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Job Description Working in tandem with the Executive Director, Meeting Manager and Communications Manager for several national non-profit associations (Association for Applied Sport Psychology, Institute of Nuclear Materials Management, Pacific Dermatologic Association and Society for Redox Biology & Medicine), the Membership / Meeting / Registration Coordinator provides valuable support to association members, assists manages registration for meetings and assists in planning and executing national association meetings. Key Responsibilities: · Frontline customer service for association members · Processing membership applications and renewals · Coordinate registration for meetings · Plan & coordinate virtual meetings such as webinars and committee meetings · Support various aspects of meetings, registration set-up and assisting the administrative needs of the Meeting Manager · Support for association committees · Support of client certification and accreditation programs · Update and maintain association Policies and Procedures and Strategic Plans · Process monthly membership and meeting financial reports · Plan and execute some member marketing and communications · Assist with maintaining association websites, and email programs · Database Management (FileMaker Pro) Requirements: · Bachelor’s degree · Excellent communication skills with a strong focus on customer service · Ability to work well in a team and independently · Excellent organizational and time management skills · Ability to work well under pressure and firm deadlines · Strong problem-solving skills · Computer literacy with expert knowledge of Microsoft Office · Previous MAC experience preferred (we are a MAC only office) Travel: · 2-3 weeks per year · November 2025, Washington DC · May 2026, Scottsdale, AZ · August 2026, Lake Tahoe, CA Benefits: Medical/Dental/Vision benefits, 401K, paid holidays and access to on-site fitness center. Hybrid work environment – 3 days in office / 2 days remote. To Apply: Send resume and cover letter by Monday, September 8. No phone calls please. Company DescriptionFor 40 years, HollandParlette has been providing management and specialized administrative services to professional societies and trade associations using a for-profit approach that runs not-for-profit associations like businesses. We manage associations of varying sizes and annual budgets. Within the AMC model, HollandParlette affords association clients the characteristics of economies of scale, experience in the association marketplace, flexibility and adaptability, buying power and centralized facilities. Office located in Keystone at the Crossing in north Indianapolis.For 40 years, HollandParlette has been providing management and specialized administrative services to professional societies and trade associations using a for-profit approach that runs not-for-profit associations like businesses. We manage associations of varying sizes and annual budgets. Within the AMC model, HollandParlette affords association clients the characteristics of economies of scale, experience in the association marketplace, flexibility and adaptability, buying power and centralized facilities. Office located in Keystone at the Crossing in north Indianapolis.

Job Description The field of gene therapy is growing rapidly and Genezen is here to meet the exacting needs of our clients. We provide process development, produce GMP viral vectors, and provide cell transduction for gene and cell therapy clinical trials and are proud to be a part of the process that leads to new cures. WORKING AT GENEZEN Many people have worked in environments where you feel like just another nameless part of an enormous machine. Genezen is different. We want our employees to be innovative, collaborative problem solvers who are dedicated to meeting the challenges of working at a fast-growing company. We are dedicated to empowering our employees to be their best and making Genezen a rewarding place to work. Every employee contributes to the success of the company and you can be part of that team. JOB SUMMARY Responsible for leading routine performance of downstream manufacturing operations including advanced laboratory techniques related to viral vector production and analytics as well as basic laboratory functions. Responsibilities and laboratory techniques required for this position include aseptic technique, preparing solutions and media, molecular biology techniques, cell culture techniques, and general cleanroom sanitization/area maintenance. The position requires working both independently and serving as the manufacturing Downstream SME for client processes, but also under the supervision of the Manufacturing Manager. ESSENTIAL JOB FUNCTIONS • Serve as the lead Downstream operator for coordinating team responsibilities and peforming hands on manufacturing processes related to viral vector production including downstream manufacturing tasks under the guidelines of established procedures and batch records, • Lead manufacturing activities within a team environment related to clarification, chromatography, TFF and filling activities, • Serve as a liason with downstream process development SMEs to understand the latest downstream process development processes/practices and ensure feasibility of translation of said processes/practices to a GMP manufacturing environment, • Maintain manufacturing material supply, primarily ensuring manufacturing spaces are adequately stocked and prepared, • Assist in the maintenance of laboratory equipment and laboratory support operations, • Lead in the creation, review, and revision of SOPs, batch records, and forms in coordination with management, PD and Quality Assurance, • Ensure roles and responsibilities for executing downstream manufacturing processes are clear to the operators assigned to the processes and assist with coaching/training operators as needed, • Follow detailed instructions with a high level of focus and attention to detail, • Complete documentation accurately and in a timely fashion, • Maintain up to date training status, • Use, clean, and maintain laboratory spaces and manufacturing equipment, • Lead in troubleshooting of downstream manufacturing issues, with assistance from Manufacturing Management as needed, • Train new staff members and fellow employees in all relevant downstream manufacturing processes, • Comply with all established policies and SOPs, • Perform safety inspections and maintain a safe working environment, • Use industrial equipment such as pallet jacks, • Perform area sanitization and collect/dispose of waste per established procedures, • Help collect process data for metrics/trending, • Assist in tasks required to be performed in a BSL-1, -2, or -3 environment., • Contribute to the support, optimization, and improvements of GMP products, • Assist in specification development and review via Corrective and Preventive Actions (CAPA) and/or change controls, • Adaptability required as work schedule may change based on business needs, • Criminal background check required EDUCATION / CERTIFICATIONS / LICENSES Essential/Desired BS degree in Biology, Biochemistry, Molecular Biology, or similar field Essential ON-THE-JOB EXPERIENCE Minimum 2 years of post-graduation experience in a GMP environment Essential 2 years of experience operating in a GMP laboratory using aseptic technique and risk mitigation strategies Essential 2 years of experience with at scale Clarification, Chromatography, and TFF platforms Essential Experience in cell and gene therapy DS/DP manufacturing, specifically viral vectors Strongly Desired SKILLS / ABILITIES Excellent computer, verbal, and written communication skills Essential Ability to work independently with minimal supervision as well as within in a team, specifically as the lead operator during manufacturing activities Essential Able to adapt quickly to changing ideas, responsibilities, strategies, and other processes Essential Willing to work in an environment where individual initiative, collaboration, and accountability are valued Essential PHYSICAL DEMANDS While performing the duties of this job, the employee is required to meet the following physical demands: Work Environment • Frequently required to work in a BSL 2 environment with personal protective equipment/aseptic gowning, • Regularly required to work around large machinery and typical utilities seen in pharmaceutical facilities, • Occasionally exposed to moving mechanical parts; high, precarious places; toxic or caustic chemicals; hazardous waste; and risk of electrical shock, • Frequently required to stand; sit; walk; balance; stoop; kneel; crouch; use hands to finger, handle, or feel; reach with hands and arms, • Frequently lift and/or move up to 25 pounds, • Frequently required to communicate by talking, hearing, using telephone and e-mail GENEZEN'S CURES VALUE-BASED COMPETENCIES Committed to Science We are committed to scientific excellence, staying current with industry developments, making data-driven decisions, and pursuing innovation to advance healthcare. Urgency in action for the patients We operate with urgency and a commitment to delivering timely treatments to patients by accelerating our partners' programs. Resilience & Grit in operations We are committed to overcoming challenges, learning from failures, and persistently striving for success. Execute with Excellence & Integrity We are dedicated to delivering quality results and upholding ethical principals. Solutions driven for our partners We are committed to being a proactive, collaborative, creative and open-minded partner. GENEZEN'S BENEFITS • Paid vacation days, amount based on tenure, • Paid sick time, • 10 observed holidays + 2 floating holiday + 1 volunteer day, • 401(k) plan with company match up to 6% of salary, vested immediately, • Share Appreciation Rights, • Choice of several healthcare plans, • FSA and HSA programs, • Dental & vision care, • Employer-paid basic term life/personal accident insurance, • Voluntary disability, universal life/personal accident insurance, • Nothing in the job description for this role restricts management's right to assign or reassign duties and responsibilities to this job at any time., • This position requires a criminal background check., • Genezen is an Equal Opportunity Employer., • Genezen participates in EVerify. Fishers is a suburb of Indianapolis. Fishers was named the #1 place to live in the US by Money Magazine in 2017 for its livability, safety and entrepreneurship. Fishers is one of the fastest growing communities in Indiana and is dedicated to supporting a high quality of life for all its residents. Nearby Indianapolis is home to professional and college sports teams, the Indy 500, a growing art community and the world's largest children's museum--to name just a few reasons why this area is a great place to live. Lexington, Massachusetts, located just northwest of Boston, is renowned as a historic suburb with a rich cultural heritage. It boasts picturesque New England charm, tree-lined streets, and a vibrant community. Known for its pivotal role in the American Revolution, Lexington offers visitors and residents alike a blend of historical landmarks, modern amenities, and a strong sense of community pride.

