Quality control analyst jobs in Rocky Point, NY - 77 jobs

Pride Health is seeking a second shift Distillation Chemist for a leading flavor and fragrance supplier in Danbury, CT. Job Title: Distillation Chemist Job Type: Direct Hire Shift: 2nd shift, Mon - Fri, 2:30pm - 11:00pm (shift differential included) Salary Range: $55K - $60K/year Overview: This function provides purification of organic chemicals using distillation techniques and related support systems. This involves a range of activities including: Sets up and adjusts distillation equipment. May operate heating, cooling, vacuum and pressure systems. Uses analytical equipment for assessing quality of distillation cuts and final products. Understands principles of operation of the equipment and, with supervision, interprets results. Transport, weigh, mix and pump chemical materials. Monitoring of process parameters to ensure product quality, yields and lot consistency. Proper care, safety, maintenance and usage of technology, equipment, and/or systems. May serve as a technical resource for Distillation Technician. Maintain all necessary production, safety, inventory, training, and other records and/or logs as required, in written and /or computer format. Complies with all BRI environmental and safety policies and procedures. Requirements: Knowledge of the principles and techniques of distillation and analytical chemistry. BS in Chemistry or related field and one to five years' experience in distillation. Ability to use interchangeably metric and U.S. standards of weights and measures and its application in determining molar quantity Skill in the operation of distillation and support equipment. Knowledge of piping and valve operations to control processes. Ability to conduct gas chromatographic analyses and interprets results. Evaluate materials by odor. Apply Today! If you are interested in the position, please email your resume to **************************** for immediate consideration.

NOTICE: The posting for local applicants only - is not for those applying for a global assignment and/or for employees working outside of Cipla's U.S. Subsidiaries or Affiliates. Job Title QC Chemist III Organization Name InvaGen Pharmaceuticals, Inc. Employment Type Full Time - Salary/Exempt Salary Range $72,800 - $93,600 Benefits In addition to a fulfilling career and competitive salary, the Company offers a comprehensive benefits package to include a 401(k) savings plan and matching, health insurance - medical/dental/vision, health savings account (HSA), flexible spending account (FSA), paid time off (PTO) - vacation/sick/flex time, paid holidays, short-term disability (STD), long-term disability (LTD), parental leave, paid and unpaid family leave, employee discounts, and other benefits. Work Hours/ Shift/ Remote 8:30 AM - 5:00 PM (General Shift) Job Summary The job of the "Chemist" is simple 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. Responsibilities/ Accountabilities * 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. * Participate in investigation activities. * Ensure compliance to all data integrity and cGMP practices, procedures, and expectations * Ensure compliance with all good documentation practices. * Other duties and responsibilities as assigned by the Head of the Department Education Qualifications/Experience * Bachelor's degree (BS or BA), physical sciences preferred * Masters or (MS) or Doctorate (PhD) * 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. 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-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. About Cipla 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. Driven by the purpose 'Caring for Life', Cipla's focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world. In the last 85 + years, Cipla has emerged as one of the most respected pharmaceutical names in India as well as across more than 100 countries. Cipla is a fast-growing pharmaceutical company with a continued focus on the expanse of our strong legacy. Over the last five years, Cipla has significantly expanded its portfolio and presence in the U.S. with both a generic and brand division. InvaGen Pharmaceuticals, Inc. InvaGen Pharmaceuticals is a Cipla subsidiary 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. In October 2020, InvaGen established its project site in Fall River, Massachusetts to support the launch of Cipla's respiratory business in the United States. Equal Opportunity Employer Cipla is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Cipla, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require reasonable accommodation to make your application or interview experience a great one, please contact the recruiter. About the Salary/ Pay Range: The salary range mentioned above is an anticipated base salary range for this position. Exact salary depends on several factors such as experience, skills, education, and budget. Salary range may vary based on geographic location. In addition to base salary, this position may be eligible for benefits and participation in a bonus program based on performance and company results.

NOTICE: The posting for local applicants only - is not for those applying for a global assignment and/or for employees working outside of Cipla's U.S. Subsidiaries or Affiliates. Job Title QC Chemist III Organization Name InvaGen Pharmaceuticals Location 7 Oser Ave, Hauppauge, NY 11788 Employment Type (Hourly/ Full Time) Full-Time - Salary/Exempt Benefits In addition to a fulfilling career and competitive salary, the Company offers a comprehensive benefits package to include a 401(k) savings plan and matching, health insurance - medical/dental/vision, health savings account (HSA), flexible spending account (FSA), paid time off (PTO) - vacation/sick/flex time, paid holidays, short-term disability (STD), long-term disability (LTD), parental leave, paid family leave, employee discounts, and other benefits Work Hours/ Shift/ Remote 8:30 AM - 5:00 PM General Salary Range $73,000 - $93,000 Responsibilities/ Accountabilities The job of the "Chemist" is simple 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. The general duties and responsibilities of the "Chemist" 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. Participate in investigation activities. Ensure compliance to all data integrity and cGMP practices, procedures, and expectations. Ensure compliance with all god documentation practices. Other duties and responsibilities as assigned by the Head of the Department. Education Qualifications Bachelor's degree (BS or BA), physical sciences required. Masters or (MS) or Doctorate (PhD) 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 Must have a minimum of eight (8) years of Pharmaceutical QC lab experience. Must have a background within the pharmaceutical industry. Understanding of lab equipment and QC testing techniques required. Experience in Inhalation products (DPI) is a plus Skills/ Competencies UV, HPLC, DSC, and other tests. Know how to use dissolution instruments. LIMS and Empower 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. Other Information 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. No remote work available. Relocation negotiable. About Cipla 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. Driven by the purpose ‘Caring for Life', Cipla's focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world. In the last 85 + years, Cipla has emerged as one of the most respected pharmaceutical names in India as well as across more than 100 countries. Cipla is a fast-growing pharmaceutical company with a continued focus on the expanse of our strong legacy. Over the last five years, Cipla has significantly expanded its portfolio and presence in the U.S. with both a generic and brand division. InvaGen Pharmaceuticals, Inc. InvaGen Pharmaceuticals is a Cipla subsidiary 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. In October 2020, InvaGen established its project site in Fall River, Massachusetts to support the launch of Cipla's respiratory business in the United States. Equal Opportunity Employer Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Cipla, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require reasonable accommodation to make your application or interview experience a great one, please contact the recruiter. About the Salary/ Pay Range: The salary range mentioned above is an anticipated base salary range for this position. Exact salary depends on several factors such as experience, skills, education, and budget. Salary range may vary based on geographic location. In addition to base salary, this position may be eligible for benefits and participation in a bonus program based on performance.

