Eurofins jobs in Piscataway, NJ - 65 jobs

South Brunswick Township, NJ, USA Full-time ** Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. **Job Description** + Assist in performance of all Quality Assurance functions as outlined in the GLPs and PSL SOPs. Assist the Quality Assurance Director as needed during inspections by EPA, FDA or clients. Prepare records and assemble copies of documents requested by inspectors when advance notice is given and Sponsor and/or Laboratory Director approval is obtained. + Conduct in-process study inspections and general facility inspections in the toxicology and chemistry laboratories as directed. + Audit raw data and proofread report and tables against raw data for accuracy and for typing corrections. Audit final report to verify corrections. + Amend and update Standard Operating Procedures as required using word processing system. File all QAU-related paperwork as directed. + Select intervals for inspection for any regulatory test under the auditor's responsibility or as directed by QA Director, Laboratory Director, or President. Perform such inspections in accordance with the test schedule. When the time for conduct of intervals requiring inspection falls outside of normal working hours, this will be brought to the attention of the Study Director or QA Director in order that a suitable arrangement may be made. + Ability to safely wear a respirator required. + Other duties as assigned. **Qualifications** + QA auditors will have experience in a laboratory regulated by FDA/EPA GLP standards. Experience in other quality standards such as cGMP or GCP will also be considered. + Experience with acute toxicology, analytical chemistry, and/or general laboratory procedures is preferred. B.S. degree in biology, toxicology, animal science or related field and/or AALAS certification at the Technician level is also preferred. Experience in computer system validation and electronic data capture is desirable but is not required. + The individual holding this position must be of the highest integrity and have a very strong sense of responsibility. Attention to detail is essential. He/she must be well organized, tactful, be able to work independently and maintain all records, documents, and schedules associated with quality assurance procedures and studies. Communication skills, especially written, are necessary. Proficiency with MSWord and Excel is required. He/she must have a current tetanus vaccination if required to access the vivarium. **Additional Information** Position is full-time, Monday-Friday 8am-5pm. Candidates within a commutable distance of South Brunswick, NJ are encouraged to apply. Compensation: $22.50-$25.50/hr Excellent full-time benefits including: + Comprehensive medical coverage, dental, and vision options. + Life and disability insurance + 401(k) with company match + Paid vacation and holidays **Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.**

The Transdermal Operator II (3rd Shift) responsibilities include equipment start-up, participation in ANDA batch production and commercial batch manufacturing. Primary responsibilities include in process checks, operating Transdermal machines. This role follows a 12-hour rotating schedule, working from 6:00 PM to 6:30 AM. Essential Functions: Perform equipment set-up, IQ/OQ/PQ, and commercial batch activities. Monitor automatic and semi-automatic equipment to manufacture transdermal products. Operate complex machines, i.e. Delta, to conduct mixing, coating, converting, pouching and cartoning operations. Set-up, run and clean equipment in a GMP compliant environment. Work with team to troubleshoot and resolve manufacturing issues as they arise. Report issues/concerns or potential issues/concerns, that may negatively impact the outcome of the successful execution of a batch, to the department Supervisor. Immediately notify the department supervisor of any action or activity that is a violation of cGMPs, SOP, or Safety procedures. Ensure that all processing equipment, room, scale, and environmental log books are promptly and accurately filled in - recording all activities. Responsible for 100% documentation accuracy on all GMP documents, such as bath records, log books, training records, in-process forms. Conduct R&D and commercial scale-up activities. cGMP's, SOP's, OSHA, regulations are followed at all times during the execution of the batch. Additional Responsibilities: R&D and commercial scale-up activities Other duties as assigned. Education: High School or GED - Required Experience: 3 years of experience in Manufacturing or GMP environment - Required 3 years of experience in Pharmaceutical Manufacturing - Preferred Skills: Must be able to understand and communicate in English. - Advanced Strong math and mechanical skills. - Advanced Ability to use computer systems for data entry. - Advanced Ability to work as part of a team. - Advanced Great attention to detail, ability to be accurate and apply good documentation practices. - Advanced Specialized Knowledge: Strong knowledge of converting (die cutting) and packaging Additional Requirements: Flexible to work extended hours when required. This position requires successful completion of an OSHA-compliant Respirator Fit Test. The hourly rate for this position ranges from $19.50 to $26.50 per hour. In addition, Amneal offers a short-term incentive opportunity, such as a bonus or performance-based award, as well as a long-term incentive award, such as restricted stock units, with this position within the first 12 months. Amneal ranges reflect the Company's good faith estimate of what 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, experience, 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 help you enjoy your career alongside life's many other commitments and opportunities.

The Mixing Operator III is responsible for operating industrial mixing equipment in full accordance with Company Standard Operating Procedures (SOPs) and maintaining 100% cGMP compliance to ensure the consistent production of high‑quality pharmaceutical products. Essential Functions: * Perform and verify complex equipment cleaning and operate various types of industrial‑scale mixing equipment. * Monitor production activities to ensure batches are completed on schedule and equipment is running safely and efficiently. * Review Production Batch Records (PBRs) for accuracy upon completion of mixing activities, sign off, and submit to the Supervisor. * Ensure all equipment within the department is properly grounded prior to initiating any batch. * Follow the daily production schedule and assign tasks accordingly to support workflow and production targets. * Assess the performance and skill levels of Mixing Operators I and II and provide recommendations for development or improvement.