Job Description IMMEDIATE OPENING: Clinical-Biology Lab Tech Interested in this role? Reach out directly to mrichey@actalentservices .com or CALL 317 567 6591 with an updated resume to apply (HIRING NOW) Position Summary: Join our team as a Clinical Lab Technician where you will perform diagnostic clinical and clinical contract research testing under direct supervision. This role involves preparing samples through sample management and testing on various analyzers to deliver accurate customer results, supporting laboratory reagent preparation, and maintaining equipment. Essential Functions and Responsibilities: • Under direct supervision by department leadership, be a lead tech to perform diagnostic clinical and clinical contract research testing., • Prepares samples through sample management and tests samples on 4 different analyzers for customer results., • Supports clinical diagnostic testing, preparation of laboratory reagents, releasing final results, and routine maintenance of laboratory equipment., • Understands and performs to all applicable regulatory and compliance requirements., • Performs diagnostic testing, as scheduled (500-1,500 samples per analyzer in a given shift) on one of 4 analyzers., • Supports the sample management team with sample identification/evaluation, labeling, processing, and centrifuging samples when there are high volumes of samples or a decrease in tests needed., • Performs reagent preparation, as scheduled, and supports maintenance of reagents., • Operates, troubleshoots, and performs routine maintenance and calibration on equipment and may participate in validations. Qualifications • Required: B.S. in Life Science (biology, chemistry, biochemistry, etc.), • OR Medical Lab Tech (MLT) with ASCP certification or Clinical Lab Science (CLS) schooling with 4+ years of hands-on testing experience., • OR Masters degree with 2+ years of hands-on testing., • Human biological testing experience (blood, tissue, urine, etc.)., • Blood banking experience., • Biology lab internship., • Leadership skills, • Lab Training and Development, • Diagnostic clinical testing, • Sample management, • Operation and maintenance of laboratory equipment, • Reagent preparation, • Attention to detail, • Team collaboration, • Time management, • Regulatory compliance, • I am scheduling interviews, with phone screenings available as early as today. If interested, apply within 24 hours for priority consideration to Max Richey., • HOW TO APPLY DIRECTLY: Email your updated resume, brief intro about your interest, preferred method of communication for you (i.e., call, email, text) to mrichey@ actalentservices.com or CALL/TEXT: 317 567 6591 Pay and Benefits The pay range for this position is $22.75 - $26.50/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision, • Critical Illness, Accident, and Hospital, • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available, • Life Insurance (Voluntary Life & AD&D for the employee and dependents), • Short and long-term disability, • Health Spending Account (HSA), • Transportation benefits, • Employee Assistance Program, • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Indianapolis,IN. Application Deadline This position is anticipated to close on Sep 17, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email for other accommodation options.

Job DescriptionCompany 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 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 • Provide technical leadership on Effector Function Testing for Biologics, • Perform cell-based assays to support preclinical development of the molecules, • Identifying and helping troubleshoot issues, • Biology experience, including, but not limited to, the following: mammalian cell culture techniques and cell-based assay development, • ELISAs and luciferase reporter assays, • Flow cytometry, • Capable of balancing multiple tasks at once while delivering the highest standard of quality data., • Experience:, • Transient and/or stable cell line generation, • Experience with automation of cell-based assays on Hamilton or other Liquid handlers., • Characterizing protein structure and function using various biochemical/biophysical approaches such as SPR, • Characterizing protein: protein interactions, • Microsoft Office software (Excel, PowerPoint, etc.), • Graphing data in GraphPad Prism, • Strong interpersonal skills; able to foster an environment for learning and open/honest communication, • Ability to identify and implement operational and organizational improvements, • Analytical/Problem-Solving skills, • Supervision of others:, • Coach, train, and develop others within the group with respect to their personal development and effective implementation of operational improvements, • Foster motivation and morale, • Coordinate workflow and perform daily monitoring to meet TAT, • Prepare and review job plans, conduct semiannual performance reviews, interview applicants, keep training records up to date for assigned employees, perform succession planning in preparation for growth, • Laboratory maintenance (e.g. cleaning and sanitizing of laboratory), • Demonstrates strong client service skills, teamwork, and collaboration, • Proactively plans and multitasks to maximize productivity, • Ensure that the quality policy program is understood, implemented, and maintained at all levels of the organization; identify, prevent, or correct any departures from the quality system, • Develop and implement operational improvements, • Monitor and approve employees’ time worked through time-entry system, • Support and promote company policies and proceduresQualifications, • Strong computer and organizational skills and experience with Excel and QualityDocs (controlled content management platform), • Ability to learn, prioritize multiple tasks, keep accurate records, follow instructions, and comply with company policies, • Ability to work independently and as part of a team with internal and external clients, self‑motivation, adaptability, and a positive attitude, • Bachelor's degree in biology, chemistry, or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major), • Leadership experience, • 4+ years related lab experience, • Excellent written and verbal communication skills and experience interacting with people from a wide range of skill levels and experience, • Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies, • Demonstrated ability to work as an independent, self-motivated, detail-oriented, result-driven and highly flexible team-player in a fast-paced working environment, • Strong focus on quality, teamwork, and productivity, • Proactive, positive, solution-oriented leadership style with ability to prioritize and coordinate simultaneous projects with varying deadlines, • Strength in employee engagement, morale, and retention, • Authorization to work in the United States indefinitely without restriction or sponsorship Additional Information • Position is full-time, 8:00 am- 5:00 pm Overtime as needed., • Candidates currently living within a commutable distance of Indianapolis, IN, are encouraged to apply, • 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, • #LI-EB1 Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Job Description Company: Davey Resource Group, Inc. Locations: Indianapolis, IN, South Bend, IN Additional Locations: NA Work Site: Hybrid Req ID: 212455 Position Overview DAVEY RESOURCE GROUP, Inc., has openings throughout South Bend, Indianapolis, and the Great Lakes region for experienced environmental consulting professionals. We are seeking teamwork-oriented individuals with excellent written and oral communication skills. Candidates should possess a professional work ethic with attention to detail and safety. Position Description and Responsibilities Selected candidates will work collaboratively with Davey Resource Group project developers, biologists, and project managers on a variety of ecological restoration projects. The position involves preparing and supervising client proposals, technical report writing, and plan development for ecological restoration of upland, wetland and stream environments. Additional experience in environmental planning, permitting, monitoring, construction, wetland delineation and section 401/404 permitting is also a plus. The primary focus of this position is to not only provide senior level project management and expertise, but also perform a key role in the development of new projects, grant writing, networking and identifying new client relationships and project opportunities. This may include attending conferences/workshops and public speaking. Required Qualifications • Minimum of a four-year degree in biology, ecology, conservation, environmental science, or related fields., • At least eight years of experience working in the natural resources field performing ecological consulting work., • Proficient with state laws and environmental regulations., • Valid driver's license and have a good driving record The successful candidate will demonstrate proficiency with stream/wetlands restoration design work, including modeling and plan development; have experience performing construction oversight of restoration projects; be capable of managing large projects with multiple subcontractors; and maintain an existing network of clients and contacts within the ecological consulting industry. Additional Information What We Offer:* • Paid time off and paid holidays., • Opportunities for advancement., • All job specific equipment and safety gear provided., • 401(k) retirement savings plan with a company match., • Employee-owned company and discounted stock purchase options., • Group Health Plan., • Employee Referral Bonus Program: Send-A-Friend., • Locations throughout the United States in major cities and desirable areas., • Career Development Program supported by industry expert safety specialists and skilled trainers., • The Davey Tree Family Scholarship for children of employees. What We Offer:* • Paid time off and paid holidays., • Opportunities for advancement., • All job specific equipment and safety gear provided., • 401(k) retirement savings plan with a company match., • Employee-owned company and discounted stock purchase options., • Group Health Plan., • Employee Referral Bonus Program: Send-A-Friend., • Locations throughout the United States in major cities and desirable areas., • Career Development Program supported by industry expert safety specialists and skilled trainers., • The Davey Tree Family Scholarship for children of employees. Davey Resource Group, Inc., is a leader in the natural resource, environmental, and forestry consulting industries throughout the United States. The Davey Tree Expert Company provides research-driven tree services, grounds maintenance and environmental consulting for residential, utility, commercial and environmental partners in the U.S. and Canada. We care about our clients, each other and the world around us. We offer the resources, size and stability of a big company while maintaining the culture, entrepreneurial spirit and feel of a small one. We invest in our employees by offering industry-leading training, technology and benefits that lead to a rewarding and safe work experience at all levels. Wherever you want to grow your career, there’s a place for you at Davey. To learn more, visit Davey.com. Accommodations: If requested by employee or otherwise as required by law, reasonable accommodations will be made to enable employees with disabilities to perform essential job functions. If you need assistance at any time, please contact us at 1-877-411-7601 or at . Employment Type: Permanent Job Type: Full Time Travel Expectations: Up to 50%