Part-time Description The Part-Time Quality Associate supports the Quality Department at the Wallingford Distribution Center. This role receives and manages components and retain samples, conducts sampling and inspections, and executes release decisions for third-party co-manufactured finished goods, packaging components, and received retains. The position maintains retain sample storage and logs, pulls retains for complaint investigations, reviews manufacturing jobs performed at Wallingford, and manages local document control. The associate also coordinates closely with the Middletown manufacturing facility (Production, Shipping/Receiving, and Quality) and maintains compliance with cGMP/GDP requirements under 21 CFR Part 111. MAJOR RESPONSIBILITIES: · Compliance with Standard Operating Procedures, GMPs and related systems that ensure company compliance and applicable regulations · Receive, log, and stage incoming components and retain samples in accordance with SOPs. · Maintain retain sample storage conditions, inventory, and chain-of-custody; pull retains to support complaint investigations. · Perform sampling and visual/physical inspections of incoming materials and finished goods per approved methods. · Review documentation (e.g., COAs, specifications, receiving records) and determine release/hold status for third-party co-manufactured finished goods, packaging components, and received retains. · Perform quality approval and documentation review for manufacturing jobs executed at the Wallingford Distribution Center (e.g., kitting, rework, relabeling). · Verify completion, legibility, and GDP compliance of all associated records; ensure line clearance and reconciliation requirements are met. · Review and maintain quality documentation and logbooks for the Wallingford team. · Execute local document control activities (issuing/archiving controlled documents and forms, processing requests from Middletown, ensuring current versions are in use). · Coordinate with Middletown Production, Shipping/Receiving, and the main Quality team on releases, holds, investigations, and material movements. · Escalate deviations, complaints, and potential quality issues promptly per SOP. · Adhere to cGMP and GDP practices and maintain required training to ensure compliance with 21 CFR Part 111. · Support internal/external audits and maintain inspection-ready work areas and records. · Follow site safety, housekeeping (5S), and PPE requirements. · Destruction of rejected/expired materials following company SOP's and guidelines · Operate forklift and other power equipment as needed · Must prepare and complete required documentation · Perform additional duties as assigned KNOWLEDGE/SKILLS/EXPERIENCE: · Must have a high school diploma or general education degree (GED); Associates degree strongly preferred in Food Science, Nutrition, Biology, or Chemistry · Experience in · Ability to read, write, and communicate about work instructions and safety information written in English · Understanding of basic mathematical concepts · Ability to analyze and interpret technical information · Computer skills including MS office and material control programs · Advanced organizational skills · Ability to follow and interpret instructions whether written or spoken · Ability to work well in a team · Strong communication and interpersonal skills · Punctual and reliable in work attendance PHYSICAL REQUIREMENTS: · Must be able to lift up to 50 pounds on a regular basis · Operation of forklift and other power equipment · Works near moving mechanical parts · Vision requirements: Requires distance vision, color visions, peripheral vision, depth perception and ability to focus · Must wear PPE and GMP appropriate for the position: non-slip footwear (boots), hair net, beard net (if applicable), face masks, nitrile food-grade gloves Blueroot Health™ is an Equal Opportunity Employer. Employment opportunities at Blueroot Health™ are based upon one's qualifications and capabilities to perform the essential functions of a particular job. All employment opportunities are provided without regard to race, religion, sex, national origin, age veteran status, disability, genetic information, or any other characteristic protected by law. This Equal Employment Opportunity policy governs all aspects of employment, including, but not limited to, recruitment, hiring, selection, job assignment, promotions, transfers, compensation, discipline, termination, layoff, access to benefits and training, and all other conditions and privileges of employment.