Reporting to the Senior Director, Institutional Marketing & Sales Operations, the Digital Marketing Manager will help develop, deploy, and optimize subscriber acquisition campaigns for the Amneal Direct Portal. This role manages digital campaigns across email, SEM, paid social, display retargeting, and content marketing networks while overseeing the creation of marketing assets. The manager will track and report on campaign performance, analyze data across advertising and customer platforms, and deliver actionable insights. They will also lead onsite acquisition tactics and optimize campaigns through testing strategies, partnering with vendors as needed. Essential Functions: Monitor, analyze and report on the performance of digital marketing campaigns, using data from ad platforms for reporting views, often presented in spreadsheets and decks, pulling in campaign data from advertising, analytics and customer data platforms to analyze, interpret and present campaign/acquisition learnings. Manage the collective onsite customer acquisition tactics, onsite marketing solutions and house advertising inventory. Experience optimizing campaigns via A/B and multivariate testing of creative, landing pages, media buying and audience targeting Work with vendors who support various marketing/acquisition channels Education: Bachelors Degree (BA/BS) Business, Marketing, Communications or a related field - Required Experience: 5 years or more in Digital marketing/eCommerce, with a strong track record in pharmaceuticals, healthcare, or a related industry. Skills: Competent knowledge of the pharmaceutical industry in Digital/eCommerce channels - Proficient Competency with presentation decks (PowerPoint, Google Slides), website analytics (Google Analytics or Adobe Analytics) and spreadsheets (Microsoft Excel and Google Docs) - Proficient Sound understanding of digital and social media advertising. - Proficient Sound understanding of digital marketing technology aspects and conventions (e.g. ad serving, creative tracking, etc). - Proficient The base salary for this position ranges from $130,000 to $145,000 per year. In addition, Amneal offers a short-term incentive opportunity, such as a bonus or performance-based award, with this position within the first 12 months. Amneal ranges reflect the Company's good faith estimate of what 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, experience, 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 help you enjoy your career alongside life's many other commitments and opportunities.

The Scientist-2 is a mid-level analytical scientist opportunity supporting the analytical development of pharmaceutical oral dosage form. The individual in this capacity performs analytical methods qualifications/validations, analyzes active pharmaceutical ingredients, excipients, and finished dosage forms using appropriate analytical methods and maintains/qualifies analytical equipment. Essential Functions: * Performs analysis and release of active pharmaceutical ingredients, excipients, in-process materials, and finished drug products to support the formulation development team, maintaining full compliance with all applicable US FDA - cGMP regulations and internal SOPs. * Develops and optimizes new and existing analytical methods for qualification and release testing of products. Develops stability indicating methods and performs methods validation. * Provides timely responses to all internal and external inquiries. * Ensures deadlines are met for product development schedules, and checks that technical and compliance requirements are met. * Evaluates, recommends, and implements new analytical technologies and instrumentation for testing. * Assists with training other members of the analytical development team. Additional Responsibilities: * Stays abreast of new developments in analytical technologies. Contributes to improvement in laboratory operations to increase efficiency and GMP compliance.

Laboratory operations assistant will play a vital role in maintaining the cleanliness and organization of the laboratory. Preliminary responsibilities include cleaning and arranging the laboratory glassware, keeping the laboratory area clean and organized. Be able to lift 20 lbs. Essential Functions: * Wash and clean glassware. Arrange clean glassware in designated area after cleaning. * Dust and mop thoroughly in the lab and adjoining areas. * Clean benchtops, glassware storage, chemical storage cabinets and fume hoods. * Clean and wash the Dissolution baths and Sonicators. * Removal of accumulated garbage and disposal of cardboard. * Lab cleanliness round with floor Supervisors. Additional Responsibilities: * Order needed sanitary items and detergents in a timely manner. * Help Sample coordinators during product disposal. * Help Sample coordinator and Lab coordinators to transfer the lab resources from Warehouse to Laboratory.

The Automation Engineer is responsible for overseeing and optimizing automation systems to improve production efficiency and reduce operational costs. This position involves designing, integrating, and implementing advanced hardware and software solutions within pharmaceutical manufacturing facilities. Essential Functions: * Develop Control Systems based on coordination with OEM, in order to automate upstream and downstream processing equipment, including Mixers, Coaters, Pouches, Cartoners, Packaging Lines, Laboratory equipment, facility systems, stability Chambers, BMS, CIP (Clean in Place) and SIP (Steam in Place), Water System Controls, Tablet Press, Fluid Bed Dryers, Granulators, Vision System etc. * Perform programming, qualification and validation of digital process automation systems. Provide 24x7 on-call Automation Support, including technical support and troubleshooting functions. * Perform formal systems acceptance testing, including software simulation and hardware and equipment acceptance in pharmaceutical manufacturing facilities. * Properly complete documentation for accurate recordkeeping, according to the Engineering Department's procedures, Assist with updating departmental procedures; monitor equipment, and ensure preventative maintenance is being done, handle calibration monitoring, engineering analysis. Assist with training coworkers on using equipment. * Read, understand, verify and develop P&ID, Engineering Layout, Engineering Drawings and Engineering documents. * Implement projects according to Good Automated Manufacturing Practice (GAMP) guide for validation of automated systems in pharmaceutical manufacture. * Handle logistics and coordination of electrical construction activities as per engineering standards, vendor development, with the various departments like manufacturing, QA, QC, R&D for the engineering and Validation Aspects; maintain VMP and other GMP documents, Support Process Validation and Development Studies. Coordinate and ensure Safety Aspects. * Perform hands on field installation, operational start-up, calibration, and commissioning activities. * Support Change Control Management, updating documentation for client, including test plans and production implementation. * Apply batch coding standards to automation process, including design of batch operations, unit procedures, and procedural recipe components to aforementioned processes. Additional Responsibilities: * Assists with engineering projects and performs other duties as assigned.

