Quality control analyst jobs in New Bedford, MA - 137 jobs

Industry: Pharmaceuticals Title: Quality Control Analyst II Duration: 11 months contract (+Possibility of extension) This is an onsite role in Norton, MA, with occasional responsibilities at other Client locations. Weekend coverage is required. First shift, Friday-Monday (4 x 10 hours), with initial Monday-Friday training. Description: The Quality Control Operations (QCO) Analyst II Contractor supports maintaining high standards of quality and compliance from development through commercialization. The role includes performing routine and non-routine testing, participating in data trending, investigations, and lab operations, and supporting method transfers, qualification/validation, verification, and implementation. This position enhances QC efficiency and effectiveness. Key Responsibilities' Perform routine/non-routine analytical (HPLC/UPLC) and/or microbiological assays for raw materials, in-process samples, product release, and stability studies following SOPs. Support weekend lab operations and maintain training records. Assist in lab equipment and inventory maintenance, including reagent and sample prep. Review data timely and qualify as a data reviewer. Perform operational assignments (raw material processes, environmental monitoring, in-process testing). Contribute to updating controlled documents (SOPs, work instructions, test methods). Follow internal policies, SOPs, and regulatory standards (GMP, GLP, ICH). Participate in continuous improvement initiatives and cross-functional collaboration. Support regulatory submissions, inspection readiness, and audits Qualifications: B.S. in chemistry, biology, biochemistry, or related field. 4-8 years of pharmaceutical/biotech experience in GMP QC or equivalent. Experience in method transfer/implementation; understanding of method lifecycle management preferred. Strong technical writing, data analysis, problem-solving, and organizational skills. Excellent communication and teamwork. Proficiency in LabWare LIMS, Excel, Word, and PowerPoint preferred

Quality Control Analyst II Norton 45 per hour This is an onsite role in Norton, MA. First shift, Friday-Monday (4 x 10 hours), with initial Monday-Friday training. Perform routine and non-routine analytical (HPLC/UPLC) and/or microbiological assays for raw materials, in-process samples, product release, and stability studies in accordance with SOPs Support weekend laboratory operations and maintain required training records Assist with laboratory equipment and inventory maintenance, including reagent and sample preparation Review data in a timely manner and serve as a qualified data reviewer Perform operational assignments such as raw material processing, environmental monitoring, and in-process testing Contribute to the creation and updating of controlled documents, including SOPs, work instructions, and test methods Follow internal policies, SOPs, and applicable regulatory standards (GMP, GLP, ICH) Participate in continuous improvement initiatives and cross-functional collaboration Support regulatory submissions, inspection readiness, and audits Qualifications Bachelor's degree in Chemistry, Biology, Biochemistry, or a related field 4-8 years of pharmaceutical or biotech experience in GMP QC or equivalent environments Experience with method transfer and implementation; understanding of method lifecycle management preferred Strong technical writing, data analysis, problem-solving, and organizational skills Excellent communication and teamwork abilities Proficiency in LabWare LIMS, Microsoft Excel, Word, and PowerPoint preferred

Title: QC Investigations Specialist Employment Type: Contract Status: Accepting Candidates About the role This role supports real-time manufacturing operations by leading investigations, resolving on-floor issues, and ensuring high-quality documentation. You'll partner closely with manufacturing, QC, materials, and facilities teams to maintain operational continuity and compliance. Key Responsibilities • Triage manufacturing issues and lead analytical investigations and root cause analysis. • Write clear, compliant quality documentation including deviations and CAPAs. • Coordinate with SMEs to determine immediate actions, containment, and impact assessments. • Interpret data to support structured problem-solving and continuous improvement. • Provide technical operations support across manufacturing and QC functions. Qualifications • 6+ years pharmaceutical or biotech manufacturing experience. • 4+ years analytical investigation and QC-focused experience. • Strong background in RCA, deviation management, and GxP documentation. • Ability to interpret analytical data and think scientifically under time-sensitive conditions. • Experience partnering cross-functionally with manufacturing, QC, materials, and facilities teams. Compensation (MA Pay Transparency): • Estimated hourly range: $50-$55/hr (W-2). • Final rate within this range will be based on skills, experience, and interview results.