As an essential business, Anomatic produces innovative and sustainable packaging for today's biggest brands. By leveraging over five decades of manufacturing expertise and employing an extensive technologies portfolio, we design, manufacture, and finish incomparable stock and customized solutions for numerous markets. Position: Quality Control Inspector Location: Naugatuck, CT Department: Quality Shift: First Shift 6am - 2:30pm JOB SUMMARY QC Stamping Inspector's primary function is the quality evaluation through gauging and inspection to validate the acceptability of stamping production, the capture of nonconforming product and the documenting of that acceptability. Evaluation is conducted as specified through provided gauging and inspection standards. QC Stamping inspectors also provide general “Quality” training, support and guidance to Stamping Department Personnel ESSENTIAL FUNCTIONS Gather samples from each stamping press twice per shift, performs visual and dimensional inspection, recording dimensional results in Mongoose (stamping inspection system of record) as well as on the Stamping Inspection Shift Report (excel file) Conduct proper defect containment, inform the Press Operators of any defects identified, as well as Set-Up personnel, Toolmakers, Tooling Engineer and/or Stamping Dept. Manager as applicable. Record actions (i.e. scrap, hold, etc..) on the Stamping Inspection Shift Report Receive QC LAB (also receiving inspection group) anodizing report, as well as supporting defect samples and address quality issues specified in their report Conduct “outgoing” (from stamping) skid audits for product from presses identified by the Stamping Q.E. Report data as specified Provided training to Stamping Department personnel as a qualified TWI trainer (Includes but not limited to developing TWI instructional break downs, providing individual training for TWI, documenting & tracking provided training, auditing TWI tasks as indicated by management) For Start-up ensure that proper documentation and standards are at each press (gauge plan, part drawing, skid tags, skid labels, and standard boards) Perform “Start-Up” inspection using applicable gauge plan, applicable standard boards and past start-up retains. Record all results on Stamping Inspection Report Maintain “Start-Up Retains Bank” located in the Toolmaker work area. As startups are approved, one raw and one anodized sample from the Start-up will be marked with the approval date and placed in the appropriate bin to be referenced on future start ups At the beginning of each shift Stamping Q.C. Inspectors will review each press and ensure correct labels, gauge plan, part drawing and correct skid tags are being used Keep Department QC Stations and/or QC Work Areas orderly at all times. Double check to make sure proper prints, gauging and inspection plans are at each press and in the QC areas as assigned. Inspect and report inspection results for New Product Development (NPD) by completing the applicable Stamping Quality portion of the First Piece Submission Routing Form Any other duties that may be assigned, including data entry, QC checks on discrepant materials, production and quality reporting, filing and maintaining paperwork, etc. Assist with any other duties and projects as required QUALIFICATIONS Must be proficient in gauging methods and procedures. Must maintain an excellent attendance record. Must be able to work independently without constant supervision and be able to work overtime as needed to cover absences. Must be proficient in the use of Microsoft Office Applications (Outlook, Excel, Word and Power Point at a minimum). Must have basic knowledge of or be trainable on Syteline. Must be able to wear prescribed safety equipment and promote a safe work environment. #1Anomatic

Nature and Scope This position is centered on testing of raw materials, in-process, and finished product samples accurately and efficiently to determine chemical identity, potency and purity of pharmaceutical products manufactured by American Regent, Inc. The QC Chemist I will perform analytical testing according to current guidance and established procedures for analysis of stability samples in the Quality Control Laboratories. Essential Duties and Responsibilities Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to this job at any time. * Successfully operate all instruments including: pH meter Balances Autotitrator / Karl Fischer Titrator HPLC / GC ICP-OES / ICP-MS UV-VIS Spectrophotometer Osmometer Polarograph * Perform testing of raw materials, in-process, and finished product samples. * Perform all wet chemistry procedures including titrations, extractions, etc. * General glassware and laboratory cleaning. * Maintain GMP documentation of all activities. * Perform calibration, basic troubleshooting and maintenance on laboratory instruments. * Perform any other tasks/duties as assigned by management. Education Requirements and Qualifications To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required. * Bachelor's degree in Science, Chemistry, Biology or related field required. * Good oral and written communication skills, detail oriented, capable of multi-tasking. * Knowledge of HPLC instrumentation and software. * Knowledge of MS Word, Excel. * Ability to work overtime as needed. Physical Environment and Requirements * Specific vision requirements include 20/40 near vision (can be corrected with eyeglasses or contacts) and color vision. Expected Hourly Rate: $33.70 - $37.00 The hourly rate displayed is the hourly rate of compensation for the role that the employer in good faith believes to be accurate at the time of the posting of an advertisement for the role. Actual compensation for the role will be based on a number of different factors including but not limited to the candidate's qualifications, education, knowledge, skills and experience. American Regent also offers a competitive total rewards package which includes healthcare, life insurance, profit sharing, paid time off, matching 401k as well as a wide range of other benefits. American Regent celebrates diversity and we are committed to creating an inclusive environment for all employees. We are an Equal Opportunity Employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, or protected veteran status. Applicants have rights under Federal Employment Laws. * FMLA poster: ********************************************************** * Know Your Rights: Know Your Rights: Workplace discrimination is illegal (eeoc.gov) * Employee Polygraph Protection Act: ********************************************************* Alert: We're aware of individuals impersonating our staff to target job seekers. Please note: * All legitimate communication will come directly from a verified ARI recruiter either by phone or via an americanregent.com email address. * Our recruiting process includes multiple in person and/or video interviews and assessments. * If you are unsure about the legitimacy of a message, contact John Rossini at *************************** before responding. * We never request payment, bank information, or personal financial details during our offer process. Your security is important to us, and we encourage you to stay vigilant when job searching. American Regent Inc. endeavors to make *********************************** accessible to any and all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please email **************************************.

Kit QC Inspector- Farmingdale, NY on site ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. Job Advert Posting At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives. Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development. That's our vision. We're driven by it. And we need talented people who share it. If you're as driven as we are, join us. You'll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry. Kit QC Inspector- Farmingdale, NY onsite The role: To ensure the quality and correctness of all visit kits distributed to investigator sites. Inspect all visit kits according to SOP prior to packing and transfer to the shipping department. Perform quality control of all visit kits as required by the SOP. Ensure all errors are corrected & logged appropriately. Inform the QC supervisor of any issues or delays. Achieve daily/weekly departmental Quota assigned. Perform additional responsibilities as requested by Management To be successful you will need: 2 to 3 years of QC experience Skills - Detail oriented, excellent organizational skills, Commutations skills and the ability to deal well with stress. Basic computer skills including knowledge in MS Outlook, of MS Word, Excel and typing skills. High School or Equivalent (Required) Hourly Rate range: Up to 23.50 hour Actual compensation will be determined based on factors such as geographic location, work experience, education/training, and skill level. You may be eligible for a bonus, stock compensation and commissions in some cases depending on your role and performance. Visit our careers site to read more about the benefits ICON offers. #LI-FL1 Benefits of Working in ICON: Our success depends on the quality of our people. That's why we've made it a priority to build a culture that rewards high performance and nurtures talent. We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours. We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead. But beyond the competitive salaries and comprehensive benefits, you'll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change. ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below. What ICON can offer you: Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: * Various annual leave entitlements * A range of health insurance offerings to suit you and your family's needs. * Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. * Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being. * Life assurance * Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles. Salary range: - Bonus, Com, Stock, Benefits & Disclaimer verbiage: Actual compensation will be determined based on factors such as geographic location, work experience, education/training, and skill level. You may be eligible for a bonus, stock compensation and commissions in some cases depending on your role and performance. Are you a current ICON Employee? Please click here to apply