Responsible for the upkeep, repair, and efficient operation of facility infrastructure and utility equipment. This role ensures all systems are functioning safely and reliably, supporting continuous operations through preventive maintenance, troubleshooting, and coordination with internal teams and external contractors. Essential Functions: Performs plumbing maintenance (e.g. replacement or repair of leaks in drains and faucets, unclogging of drains, trenching and laying new lines, replacing drain hoses on washers and similar devices, etc.) to provide operable and efficient plumbing capabilities to department personnel. Maintains and repairs all building finishes and associated support equipment including but not limited to: wall, floor and ceiling finishes, electric systems, plumbing systems and fixtures. Installs insulation to building walls, ceilings and floors to provide sound and thermal barriers using various tools and materials (e.g. wire, knives, dust masks, etc.) Performs painting, carpentry and masonry work (e.g., preparing surfaces and using brush, sprayer, or roller to apply paints, stains, and varnishes, hanging doors, fitting locks and handles, etc.) to provide operable and efficient facilities for department personnel. Conducts repairs and performs preventive maintenance tasks on all utility equipment in the physical plant, in a safe and proper manner and in accordance with SOPs and departmental policies and procedures. Including purifies water system, preparation of pretreatment solutions. Basic computer knowledge to execute work order requests, pm and online documentation. Is proficient in filter installation, maintenance, and testing. Maintains, repairs, installs, lubricates, and adjusts all types of utility equipment. Conducts data recording assignments as required. Prepares and maintains detailed equipment, plant operations, and preventive maintenance records involving all plant equipment for cGMP compliance. Monitors and adjusts building environmental and equipment operational set points. Responds to out of specification situations as required. Identifies and analyzes operating, maintenance, and repair problems and recommends corrective action. Performs minor electrical maintenance to include but not be limited to: replacement or repair of fixtures (e.g., wall switches and outlets, incandescent and fluorescent bulbs and tubes, ballast, sockets, fuses, minor appliances, cords, etc.) Conducts daily/monthly inspections of facility equipment and services. Manage daily and monthly logs for facility inspections. Wear proper PPE - a must Additional Responsibilities: Additional responsibilities that management may assign. Education: High School or GED - Required Experience: 2 years or more in Facility maintenance or related experience 2 years or more in Pharmaceutical, production and/or laboratory environment Skills: Ability to follow safety standards while working with multiple services, tools and equipment - Intermediate Able to observe, record, and report unsafe working conditions - Intermediate Able to read and interpret blueprints, sketches and schematics as they relate to building and utilities services systems - Intermediate Able to follow orders and complete work assignments with a minimum of supervision - Intermediate Apply methods, practices, and procedures in preventative maintenance, inspection, repair, renovation, and minor construction of buildings and utilities - Intermediate Basic computer literacy with the ability to use web browsers, typing applications, Microsoft Office, and related communication tools - Intermediate The hourly rate for this position ranges from $23.00 to $33.00 per hour. In addition, Amneal offers a short-term incentive opportunity, such as a bonus or performance-based award, with this position within the first 12 months. Amneal ranges reflect the Company's good faith estimate of what 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, experience, 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 help you enjoy your career alongside life's many other commitments and opportunities.

The Associate Process Engineer reports to the Technical Lead or head of Technical Services. Executes Process/Cleaning Validation/Study assignments as per directives. Creates protocols, data collection and analysis and prepare reports under supervision. Essential Functions: Prepare validation protocols & reports for manufacturing process and cleaning process qualification; data analysis and prepare reports; execute manufacturing process and cleaning process qualification/validation/study Analyzes statistical data, product or functional specifications to determine conformance with standards and established quality requirements Prepare and review manufacturing batch record and other engineering qualification documents as required Coordinate/oversee the development of new processes or troubleshoot existing ones Review Annual Product Review reports and plot trend analysis & APR reports Assist in deviation/investigations to identify root causes and define corrective and/or preventative actions (CAPA) Assist in various audits Additional Responsibilities: Performs other functions as required or assigned. Complies with all company policies and standards. Initiation of Change Controls and Planned Deviations when required Reviews manufacturing/ Packaging batch records and Engineering qualification documents Performs other functions as required or assigned. Complies with all company policies and standards. Qualifications Education: Bachelors Degree (BA/BS) Pharmaceutical/Chemical Engineering - Required Master Degree (MS/MA) Pharmaceutical/Chemical Engineering - Preferred Experience: 1 year or more in Pharmaceutical/Manufacturing Industry Skills: Excellent verbal and written communication skills. - Advanced Proficiency in MS Word/Excel/Powerpoint. - Advanced Multi-tasking. - Specialized Knowledge: Basic Analytical Knowledge desirable. 21 CFR, cGMP, basic manufacturing process knowledge. The salary for this position ranges from $65,000 to $80,000. In addition, Amneal offers a short-term incentive opportunity, such as a bonus or performance-based award, as well as a long-term incentive award, such as restricted stock units, with this position within the first 12 months. Amneal ranges reflect the Company's good faith estimate of what 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, experience, 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 help you enjoy your career alongside life's many other commitments and opportunities.