Location: Rochester MA (100% On-site), 1st shift only 6:30A-3:30P M-F, salary range $72K-$82K, full-time role: health insurance with an HRA, dental, vision, LTD, and a 401(k) retirement plan with an employer match. 3 weeks PTO, 1 week sick. Generous relocation package offered. Qualified candidates are encouraged to apply. Large precast concrete supplier in Massachusetts and New Hampshire, providing high-quality products for over 70 years. Their extensive product range includes septic tanks, manholes, drainage structures, bulkheads, curbing, residential steps, and retaining wall systems, all crafted to precise specifications. They cater to engineers, contractors, and homeowners, emphasizing superior performance and exceptional customer service. The Quality Control Technician (“QC Technician”) will work within the 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. 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. Housekeeping - maintain a clean work area. Including cleanliness within breakroom, restroom, and general facility areas. 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) NPCA PQS Training 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 in order to perform tasks. Ability to read blueprints and sketches.

We are seeking an enthusiastic Associate Synthetic Chemist to support the discovery of small molecules for next-generation 3D printing resins. You will work hands-on in the lab, executing syntheses of novel molecules, characterizing products, and exploring photochemical and photophysical structure-property relationships. This role is ideal for highly motivated early-career chemists who love synthesis and are excited to accelerate innovation through fast, iterative chemistry. You will be closely mentored by experienced synthetic chemists and will collaborate with analytical scientists and engineers developing our printing systems. Responsibilities Design, execute, and troubleshoot small molecule synthetic routes, with a focus on divergent or modular approaches to rapidly generate lead candidates. Purify products using chromatography and crystallization techniques. Characterize compounds via UPLC, NMR, UV/Vis and IR spectroscopy, and mass spectrometry. Work with cross-functional teammates to explore photochemical and photophysical structure-property relationships that drive 3D printing performance. Maintain excellent electronic lab notebook documentation. Contribute to management of chemical databases (e.g., commercial, proprietary, and virtual compound libraries). Minimum Qualifications Bachelor's degree in Chemistry or a closely related field with equivalent advanced chemistry coursework. ≥2 years of intensive organic synthesis laboratory experience (academic research and/or industrial roles). Experience with synthetic planning with chemical databases (e.g., SciFinder, Reaxys). Excellent command of synthetic and physical organic chemistry fundamentals. Experience with air-sensitive techniques (e.g., Schlenk line), purification (chromatography/crystallization), and data interpretation (NMR / LC-MS). Evidence of strong documentation and organizational skills, attention to detail, and the ability to manage multiple workflows efficiently. Evidence of strong collaboration and teamwork talents/skills. Ability to thrive in a fast-paced, collaborative R&D environment. Preferred Qualifications Command of the basics of photochemistry. Experience with heterocyclic and/or extended aromatic systems, especially those relevant to organic (opto)electronics. Benefits We offer competitive compensation packages in our VC-backed startup. Benefits include a full suite of offerings covering medical, dental, vision and 401k plan. Beautiful setting looking out over a river and seaport; outdoor seating and picnic areas. Highly collaborative work environment. Additional Information Travel: Occasional travel may be required from time to time Location: Boston, Massachusetts We value diversity in our company and are an Equal Opportunity Employer.