First shift 445am-3pm Monday - Friday with some Saturdays through the year Summary: The Quality Control Technician is primarily responsible for quality assurance of all products through administration of HACCP, GMP's, Sanitation, Pest Management and other programs that ensure regulatory compliance and education of staff. The position supports the Quality, Food Safety and SQF initiatives outlined in the Quality Manual and SQF Program. Essential Job Functions : Ensures specifications are met by measuring, recording, analyzing data and working with equipment and production personnel to improve results. Perform and document daily pre-op inspections and related checks. Assist Production Supervisor with daily line set up. Calibrate scales, thermometers, and water meters daily. Prepare all the necessary paperwork needed to complete documentation of all products and processes. Test, analyze, record, and control all product and component weights as well as sensory evaluations according to specified time intervals. Record and document all HACCP related processes. Report problems or deficiencies in quality or related processes to QA Manager and Shift Supervisor. Maintain USDA, HACCP, GMP guidelines on the production floor. Interact with USDA Inspectors. Work with Production Supervisors and personnel to maintain quality /customer standards. Pre-operations testing to ensure production is authorized to start. Ensure sufficient supply of items such as gloves, hairnets/beard nets, hearing protection, aprons, hand and shoe sanitizing stations, soap, and paper towel stations. Monitor all freezer and cooler temperatures. Monitor the temperature of the meet during cooking and cooling. Monitor the pasta hydration. Ensure all metal detection/X-ray devices are operating properly. Interact with outside technicians for scale and metal detection calibrations. Take product samples at scheduled times. May participate as member of Safety Committee. Participate in Allergen and Pest Management Program. Provide support for other positions when needed. Check and record sanitizer concentrations. Verify ingredients, lots, and quantities in production batches. Other duties as assigned. Job Requirements: High School diploma or equivalent. English, Bilingual preferred. 1-2 years of Production Line Experience within the food industry a plus. Product knowledge: Acquire and maintain full knowledge of USDA and FDA codes, rules, and regulations. Proficiency in follow-up; ability to meet deadlines. Team player, positive can-do attitude. Ability to assess situations and make independent decisions to achieve success. Ability to bend, sit and stand. Ability to perform multiple complex tasks concurrently. Ability to communicate both verbally and in writing. Ability to see and walk for inspections of plant sites. Ability to hear. Ability to lift at least 25 lbs.

Job DescriptionBenefits: 401(k) matching Dental insurance Health insurance Paid time off Structural Steel Certified Welding Inspector (CWI)/QC) Structural steel fabricator in Calverton NY is seeking an experienced Certified Welding Inspector (CWI). We are looking for a team player with experience in AISC standards and audits. This is a non-traveling position, which reports to the QC Manager. EDUCATION EXPERIENCE: High school diploma or equivalency certificate. 3+ years of experience as a certified welding inspector in a structural steel fabrication facility, as well as experience in Quality Assurance. Current American Welding Society certified welding inspector (CWI). Ability to read and understand drawings plans and specifications. Ability to perform physical activities that require frequent bending at the waist, squatting, climbing, kneeling and reaching about the head. Must be detail-oriented, extremely organized and have a good work ethic. Microsoft Office skills, including Excel, required. Experience working in fabrication shop UT and MT certification is required AISC standards/audit experience highly preferred. RESPONSIBILITIES: Maintain Quality Control Manual, including compliance to all AISC standards. Position involves visual inspection of structural steel, including bolted and welded connections, and performing non-destructive testing. Interpret codes and specifications in accordance with the drawing requirements. Use a computer to compile and submit data of acceptance or rejection of inspections, as well as for inter-office communications and audit program management. Recommend and approve repairs as well as perform visual inspection of work in progress and completed work. Review and verify welding procedures and welder qualifications. Review Mill test reports and certifications

