager Salary Range: $72,800 - $93,600 Purpose The job of the "Chemist" is simply described as an individual contributor who performs testing of samples of various types using various techniques or equipment in the QC laboratory. The job itself may be further modified with respect to the department, group, etc., as exemplified in the "Department" on an individual assigned basis to a sometimes-specific testing group. The role may be further modified based upon individual education, training, experience or a combination of all three. Generally, modifier designation with respect to experience for Chemist are as follows. However, a combination of education, training, and special skills will determine the assignment of Level to a specific individual: Duties and Responsibilities The general duties and responsibilities of the "Chemist" include but are not limited to the following: • Calibration and preventive maintenance of instruments. • Communications with vendors for installation, qualification and maintenance. • 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 • 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 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. The role may be assigned on a work-shift basis, where required (Day, Evening, Night). Weekend or Holiday work may be requested or 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. Professional and Behavioral Competencies • Must be willing to work in a pharmaceutical packaging setting. • Must be willing and able to work any assigned shift ranging from first or second shift. Work schedule may be Monday to Friday. • Must be willing to work some weekends based on business needs as required by management. • No remote work available • No employment sponsorship or work visas. 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 NEW YORK (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 a range of therapeutic areas, including cardiovascular, anti-infective, CNS, anti-inflammatory, anti-diabetic, and anti-depressants. 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. EEO Statement Cipla is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, sex, sexual orientation, gender identity, religion, national origin, genetic information, disability, or protected veteran status.

Shea Concrete, New England's Premier Precaster, is currently hiring for a Quality Control (QC) Technician at our year-round plant located in Rochester, MA. This is a year round facility in a fast paced environment. $25-$30/hr based on experience. The Quality Control Technician (“QC Technician”) will work within Shea Concrete's production plant and is ultimately responsible for product testing. The QC Tech will assist in the execution of quality control processes, procedures and protocol associated with the production of pre and post concrete pours. QC Experience required, Precast experience preferred. Come see what we are all about (click on video): ************************************************** Responsibility Responsible for ACI concrete field tests Responsible for quality control inspections in manufacturing plant Inspect forms before pouring (Pre-Pour). Inspect product after removed from forms (Post-Pour) Notifies Production Supervisor if deficiencies are found. Perform and/or schedule repairs on products as needed. Expected to maintain knowledge of precast plant techniques and procedures. May assist with precast production operation as needed. Characteristics Always committed to safety. Maintain a safe work area. Follow safe work practices as outlined in the Safety Program. Always committed to quality. Follow and implement quality control measures. Excellent attendance. Reliable means of transportation to and from work. Ability to learn, organize and prioritize work and handle multiple tasks. Outstanding attitude, honesty, and ethic at all times. Expected to use sound judgment, diplomacy, and discretion. Work independently or cooperatively with others. Self-drive in carrying out the functions of the job. Requirements: ACI Concrete Field-Testing Grade 1 Certified (preferred but not required) NPCA PQS Training (preferred) Must be at least 18 years of age per federal guidelines. Good communication skills, both verbal and written to all levels of staff Ability to remain focused in busy environment. Computers and tablets skills are required in order to perform tasks. Ability to read blueprints and sketches. Physical Demands Ability to stand/bend/stretch/reach/kneel/crawl, etc. Must be able to be on your feet for extended periods of time throughout work shift. Ability to lift and carry 50lbs. Must be able to work with heights up to 10 feet. Must wear proper PPE at all times in a production plant environment