Whirlpool is currently seeking qualified candidates for a Quality Control Technician. This role is for our Fall River, MA site. The role of the 1st Shift Quality Tech is to help solve quality problems on dryers by taking measurements, doing testing and effecting repairs. Additionally, will assist in certifying materials or machines to reduce the End of line (EOL) testing and field failures. Areas can be main line or medium large assembly or fabrication as required by the problems. Tasks will vary day by day based on the needs of Quality and production. Flexibility in work hours as needed. Reports to Metrology/Fabrication Engineer. Pay Rate $27.05 an hour Your responsibilities will include * Working with test booth operators to understand and aid in the problems * Understanding of the EOL inspections and helping to improve in line inspection to reduce failures at EOL and in the field. * Inspecting and taking measurements on dryers in the line * Performing inspections of materials required to run the next day (in line, fabrication, incoming material from suppliers). * Performing repairs or some assembly operations on the Line to stage the line for success the next day. * Run dryers through the Main Line Customer Assurance Lab (CAL) test as required when it is installed. * Performing process audits as required on the off shift. * Will need to have the ability to plan and perform work and the making of decisions involving the use of considerable judgment and initiative. * Lead problem solving using World Class Manufacturing (WCM) tools. * Learn new skills as needed * Follow all Whirlpool Safety policies when working in the plant. * Will add, subtract, divide and multiply decimals and fractions, use measuring devices, read simple drawings, and interpret production schedules and inspection reports. * Will be lifting parts and doing assembly operations in a safe manner. * Support cost and quality projects by providing data and evaluation. * Evaluate parts and products for Non-conformances * Report issues with accuracy of BOMs * Track/Understand CN's * Understand and support the APQP and QMS process as needed. * Communicate directly with suppliers & operations concerning APQP issues * Perform fit / function evaluations * Uses all designated safety equipment, observes all safety rules, and follows recognized rules of safe practice. Performs duties of a similar or lesser skill to facilitate the flow of work in the department. Minimum requirements * High School Diploma / GED * 6+months of experience doing manufacturing quality inspections and running tests. * Lift 40+ pounds * Be able to be Preferred skills and experiences * Attention to detail. * Ability to operate complicated equipment safely including electrical and gas hookups. * Self motivated and able to work on their own. This role in summary [ACTION REQUIRED - DO NOT POST AS IS]In 1-2 sentences, provide an overview of the purpose, priorities, deliverables and expected outcomes of the role. Your responsibilities will include [ACTION REQUIRED - DO NOT POST AS IS] Describe the main responsibilities of this position. We recommend up to 8 bullet points, preferably starting each statement with a verb. Minimum requirements [ACTION REQUIRED - DO NOT POST AS IS]Describe what is absolutely required for the role, meaning that the candidate cannot be hired if they do not have these requirements. We recommend no more than 3 items and suggest prioritizing:Years of experience Education (majors, minimum degree, etc.) Language skills CertificationsSystems/Technical knowledge Preferred skills and experiences [ACTION REQUIRED - DO NOT POST AS IS]Describe the desirable background and experiences which will be a plus if the candidate possesses them. We recommend no more than 5 items, and suggest including:Years of experience Education (majors, minimum degree, etc.) Language skills CertificationsSystems/Technical knowledge We strongly recommend NOT including behavioral traits in this section. Why should you apply? [ACTION REQUIRED - DO NOT POST AS IS]Describe the benefits and/or advantages of working in that particular location, such as core benefits, vacation days, home office days, on-site daycare, work environment, etc Additional information [ACTION REQUIRED - DO NOT POST AS IS]Use this section to include any other information that was not mentioned in the previous sections. If there is nothing to add, this section should be deleted. Whirlpool Corporation (NYSE: WHR) is the number one major appliance manufacturer in the world, with approximately $21 billion in annual sales, 97,000 employees and 70 manufacturing and technology research centers. The company markets Whirlpool, KitchenAid, Maytag, Consul, Brastemp, Amana, Bauknecht, Jenn-Air, Indesit and other major brand names in nearly every country throughout the world. We stay true to our philosophy that says good business begins by not following but leading. Our brands and products help people make the most of time so they can focus on making the most of moments that matter. At Whirlpool Corporation, we believe that all people matter. Celebrating diversity and including thousands of perspectives empower us to create products that blend into every concept of home. Whirlpool Corporation is committed to equal employment opportunities regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status. Additional information about our company can be found at ***************************** Follow us on LinkedIn or join the conversation @ HYPERLINK "********************************** HYPERLINK "********************************** HYPERLINK "*********************************

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

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.