This role is responsible for monitoring and ensuring that all incoming raw materials, packaging components, and returned goods are properly sampled, inspected, and tested, as applicable, to confirm compliance with established specifications. To monitor and ensure all phases of drug manufacturing are in compliance with established specifications. To receive, inspect, release and control of labels and outserts. To ensure quality compliance before, during and after each packaging run. Essential Functions: Perform inspection, sampling, and testing (where applicable) on all incoming raw materials, packaging components, and returned goods following detailed written procedures. Prepare samples for chemical and microbiological analysis (where required) and deliver them to the QC lab. Inspect and test packaging components using various measuring devices such as scales, micrometers, and height gauges to determine conformance to specifications. Maintain detailed records of sampling, inspections, and testing activities. Assign and verify expiry dates and retest dates for all GMP raw materials through vendor COA and in-house COA. Collect packaged product samples for annual stability. Perform room, equipment, and packaging line checks (where applicable) prior to each stage of manufacturing following detailed written procedures. Conduct in-process testing per manufacturing and packaging batch record instructions. Prepare controlled/uncontrolled/packaged finished product samples for QC lab and QA retains, following detailed documentation procedures. Maintain standard weights required to perform daily verification of balances. Handle labeling component receipt, visual examination, counting, preliminary inspection, and sampling. Prepare labeling components/outserts inspection reports; quarantine and release labels; maintain incoming components log and corresponding inventory cards. Issue labeling components/outserts according to packaging order and regularly monitor and audit the label room. Complete QA final labeled product inspection report and final line clearance, including labeling and packaging reconciliation paperwork. Ensure compliance of warehouse areas in terms of isolation of Quarantine, Released, In-Process, Finished Product, Packaged Product, Returned Goods, and Rejected areas. Ensure proper isolation of rejected material generated during batch process and accountability in the batch record. Monitor facility and product environmental operating conditions. Review engineering records (temperature and humidity data, calibration and PM records, pest control records, and contractor-related functions). Review online batch records for completeness of signatures, entries, and reconciliation/yields prior to initiation of the next processing step. Verify functionality of all equipment and associated controls during the batch run. Maintain retention sample room and monitor temperature and humidity; replace chart records as per schedule; review logs and disposition of samples. Additional Responsibilities: Disposition of rejected material and returned drug products as per SOP Performs environmental monitoring in accordance with established schedule (where applicable) Perform applicable testing and prepare report for customer complaints Other duties that management may assign. Education: High School or GED - Required Experience: Must have 2 years or more experience in QA or related field Skills: High energy level and organizational skills. - Advanced A certain degree of creativity and latitude - Advanced Basic computer skills (Word and Excel) - Intermediate Specialized Knowledge: Good basic math knowledge and excellent attention to details. Records observations for improving processes. The hourly rate for this position ranges from $20.00-$27.00 per hour. In addition, Amneal offers a short-term incentive opportunity, such as a bonus or performance-based award, as well as a long-term incentive award, such as restricted stock units, with this position within the first 12 months. Amneal ranges reflect the Company's good faith estimate of what 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, experience, 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 help you enjoy your career alongside life's many other commitments and opportunities.

Director, Business Development - Clinical Research Director, Clinical Business Development Full Time Remote-USA Based Reports to: Senior Vice President, Clinical Services Frontage Laboratories Inc. Frontage Laboratories Inc. (Frontage) is a global contract research organization with broad expertise in supporting pre-clinical and clinical drug development. Frontage operates out of several different locations within the USA, Canada, and China. Frontage's core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, clinical research, and core laboratory services for clinical trials. Frontage Clinical Services At Frontage, we leverage more than 25 years of experience to develop a unique approach to overcome the challenges of every clinical study, while maximizing efficiency and mitigating risk. We apply best practices in study design and execution to advance each study to completion. Responsibilities: Secure and retain business through professional, consultative, and proactive sales activities directed at key decision makers Strong negotiating skills, knowledge of legal contracts and experience with RFIs/RFPs and competitive bidding processes Analyze potential opportunities and develop sales plans for each target account, develop in-depth knowledge of the customer organization Ensure appropriate strategy/solution is proposed to clients Monitor actions and results against plans Lead client visits to the Frontage facilities Coordinate with scientific and operations staff to prepare and lead the sales presentations, present comprehensive proposals, and lead follow-up activities Monitor sponsor satisfaction by regular communication with the clients/sponsors Record all client/sponsor sales related (opportunities, CDA, MSA, Site Visits, Face to Face Meetings, etc.) activities in CRM (sales f orce) system Represent Frontage at trade shows and other meetings Education, Skills and Experience Required: BS degree or above, life science preferred. 3+ years' experience in a clinical operation role and /or 1+ years' experience selling early-stage clinical research services. Solid understanding of the principles of drug discovery and development. Knowledge and experience in DMPK & Safety Toxicology Knowledge and understanding of FDA, GCP, and ICH regulations and guidance Highly proficient in using Microsoft Office Suite: MS PowerPoint, MS Word, and MS Excel. Attention to detail and ability to work simultaneously on multiple priorities. Able to adapt and be flexible to changing priorities. Excellent oral and written communication skills. Ability to travel. Established industry client network is a plus. Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies. Job Description The Sales Account Executive is a client facing outside sales role operating within an assigned region of the Northeast. This involves identifying and managing client accounts and business opportunities for Eurofins Built Environment Testing Division. Built Environment is a group of laboratories that provides Indoor Air Quality (IAQ) testing for things such as mold, asbestos, Legionella, etc. The Account Executive will travel throughout the region to meet with clients. This individual must be comfortable with cold calling and taking initiative to bring in new business as well as cultivate existing relationships. Knowledge and understanding of environmental laboratory testing is ideal, specifically in indoor air quality testing, USP797 testing or Legionella testing. As part of the sales team, you will focus on: * Maximizing market share, profitability, competitive advantage and capacity utilization in the environmental analytical services market. * Establish and maintain productive relationships with Eurofins clients. * Provide vision and acquire new accounts to sustain growth of the business by representing Eurofins, clearly communicating Eurofins services to new customers and markets. * Identify opportunities and profitable work by following up on leads, negotiating, and closing. * Provide a valuable interface between the customer and Eurofins by communicating the customer's needs to the internal organization and fulfilling the role of customer advocate while teaming with a strong internal team from management, operations, technical staff, quoters, and project managers. Account Executive responsibilities include, but are not limited to, the following: * Responsible for meeting individual revenue as well as the goal for assigned region. * Establishes and maintains a productive working relationship between the client and laboratory. * Ensures customer awareness of Eurofins Environment Testing capabilities and services to improve selling opportunities. * Provides sales plan forecast for assigned region. * Reviews credit status of both new and existing customers prior to submitting bids or proposals for new work. * Monitors accounts receivable status for accounts assigned and resolves collection issues as required. * Develops and recommends strategies to facilitate pricing and bid/no bid decisions, establish Master Service agreements and provide budgetary information. * Develops client profiles and determines potential and ability to fund work. * Develops, qualifies, tracks, and closes leads to increase revenue. * Reports sales activity within assigned area. * Updates customer databases to identify business opportunities. * Maintains productive relationships between customers and the Eurofins Environment Testing organization. * Develops and implements account plans detailing specific clients, revenue goals and related account objectives to attain regional revenue quotas. * Identifies key target markets and major accounts and develops strategies within assigned area of responsibility to attain market position for Eurofins Environment Testing and maintain profitability. * Establishes, coordinates, negotiates, and completes Master Service * Agreements with customers which both defines customers' specific needs and streamline processes. * Within area of market responsibility collects and documents information to establish pricing and evaluate Eurofins Environment Testing's ability to meet customer requirements to meet win/loss ratios, average discount percentages and profitability. * Effectively communicates customer needs and wants to Eurofins Environment Testing * Customer Service Managers and Project Managers to facilitate successful completion of work. * Completes summaries of sales development activities as directed by GM. * Communicates all business opportunities (e.g. bids, quotes, proposals, and pricing inquires) by providing copies or entering information into Eurofins Environment Testing's database. * Follows up on all outstanding bids, quotes, proposals, and price inquiries in order to achieve successful completion of the sales cycle. * Negotiates pricing and contractual issues within area of responsibility with the approval of the GM. * Presents Environment Testing as a network of laboratories not limited to lab facilities within a geographical region to improve operational efficiencies. * Controls expenses with respect to the selling function pursuant to Eurofins Environment Testing's policy and with approval by GM. * Assumes role as "sponsor" for National Accounts as needed. * Provides feedback on market conditions within area of responsibility to facilitate the development of new products and services. * Maintains relationship with one or more of Eurofins Environment Testing's network facilities to sustain awareness of operational issues related to Eurofins Environment Testing's ability to meet customer requirements. * Provides information concerning business opportunity outcomes with respect to win/lose ratios and future pricing strategies. * Provides forecasting information to Customer Service Managers to assist operational staff with resource and operational planning. * Assists with the development of sales materials. * Gathers and communicates intelligence information on competitors within area of responsibility. * Identifies and communicates opportunities for new products and services within assigned region. Qualifications Basic Minimum Qualifications: * Degree in Sciences or related field preferred but not required * Minimum 2-3 years progressively successful sales experience in a service industry * Ability and willingness to travel throughout the assigned territory. Some overnight travel may be required. * Environmental industry knowledge. * Valid driver's license The ideal candidate would possess: * Sales specific skills of identification of prospects, interviewing, negotiating, and closing * Strong interpersonal skills * Excellent written and verbal communication skills * Sales acumen/sales skills * Lab experience and exposure to environmental industry preferred. * Writing sales and account plans * Working computer skills * Familiarity with lab functions and terminology * Analytical skills * Planning skills * Self-directed * Ability to work in an unstructured environment Additional Information Requirements: * Authorization to work in the United States indefinitely without restriction or sponsorship * Professional working proficiency in English is a requirement, including the ability to read, write and speak in English This position will be a full-time role, Monday - Friday. Candidates residing within the Northeastern U.S. are encouraged to apply. Salary Range: minimum of $70,000/yr base + Commission with benefits, PTO and company matching 401K plan. Salary range could be higher for candidates with specific sales experience in environmental testing, especially Indoor Air Quality (IAQ) testing. Eurofins Environment Testing (USA) provides a compensation range for informational purposes, the actual base salary may vary based upon, but not limited to, relevant experience and skill set, base salary of internal peers, business sector, and geographic location. As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work. we offer excellent benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays, paid time off, and dental and vision options. * The benefits package offered will vary based on the employee's full-time or part-time regular status. To learn more about Eurofins, please explore our website ******************* We support your development! Do you feel you don't match 100% of the requirements? Don't hesitate to apply anyway! Eurofins companies are committed to supporting your career development. We embrace diversity! Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique. Sustainability matters to us! We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal! Find out more in our career page: ***************************** Company description: Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and Eurofins Scientific 2/2 March 2023 agroscience contract research services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2022, Eurofins generated total revenues of EUR 6.7 billion, and has been among the best performing stocks in Europe over the past 20 years. Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.