Job Description Job Details Shifts: day Location: Indianapolis, Indiana Medical benefits-eligible first of the month following 28 days of employment. All other benefits-eligible first of the month following 90 days of employment. Benefits: 401(k) Dental insurance Health insurance Paid time off Employee Discount Vision insurance Position Overview: The Microbiologist is responsible for monitoring and qualitative/quantitative testing of process and product attributes to ensure food safety and food quality. Ensure compliance with all applicable regulations. Compliance with all applicable standards such as Safe Quality Foods (SQF), Third party audits, Kosher, and Organic requirements. Interpretation of testing results to release of product that has met specifications. Process documentation for non-conforming product and communicate information to plant management. Language Skills: English proficiency required. Spanish is a plus. Supervisory Responsibilities: None. Amount of Travel Involved: None. Essential Duties and Responsibilities: • Follow all safety procedures and work as safe as possible at all times., • Maintain Good Manufacturing Practices (GMP’s)., • Maintain Good Laboratory Practices (GLP’s)., • Daily operation of equipment which includes Autoclave, Air Sampler, and all other related equipment., • Responsible for microbiological testing/documentation of finished product, water, swabs, ingredient and or other material as needed., • Interpret the results and retest/report abnormalities as needed; Generate standard report of results., • Standardizes equipment prior to use, ensures reagents and other materials are available., • Performs analysis on products to ensure compliance to customer and regulatory agency guidelines., • Ensures that all products not meeting microbiological specification is communicated to QA Manager for further review., • Ensure that all-pertinent analytical results into the data collections system on a timely basis, immediately informs supervision of any deviations., • Review, creates, maintains, files, and scan logs, charts, finished goods/ingredients/packaging microbiological results and other reports., • Manage the laboratory operations, maintain lab equipment and supplies., • Maintain lab equipment and order supplies., • Release products that have met microbiological specification in ILS., • Conduct work processes with the use of chemicals. Evaluate the physical properties of ingredients and products., • Train Analytical Technician, QA Lead, on plating, reading, documenting, filing, and scanning microbiological sampling and results., • Provide management with microbiological expertise as needed., • Create Certificate of Analysis (COA) and submit microbiological results to customers., • Other duties as assigned at discretion of management, • Maintain a positive work atmosphere and interaction with customers, co-workers, and management., • Regular and punctual attendance., • Work scheduled shift, weekends, and extended hours as required., • Must be accurate and precise in testing procedures., • Must possess strong oral and written communication skills., • Must be able to read, write and interpret documents such as, procedure manuals., • Must have the ability to read, comprehend and follow technical instructions., • Ability to effectively present information in one-on-one and small group situations to customers, clients and other employees of the organization., • Must be able to speak and understand English fluently., • Must have the ability to apply commonsense understanding to carry out detailed and involved written or oral instructions., • Must have the ability to calculate figures and amounts such as proportions, percentages, averages, and ratios., • Must have the ability to prioritize and organize., • Must demonstrate superb decision-making ability to determine best course of action in assessing test results., • Bachelor of Science degree in Microbiology Biology, or Food Science, required., • Two years of laboratory with microbiology and chemistry experience required., • Or equivalent combination of education and experience., • At least 1 year in a food or beverage production environment preferred., • Upholds mental, spiritual and physical safety, • Asks for and provides feedback, • Holds self and others accountable, • Supportive and collaborative of team members, • Participates in self-development and encourages the development of those who report/to him or her and peers While performing the duties of this Job, the employee is regularly required to talk or hear. The employee is frequently required to sit; use hands to finger, handle or feel and reach with hands and arms. The employee is frequently required to stand; walk and stoop, kneel, crouch or squat. The employee must regularly lift, pull and/or move up to 10 pounds, frequently lift, pull and/or move up to 25 pounds and occasionally lift, pull and/or move up to 50 pounds. Specific vision abilities required by this job include close vision and ability to adjust focus. Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. While performing the duties of this job, the employee is occasionally exposed to moving mechanical parts. The noise level in the work environment is usually moderate but may be exposed to loud noises from production equipment. The employee is occasionally exposed to fumes or airborne particles; toxic or caustic chemicals; extreme cold and extreme heat. Manna Beverages is an equal opportunity employer-----M/F/D/V