The Scientist 3 - QC is responsible to perform testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, calculate and report results on applicable specification documents, participate in method transfer activities within departments or between facilities or organizations. This role will also provide feedback on systems and analytical procedures to promote continuous improvement and enhancement of compliance posture. Essential Functions: Perform physical and chemical analysis of raw materials, in-process, and finished pharmaceutical products, including products on stability, according to written methods, material specification, and company policies as identified in standard operating procedures (SOPs). Comply with cGMps, SOPs, and STPs to avoid out-of-specification situation. Assure compliance with state and federal regulations. Actively participate in any project work as and when assigned. Perform process validation and cleaning validation/verification testing on various drugs. Assist other scientists with analytical, instrument and software related problems as required. Use sonic sifter, laser diffraction, Karl Fischer, UV-Vis spectrophotometer, Infra-red spectrophotometer, HPLC with UV detection as well as with conductivity detection, TLC, pH meter, and dissolution. Calibrate HPLC, Dissolution apparatus equipped with auto-sampler and /or in-line UV, pH meters, analytical balances, and Karl-Fischer titrator. Document steps followed during analysis execution, calculate and report results. Actively participate in investigation of laboratory results. Review laboratory analysis data for completeness, specification compliance, and compliance with company's written policies. Report any abnormal findings to the Supervisor. As assigned, perform in-depth review of analytical records/reports to assure that calculations and other data are technically correct and compliant to relevant specifications. Additional Responsibilities: Assist the laboratory supervisor with handling non-routine special projects requiring activities such as out-of-specification investigations and out-of-alert limit investigations in the laboratory. Ensure that expired chemicals and reference standards are removed from laboratory area. Perform calibration of HPLC, GC, and other equipment as assigned by the supervisor. Assist with hands-on training of newly hired Technicians or Scientists 1 and 2 levels. Education: Bachelors Degree (BA/BS) Chemistry or related science discipline - Required Master Degree (MS/MA) Chemistry or related science discipline - Preferred Experience: With a Bachelors Degree (BA/BS) -5 years or more of testing of chemicals/pharmaceutical products With a Masters Degree (BA/BS) -3 years or more of testing of chemicals/pharmaceutical products Skills: Must be precise and consistent in day to day analysis, easily trainable and ready to learn. - Advanced Must be able to work in a team environment and be flexible to easily adapt to changes in assignments. - Advanced Must be able to execute compendial procedures involving complexity with no or minimal supervision. - Intermediate Must be able to effectively communicate results, problems or issues, verbally as well as in writing. - Intermediate Must be able to assume a role of a leader in team environment as and when required. - Intermediate Must be computer literate and savvy with MS office applications, software programs related to LIMS. - Intermediate Must be willing to work extended hours, including weekends, as and when required. - Intermediate Must follow safe practices as identified in appropriate MSDS during working with chemicals, and must follow applicable state and federal regulations. - Advanced Must be capable of maintaining clear and concise laboratory records and communicating clearly both within and between departments. - Advanced Must be thoroughly familiar with cGMP applicable to laboratories in pharmaceutical settings and with method verification/validation concepts. - Advanced Must be able to review laboratory records to ascertain compliance with applicable specifications, methods, and SOPs. - Intermediate Specialized Knowledge: Must possess in-depth knowledge of analytical chemistry techniques, such as spectrophotometric, dissolution and drug release, chromatographic techniques (standalone or hypenated) and measuring physical parameters (viscosity, particle size or droplet size by laser diffraction, melting point by DSC, water content by TGA, identification by XRPD, and other techniques). Must be able to follow compendial (USP/EP/BP/JP) procedures for analysis. Must understand and apply cGMP requirements applicable to quality control laboratory. Must have ability to apply advanced technical skills to troubleshoot and resolve complex analytical and instrument-related problems effectively and in a timely manner and report actions to the laboratory management in a timely manner. Must be able to identify trends in analytical data. The base salary for this position ranges from $90,000 to $95,000 per year. Amneal ranges reflect the Company's good faith estimate of base salary that Amneal reasonably believes that it will pay for said position at the time of the posting. Individual compensation will ultimately be determined based on a variety of relevant factors, including but not limited to, qualifications, geographic location and other relevant skills. At the heart of our Total Rewards commitment is a comprehensive, flexible and competitive benefits program for eligible positions that enables you to choose the plans and coverage that meet your personal needs. This includes above-market, diverse and robust health and insurance benefits to meet the varied needs of our employees as well as a significant 401(k) matching contribution to help our employees save for retirement. We also promote employee well-being with programs that helps you enjoy your career alongside life's many other commitments and opportunities.

Hourly : 22.72 What do you get when you bring together a team of bright individuals and place them into an environment where “work” means making a difference in the lives of people across the globe? You get Sciolex Corporation, a fast-growing defense contractor focused on providing the U.S. Government a level of service that surpasses the epitome of excellence. Our core services include systems engineering technical advice, technical support, and administrative assistance. From our humble beginning as a small Service Disabled, Veteran Owned Small Business in Chantilly, VA, Sciolex Corporation is now the home for over 1,000 employees across the U.S. Over the past 19 years, Sciolex Corporation has constructed an environment that celebrates diversity and encourages a positive work/life balance, all while supporting government missions that our employees are proud to be a part of. When you work for Sciolex Corporation, you are working for a stable company that values you and is committed to ensuring you receive the utmost employee care. Responsibilities The Quality Control Inspector (QCI) supports the overall mission of the U.S. Citizenship and Immigration Services (USCIS) by facilitating the operations of a local Field Office. As a QCI, your responsibilities would include: Verifies compliance with work standards, SOPs, ROH, and other requirements documents, Pays particular attention to the timeliness and accuracy of work performed, Screens documents to determine accuracy of data contained in them and determines which need corrective action, Keeps various logs and uses random sampling to evaluate process efficiency, accuracy, and timeliness, Responsible for recognizing problems that might invalidate samples, investigating complaints, reviewing violations found by USCIS personnel, and preparing reports of findings and actions needed or taken, Recommends changes that will improve contract performance, Other duties as assigned. Qualifications & Physical Requirements High school diploma or equivalent Must be able to obtain a Public Trust/Suitability Clearance under the Department of Homeland Security from the United States Citizenship and Immigration Services Ability to read and understand proficiently in English Ability to lift and carry up to 45 lbs. or more in a physical environment Ability to perform tasks while bending, stooping, climbing, and reaching At Sciolex Corporation, our top priorities and most valuable resources are our employees, which is why we offer a competitive total compensation package. We are a proud Equal Opportunity Employer (EOE) who celebrates diversity in and out of our organization. Come see where your opportunities for success can flourish. NOTICE: Sciolex Corporation NEVER asks job applicants to issue any payment, service fees, or banking information to Sciolex Corporation or its recruiters as part of our application process. Before providing any personal information to outside parties, verify that the job you are applying for appears on our Careers site.