Rahway, NJ, USA Full-time ** Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years. **Job Description** **_This role involves investigating and characterizing the solid forms of active pharmaceutical ingredients (APIs), including polymorphs, salts, co-crystals, and amorphous forms. Some of the responsibilities include designing and executing solid form screening studies to identify optimal forms for drug development based on properties, other responsibilities include growing single crystals or conducting high throughput screening._** + Physical form screening with established protocols to identify novel crystalline forms including polymorphs, solvates, salts and cocrystals under the guidance of a scientific supervisor. + Physical measurements on samples to support chemical process and pharmaceutical formulation development. + Independently execute laboratory experiments and present results in a contextualized manner. + Data processing, interpretation and documentation. + Maintain stock salt solutions, solvents and chemicals up to date. + Calibration and routine maintenance of common laboratory equipment. + Ensure a safe and organized laboratory environment by following all applicable safety protocols and guidelines. **Qualifications** + Completed Bachelors degree in a scientific concentration + 3+ years of experience working in industry lab setting + Experience with analytical techniques such as XRPD, DSC AND TGA-IR + Authorization to work in the United States indefinitely without restriction or sponsorship **Additional Information** **Position is full-time, Monday - Friday 9:00am - 5:00pm** . Candidates currently living within a commutable distance of **Rahway, NJ** are encouraged to apply. **_The compensation range is between $27-29/hr based on experience level._** Excellent full time benefits including comprehensive medical coverage, dental, and vision options. + Life and disability insurance + 401(k) with company match + Paid vacation and holidays **Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.**