Job DescriptionHeartland Food Products Group is a global leader in the consumer packaged goods (CPG) industry, producing low-calorie sweeteners, coffee, coffee creamers and liquid water enhancers. We manufacture and market Splenda, the #1 brand in the low calorie sweetener category and the most recognized in the world. We make coffee, tea and water taste better and help people live happier, healthier and longer lives by making it easy to reduce sugar. We offer an excellent compensation and benefits package. Come grow with us! This role is not a remote opportunity, it is on-site at our Manufacturing Plant in Indianapolis, Indiana. Scope: The Compliance Manager plans, directs, and coordinates all activities in accordance with current regulation and policy. Their responsibilities include the management of specifications, review of labels and claims, net contents, and supplier performance of both packaging and raw materials. This position is required to consult and provide expertise to company personnel regarding compliance and regulatory requirements. Essential Duties and Key Responsibilities: • Maintains a work environment committed to sustainable safety by enforcing safety rules, setting a safe example, and coaching and communicating to associates the reasons for safe operations., • Manages material sampling and monitoring programs to ensure the safety and compliance of materials by identifying and minimizing risks and managing contaminants., • Manages specification creation (MPSEC) and label declarations processes. This includes all Quality activities related to artwork creation, maintenance, and revisions., • Manages the receiving and Ingredient and Finished Product COA process., • Responsible for Supplier Quality pre-requisite program:, • Vendor Approval,, • Approval of RAW/PACKs,, • Vendor Performance Management and Review, aligned with Procurement. Supplier SCAR management, investigation and reporting., • Drives compliance with regulations foreign and domestic by preparing the organization with information about consumer and industry trends, emerging threats, and evolving laws and regulations. This includes establishing systems to ensure compliance with all legal requirements., • Management of Databases and Team Rooms for these processes., • Act as back up for Verification and Audit Manager, • Serve as alternate SQF practitioner, responsible and authorized for ensuring company fulfills all requirements of the current SQF code, • Responsible for driving compliance and maintenance of all certifications – including GFSI, cGMP, Kosher, Halal, Organic, Non-GMO Certified, Identity Preserved, Gluten-free, and others as needed., • Ensures compliance with Mock Recall and item traceability requirements (FDA/customer) including running trace exercises and maintaining company knowledge and resources to perform, • Assist Sales, Legal Team, International Sales, and International Quality teams with regulatory and technical inquiries, certificates, advice and program knowledge, • All other duties as assigned. Qualifications: • Bachelor’s degree in Food Science, Chemistry, Biology or related field with at least 5 years of relevant food manufacturing experience is required., • Familiarity with current good manufacturing practices and food regulation is required., • Prior experience with labeling and claims., • Six Sigma or process improvement experience and SQF practitioner certification desired., • Excellent attention to detail, • Familiar with FSMA requirements, • Previous leadership experience, • Process improvement skills (e.g. Six Sigma), • Proficient command of English and strong communication skills required – both verbal and written., • Must work well in a team environment and have strong communication skills, • Must have the ability to perform under pressure and communicate well with all departments, • Must have good computer skills, including proficiency with Microsoft Excel and Word Physical Demands: • Must be able to physically perform the functions of climbing, balancing, stooping, kneeling, crouching, reaching, standing, walking, pushing, pulling, lifting, grasping, feeling, talking, hearing, and repetitive motions, • Must be able to work seated using a computer and phone for long periods of time., • Must be available to work during extended or off-hours, • Must possess visual acuity to document company records, • Continuous walking throughout plant and distribution center., • Lifting up to 40 pounds

Job Description At Beckman Coulter Life Sciences, we know time is the most critical facet in the laboratory today: time to get life-saving therapies to patients faster; reclaiming time by automating tedious manual workflows; and saving time spent addressing erroneous or complex results. We are partners in time and accelerate answers to critical questions through the power of automation. We develop innovations for scientists by scientists, with many of our 3,300+ global colleagues coming from the laboratory. It’s all part of our time-tested approach to bringing meaningful innovations at the speed of life since 1935. And we’re just beginning. Working together, let’s put our time and talents together to advance human health for tomorrow. Learn about the Danaher Business System which makes everything possible. The Environmental Health & Safety Specialist is responsible ensuring all associates at our Indianapolis, Indiana manufacturing facility can safely help us achieve our mission and vision in scientific research, and medicine. This position reports to the EHS&S Manager, dotted to the Plant Director, and is part of the Environmental Health & Safety Team located in Indianapolis, IN and will be an on-site role. In this role, you will have the opportunity to: * Coach and serve as an EHS mentor for the site-level associates and be the point of contact for Environmental and Safety calls and supporting the EHS&S Manager. * Coordinate deployment of safety/environmental processes to maintain compliance of all legal, corporate policy, procedures and initiatives; research new or existing laws, rules, and regulations and make recommendations regarding appropriate actions. * Participate in daily management of EHS activities across the site such as audits, monthly meetings, and publishing/posting of metrics. Champion efforts to drive improvements and ensure sustainment. * Provide support and leadership in the coordination and management of the safety incident management system to include facilitating incident investigation process, conducting accident investigations and implementing corrective actions. * Lead and deliver training to ensure compliance and build functional competency; including new hire orientation, ad hoc, etc. The essential requirements of the job include: • Bachelor’s Degree in Health and Safety, Biology, Chemistry, Engineering, or related field with 5+ years of experience in EHS area., • Strong working knowledge of federal/state/local environmental regulations and policies to include OSHA, EPA etc., • Demonstrated analytical and problem-solving skills utilizing data and business insights to drive tangible results in the environmental and safety space., • Established communication and presentation skills for training, and working with associates in driving site based EHS programs/projects., • Experience driving projects using lean and six sigma tools for problem-solving, daily management, and Kaizen events., • The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions., • While performing the duties of this job, the employee is occasionally required to reach with hands and arms. The employee is constantly required to sit. The employee may occasionally squat, turn/twist, or reach. The employee is constantly using hands to: finger, handle, feel or operate objects, and computer keyboards. The employee is occasionally required to walk, stand, climb, balance, stoop, bend, kneel, crouch or crawl, and talk, hear, and smell., • The employee must frequently lift, carry, push or pull up to 20 pounds and occasionally lift, carry, push or pull up to 50 pounds., • Bachelor's Degree, • Experience in a Manufacturing Environment

Job DescriptionJob Title: Quality Assurance Auditor I INTERVIEWS AVAILABLE THIS WEEK Interested in this role? Reach out directly to mrichey@actalentservices .com or CALL 317 567 6591 with an updated resume to apply (HIRING NOW) Job Description Join a dynamic organization at the forefront of innovation in solid dosage manufacturing support. We specialize in providing advanced formulation technologies, regulatory expertise, and quality systems that empower pharmaceutical, nutritional, and animal health companies around the globe. We’re seeking a detail-oriented and collaborative Quality Assurance Auditor I to support our quality operations. This role plays a key part in ensuring compliance, product integrity, and continuous improvement across our manufacturing and laboratory processes. Responsibilities • Maintain compliance with current Good Manufacturing Practices (GMPs) and Good Laboratory Practices (GLPs)., • Conduct batch record reviews and product release activities for site-manufactured materials., • Prepare documentation for samples submitted to internal and external quality control laboratories., • Assist in the coordination and execution of internal audits., • Perform audits of incoming raw materials and finished goods to ensure quality standards are met., • Conduct investigations into product quality complaints, non-conformance events, and manufacturing deviations., • Collaborate cross-functionally with teams in operations, engineering, maintenance, safety, and supply chain to identify root causes and implement corrective actions., • Promote a culture of quality through thorough investigations and actionable solutions., • Document investigation findings in detailed, timely reports using internal quality systems., • Initiate and manage service requests related to non-conformance issues., • Generate and manage quality documentation for operational activities., • Participate in onboarding and training of new team members., • Experience in quality assurance, quality auditing, and quality specialist roles (1-4 years)., • Proficiency in quality control, audit, batch record review, and document control., • Knowledge of GMP, FDA regulations, and inspection processes., • Experience with CAPA, SOPs, and quality checks., • Strong verbal and written communication skills across all organizational levels., • Technical writing experience is highly valued., • Exceptional attention to detail and organizational skills., • Bachelor’s degree in a science discipline (preferred), Minimum High School Diploma Required., • Comfortable working in a manufacturing environment. The position is set in a manufacturing environment where adherence to safety and quality standards is paramount. Employees are expected to wear appropriate personal protective equipment and comply with all safety regulations. The organization supports a purpose-driven culture with opportunities to engage in community outreach and sustainability efforts. The work schedule offers flexibility to support work-life balance, and employees have access to performance incentives, health coverage, dental care, vision support, wellness programs, mental health services, financial assistance for education, retirement planning, generous paid time off, and paid holidays. Job Type & Location This is a Permanent position based out of Indianapolis, Indiana. INTERESTED IN THIS ROLE? SEE BELOW TO APPLY NOW FOR IMMEDIATE CONSIDERTATION: I am scheduling interviews for this position ASAP and conducting phone interviews as early as today. All candidates will be considered immediately within 24 hours of applying directly to Max Richey HOW TO APPLY DIRECTLY: Email your updated resume, brief intro about your interest, preferred method of communication for you (i.e., call, email, text) to mrichey@actalentservices. com or CALL 317 567 6591 Pay and Benefits The pay range for this position is $50000.00 - $70000.00/yr. What We Offer Our Team We believe that supporting our people—both professionally and personally—is key to building a thriving workplace. Our benefits package reflects that commitment, with a wide range of resources designed to promote health, growth, and balance: Performance Incentives: All team members are eligible for annual rewards based on collective success. Health Coverage Options: Choose from multiple comprehensive medical plans tailored to different needs. Dental Care at No Cost: Full dental coverage provided for employees and their eligible family members. Vision Support: Optional vision plans available to help keep life in focus. Wellness Matters: Access to fitness programs and holistic health initiatives. Confidential Support: Mental health and personal counseling services available through our employee support network. Purpose-Driven Culture: Opportunities to engage in community outreach and sustainability efforts. Family First: Paid leave available for new parents to bond and care for their growing families. Invest in Learning: Financial assistance for continued education Retirement Planning: Employer contributions to your retirement savings to help you plan for the future. Recharge Time: Generous paid time off to relax, travel, or simply unwind. Celebrating Together: Paid holidays to enjoy time with loved ones and mark special occasions. Workplace Type This is a fully onsite position in Indianapolis,IN. Application Deadline This position is anticipated to close on Sep 19, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email for other accommodation options.