Changing lives. Building Careers. Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging what's possible and making headway to innovate new treatment pathways to advance patient outcomes and set new standards of care. ESSENTIAL DUTIES AND RESPONSIBILITIES: The Quality Control Technician II will be responsible for performing quality control Analytical laboratory testing of in-process, finished goods, validation studies, and adherence to all applicable regulations, policies, and procedures purchased components, manufactured sub-assemblies and final product. Must have working knowledge of U.S. Food and Drug Administration regulations, ISO 13485, and other applicable regulatory agencies as they pertain to laboratory testing. Responsible for performing Analytical testing such as TOC, Conductivity, Osmometry and pH testing. Perform mechanical testing, DSC (Differential scanning calorimeter) and DBT (Burst testing). Inspection and testing of raw materials, in-process, and final product testing. Monitors equipment and instrumentation used daily to ensure proper operation and calibration. Assists in the writing and updating of analytical test procedures, protocol, logbooks, and checklists. Responsible for identifying and alerting a supervisor of issues on instruments and/or test executions; makes initial recommendations for possible solutions and/or corrective actions. Develops and revises SOPs and trains appropriate new hires. Maintains a working inventory of all components and archived materials and solutions as needed. Assist as needed in test method validation, investigation studies or other product development studies. Provides database support, generates reports, and analyzes the data as needed. Assist in Out of Specification (OOS) Investigations, Non-conformances, and Corrective Action/Preventive Actions (CAPAs). Assist in preparing for and participating in FDA audits, customer audits, etc. All other duties as assigned. DESIRED MINIMUM QUALIFICATIONS: The requirements listed below are representative of the knowledge, skill, and/or ability required for this position. Bachelor's Degree in the biological or chemical sciences or equivalent with related work experience is required. A minimum of 2-4 years' experience in a medical device, pharmaceuticals, Quality/Regulatory Compliance, or other cGMP regulated product preferred environment. Familiarity with application of FDA and/or ISO quality standards in a government regulated industry. Quality Certification (e.g., CQE, CQA, Six Sigma) preferred. Proficient computer competence, including experience with database and Microsoft Office software to create reports, spreadsheets, analyze data and prepare presentations. Experience with performing Instron, DSC and DBT testing preferred. Working knowledge of standard laboratory practices and safety. Ability to follow instructions precisely, recognize deviations, and recommend corrective action. Experience working in ISO Class 7 cleanrooms preferred. Experience with Microsoft Office software to create reports, spreadsheets, analyze data and prepare presentations. TOOLS AND EQUIPMENT USED: Working knowledge and understanding of instruments including pH, Conductivity, Total Organic Carbon Water, Osmometry, Instron, Deferential Scanning Calorimeter, Identification of Raw Materials, and the visual inspection of raw material in-process and final product samples. PHYSICAL REQUIREMENTS: The physical requirements listed in this section include but are not limited to the motor/physical abilities and skills required of this position to successfully undertake the essential duties and responsibilities of this position. In accordance with the Americans with Disabilities Act (ADA), reasonable accommodations may be made to empower individuals with disabilities to undertake the essential duties and responsibilities of the position. While undertaking the essential duties and responsibilities of the position, the employee must speak and write in English. The employee is required to go to all areas of the company. The employee may be required to periodically lift and/or move up to 25lbs. ADVERSE WORKING CONDITIONS: The adverse working conditions listed in this section include, but are not limited to, those environmental conditions to which the employee may be exposed while undertaking the essential duties and responsibilities of this position, which is that of a general plant environment. Adverse exposure may result from the handling of hazardous and biohazardous materials that include, but are not limited to, flammable and corrosive liquids, compressed gases, sharps, and medical wastes. Salary Pay Range: $26.21 - $35.38 USD Hourly Our salary ranges are determined by role, level, and location. Individual pay is determined by several factors including job-related skills, experience, and relevant education or training. In addition to base pay, employees may be eligible for bonus, commission, equity or other variable compensation. Your recruiter can share more about the specific salary range for your preferred location during the hiring process. Additional Description for Pay Transparency: Subject to the terms of their respective plans, employees and/or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance, and savings plan (401(k)). Subject to the terms of their respective policies and date of hire, Employees are eligible for the following ******************************************* Integra LifeSciences is an equal opportunity employer, and is committed to providing equal employment opportunities to all qualified applicants and employees regardless of race, marital status, color, religion, sex, age, national origin, sexual orientation, physical or mental disability, or protected veteran status. This site is governed solely by applicable U.S. laws and governmental regulations. If you'd like more information on your rights under the law, please see the following notices: EEO Is the Law | EOE including Disability/Protected Veterans Integra LifeSciences is committed to provide qualified applicants and employees who are disabled veterans or individuals with disabilities with needed reasonable accommodations in accordance with the ADA. If you have difficulty using our online system due to a disability and need an accommodation, please email us at ***********************. Unsolicited Agency Submission Integra LifeSciences does not accept unsolicited assistance from search firms for employment opportunities. All CVs/resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. A formal written agreement is required before engaging any agency, and it must be executed and authorized by the Vice President, Talent Acquisition. Where agency agreements are in place, introductions (the initial sharing of a candidate's name, resume, or background) are position-specific and may only occur within the scope of that approved agreement. Please, no phone calls or emails. Integra - Employer Branding from Integra LifeSciences on Vimeo