The Packaging Supervisor is responsible for supervising all packaging department activities on a daily basis. This position supervises the production, quality, and warehousing of packed product in a manner that is consistent with company standards, service and cost objectives. The Packaging Supervisor must communicate, motivate, supervise employees, and also work closely with HR/Upper management to counsel and discipline direct reports as needed. Essential Functions: Motivate a diverse workforce of all employees to exceed department goals, which include safety, quality, and productivity. Supervise all packaging lines, ensuring daily targets are met. Coordinate and interface with engineering for equipment preventive maintenance and validation such as IQ, OQ and PQ. Manage department audits to ensure all department operations are in compliance with cGMP and related SOPs. Audit employee training data and production batch record. Provide training and develop staff to ensure good manufacturing practices (cGMPs) and Standard Operating Procedures (SOP's) are followed. Responsible for Packaging Planned deviation, CAPA, Change control. Write and update Standard Operating Procedure (SOP). Investigate customer complaints. Perform regular inspections of the department facilities and equipment to assess and ensure compliance with SOPs, cGMPs and safety requirements. Schedule and issues work orders to maintenance department for maintenance and repair of encapsulation and ancillary machines to minimize breakdowns and improve efficiency and productivity. Coordinate and interface with Engineering for equipment changes and upgrades. Supervise, develop, mentor, engage and evaluate employees. Conduct annual performance reviews and complete appropriate documentation, training, and disciplinary action as needed. Ensure packaging line clearance after cleaning as per SOP Responsible for Global Serialization System and assist in troubleshooting when needed. Ensure the efficient operation of the entire packaging line, in process and challenge test as per the packaging procedure. Provide input during NOI investigation and CAPA. Work Hours: 3pm - 11:30pm Additional Responsibilities: Performs other functions as required or assigned. Adhere to company policies, standards, rules and regulations. Complies with all company policies and standards. Education: High School or GED 7 years of related work experience - Required Associate Degree 5 years of related work experience - Preferred Bachelor's Degree (BA/BS) 3 years of related work experience - Preferred Experience: 7 years or more in HS 7 years -manufacturing experience including supervisory experience in Pharmaceutical & Manufacturing and Packaging 5 years or more in AS 5 years -manufacturing experience including supervisory experience in Pharmaceutical & Manufacturing and Packaging 3 years or more in BS 3 years -manufacturing experience including supervisory experience in Pharmaceutical & Manufacturing and Packaging Skills: Ability to read, write, and communicate in English at a level to facilitate the understanding terminology of the job. - Advanced Ability to comprehend and follow written and verbal procedures or instructions - Advanced Have math and mechanical skills knowledge - Advanced Specialized Knowledge: Knowledge of 6 sigma and Lean Principles is preferred: to reduce cycle time and cost while maintaining or increasing Production Quality standard. Require technical knowledge of Global Serialization. The base salary for this position ranges from $80,000 to $90,000 per year. In addition, Amneal offers a short-term incentive opportunity, such as a bonus or performance-based award, with this position within the first 12 months. Amneal ranges reflect the Company's good faith estimate of what 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, experience, 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 help you enjoy your career alongside life's many other commitments and opportunities.

The Senior Manager, Corporate Counsel will be an integral member of the Amneal Legal team and will serve as a trusted legal advisor for all commercial activities involving the company's specialty, biosimilar and generic products. The incumbent will serve as a member of Amneal's promotional assets review committee (PARC), draft/review/negotiate general commercial and other types of contracts, and handle market access/customer-facing contracting. This is a hybrid position and must be in the Bridgewater, NJ office 3 days per week. Essential Functions: Advise on a broad array of issues related to the marketing and promotion of pharmaceutical products and actively represent Legal on the company PARC to review promotional/non-promotional materials and strategies covering multiple topics (disease awareness, patient education/access/support, press releases interactions with HCP and payers,etc.) to ensure that materials and strategies are compliant with legal and regulatory requirements as well as with internal company policies. Counsel on FDCA and other applicable laws and regulations (including federal and state anti-kickback statues, FDC, FCPA, FDA regulations, OIG guidance, PhMRA Code, Federal health care programs, state drug transparency laws, HIPAA/privacy, etc.) Negotiate, draft, review general commercial and other contracts including HCP consultant and speaker agreements, vendor and service provider MSAs and SOWs such as licensing agreements, software agreements, standard confidentiality and non-disclosure agreements, R&D and clinical trial agreements Negotiate, draft and review market access/customer-facing contracts including product purchase, supply, distribution, PBM, GPO, wholesaler/distribution, rebate/discount, and specialty pharmacy agreements. Provide legal guidance on contracting and strategy for established and newly launched products. Qualifications Education: Bachelors Degree (BA/BS) - Required Juris Doctor L.L.M. or J.D. from accredited U.S. law school - Required Experience: Must have at least 5 years of legal experience with proven ability to work independently or with minimal supervision from attorneys. 4 years of pharmaceutical experience with experience reviewing promotional material and drafting, reviewing, negotiating a wide array of contracts. Skills: Highly organized and able to independently administer department procedures and carry out projects with minimal supervision under pressured circumstances. - Advanced Strong ability to independently problem solve, take initiative to assist others and find creative solutions. - Advanced Strong ability to manage a complex project from inception to completion with limited guidance and oversight. - Advanced Ability to maintain strict confidentiality, exercising discretion and independent judgment on matters of significance. - Advanced Superior communication and interpersonal skills and ability to effectively communicate with all levels of individuals within and outside the company, including an in international environment. - Advanced Expertise in performance of legal analysis and problem solving. - Advanced Ability to multi-task and handle multiple interruptions and adjustments to priorities throughout the day, including the ability to perform multiple projects for a variety of people while organizing and meeting deadlines. - Advanced Team player willing to pitch in as needed in all department matters. - Advanced Ability to gather and analyze due diligence and other legal materials, such as statutes, decisions, and legal articles, codes, and documents. - Advanced Highly detail oriented and able to quickly and independently identify gaps or risk areas in a complex project. - Advanced Expertise in MS Word, Excel, PowerPoint, Outlook, Adobe Acrobat, and Cloud based file sharing programs including databases. - Advanced Exercises independent judgment - Advanced The annual salary for this position ranges from $156,000 to 170,000 per year. In addition, Amneal offers a short-term incentive opportunity, such as a bonus or performance-based award with this position within the first 12 months. Amneal ranges reflect the Company's good faith estimate of what 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, experience, 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 help you enjoy your career alongside life's many other commitments and opportunities.