Sr. Scientist - FSP - Quality Control Shift: Full-Time; Monday - Friday; 8am-5pm EST ONSITE: This is a fully onsite role based at our customer's site in (Boston, MA). We welcome applicants from all locations within the US. Please note that relocation assistance is not provided for this position, and any relocation costs will be the responsibility of the candidate. Must be legally authorized to work in the United States without sponsorship. Must be able to pass a comprehensive background check, which includes a drug screening. At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future. Thermo Fisher's clinical research business is a leading global contract research organization and world leader in serving science. We are passionate, deliberate, and driven by our mission - to enable our customers to make the world healthier, safer, and cleaner. Our Laboratories Functional Service Partnership (FSP) team plays a direct role in advancing drug development by creating sustained groups of talent within our customers' organizations to provide long-term support. Through this collaborative approach, our professionals bring their commitment to excellence, industry knowledge, and operational strength directly into customer environments, helping to enhance capabilities and advance the delivery of life-changing therapies. Key responsibilities: Perform in-process, release, and stability testing and/or review independently following established methodology, procedures and SOPs Maintain accurate testing records and adhere to cGMP/GDP expectations May participate in executing method validations and/or method transfers Assist in troubleshooting of analytical methods with the assistance of manager when necessary May participates in author and review of data, SOPs, analytical methods, protocols and reports May participate in compliance related teams working towards the goal of continuous improvement. Report OOT/OOS results and other deviations to area management. Perform other laboratory duties as assigned. Education and Experience: Bachelor's degree in lab sciences such as Chemistry, Biochemistry, Material Science, Immunology, Biology, Molecular Biology or similar Sr. Scientist: Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 4+ years') OR Masters degree and previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years') OR PhD In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role. Knowledge, Skills and Abilities: Understands cGMP concepts and general practices Knowledge and experience in chromatography, dissolution, and Karl Fisher Knowledge of various complex laboratory equipment including HPLC, GC, KF, dissolution, TOC, UV, IR, pH meter, and balance Strong attention to detail Demonstrate good communication skills both oral and written. A minimum of a Bachelor Degree in science or related discipline is required. Typically requires 4 years of experience in GMP pharmaceutical/biopharmaceutical industry Working Environment: Below is listed the working environment/requirements for this role: Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner. Able to work upright and stationary and/or standing for typical working hours. Able to lift and move objects up to 25 pounds Able to work in non-traditional work environments. Able to use and learn standard office equipment and technology with proficiency. May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments. Able to perform successfully under pressure while prioritizing and handling multiple projects or activities. Benefits We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation! Compensation and Benefits The salary range estimated for this position based in Massachusetts is $95,000.00-$110,000.00. This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes: A choice of national medical and dental plans, and a national vision plan, including health incentive programs Employee assistance and family support programs, including commuter benefits and tuition reimbursement At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount For more information on our benefits, please visit: *****************************************************

Title: QC Equipment Technician Employment Type: Contract Duration: 6+ months Status: Accepting Candidates About the role Support a regulated laboratory or manufacturing team by ensuring equipment operates reliably, efficiently, and in compliance with quality standards. Key Responsibilities Investigate and resolve issues related to equipment failures, system deficiencies, deviations, and troubleshooting activities Author and support quality system records, including deviations, change controls, and CAPAs, as required Monitor and coordinate equipment lifecycle activities, including acquisition, qualification/validation, implementation, and decommissioning Track and communicate equipment timelines using project management tools Ensure equipment documentation complies with cGMP, GDP, and data integrity requirements Qualifications BS degree with a minimum of 3 years of relevant experience, or 3+ years of experience in a GMP laboratory setting Demonstrated ability to quickly learn and apply GxP principles Strong attention to detail and documentation practices Experience supporting regulated laboratory or manufacturing equipment preferred Compensation (MA Pay Transparency) Estimated hourly range: $30-$35/hour (W-2) Final rate within this range will be based on skills, experience, and interview outcomes