Since 2009, Info Way Solutions has earned a reputation as a full-service staffing firm that excels in a fast-paced marketplace. We have placed highly skilled professionals on a temporary, temporary-to-hire and direct-hire basis in the fields of accounting and finance, IT technology,office administration, marketing and design. Info Way Solutions is dedicated to providing you quality professionals with well-matched skills to your unique hiring requirements and workplace environment. We collaborate with customers to consistently and cost-effectively plan, execute and deliver high-quality services and results.Our consultants are seasoned professionals who build long-term,trusted relationships that bring about a high level of energy, integrity, experience and value to our client's work. Our superior client-consultant relationships and in-depth insight of services have resulted in significant repeated business with clients. In addition, we are partners with best-in-class technology vendors that enable us to best determine the most appropriate hardware, software and services to cater to any of our client's business needs. We have often collaborated with them to make optimal use of today's technology while also planning for the future. More than 50 customers - including mid-market leaders and many of the Fortune 500 Companies - rely on our expertise to leverage their investments. Job Description Responsible for cleaning\decontamination of returned product samples. After processing of samples, responsible for shipping samples to appropriate manufacturing location. Must be able to handle lifting of boxes on a daily basis. Will be responsible for lifting Biohazards shipping boxes with assistance from a second person to be placed on a designated cart; these boxes can weigh upwards of 55 pounds. Analyze samples using specific procedures and instrumentation. Maintain documentation. May provide assistance in troubleshooting results outside of predefined specifications. SUMMARY OF POSITION: The candidate will support the Post Market Vigilance Investigations team's activities for the Patient Monitoring and Recovery (PMR) Division. These activities include; assist in managing the receipt of incoming physical complaint product, conducting follow ups with accounts and/or International Subsidiaries to rectify discrepancies with product receipt, assisting in managing the process flow of complaint investigations, performing Device History Record Reviews, and performing root cause analysis on PMR Product customer returns to ensure high levels of quality, reliability, safety, and efficacy. Additional responsibilities include management of clinically applied medical device retains and associated paper records in accordance with Covidien Medtronic Record Retention Policies and support staffing needs. ESSENTIAL FUNCTIONS: • Assist PMV Investigations Coordinator with managing receipt of physical complaint product samples, in addition to corresponding with domestic and international accounts to rectify discrepancies in product receipt. • Assist in the coordination of sanitization of clinically applied medical device returns and shipment to respective Medtronic Manufacturing facilities, as well as coordinating the investigation process with internal Engineering and Quality groups. • Test and thoroughly evaluate clinically applied surgical medical devices of various degrees of complexity to determine root cause analysis within a closely monitored time frame. • Identifying the appropriate test method/regiment from existing Standard Operating Procedures for complaint sample evaluation, execute the method, and interpret the data (technical) for definitive root cause analysis determination. Test methods may include dimensional and/or tensile testing and interpretation of the technical data yielded in accordance with USP/EP/ASTM standards. • Replicate reported failure mode with bench top or in vivo test methods and document observations accordingly. • Initiate and distribute Corrective Action Requests to Manufacturing or Engineering Departments as needed. • Prepare technical investigation reports based on results of evaluation and/or review of the manufacturing plant reports to be documented in the QA (Quality Assurance) Department complaint database and incorporated into customer response letters. • Certification with OSHA's BloodBorne Pathogens Standard 29 CFR 1910.1030 and adherence to Corporate and Local Environmental Health and Safety Policies. MINIMUM REQUIREMENTS: Minimum Experience: 2 to 3 yrs • Academic or work experience in a laboratory or manufacturing environment. Experience with laboratory equipment or test equipment or manufacturing equipment highly desirable. • Experience with medical devices preferred but not required. Skills/Qualifications: • Must be proficient with MS Office (with emphasis on Excel and Word). • Critical independent thinking and timely follow up. • Time management skills. • Excellent written and verbal skills necessary. QD003425-001, Rev A ORGANIZATIONAL RELATIONSHIPS/SCOPE: • Quality Assurance • Manufacturing • Engineering • Research and Development • Regulatory Affairs • Legal • Marketing/Sales WORKING CONDITIONS: Biohazardous laboratory environment requiring use of personal protective equipment in accordance with CDC and OSHA regulations. Responsible for cleaning\decontamination of returned product samples. After processing of samples, responsible for shipping samples to appropriate manufacturing location. Must be able to handle lifting of boxes on a daily basis, some boxes weigh upwards of 50 pounds each. Must be able to handle lifting of boxes on a daily basis. Will be responsible for lifting Biohazards shipping boxes with assistance from a second person to be placed on a designated cart; these boxes can weigh upwards of 55 pounds. Analyze samples using specific procedures and instrumentation. Maintain documentation. May provide assistance in troubleshooting results outside of predefined specifications. Qualifications Education: BS Degree in a Science or Engineering discipline.