Eurofins Scientific is an international life sciences company which provides a unique range of analytical testing services to clients across multiple industries. The Group believes it is the world leader in food, environment and pharmaceutical products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and for supporting clinical studies. In addition, Eurofins is one of the key emerging players in specialty clinical diagnostic testing in Europe and the USA. Group's key figures are approx. 6.95 billion Euros turnover, over 950 laboratories across 60 countries and about 63,000 staff. Job Description Join the leader in Environment Testing. Eurofins Environment Testing has a fulltime entry level opportunity with benefits. The Laboratory Technician I, using general laboratory methods, techniques, equipment, and instrumentation in compliance with Eurofins Environment Testing America's Quality Assurance programs and standard operating procedures, supports laboratory operations through general maintenance of laboratory and supply storage areas, equipment, instruments, and supplies. Shift & Hours: Full time- Monday-Friday schedule 7:00am-4:00pm plus overtime as needed and required. Compensation- $17.50 an hour + benefits ***This is an entry level position for those interested in starting their career in a laboratory setting. College degree not needed. Essential Duties and Responsibilities Retrieves samples from Sample Control for analysis. Performs sample preparation which may include, but is not limited to, a combination of the following methods: Aliquot samples o Spike and trace samples o Prepare reagents o Bottle samples o Prepare concentrations o Separation o Sonication o Liquid rack set up Resolves discrepancies and anomalies to ensure samples are properly labeled. Prepares general laboratory paperwork such as recording analysis results, tracking samples, bench sheets, and laboratory logbooks. Washes laboratory glassware to prepare for next day's samples. Stocks laboratory supplies. Cleans work area(s) to maintain a safe working environment. Assists other laboratory areas as needed. Ability and/or Skills General knowledge of chemistry and/or general science Comfortable in a fast paced environment Mechanically inclined and enjoys instrument troubleshooting Comfortable with a flexible schedule (8 hour shift may become 12 hour shift in busy season) Detail Oriented Basic mathematical skills Production work Great organizational skills Great communication skills Problem solving skills Ability to muti-task Quick learner Work independently Work within time constraints This position description is written as a guideline to inform employees of what is generally expected of them at each job level. The description is not intended to be all encompassing or limiting in any manner; rather, it is hoped it will add understanding and better reflect the work performed at all levels of employment. Duties and responsibilities other than those listed may be included as needed within the work group or the company as a whole. Qualifications Requirements Education: High school Chemistry coursework a must, basic laboratory experience Experience: Laboratory experience helpful Previous production-oriented work helpful (awareness and ability to meet deadlines) Authorization to work in the United States indefinitely without restriction or sponsorship Professional working proficiency in English is a requirement, including the ability to read, write and speak in English. Must be able to lift up to 25 lbs frequently, and up to 50 lbs occasionally Candidates with a BA or BS or without a college degree would excel in this position. Perform other duties as assigned Physical Requirements Lifting and Carrying: Lifting up to 50 pounds and carrying up to 30 pounds when moving samples and disposing of waste Pushing and Pulling: Pushing and pulling up to 200 pounds when moving sample carts and gas tanks Body Positions: Approximately 60% of time standing when analyzing samples, 10% walking when moving about laboratory, and 30% sitting when working at computer, doing paper work, or analyzing samples. These percentages vary significantly Page 4- Analyst I depending upon duties being performed. Must be able to sit, stand, or stoop for long periods of time. Body Movements: Stooping, kneeling, crouching, and reaching when getting samples and performing analyses Smelling: For unusual odors, leakage, contamination Hand Use: Handling samples, operating instruments, data entry Hearing: Conversational hearing ability Vision: Performing analyses, viewing computer screen, doing paperwork Speaking: Conversational speaking ability. "All offers of employment are contingent upon a successful completion of a pre-employment drug screen and background check." Additional Information Please note - Eurofins Environment Testing (USA) provides a compensation range for informational purposes, the actual base salary may vary based upon, but not limited to, relevant experience and skill set, base salary of internal peers, business sector, and geographic location. As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work. We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays, paid time off, and dental and vision options. We do not offer Visa Sponsorship for this role. We support your development! Do you feel you don't match 100% of the requirements? Don't hesitate to apply anyway! Eurofins companies are committed to supporting your career development. We embrace diversity! Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique. Sustainability matters to us! We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal! Find out more in our career page: ***************************** Company description: Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and Eurofins Scientific 2/2 March 2023 agroscience contract research services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2022, Eurofins generated total revenues of EUR 6.7 billion, and has been among the best performing stocks in Europe over the past 20 years. Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer. Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer. Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.

The Senior Manager, IT Application Support will lead global support for Amneal Pharmaceuticals' enterprise and critical business applications, ensuring availability, performance, compliance, and user satisfaction across manufacturing, quality, R&D, supply chain, commercial, and corporate functions. This role manages a distributed team and strategic partners to deliver secure, compliant 24x6 support. The ideal candidate brings expertise in application operations, ITIL, vendor management, and regulated industry standards (FDA, SOX, GxP), with strong cross-functional collaboration skills. Essential Functions: Global Application Support Leadership Lead Level 2 and 3 support teams across the US, India, and Ireland. Ensure 24x7 coverage for critical applications with effective on-call and escalation protocols. Oversee incident, problem, and change management in alignment with ITIL standards. Application Portfolio & Service Ownership Maintain operational health, upgrades, patches, and performance of global applications, including: ERP: JDE, SAP Business Objects Quality: Caliber QMS, LIMS Supply Chain: Coupa P2P, Manhattan WMS, Liaison EDI Commercial: Veeva CRM, corporate and marketing websites Process Excellence & Continuous Improvement Standardize support processes, runbooks, and documentation for global consistency. Drive root cause analysis and implement preventive actions. Promote automation, monitoring, and self-service to reduce manual effort and improve resolution speed. Stakeholder & Business Engagement Act as the primary escalation point for application performance and support concerns. Additional Responsibilities: Conduct regular service reviews with business units to assess satisfaction, gather feedback, and align on priorities. Work closely with IT business partners to understand evolving needs and integrate them into support strategies. Ensure application support activities comply with SOX, FDA, GxP, and ITGC requirements. Maintain auditable change controls, incident records, and access management processes. Support internal and external audits with timely and accurate evidence. Qualifications Education: Bachelors Degree (BA/BS) Engineering - Preferred Experience: 10+ years managing enterprise application support in a global environment. 8+ years leading distributed teams and overseeing vendor-managed services. Skills: Strong knowledge of ITIL processes (Incident, Problem, Change, Release). - Expert Experience in regulated industries (pharmaceutical, biotech, or similar) with compliance frameworks like FDA, SOX, and GxP. - Advanced Specialized Knowledge: ITIL v4 certification. Familiarity with DevOps practices and agile methodologies. Background in ERP, quality systems, and integration platforms. The base salary for this position ranges from $155,000 to $170,000 per year. In addition, Amneal offers a short-term incentive opportunity, such as a bonus or performance-based award, with this position within the first 12 months. Amneal ranges reflect the Company's good faith estimate of what 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, experience, 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 help you enjoy your career alongside life's many other commitments and opportunities.