Hamilton Connections is seeking candidates for a quality control inspector operating at a manufacturing company in Danbury, CT. The quality control inspector is responsible for testing, evaluating and documenting the quality of manufactured products. The hours are 3:30 p.m.-12 a.m., Monday-Friday. The job pays $28-$32 an hour, depending on experience. Job Responsibilities: Perform first piece, final and first article inspections of products to inspect for damage and/or defects Use measuring tools like calipers, micrometers and gages to inspect products Measure products for accuracy according to blueprint specifications Maintain accurate documentation and reporting Other duties as assigned Job Requirements: 5 or more years of quality control experience, including first piece, final and first article inspections Experience with precision measuring instruments, including calipers, micrometers, height gages, plug gages and thread gages Able to read blueprints Coordinate Measuring Machines (CMM), vision system and/or optical comparator experience Geometric Dimensioning and Tolerancing (GD&T) experience Familiar with ISO procedures a plus Organized, responsible and self-driven High school diploma or equivalent Able to pass pre-employment screenings

Job Advert Posting At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives. Our ‘Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development. That's our vision. We're driven by it. And we need talented people who share it. If you're as driven as we are, join us. You'll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry. Kit QC Inspector- Farmingdale, NY onsite The role: To ensure the quality and correctness of all visit kits distributed to investigator sites. Inspect all visit kits according to SOP prior to packing and transfer to the shipping department. Perform quality control of all visit kits as required by the SOP. Ensure all errors are corrected & logged appropriately. Inform the QC supervisor of any issues or delays. Achieve daily/weekly departmental Quota assigned. Perform additional responsibilities as requested by Management To be successful you will need: 2 to 3 years of QC experience Skills - Detail oriented, excellent organizational skills, Commutations skills and the ability to deal well with stress. Basic computer skills including knowledge in MS Outlook, of MS Word, Excel and typing skills. High School or Equivalent (Required) Hourly Rate range: Up to 23.50 hour Actual compensation will be determined based on factors such as geographic location, work experience, education/training, and skill level. You may be eligible for a bonus, stock compensation and commissions in some cases depending on your role and performance. Visit our careers site to read more about the benefits ICON offers. #LI-FL1 Benefits of Working in ICON: Our success depends on the quality of our people. That's why we've made it a priority to build a culture that rewards high performance and nurtures talent. We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours. We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead. But beyond the competitive salaries and comprehensive benefits, you'll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change. ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below. Are you a current ICON Employee? Please click here to apply: link

Job Advert Posting At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives. Our ‘Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development. That's our vision. We're driven by it. And we need talented people who share it. If you're as driven as we are, join us. You'll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry. Kit QC Inspector- Farmingdale, NY onsite The role: To ensure the quality and correctness of all visit kits distributed to investigator sites. Inspect all visit kits according to SOP prior to packing and transfer to the shipping department. Perform quality control of all visit kits as required by the SOP. Ensure all errors are corrected & logged appropriately. Inform the QC supervisor of any issues or delays. Achieve daily/weekly departmental Quota assigned. Perform additional responsibilities as requested by Management To be successful you will need: 2 to 3 years of QC experience Skills - Detail oriented, excellent organizational skills, Commutations skills and the ability to deal well with stress. Basic computer skills including knowledge in MS Outlook, of MS Word, Excel and typing skills. High School or Equivalent (Required) Hourly Rate range: Up to 23.50 hour Actual compensation will be determined based on factors such as geographic location, work experience, education/training, and skill level. You may be eligible for a bonus, stock compensation and commissions in some cases depending on your role and performance. Visit our careers site to read more about the benefits ICON offers. #LI-FL1 Benefits of Working in ICON: Our success depends on the quality of our people. That's why we've made it a priority to build a culture that rewards high performance and nurtures talent. We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours. We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead. But beyond the competitive salaries and comprehensive benefits, you'll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change. ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below. Are you a current ICON Employee? Please click here to apply: link

Job Description Schivo Medical, located in Plainview , NY, is a contract manufacturer that make medical components that enhance and save people lives. ***We are hiring a quality control inspector with knowledge in the manufacturing of medical and surgical tools*** Quality Control Inspector Job Overview: Quality Control related tasks such has verifying components that are produced to print and relate the results to appropriate personal. Quality Control Inspector Knowledge, Skills and Abilities Required: Perform in-progress inspection for all machined components. Operate CMM machines, Keyence and visions systems Review operator inspection reports and traveler information. Submit reports to shift supervisor and communicate the results to machine operators. Perform First Article Inspection for new parts (set ups) Follows established departmental policies, procedures, and objectives, continuous quality improvement objectives, and safety, environmental, control standards. Detail knowledge of inspection techniques, tools and methodology Experience using measuring tools a plus Ability to read and interpret engineering drawings and blueprints Must possess the ability to use a wide variety of measuring devices to perform dimensional inspection of components produced. Must be dependable and possess a willingness to learn new techniques. Medical and Aerospace manufacturing experience with emphasis on FAIR Follow the quality standards of ISO-13485 Knowledge of GD& T helpful Minimum Job Requirements & Education* Completed AAS degree(s) from an accredited institution that are above the minimum education requirement may be substituted for experience on a year for year basis. Concentration on taking classes based in quality and metrology plus High school diploma or GED; at least 2 years of experience in a CNC Manufacturing environment Benefits:* 401(k) 401(Match) Dental insurance Health insurance Vision insurance Generous Paid time off EAP Program Employee referral ******Must be authorized to work in the United States********* Schivo Medical is an Equal Opportunity Employer. All qualified applicants will receive employment consideration without regard to race, color, age, sex, sexual orientation, gender identity, religion, national origin, genetic information, disability, or protected veteran status.