Job DescriptionCompany 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 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 Responsibilities include but are not limited to: • Perform and document qualifications on laboratory instrumentation (i.e. HPLC, GC, KF, UV-Vis, etc.), • Perform urgent/priority repairs including user accessible consumables (i.e. lamps, pumps, seals, tubing, etc.), • Experience with chromatography data processing software (e.g. Empower), • Verify system readiness for open access instruments, • Execute scheduled and post-maintenance instrument qualifications, • Troubleshoot routine instrument issues (limited to calibration issues), • Assist in testing activities during instrument upgrades, • Report on metrics and appropriate document service on instruments, • Coordinate and escort vendors on-site to perform maintenance activities on instruments on contract, • Interface with the client and project resources as necessary to provide asset management functions and data management services, • Maintain accurate instrument files (work orders, qualification records, etc.), • Input data into electronic asset management system (GMARS)Qualifications, • Bachelor’s degree in life science concentration (chemistry, biology, or related fields) and greater than over 4 years of directly related industry experience or a MS/PhD degree in a life science concentration (chemistry, biology, or related fields) and 2 years of directly related industry experience., • Strong computer, scientific, and organizational skills, • Excellent communication (oral and written) and attention to detail, • Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude, • Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Additional Information • Position is full-time, Monday- Friday 8 am-5 pm, • May be requested to work on weekends, overtime, and holidays based on business needs., • Candidates currently living within a commutable distance of Indianapolis, IN are encouraged to apply., • 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, • #LI-EB1, • Authorization to work in the United States indefinitely without restriction or sponsorship Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Job DescriptionCompany 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 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 • Perform cell-based bioassays and surrogate bioassays such as ligand-binding ELISA assays in plate-based format in a GMP environment, • Perform qualification and transfer of analytical test methods in the GMP environment, • Document laboratory work in notebooks/electronic notebooks and log books, perform data integrity checks, data verification reviews, and communicate final results through electronic systemsQualifications, • Bachelor’s degree in life science concentration (chemistry, biology, or related fields) and greater than 4 years of directly related industry experience or a MS degree or a PhD in a life science concentration (chemistry, biology, or related fields) with 2 years of directly related industry experience, • Strong computer, scientific, and organizational skills, • Experience with reporter-gene assay, cell biology skills such as cell culturing, cell counting, cell banking; GMP quality system and lab operations experience, • Excellent communication (oral and written) and attention to detail, • Ability to work independently and as part of a team with internal and external clients, self‑motivation, adaptability, and a positive attitude, • Ability to learn new techniques, keep accurate records, follow instructions, and comply with company policies Additional Information • Position is full-time, Monday-Friday, 8:00 am - 5:00 pm., • Candidates currently living within a commutable distance of Indianapolis, IN are encouraged to apply, • 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, • #LI-EB1, • Authorization to work in the United States indefinitely without restriction or sponsorship Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Job Description Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services. We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position: Key Responsibilities: • Develop and maintain the Contamination Control Strategy (CCS) in alignment with EU Annex 1, FDA Guidance, and industry best practices., • Provide technical oversight for aseptic processing, cleanroom qualification, and sterilization processes (e.g., moist heat, dry heat, radiation, filtration)., • Lead and support media fill (aseptic process simulation) planning, execution, and evaluation., • Review and approve environmental monitoring (EM) and cleanroom classification protocols and data trends., • Serve as the subject matter expert (SME) during regulatory inspections and internal audits related to sterility assurance., • Evaluate and recommend improvements in facility design, airflow patterns, and personnel/material flow for aseptic areas., • Provide input into the design qualification and validation of sterilizers, cleanroom HVAC systems, isolators, RABS, and barrier technologies., • Participate in deviation investigations, CAPAs, and risk assessments involving microbiological contamination or sterility failures., • Author and maintain SOPs, risk assessments, protocols, and reports related to sterility assurance., • Support training programs for aseptic technique, gowning, and microbiological control., • Collaborate with Quality, Validation, Engineering, and Manufacturing to ensure a holistic approach to sterility assurance. Required Qualifications: • Bachelor’s or Master’s degree in Microbiology, Biology, Pharmacy, Biotechnology, or related field., • 5+ years of experience in a GMP-regulated environment, preferably in aseptic processing or microbiology QA/QC., • In-depth knowledge of GMP, USP <71>, <85>, <1116>, EU Annex 1, ISO 14644, and PDA technical reports., • Experience with cleanroom operations, aseptic technique, sterilization methods, and EM programs., • Strong problem-solving, risk assessment, and technical writing skills., • Excellent communication skills and ability to work cross-functionally. Preferred Qualifications: • Experience with isolator technology or advanced aseptic processing (e.g., closed RABS, automated filling lines)., • Knowledge of terminal sterilization validation, biological indicators, and sterility test validation., • Familiarity with Lean/Six Sigma or Quality by Design (QbD) principles in sterility assurance., • Prior participation in regulatory inspections (FDA, EMA, MHRA, etc.) as SME.