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.**

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.

We are seeking a Quality Control Inspector with experience in conducting first article inspection processes to ensure the quality of finished products. The ideal candidate will have some prior experience with FAI, knowledge of quality assurance techniques, and the ability to interpret engineering drawings and technical documents. Responsibilities: Assist in Conducting First Article inspection (AS9102) processes and document activities Interpret test results for acceptance or rejection Record test results and compile nonconforming output report Mechanical Inspection Electrical Point to Point wiring continuity testing Maintain calibration logs Qualifications: Minimum experience with first article inspection processes (Will Train) Knowledge of quality assurance techniques and functions Previous experience with calipers and micrometers Ability to read and interpret engineering drawings, specs, and other technical documents Mechanical aptitude Excellent communication skills both verbally and in writing

Nexus Staffing Specialists is a dynamic, fast growing company with tremendous advancement opportunity. We are presently searching for a Bilingual - Spanish , Talent Acquisition Specialist for our new flagship office at 330 Lynnway in Lynn, MA. This state of the art, custom designed location is our 4th office. If you are looking for an energetic organization with a mentoring spirit and significant advancement opportunity, you have found a home with Nexus Staffing Specialists. Nexus Staffing Specialists has combined experience of over 20 years in staffing and providing talent globally. Our professional staff of recruiters based in the Boston and NY area provides comprehensive staffing needs including temporary, temporary to hire, and professional placement in the areas of manufacturing, engineering, IT, finance, logistics and warehouse, supervisory, operations and more.. Job Description Position Summary Monitor standards and controls in relation to the manufacturing of high quality soup, dip and salad products in a dynamic, fast paced USDA, FDA food manufacturing facility. In event of absence, position will be filled by adequately trained personnel Position Responsibilities (Other duties may be assigned) Monitor and enforce quality control points. Possess and promote the highest product and process quality standards. Complete audits to ensure quality standards are kept within specifications. Complete process related audits to assure that process instructions are being followed. Complete updates on stock status via inventory control software when placing non-conforming material on hold or assigning a disposition of currently held product in the system. Updating all reporting databases with pertinent information of all non-conforming products. Performing a cause and effect/root cause analysis on all non-conforming product to assist in creating further planned actions or prevention methods. Perform viscosity and solids data testing. Perform packaging verification audits. Partake in quality systems development. Sensory evaluation of key ingredients and attributes. Analyze data and use information to enact quality improvements. Maintain, create and communicate quality control reporting data quickly and effectively. Identify and take part in continuous improvement opportunities. Qualifications Candidate should have a developed palette and be able to use that ability to monitor the consistency of a wide variety of products. Must be an agent of change and emanate a positive and upbeat attitude. To perform this job successfully, the individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Education and/or Experience 2+ year college degree and 2+ years manufacturing experience preferably in a food environment, or equivalent combination education work experience. Certification of Quality Inspector by ASQ a plus. Candidate must have above average mathematics skills, as well as familiarity with statistical process control and quality control concepts and tools. Candidate must possess a thorough knowledge of computers and their programs. Must be detail oriented with above average organizational skills. Must have excellent verbal and written communication skills. Candidate must be able to interact in a dynamic team environment while displaying tact and diplomacy with peers and management. Language Skills Level II: the ability to communicate effectively both written and verbally in English as it pertains to individual position. Physical Demands Must be able to occasionally lift up to 35 pounds Extended periods of standing, walking Additional Information All your information will be kept confidential according to EEO guidelines.