The Chemistry Department at Farmingdale State College is seeking to fill a part-time Lab Technician vacancy for its academic laboratory program. * Assembly and disassembly of laboratory setups * Monitoring of a laboratory class, in conjunction with a faculty member, to ensure adherence to procedures, * laboratory safety, and waste disposal * Preparation of materials for laboratory sections * Maintaining general safety and cleanliness of laboratory rooms This position will require learning the laboratory preparations and assisting in laboratory observation for the Department's one year general chemistry course as well as the one-semester general and organic chemistry courses. Work schedule would consist of day and evening hours for a total of 15-20 hours per week. The college particularly welcomes candidates with knowledge, skills and abilities that include: * Commitment to diversity and university initiatives supportive of diversity and inclusion. * Interest in participating in student-centered service activities. * Desire to apply expertise in promoting civic engagement with the College's many community partners. Requirements: MINIMUM REQUIRED QUALIFICATIONS: * BS in Chemistry or a related field * Minimum of 2 years experience in a laboratory environment Additional Information: This is a part-time, temporary UUP position. * SALARY: $23.33/hour The State University of New York offers excellent fringe benefits including health insurance options and retirement plans. Click here for New York State PT UUP Benefits Summary Visit our Why Work at FSC page to learn more about FSC and the total rewards we offer. VISA SPONSORSHIP IS NOT AVAILABLE FOR THIS POSITION The Consumer Information web page can be viewed at the following link *********************************************************** This page describes various services, information and statistics on many different aspects of the College's operations. Farmingdale State College's commitment to inclusive excellence is an important part of our mission of public education and our culture. At Farmingdale State College, we continue to work on building a community that supports freedom, mutual respect, and civility. We seek others who support these values of diversity and inclusiveness and candidates of all diverse backgrounds who wish to participate in our cultural aspirations are welcome and encouraged to apply. The College is an Equal Opportunity/Affirmative Action employer and does not discriminate on the basis of race, color, national origin, religion, creed, age, disability, sex, gender identity, sexual orientation, familial status, pregnancy, predisposing genetic characteristics, military status, domestic violence victim status or any other legally protected status. Application Instructions: Interested candidates may apply by clicking on the "Apply Now" link at the top or bottom of this page. The following documents are required for all positions: * Cover Letter * Resume/C.V. Only applications made through Farmingdale's electronic application system will be accepted. Once you successfully apply you will receive an email as confirmation. Returning applicants may login to their Farmingdale State College Careers Account to apply for this position. See the FAQ for using our online system. Please contact us if you need assistance applying through this website.

NOTICE: The posting for local applicants only - is not for those applying for a global assignment and/or for employees working outside of Cipla's U.S. Subsidiaries or Affiliates. Job Title QC Chemist III Organization Name InvaGen Pharmaceuticals Employment Type (Hourly/ Full Time) Full-Time - Salary/Exempt Benefits In addition to a fulfilling career and competitive salary, the Company offers a comprehensive benefits package to include a 401(k) savings plan and matching, health insurance - medical/dental/vision, health savings account (HSA), flexible spending account (FSA), paid time off (PTO) - vacation/sick/flex time, paid holidays, short-term disability (STD), long-term disability (LTD), parental leave, paid family leave, employee discounts, and other benefits Work Hours/ Shift/ Remote 8:30 AM - 5:00 PM General Salary Range $73,000 - $93,000 Responsibilities/ Accountabilities The job of the "Chemist" is simple 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. The general duties and responsibilities of the "Chemist" 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. * Participate in investigation activities. * Ensure compliance to all data integrity and cGMP practices, procedures, and expectations. * Ensure compliance with all god documentation practices. * Other duties and responsibilities as assigned by the Head of the Department. Education Qualifications * Bachelor's degree (BS or BA), physical sciences required. * Masters or (MS) or Doctorate (PhD) 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 * Must have a minimum of eight (8) years of Pharmaceutical QC lab experience. * Must have a background within the pharmaceutical industry. * Understanding of lab equipment and QC testing techniques required. * Experience in Inhalation products (DPI) is a plus Skills/ Competencies * UV, HPLC, DSC, and other tests. * Know how to use dissolution instruments. * LIMS and Empower 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. Other Information 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. No remote work available. Relocation negotiable. About Cipla 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. Driven by the purpose 'Caring for Life', Cipla's focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world. In the last 85 + years, Cipla has emerged as one of the most respected pharmaceutical names in India as well as across more than 100 countries. Cipla is a fast-growing pharmaceutical company with a continued focus on the expanse of our strong legacy. Over the last five years, Cipla has significantly expanded its portfolio and presence in the U.S. with both a generic and brand division. InvaGen Pharmaceuticals, Inc. InvaGen Pharmaceuticals is a Cipla subsidiary 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. In October 2020, InvaGen established its project site in Fall River, Massachusetts to support the launch of Cipla's respiratory business in the United States. Equal Opportunity Employer Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Cipla, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require reasonable accommodation to make your application or interview experience a great one, please contact the recruiter. About the Salary/ Pay Range: The salary range mentioned above is an anticipated base salary range for this position. Exact salary depends on several factors such as experience, skills, education, and budget. Salary range may vary based on geographic location. In addition to base salary, this position may be eligible for benefits and participation in a bonus program based on performance.