Job DescriptionCompany 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 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 • Perform cell-based bioassays and surrogate bioassays such as ligand-binding ELISA assays in plate-based format in a GMP environment, • Perform qualification and transfer of analytical test methods in the GMP environment, • Document laboratory work in notebooks/enotebooks and log books, perform data integrity checks, data verification reviews, and communicate final results through electronic systems, • Coach, train, and develop others within the group with respect to their personal development and effective implementation of operational improvements, • Coordinate workflow and perform daily monitoring to meet TAT, • Prepare and review job plans, conduct semiannual performance reviews, keep training records up to date for assigned employees, perform succession planning in preparation for growth, • Collaborate closely with leaders and clients in implementing overall business directivesQualifications, • Experience with reporter-gene assay, cell biology skills such as cell culturing, cell counting, cell banking; GMP quality system and lab operations experience, • Excellent communication (oral and written) and attention to detail, • Ability to work independently and as part of a team with internal and external clients, self‑motivation, adaptability, and a positive attitude, • Ability to learn new techniques, keep accurate records, follow instructions, and comply with company policies, • Bachelor's degree in biology, chemistry, or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major), • Leadership experience, • 4+ years related lab experience, • Authorization to work in the United States indefinitely without restriction or sponsorship, • Strong computer, scientific, and organizational skills, • Excellent written and verbal communication skills and experience interacting with people from a wide range of skill levels and experience, • Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies, • Ability to work independently and as part of a team, and possess self-motivation, adaptability, and a positive attitude, • Demonstrated ability to work as an independent, self-motivated, detail-oriented, result-driven and highly flexible team-player in a fast-paced working environment, • Strong focus on quality, teamwork, and productivity, • Proactive, positive, solution-oriented leadership style with ability to prioritize and coordinate simultaneous projects with varying deadlines, • Strength in employee engagement, morale, and retention Additional Information • Position is full-time, Monday-Friday, 8:00 am - 5:00 pm., • Candidates currently living within a commutable distance of Indianapolis, IN are encouraged to apply, • 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, • #LI-EB1, • Authorization to work in the United States indefinitely without restriction or sponsorship Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Job DescriptionCompany 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 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 Responsibilities include but are not limited to: • Supervise others in performing client’s service requirements, • Coach, train, and develop others within the group with respect to their personal development and effective implementation of operational improvements, • Foster motivation and morale, • Coordinate workflow and perform daily monitoring to meet TAT, • Prepare and review job plans, conduct semiannual performance reviews, interview applicants, keep training records up to date for assigned employees, perform succession planning in preparation for growth, • Interface with the client and project resources as necessary to provide asset management functions and data management services, • Perform and document qualifications on laboratory instrumentation (i.e. HPLC, GC, KF, UV-Vis, etc.), • Perform urgent/priority repairs including user accessible consumables (i.e. lamps, pumps, seals, tubing, etc.), • Execute scheduled and post-maintenance instrument qualifications, • Participate in instrument onboarding activities, • Report on metrics and appropriate document service on instruments, • Coordinate and escort vendors on-site to perform maintenance activities on instruments on contract, • Input data into electronic asset management system (GMARS), • Assist with change controls and investigations as neededQualifications, • Bachelor’s degree in life science concentration (chemistry, biology, or related fields) and 2 or more years of directly related industry experience, • Strong computer, scientific, and organizational skills, • Excellent communication (oral and written) and attention to detail, • Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude, • Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Additional Information • Position is full-time, 8:00 am- 5:00 pm Overtime as needed., • Candidates currently living within a commutable distance of Indianapolis, IN, are encouraged to apply, • 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, • #LI-EB1, • Authorization to work in the United States indefinitely without restriction or sponsorship Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Job DescriptionCompany 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 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 • Perform cell-based bioassays and surrogate bioassays such as ligand-binding ELISA assays in plate-based format in a GMP environment, • Perform qualification and transfer of analytical test methods in the GMP environment, • Document laboratory work in notebooks/electronic notebooks and log books, perform data integrity checks, data verification reviews, and communicate final results through electronic systemsQualifications, • Bachelor’s degree in life science concentration (chemistry, biology, or related fields) and greater than 4 years of directly related industry experience or a MS degree or a PhD in a life science concentration (chemistry, biology, or related fields) with 2 years of directly related industry experience, • Strong computer, scientific, and organizational skills, • Experience with reporter-gene assay, cell biology skills such as cell culturing, cell counting, cell banking; GMP quality system and lab operations experience, • Excellent communication (oral and written) and attention to detail, • Ability to work independently and as part of a team with internal and external clients, self‑motivation, adaptability, and a positive attitude, • Ability to learn new techniques, keep accurate records, follow instructions, and comply with company policies Additional Information • Position is full-time, Monday-Friday, 8:00 am - 5:00 pm., • Candidates currently living within a commutable distance of Indianapolis, IN are encouraged to apply, • 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, • #LI-EB1, • Authorization to work in the United States indefinitely without restriction or sponsorship Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Job Description Job Duties/Responsibilities: Work environment/department will be listed in requirement. Determine the acceptability of specimens for testing according to established criteria. Perform routine and complex technical procedures and functions according to departmental Standard Operating Procedures. Monitor, operate and troubleshoot instrumentation to ensure proper functionality. Demonstrate the ability to make technical decisions regarding testing and problem solving. Prepare, test, and evaluate new reagents or controls. Report accurate and timely test results to deliver quality patient care. Perform and document preventive maintenance and quality control procedures. Identify and replenish testing bench supplies as necessary. Assist with processing of specimens when needed. Maintain a safe work environment and wear appropriate personal protective equipment Requirements: Associate degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requirements. Minimum 2-4 years of clinical laboratory testing experience is required. State Medical Technician license may be required (will be listed in requirement if its needed). ASCP or AMT certification is either preferred or required (will be listed in requirement if its required). Ability to work independently and within a team environment. Proficient with computers; Familiarity with laboratory information systems is a plus. High level of attention detail along with strong communication and organizational skills. Must be able to pass a standardized color vision screen. Flexibility to work overtime or other shifts depending on business needs

Job Description VitaCyte is a leading manufacturer of purified-defined bacterial collagenase and associated protease enzymes for enzyme-mediated cell isolation and other biotherapeutic applications. The company has established a Quality Management System (QMS) to comply with ISO-9001 and aligned with industry standards and regulations. • Job Purpose, • Maintain the QMS to ensure compliance with ISO 9001 and applicable regulatory standards in a state of inspection readiness under the direction of the Director of Quality Assurance., • Duties & Responsibilities, • Ensures VitaCyte personnel comply with an ISO 9001 certified QMS and applicable regulatory requirements., • Owns and delivers the training program for the site while ensuring compliance with the QMS and applicable regulatory requirements. Management of the training program may include facilitation of course creation & revision, course instruction & remediation, coordination of the training schedule, maintaining employee training files, and periodic metrics trending and reporting., • Owns the site inspection readiness program, which includes periodic self-assessments, customer audits, and external agency inspections. Management of the inspection readiness program includes but is not limited to the facilitation of inspection planning, executing, reporting, appropriate escalation/notification to management, closing & executive summaries, and tracking and evaluating the effectiveness of any performed remediation by the audited party., • Owns and executes the vendor management program for the site while ensuring compliance with the QMS and applicable regulatory requirements. Vendor management may include negotiating terms of Quality Assurance Agreements, creation & revision of the vendor management procedure & risk classification procedure, vendor inspections, vendor classifications, onboarding, performance monitoring, metric reporting, and termination., • Owns the non-conformance management process, which includes deviation, corrective actions, root cause investigations, and documentation management, • Support equipment and facility maintenance and calibration records, • Support change management processes and records, • Qualifications, • Education/Experience, • Bachelor’s Degree in Chemistry, Biochemistry, Biology, or Biotechnology, or related field, • Minimum 3-years experience working with a quality management system, • Knowledge of applicable standards and regulations (ex. ISO 9001, ICH Q7, 21 CFR Part 210/211), • Maintaining ISO certification is preferred., • Experience with eQMS and/or CMMS software preferred., • Auditing experience preferred., • Skills/Abilities, • Comfortable working in a laboratory environment including lab safety, general chemical knowledge, clean room attire and recording results in controlled documents, • Strong computer skills including comfort using web-based software tools, • Strong documentation, interpersonal, communication and problem-solving skills while working in a team environment, • Average physical strength and ability to stand for long periods, • Benefits, • Full time, permanent position including a comprehensive family medical benefit package and participation in an employer matched 401K plan., • Salary is commensurate with experience.