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

Job Description The Quality Control Technician - Troubleshooting is responsible for inspecting and testing cable and wire products and processes to ensure they meet all quality standards, specifications, and regulations. This includes performing visual inspections, dimensional measurements, electrical, and functional tests. The primary function of this role is to evaluate nonconforming products and to determine the necessary actions to rework the product. The QC Technician must also be able to read and interpret blueprints, engineering drawings, and specifications. This position requires the use of High Voltage, all safety guidelines, procedures, and regulations to prevent accidents and ensure a safe working environment must be followed. The Quality Control Technician - Troubleshooting is a respectful team-player that works well with diverse internal team members. This position is ambitious, self-motivated, results-driven, and demonstrates problem solving skills with sound judgment. This role is also responsive, flexible, accessible, detail oriented, willing to embrace change and proactively adjust plans. Partnering with and elevating others by communicating with peers to increase awareness and ensure team success. Essential Duties and Responsibilities: Troubleshoot nonconforming cables, fill out nonconformance reports and communicates findings to Production Quality Supervisor and Quality Manager Detect and report unusual or non-conforming documentation, materials, conditions, or product to Production Quality Supervisor and Quality Manager. Assist and sometimes lead Root Cause and Corrective Action efforts. Inspect materials, components, and final product to ensure they meet quality standards. Measure dimensions of cable and wire products to ensure they meet specifications. Conduct visual and electrical tests on cable and wire products to ensure they meet performance requirements and identify any defects. When required, perform functional tests on cable and wire products to ensure they operate as designed. Document the results of all tests and inspections. Create, update, compile, save and maintain documentation into internal database. Work with various internal personnel and departments to communicate and resolve quality issues. Comply and support company policies and quality management system. Maintain and create a clean, uncluttered environment that reduces waste and optimizes productivity by following the 5S steps: sort, set in order, shine, standardize, and sustain. When required, help with continuous improvement efforts. More additional responsibilities may be applicable per the Quality Manager. Qualifications: High school diploma or equivalent. 1+ year of experience in quality control, preferably in the cable and wire manufacturing industry. Experience with visual inspection and dimensional measurement. Basic understanding of Microsoft Office and Adobe. Ability to read and interpret blueprints, engineering drawings, and specifications. Strong attention to detail. Ability to work independently and as part of a team. Strong communication skills. Proficient with computers and comfortable using Microsoft Office Suite (Word, Excel, etc.). Physical Qualifications: The physical demands described are representative of those that must be met by an employee to successfully perform the essential function of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this Job, the employee is regularly required to sit; stand; crouch; stoop; walk; talk; hear; use hands to handle or feel assemblies; reach with hands and arms for materials and tools. The employee must occasionally lift and/or move up to twenty-five (25) pounds. They must also have the ability to see details at close range (within a few feet of the observer), color vision, depth perception and ability to focus. This position requires use of information or access to hardware and documents which are subject to the International Traffic in Arms Regulations (ITAR). All applicants must be U.S. persons within the meaning of ITAR. ITAR defines a U.S. person as a U.S. Citizen, U.S. Permanent Resident (i.e. 'Green Card Holder'), Political Asylee, or Refugee. Benefit Conditions: Waiting period may apply Only full-time employees are eligible This Job Is: A job for which military experienced candidates are encouraged to apply Job Type: Full-time Salary: $20.00 - $25.00 per hour Benefits: 401(k) Dental insurance Health insurance Paid time off Vision insurance Experience level: 1 year Schedule: 8 hour shift Day shift Monday to Friday Overtime Work setting: In-person Experience: Blueprint reading: 1 year (Required) Quality control: 2 years (Preferred) Work Location: In person