The Supervisor will oversee the operations and staff throughout the manufacturing floor. The supervisor will also assist with equipment start-up, participate in ANDA batch production and commercial batch manufacturing. This role follows a 12-hour rotating schedule, working from 6:00 AM to 6:30 PM. Essential Functions: Oversee all activities throughout the manufacturing floor. Ensure safety, quality, and effective productivity, adhering to 100% GMP compliance. Plan and schedule all manufacturing and packaging activities to ensure deadlines are met, prevent a back order situation. Work closely with the quality group to ensure constant compliance, participate in any and all investigations that may arise in the department. Support the R&D process and execution of new products is expected, will be a key contributor of information during the process. Act as a "Working Supervisor" to manufacture the various R&D large/small scale batches, train operators in the processing and equipment capabilities for all production. Participate in equipment set-up, IQ/OQ/PQ, and commercial batch activities. Set-up, run and clean equipment in a GMP compliant environment. Conduct mixing, coating, converting, pouching and cartoning operations. The Working Supervisor responsibility is a key aspect of the role as it pertains to leading, performing and demonstrating the actual methods and procedures in manufacturing the products using state-of-the-art equipment and operating systems. These systems include sophisticated recipe driven controlled human interface systems. Conduct effective communication to the staff on a daily basis to ensure that everyone is up to speed with the all pertinent departmental and/or company events. Additional Responsibilities: R&D and commercial scale-up activities. Perform Continuous Improvements. Education: Bachelors Degree (BA/BS) Related field - Preferred Associate Degree Related field + 5 yrs exp leading and training staff - Required Experience: 3 years or more in Transdermal drug delivery or manufacturing GMP environment 3 years or more in Leading and training staff Skills: Strong analytical and quantitative skills with good common sense. - Intermediate Excellent oral and written communication skills. - Intermediate Able to multi-task, and advance multiple programs simultaneously. Takes thoughtful and timely action when confronted with a problem. - Intermediate Ability to adapt to changes in assignments, flexibility, and willingness to work extended hours. - Intermediate Strong team player. - Intermediate Specialized Knowledge: Transdermal, Converting, Packaging Experience with in a GMP Manufacturing Environment Additional Requirement: This position requires successful completion of an OSHA-compliant Respirator Fit Test. The base salary for this position ranges from $80,000 to $100,000 per year. In addition, Amneal offers a short-term incentive opportunity, such as a bonus or performance-based award, with this position within the first 12 months. Amneal ranges reflect the Company's good faith estimate of what 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, experience, 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 help you enjoy your career alongside life's many other commitments and opportunities.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. Job Description * Assist in performance of all Quality Assurance functions as outlined in the GLPs and PSL SOPs. Assist the Quality Assurance Director as needed during inspections by EPA, FDA or clients. Prepare records and assemble copies of documents requested by inspectors when advance notice is given and Sponsor and/or Laboratory Director approval is obtained. * Conduct in-process study inspections and general facility inspections in the toxicology and chemistry laboratories as directed. * Audit raw data and proofread report and tables against raw data for accuracy and for typing corrections. Audit final report to verify corrections. * Amend and update Standard Operating Procedures as required using word processing system. File all QAU-related paperwork as directed. * Select intervals for inspection for any regulatory test under the auditor's responsibility or as directed by QA Director, Laboratory Director, or President. Perform such inspections in accordance with the test schedule. When the time for conduct of intervals requiring inspection falls outside of normal working hours, this will be brought to the attention of the Study Director or QA Director in order that a suitable arrangement may be made. * Ability to safely wear a respirator required. * Other duties as assigned. Qualifications * QA auditors will have experience in a laboratory regulated by FDA/EPA GLP standards. Experience in other quality standards such as cGMP or GCP will also be considered. * Experience with acute toxicology, analytical chemistry, and/or general laboratory procedures is preferred. B.S. degree in biology, toxicology, animal science or related field and/or AALAS certification at the Technician level is also preferred. Experience in computer system validation and electronic data capture is desirable but is not required. * The individual holding this position must be of the highest integrity and have a very strong sense of responsibility. Attention to detail is essential. He/she must be well organized, tactful, be able to work independently and maintain all records, documents, and schedules associated with quality assurance procedures and studies. Communication skills, especially written, are necessary. Proficiency with MSWord and Excel is required. He/she must have a current tetanus vaccination if required to access the vivarium. Additional Information Position is full-time, Monday-Friday 8am-5pm. Candidates within a commutable distance of South Brunswick, NJ are encouraged to apply. Compensation: $22.50-$25.50/hr Excellent full-time benefits including: * Comprehensive medical coverage, dental, and vision options. * Life and disability insurance * 401(k) with company match * Paid vacation and holidays Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.