NOTICE: The posting for local applicants only - is not for those applying for a global assignment and/or for employees working outside of Cipla's U.S. Subsidiaries or Affiliates. Job Title QC Chemist I Organization Name InvaGen Pharmaceuticals, Inc. Location Central Islip, NY Employment Type Full Time - Salary/Exempt Benefits In addition to a fulfilling career and competitive salary, the Company offers a comprehensive benefits package to include a 401(k) savings plan and matching, health insurance - medical/dental/vision, health savings account (HSA), flexible spending account (FSA), paid time off (PTO) - vacation/sick/flex time, paid holidays, short-term disability (STD), long-term disability (LTD), parental leave, paid and unpaid family leave, employee discounts, and other benefits. Work Hours/ Shift/ Remote 8:30 AM - 5:00 PM (General Shift) Responsibilities/ Accountabilities Demonstrated ability to perform independent work requiring attention to detail, accuracy and scientific judgment and a consistent record of shifting thought processes quickly from one task to another. Strong analytical skills, attention to detail, knowledge of analytical techniques (HPLC, GC, UV-Vis etc.) and familiarity with quality control procedures. Responsible for performing routine analytical testing of raw material, in-process samples, finished products to ensure they meet quality standards and regulatory requirements. Understanding of regulatory compliance, quality management systems and document control processes, and the ability to collaborate cross-functionally and communicate effectively. Responsible for QA review and approval of the following types of documents: SOP's GMP documents Change control documents Review of system records Perform activities related to periodic audit trail review of all quality softwares, ensure compliance within the systems etc. Maintaining regulatory compliance in accordance with cGMP and Perform Data Integrity risk assessment of current Good Manufacturing Practices (cGMP) and GLP systems both manual and automated. Follow all safety procedures and guidelines to ensure a safe laboratory environment. Prioritize risks and work with IT, QA, laboratory personnel to mitigate data integrity gaps. Partnering with other members of the Quality Assurance team and/or end users of the system to Identify, Develop, and Implement Continuous Improvements to the Change Control System, Process, and associated procedures. Evaluate proposed and existing software systems that support laboratory and software applications for data integrity gaps. Works with IT and QA to resolve those gaps. Develop standard operating procedures for the administration of analytical and QC equipment. Ensuring the GMP status and the functionality of the laboratory equipment in accordance with the guidelines 21 CRF Part 11 on data integrity. Excellent written and verbal communication skills. Perform additional duties as requested. Education Qualifications/Experience Entry level position. Master's degree in chemistry, pharmaceutical or related field is required. May require 1+ years' experience in a pharmaceutical manufacturing lab. Experience and understanding of the Laboratory Information Management Systems (LIMS) is a plus. Understanding of systems such as polarimeter, IR spectroscopy, Karl Fischer etc. is expected. Proficient digital literacy in Microsoft (MS) Word, Excel, PowerPoint, and SharePoint required. Experience in Chromatographic softwares such as Empower3, Chromeleon preferred. Understanding or experience in other quality systems such as Trackwise, master control is a plus. About Cipla 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. Driven by the purpose ‘Caring for Life', Cipla's focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world. In the last 85 + years, Cipla has emerged as one of the most respected pharmaceutical names in India as well as across more than 100 countries. Cipla is a fast-growing pharmaceutical company with a continued focus on the expanse of our strong legacy. Over the last five years, Cipla has significantly expanded its portfolio and presence in the U.S. with both a generic and brand division. InvaGen Pharmaceuticals, Inc. InvaGen Pharmaceuticals is a Cipla subsidiary 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. In October 2020, InvaGen established its project site in Fall River, Massachusetts to support the launch of Cipla's respiratory business in the United States. Equal Opportunity Employer Cipla is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Cipla, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require reasonable accommodation to make your application or interview experience a great one, please contact the recruiter. About the Salary/ Pay Range: The salary range mentioned above is an anticipated base salary range for this position. Exact salary depends on several factors such as experience, skills, education, and budget. Salary range may vary based on geographic location. In addition to base salary, this position may be eligible for benefits and participation in a bonus program based on performance and company results.

Nature and Scope This position is centered on testing of raw materials, in-process, and finished product samples accurately and efficiently to determine chemical identity, potency and purity of pharmaceutical products manufactured by American Regent, Inc. The QC Chemist I will perform analytical testing according to current guidance and established procedures for analysis of stability samples in the Quality Control Laboratories. Essential Duties and Responsibilities Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to this job at any time. Successfully operate all instruments including: pH meter Balances Autotitrator / Karl Fischer Titrator HPLC / GC ICP-OES / ICP-MS UV-VIS Spectrophotometer Osmometer Polarograph Perform testing of raw materials, in-process, and finished product samples. Perform all wet chemistry procedures including titrations, extractions, etc. General glassware and laboratory cleaning. Maintain GMP documentation of all activities. Perform calibration, basic troubleshooting and maintenance on laboratory instruments. Perform any other tasks/duties as assigned by management. Education Requirements and Qualifications To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required. Bachelor's degree in Science, Chemistry, Biology or related field required. Good oral and written communication skills, detail oriented, capable of multi-tasking. Knowledge of HPLC instrumentation and software. Knowledge of MS Word, Excel. Ability to work overtime as needed. Physical Environment and Requirements Specific vision requirements include 20/40 near vision (can be corrected with eyeglasses or contacts) and color vision. Expected Hourly Rate: $33.70 - $37.00 The hourly rate displayed is the hourly rate of compensation for the role that the employer in good faith believes to be accurate at the time of the posting of an advertisement for the role. Actual compensation for the role will be based on a number of different factors including but not limited to the candidate's qualifications, education, knowledge, skills and experience. American Regent also offers a competitive total rewards package which includes healthcare, life insurance, profit sharing, paid time off, matching 401k as well as a wide range of other benefits. American Regent celebrates diversity and we are committed to creating an inclusive environment for all employees. We are an Equal Opportunity Employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, or protected veteran status. Applicants have rights under Federal Employment Laws. FMLA poster: ********************************************************** Know Your Rights: Know Your Rights: Workplace discrimination is illegal (eeoc.gov) Employee Polygraph Protection Act: ********************************************************* Alert: We're aware of individuals impersonating our staff to target job seekers. Please note: · All legitimate communication will come directly from a verified ARI recruiter either by phone or via an americanregent.com email address. · Our recruiting process includes multiple in person and/or video interviews and assessments. · If you are unsure about the legitimacy of a message, contact John Rossini at *************************** before responding. · We never request payment, bank information, or personal financial details during our offer process. Your security is important to us, and we encourage you to stay vigilant when job searching. American Regent Inc. endeavors to make *********************************** accessible to any and all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please email **************************************.