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

Job Title: Quality Control (QC) Chemist (Metrology) FLSA Classification: Full-Time, Exempt Professional Work Hours: General Shift: 8:30AM - 5:00PM (may vary based on business needs) Reports To: Quality Control Manager Salary Range: $75,400 - $93,600 Purpose: The job of the "Chemist" is simply described as an individual contributor who performs testing of samples of various types using various techniques or equipment in the QC laboratory. The job itself may be further modified with respect to the department, group, etc., as exemplified in the "Department" on an individual assigned basis to a sometimes-specific testing group. The role may be further modified based upon individual education, training, experience or a combination of all three. Generally, modifier designation with respect to experience for Chemist are as follows. However, a combination of education, training, and special skills will determine the assignment of Level to a specific individual: 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. Duties and Responsibilities The general duties and responsibilities of the "Chemist" include but are not limited to the following: * Calibration and preventive maintenance of instruments. * Communications with vendors for installation, qualification and maintenance. * 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 * 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 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. The role may be assigned on a work-shift basis, where required (Day, Evening, Night). Weekend or Holiday work may be requested or 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. Professional and Behavioral Competencies * Must be willing to work in a pharmaceutical packaging setting. * Must be willing and able to work any assigned shift ranging from first or second shift. Work schedule may be Monday to Friday. * Must be willing to work some weekends based on business needs as required by management. * No remote work available * No employment sponsorship or work visas. 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 NEW YORK (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 a range of therapeutic areas, including cardiovascular, anti-infective, CNS, anti-inflammatory, anti-diabetic, and anti-depressants. 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. EEO Statement Cipla is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, sex, sexual orientation, gender identity, religion, national origin, genetic information, disability, or protected veteran status.

Job Title: Quality Control (QC) Chemist FLSA Classification: Full-Time, Exempt Professional Work Hours: General Shift: 8 AM - 5 PM (may vary based on business needs) Reports To: Quality Control Manager Pay Range: $65,000 - 90,000 (Annually) InvaGen pharmaceuticals is looking for talent in the following areas at our manufacturing site in Fall River, MA. Purpose The job of the "Chemist" is simply described as an individual contributor who performs testing of samples of various types using various techniques or equipment in the QC laboratory. The job itself may be further modified with respect to the department, group, etc., as exemplified in the "Department" on an individual assigned basis to a sometimes-specific testing group. The role may be further modified based upon individual education, training, experience, or a combination of all three. Generally, modifier designation with respect to experience for Chemist are as follows. However, combination of education, training, and special skills will determine the assignment of Level to a specific individual: Level 1: 0 to 3 years Level 2: 3 to 5 years Level 3: 5 to 10 years Senior: more than 10 years Level 2 or above is strongly preferred. Summary of Responsibilities: Conduct routine testing or other analysis in a specific group or department setting Conduct advanced testing and/or critical testing, as required. Ensures QC Analysts receive proper training. Attends meetings to keep informed of manufacturing priorities. Ensures that safety standards are maintained. Operate specialized equipment or conduct specialized skill testing. Participate in investigation activities. Ensure compliance to all data integrity and cGMP practices, procedures, and expect ensuring compliance with all good documentation practices. Other duties and responsibilities as assigned by the Head of the Department or Section Head. Educational, Skills & Experience Requirements and Preferences: Bachelor's degree (BS or BA), in Chemistry, Biology, Pharmaceutical Sciences, or related field, and a preferred 1-year experience in the pharmaceutical or biotechnology industries preferred. Must have current Good Manufacturing Practices (cGMP) Good Laboratory Practice (GLP) knowledge Professional and Behavioral Competencies Proficiently speak, communicate, and understand (read and write) scientific work in English. Have excellent organization, learning and teaching skills required to work in teams. You enjoy working in a fast-paced environment and are flexible to changing requirements. Working knowledge of raw materials and finished product testing and instruments and techniques such as GC, High-Performance Liquid Chromatography (HPLC), Karl Fischer (KF), Dissolution, Particle Size and ICP. Lead Investigation activities Familiarity with Chromatography systems is required, Empower is a plus. Ability to understand and analyse complex data sets and must have working knowledge of Microsoft Office programs and other scientific based software. Experience in Inhalation products (MDI) is a plus. Effective interpersonal relationship skills and the ability to work individually and as a part a team. Must be a detail-oriented self-starter, demonstrate initiative and possess a positive professional attitude towards work. Must have strong organization and communication skills (written, verbal, and presentation). Must be willing to work in a pharmaceutical packaging setting. Must be willing and able to work any assigned shift ranging from first or second shift. Work schedule may be Monday to Friday. Must be willing to work some weekends based on business needs as required by management. No remote work available Physical Requirements: Work standing or walking unassisted for 75% or greater of an 8-hour period. Unassisted lifting up-to 10 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. Locations: Fall River, Massachusetts EEO Statement: Cipla is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, sex, sexual orientation, gender identity, religion, national origin, genetic information, disability, or protected veteran status.