Whirlpool is currently seeking qualified candidates for a Quality Control Technician. This role is for our Fall River, MA site. The role of the 1st Shift Quality Tech is to help solve quality problems on dryers by taking measurements, doing testing and effecting repairs. Additionally, will assist in certifying materials or machines to reduce the End of line (EOL) testing and field failures. Areas can be main line or medium large assembly or fabrication as required by the problems. Tasks will vary day by day based on the needs of Quality and production. Flexibility in work hours as needed. Reports to Metrology/Fabrication Engineer. Pay Rate $27.05 an hour Your responsibilities will include Working with test booth operators to understand and aid in the problems Understanding of the EOL inspections and helping to improve in line inspection to reduce failures at EOL and in the field. Inspecting and taking measurements on dryers in the line Performing inspections of materials required to run the next day (in line, fabrication, incoming material from suppliers). Performing repairs or some assembly operations on the Line to stage the line for success the next day. Run dryers through the Main Line Customer Assurance Lab (CAL) test as required when it is installed. Performing process audits as required on the off shift. Will need to have the ability to plan and perform work and the making of decisions involving the use of considerable judgment and initiative. Lead problem solving using World Class Manufacturing (WCM) tools. Learn new skills as needed Follow all Whirlpool Safety policies when working in the plant. Will add, subtract, divide and multiply decimals and fractions, use measuring devices, read simple drawings, and interpret production schedules and inspection reports. Will be lifting parts and doing assembly operations in a safe manner. Support cost and quality projects by providing data and evaluation. Evaluate parts and products for Non-conformances Report issues with accuracy of BOMs Track/Understand CN's Understand and support the APQP and QMS process as needed. Communicate directly with suppliers & operations concerning APQP issues Perform fit / function evaluations Uses all designated safety equipment, observes all safety rules, and follows recognized rules of safe practice. Performs duties of a similar or lesser skill to facilitate the flow of work in the department. Minimum requirements High School Diploma / GED 6+months of experience doing manufacturing quality inspections and running tests. Lift 40+ pounds Be able to be Preferred skills and experiences Attention to detail. Ability to operate complicated equipment safely including electrical and gas hookups. Self motivated and able to work on their own. This role in summary [ACTION REQUIRED - DO NOT POST AS IS] In 1-2 sentences, provide an overview of the purpose, priorities, deliverables and expected outcomes of the role.Your responsibilities will include [ACTION REQUIRED - DO NOT POST AS IS] Describe the main responsibilities of this position. We recommend up to 8 bullet points, preferably starting each statement with a verb.Minimum requirements [ACTION REQUIRED - DO NOT POST AS IS] Describe what is absolutely required for the role, meaning that the candidate cannot be hired if they do not have these requirements. We recommend no more than 3 items and suggest prioritizing: Years of experience Education (majors, minimum degree, etc.) Language skills Certifications Systems/Technical knowledge Preferred skills and experiences [ACTION REQUIRED - DO NOT POST AS IS] Describe the desirable background and experiences which will be a plus if the candidate possesses them. We recommend no more than 5 items, and suggest including: Years of experience Education (majors, minimum degree, etc.) Language skills Certifications Systems/Technical knowledge We strongly recommend NOT including behavioral traits in this section.Why should you apply? [ACTION REQUIRED - DO NOT POST AS IS] Describe the benefits and/or advantages of working in that particular location, such as core benefits, vacation days, home office days, on-site daycare, work environment, etc Additional information [ACTION REQUIRED - DO NOT POST AS IS] Use this section to include any other information that was not mentioned in the previous sections. If there is nothing to add, this section should be deleted. Whirlpool Corporation (NYSE: WHR) is the number one major appliance manufacturer in the world, with approximately $21 billion in annual sales, 97,000 employees and 70 manufacturing and technology research centers. The company markets Whirlpool, KitchenAid, Maytag, Consul, Brastemp, Amana, Bauknecht, Jenn-Air, Indesit and other major brand names in nearly every country throughout the world. We stay true to our philosophy that says good business begins by not following but leading. Our brands and products help people make the most of time so they can focus on making the most of moments that matter. At Whirlpool Corporation, we believe that all people matter. Celebrating diversity and including thousands of perspectives empower us to create products that blend into every concept of home. Whirlpool Corporation is committed to equal employment opportunities regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status. Additional information about our company can be found at ***************************** Follow us on LinkedIn or join the conversation @ HYPERLINK "********************************** HYPERLINK "********************************** HYPERLINK "*********************************

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

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: 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.

Title: QC Specialist - Chemistry Employment Type: Contract Status: Accepting Candidates About the role This role supports Quality Control Chemistry operations by leading QC Sample Management activities across multiple lab functions. You will ensure compliant, on-time sample processing while partnering with digital and quality teams in a fast-paced cGMP environment. Shift: Wednesday-Saturday, 6:00 AM-4:00 PM. Key Responsibilities • Lead QC Sample Management operations supporting Chemistry, Microbiology, Bioassay, and Raw Materials • Oversee daily schedules to ensure compliant sample processing and documentation • Author and maintain SOPs, deviations, CAPAs, and change controls • Act as primary support for audit readiness and regulatory inspections • Partner with Digital teams to optimize LIMS (LabVantage) and data workflows • Manage CTU systems, investigations, and compliance issue resolution Qualifications • BA/BS with 3-5 years or MS with 1-3 years of cGMP Quality Control experience • Strong hands-on experience with QC Sample Management • Proficiency with LIMS and Veeva Quality Systems • Working knowledge of FDA, EU, and ICH regulations • Experience with gowning, aseptic technique, and lab safety practices • Proven people management and cross-functional leadership skills Compensation (MA Pay Transparency): • Estimated hourly range: $40-$45/hr (W-2) • Final rate within this range will be based on skills, experience, and interview results.

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

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.

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.