Job Description Job Duties/Responsibilities: Responsibilities are interchangeable within job titles of medical laboratory scientist (MLS), medical technologist or clinical laboratory scientist. Work environment/department will be listed in requirement. Determine the acceptability of specimens for testing according to established criteria. Perform routine and complex technical procedures and functions according to departmental Standard Operating Procedures. Monitor, operate and troubleshoot instrumentation to ensure proper functionality. Demonstrate the ability to make technical decisions regarding testing and problem solving. Prepare, test, and evaluate new reagents or controls. Report accurate and timely test results to deliver quality patient care. Perform and document preventive maintenance and quality control procedures. Identify and replenish testing bench supplies as necessary. Assist with processing of specimens when needed. Maintain a safe work environment and wear appropriate personal protective equipment Requirements: Bachelors degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requirements. Minimum 0-2 years of clinical laboratory testing experience is required. State Medical Technologist license may be required (will be listed in requirement if its needed). ASCP or AMT certification is either preferred or required (will be listed in requirement if its required). Ability to work independently and within a team environment. Proficient with computers; Familiarity with laboratory information systems is a plus. High level of attention detail along with strong communication and organizational skills. Must be able to pass a standardized color vision screen. Flexibility to work overtime or other shifts depending on business needs

Job DescriptionCompany 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 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 Job Description • Perform analytical testing of medium to high complexity on drug substance/drug product using instrumentation including, but not limited to, compendial testing (e.g. description, EP color/clarity, VOI, osmolality), pH, HIAC, MFI, HPLC, UPLC, icIEF, GC, TOC, Karl Fischer, FTIR, UV, LC/MS, and NMR., • Initiate Trackwise events and participate in conducting investigations, • Execute method qualifications, • Document test results in notebooks and reports, • Perform technique training with new analystsQualifications The ideal candidate would possess: • Strong computer, scientific, and organizational skills, • Excellent communication (oral and written) and attention to detail, • Ability to work independently and as part of a team with internal and external clients, self‑motivation, adaptability, and a positive attitude, • Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies, • Bachelor’s or M.S. degree with a science concentration (chemistry, biology, or related fields) with at least 2 years of related industry experience, • Strong computer, scientific, and organizational skills, • Excellent communication (oral and written) and attention to detail, • Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude, • Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Additional Information • Position is full-time, Monday-Friday, 8:00 am - 5:00 pm., • Candidates currently living within a commutable distance of Indianapolis, IN are encouraged to apply, • 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, • #LI-EB1, • Authorization to work in the United States indefinitely without restriction or sponsorship Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Job DescriptionDescription: Business Development Manager Northeast Region - Remote - Frequent Travel Pay: $150k + uncapped commission Candidates must reside in the Northeast region of the U.S., as the role requires frequent travel within this area. Astoriom is seeking a dynamic and results-driven Business Development Manager to join our expanding team. This remote role is focused on driving growth and strengthening relationships with new and existing clients across the Northeast United States. The ideal candidate will be a strategic thinker with strong client-facing skills, able to identify opportunities, close new business, and support the success of key accounts. Frequent travel to client sites, industry conferences, and Astoriom offices is a critical component of this role. If you are passionate about building relationships, growing revenue, and making a measurable impact, we want to hear from you. Key Responsibilities • Proactively develop and maintain strong relationships with prospective and existing clients in the Northeast U.S. region., • Identify new business opportunities through market research, networking, and lead generation activities., • Manage the full sales cycle: prospecting, presenting solutions, negotiating contracts, and closing deals., • Collaborate with internal teams (e.g., operations, marketing, finance) to ensure alignment and support in delivering value to clients., • Attend and represent Astoriom at regional and national industry conferences, trade shows, and networking events., • Visit client sites regularly to deepen relationships, support project success, and identify upselling or cross-selling opportunities., • Maintain a robust and up-to-date CRM pipeline and provide accurate sales forecasting and reporting to leadership., • Develop territory growth strategies that align with company goals and market trends., • Provide feedback and insights from the field to influence marketing, and overall service improvement., • Bachelor's degree in Biology (or related fields), • 5+ years of proven success in business development, sales, or account management, preferably within a B2B services or technology environment., • Demonstrated experience managing a regional territory and growing client accounts., • Excellent interpersonal, communication, and presentation skills., • Self-starter with strong organizational and time management abilities., • Willingness and ability to travel frequently (up to 50%) throughout the Northeast U.S. and occasionally to Astoriom sites nationally., • Proficient in CRM usage in support of delivering territory KPIs, • Ability to work independently in a remote setting while collaborating closely with cross-functional teams. Requirements:

Pride Health is hiring a Medical Laboratory Scientist to support our client’s medical facility based in Indianapolis, IN 46214. This is a Contract job with a possible extension opportunity and a great way to start working with a top-tier healthcare organization! Location: Indianapolis, IN 46214 Job Type: 12+ Months - W2 contract - with possible extension Schedule: 1st shift. Mon – Fri. 8am – 5pm. Pay Range: $30-$37/hr. (Offered pay rate will be based on education, experience, and healthcare credentials.) Responsibilities: Responsibilities are interchangeable within job titles of medical laboratory scientist (MLS), medical technologist or clinical laboratory scientist. Work environment/department will be listed in requirement. Determine the acceptability of specimens for testing according to established criteria. Perform routine and complex technical procedures and functions according to departmental Standard Operating Procedures. Monitor, operate and troubleshoot instrumentation to ensure proper functionality. Demonstrate the ability to make technical decisions regarding testing and problem solving. Prepare, test, and evaluate new reagents or controls. Report accurate and timely test results to deliver quality patient care. Perform and document preventive maintenance and quality control procedures. Identify and replenish testing bench supplies as necessary. Assist with processing of specimens when needed. Maintain a safe work environment and wear appropriate personal protective equipment Requirements: Bachelor’s degree in biology, Chemistry, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requirements. Minimum 0-2 years of clinical laboratory testing experience is required. Ability to work independently and within a team environment. Proficient with computers; Familiarity with laboratory information systems is a plus. High level of attention detail along with strong communication and organizational skills. Must be able to pass a standardized color vision screen. Flexibility to work overtime or other shifts depending on business needs Skills required: Pipetting ELISA 96 Well Plating LIS (lab information system) knowledge Education: BACHELOR’S DEGREE IN BIOLOGY OR CHEMISTRY. Pride Global offers eligible employees comprehensive healthcare coverage (medical, dental, and vision plans), supplemental coverage (accident insurance, critical illness insurance, and hospital indemnity), 401(k)-retirement savings, life & disability insurance, an employee assistance program, legal support, auto, home insurance, pet insurance, and employee discounts with preferred vendors. About Pride Health Pride Health is Pride Global's healthcare staffing branch, providing recruitment solutions for healthcare professionals and the industry at large since 2010. As a minority-owned business that delivers exceptional service to its clients and candidates by capitalizing on diverse recruiting, account management, and staffing backgrounds, Pride Health's expert team provides tailored and swift sourcing solutions to help connect healthcare talent with their dream jobs. Our personalized approach within the industry shines through as we continue cultivating honest and open relationships with our network of healthcare professionals, creating an unparalleled environment of trust and loyalty. Interested? Apply today!