The Quality Control Technician - Troubleshooting is responsible for inspecting and testing cable and wire products and processes to ensure they meet all quality standards, specifications, and regulations. This includes performing visual inspections, dimensional measurements, electrical, and functional tests. The primary function of this role is to evaluate nonconforming products and to determine the necessary actions to rework the product. The QC Technician must also be able to read and interpret blueprints, engineering drawings, and specifications. This position requires the use of High Voltage, all safety guidelines, procedures, and regulations to prevent accidents and ensure a safe working environment must be followed. The Quality Control Technician - Troubleshooting is a respectful team-player that works well with diverse internal team members. This position is ambitious, self-motivated, results-driven, and demonstrates problem solving skills with sound judgment. This role is also responsive, flexible, accessible, detail oriented, willing to embrace change and proactively adjust plans. Partnering with and elevating others by communicating with peers to increase awareness and ensure team success. Essential Duties and Responsibilities: Troubleshoot nonconforming cables, fill out nonconformance reports and communicates findings to Production Quality Supervisor and Quality Manager Detect and report unusual or non-conforming documentation, materials, conditions, or product to Production Quality Supervisor and Quality Manager. Assist and sometimes lead Root Cause and Corrective Action efforts. Inspect materials, components, and final product to ensure they meet quality standards. Measure dimensions of cable and wire products to ensure they meet specifications. Conduct visual and electrical tests on cable and wire products to ensure they meet performance requirements and identify any defects. When required, perform functional tests on cable and wire products to ensure they operate as designed. Document the results of all tests and inspections. Create, update, compile, save and maintain documentation into internal database. Work with various internal personnel and departments to communicate and resolve quality issues. Comply and support company policies and quality management system. Maintain and create a clean, uncluttered environment that reduces waste and optimizes productivity by following the 5S steps: sort, set in order, shine, standardize, and sustain. When required, help with continuous improvement efforts. More additional responsibilities may be applicable per the Quality Manager. Qualifications: High school diploma or equivalent. 1+ year of experience in quality control, preferably in the cable and wire manufacturing industry. Experience with visual inspection and dimensional measurement. Basic understanding of Microsoft Office and Adobe. Ability to read and interpret blueprints, engineering drawings, and specifications. Strong attention to detail. Ability to work independently and as part of a team. Strong communication skills. Proficient with computers and comfortable using Microsoft Office Suite (Word, Excel, etc.). Physical Qualifications: The physical demands described are representative of those that must be met by an employee to successfully perform the essential function of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this Job, the employee is regularly required to sit; stand; crouch; stoop; walk; talk; hear; use hands to handle or feel assemblies; reach with hands and arms for materials and tools. The employee must occasionally lift and/or move up to twenty-five (25) pounds. They must also have the ability to see details at close range (within a few feet of the observer), color vision, depth perception and ability to focus. This position requires use of information or access to hardware and documents which are subject to the International Traffic in Arms Regulations (ITAR). All applicants must be U.S. persons within the meaning of ITAR. ITAR defines a U.S. person as a U.S. Citizen, U.S. Permanent Resident (i.e. 'Green Card Holder'), Political Asylee, or Refugee. Benefit Conditions: Waiting period may apply Only full-time employees are eligible This Job Is: A job for which military experienced candidates are encouraged to apply Job Type: Full-time Salary: $20.00 - $25.00 per hour Benefits: 401(k) Dental insurance Health insurance Paid time off Vision insurance Experience level: 1 year Schedule: 8 hour shift Day shift Monday to Friday Overtime Work setting: In-person Experience: Blueprint reading: 1 year (Required) Quality control: 2 years (Preferred) Work Location: In person