Who We Are Net2Source Inc. isn’t just another staffing company, we’re a powerhouse of innovation, connecting top talent with the right opportunities. Recognized for 300% growth in the past three years, we operate in 32 countries with a global team of 5,500+. Our mission? To bridge the talent gap with precision—Right Talent. Right Time. Right Place. Right Price. Title: Laboratory Technician Location: Indianapolis IN Pay Range: $19–$20 per hour Duration: 12+ months Experience Level: 0–3 years Job Description: We are seeking a motivated Lab Technician to join our team. This position supports laboratory operations in a dynamic research environment, assisting with experiments, sample preparation, and data collection. Key Responsibilities • Prepare and process biological samples for analysis., • Assist in conducting experiments under the supervision of senior scientists., • Maintain laboratory equipment and ensure a clean, safe work environment., • Record and organize experimental data accurately., • Follow standard operating procedures (SOPs) and safety protocols. Qualifications • Associate’s or Bachelor’s degree in Biology, Chemistry, Biotechnology, or related field preferred., • 0–3 years of laboratory experience (entry-level candidates encouraged to apply)., • Basic understanding of laboratory techniques (e.g., pipetting, sample prep)., • Strong attention to detail and organizational skills., • Ability to work independently and collaboratively in a team setting. Why Work With Us? We believe in more than just jobs—we build careers. At Net2Source, we champion leadership at all levels, celebrate diverse perspectives, and empower you to make an impact. Think work-life balance, professional growth, and a collaborative culture where your ideas matter. Our Commitment to Inclusion & Equity Net2Source is an equal opportunity employer, dedicated to fostering a workplace where diverse talents and perspectives are valued. We make all employment decisions based on merit, ensuring a culture of respect, fairness, and opportunity for all, regardless of age, gender, ethnicity, disability, or other protected characteristics. Awards & Recognition • America’s Most Honored Businesses (Top 10%), • Fastest-Growing Staffing Firm by Staffing Industry Analysts, • INC 5000 List for Eight Consecutive Years, • Top 100 by Dallas Business Journal, • Spirit of Alliance Award by Agile1

Eli Lilly and Company seeks a Manufacturing Scientist (R4-R5) to provide technical support for commercialization and commercial activities within parenteral manufacturing. Drive the validation and commercialization of monoclonal antibodies, biologics, and peptide therapeutics on syringe platforms. Serve as technical expert on all manufacturing products and platforms as well as commercialization, commercial, regulatory, and parenteral control strategy. Ensure consistency in manufacturing approaches and processes. Prepare, review, and approve technical documents including change controls, regulatory submissions, technical transfer plans, strategy documents, deviations, and expert opinions. Provide technical and project management oversight to post-launch optimization teams and for technical agenda projects. #LI-DNI Position requires a Bachelor's degree in Chemistry, Biochemistry, Biology, Pharmacy, Engineering, or a related field followed by 5 years of progressively responsible experience with pharmaceutical manufacturing and control strategies. Experience must include a minimum of: 5 years of experience with technical transfer and validation of drug products; 5 years of experience with providing technical oversight for post-launch commercial operations; 5 years of experience with delivering technical agendas, including yield improvements and batch size increases; and 5 years of experience with preparing and reviewing technical documents, including change controls, regulatory submissions, and deviations. Up to 5% domestic and international travel required. #LI-DNI Job location: Indianapolis, IN. To apply, please visit and enter job requisition number R-91516 when prompted. Alternatively, please send your resume, cover letter, and a copy of the ad to: Matthew Tenaglio, Lilly Corporate Center, Indianapolis, IN 46285.

Eli Lilly and Company seeks an Associate Director – Project Management (P4-P4-2) to lead technical transfers to internal or external manufacturing facilities and laboratories. Develop, manage, and facilitate technical agendas for analytical governance teams. Manage and track laboratory governance projects. Support the analytical teams in developing strategies and implementing operational plans. Resolve issues with cross-functional project teams and appropriately manage through analytical governance. Ensure strategic alignment with Business Unit and Manufacturing partners. #LI-DNI Position requires a Bachelor’s degree in Chemistry, Biology, Physiology, or a related scientific field followed by 6 years of progressively responsible experience with analytical method development and QC within pharmaceutical manufacturing. Experience must include a minimum of: 3 years of experience performing product release and stability testing; 2 years of experience managing the analytical transfer with manufacturing sites and performing risk assessment of the projects; 2 years of experience with method validations per ICH; 2 years of experience working with core analytical equipment such as HPLC, GC, dissolution, and wet chemistry; and 1 year of experience with project management in analytical chemistry projects. 10% domestic and international travel required. #LI-DNI Job location: Indianapolis, IN. To apply, please visit and enter job requisition number R-92266 when prompted. Alternatively, please send your resume, cover letter, and a copy of the ad to: Matthew Tenaglio, Lilly Corporate Center, Indianapolis, IN 46285.

Job Description Heartland Food Products Group is a global leader in the consumer packaged goods (CPG) industry, producing low-calorie sweeteners, coffee, coffee creamers and liquid water enhancers. We manufacture and market Splenda, the #1 brand in the low calorie sweetener category and the most recognized in the world. We make coffee, tea and water taste better and help people live happier, healthier and longer lives by making it easy to reduce sugar. We offer an excellent compensation and benefits package. Come grow with us! This role is not a remote opportunity, it is on-site at our Manufacturing Plant in Indianapolis, Indiana. Scope: The Sanitation & Validation Manager is responsible for managing several key prerequisite programs including – calibration of equipment, validations of preventive controls, and performance metrics measuring effectiveness of sanitation activities. These sanitation activities encompass – master sanitation, environmental monitoring and operator CILs. This individual works in conjunction with the Food Safety & Quality Assurance Manager developing policies and standards to ensure the plant is prepared for any inspection. They work across the organization to educate and drive adherence to policies and standards. Essential Duties and Key Responsibilities: • Develop and implement prerequisite programs to drive food safety around plant hygiene., • Enhance and maintain a Master Sanitation Schedule and operator Clean, Inspect, Lubricate (CILs) activities., • Work with the sanitation team and plant managers to ensure adherence to the MSS., • Lead CIP validation studies and evaluate results., • Partner with engineering to drive hygienic design., • Review, update, and develop SSOPs., • Manages the execution of the Environmental Monitoring Program and results., • Conduct investigations and perform RCA/CAPAs when out of Specification results occur., • Establish strong relationships throughout the organization. Ability to work in a collaborative environment., • Reviews calibrations of equipment and ensures appropriate actions are taken to address nonconformances., • Participates in development and execution of validation protocols for preventive controls which are scientific and thorough., • Maintains a work environment committed to sustainable safety by enforcing safety rules, setting a safe example, and coaching and communicating to associates the reasons for safe operations., • Participate in internal audits and external audits, including annual SQF recertification audit., • Communicate clearly and effectively, both orally and in writing, at all levels of the organization., • Differentiate among competing demands and establish or shift priorities as needed., • Organize and coordinate multiple tasks and to work under time pressure to meet deadlines., • Ability to multi-task and work within aggressive timeframes with minimal supervision., • Experience with HACCP Plans and an understanding of dairy / food microbiological principles., • Familiarity with microbial flora and fauna found in food (dairy) plants and monitoring and control programs associated with these., • Experience with regulatory and third party audits (e.g. SQF, BRC, FSSC 22000), • Bachelor's degree in Biology, Microbiology, and / or Food Science a minimum. Demonstrated experience with food or nutritional products manufacturing and / or quality programs required. Familiarity with food / nutritional product legislation (FDA & USDA 21CFR & 9 CFR) a plus., • HACCP, PCQI Certification, • Familiar with current good manufacturing requirements, • Good analytical and problem-solving skills; good attention to detail and ability to follow written and oral instructions., • Must work well in a team environment and have strong communication skills, • Must have the ability to perform under pressure and communicate well with all departments, • Must have good computer skills, including proficiency with MS Office, MS Project, MS Excel, Basic, • Must be able to physically perform the functions of climbing, balancing, stooping, kneeling, crouching, reaching, standing, walking, pushing, pulling, lifting, grasping, feeling, talking, hearing, and repetitive motions., • Must be available to work during extended or off-hours, • Must be able to work seated using a computer and phone for long periods of time., • Must possess visual acuity to document company records., • Continuous walking throughout plant and distribution center., • Lifting up to 40 pounds #IND2

Bachelors degree in chemistry, biology, biomedical engineering, neuroscience, pharmacy, or other medical-related discipline. Medical Science Liaison - Central Eastern US/Mid-Atlantic.