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Job Title: Clinical Research Specialist (EMT or Paramedic). Current certification as a Paramedic in Wisconsin or EMT.

Job Description Manufacturing Technician - 3rd Shift M-F 11pm-7:30am Job Description The Manufacturing Technician is responsible for preparing small batches of material for commercialization. Each day begins with a team meeting to establish priorities, and the role involves assisting with two primary processes: extracting enzymes from pig glands and using laboratory equipment such as column chromatography and UV spectrophotometry to scale small-batch products for commercial readiness. Responsibilities • Handle raw materials, including pituitary glands and pig hearts, ensuring quality assurance release and proper storage., • Assist with production scheduling and verify material availability., • Prepare and maintain the manufacturing area, including cleaning and changeovers., • Execute pilot-scale and commercial processes such as extractions, mixing, and powder finishing., • Operate equipment, including processing tanks, temperature-controlled vessels, vacuum/pressurized systems, and HMIs (touchscreen control systems)., • High School Diploma or GED, • Associate degree or above in Biotechnology field preferred, • 2+ years of experience preferred within GMP or pharmaceutical settings This role operates within a laboratory and pharmaceutical manufacturing environment consisting of one large suite and 3-4 smaller suites with benchtops. The facility is spread across one floor with areas throughout, including one area with 3 flights of stairs. The schedule involves working weekdays from 11 pm to 7:30 am (Sunday night to Friday), with an initial shift on 2nd shift (3 pm to 11:30 pm) for at least the first 3 months. Employees receive a $2.00/hour schedule incentive and a $1.50/hour 3rd shift differential. The company offers medical, dental, and vision benefits starting on the first day of employment, along with basic life insurance, short-term disability, and options for voluntary life insurance and long-term disability coverage. A 401k plan is available upon hire with company contributions, alongside 160 hours of vacation, 40 hours of sick time (pro-rated based on hire date), and 9 paid holidays. Job Type & Location This is a Permanent position based out of Waunakee, WI. Pay and Benefits The pay range for this position is $43680.00 - $51160.00/yr. Employees are eligible for Medical, Dental and Vision on day 1 of employment. The company provides Basic Life insurance, Basic AD&D insurance along with Short-term disability on all full-time employees. Employees have the option to elect Voluntary Life, Voluntary AD&D along with Long-term disability coverage. Health and Flexible spending account options. Full-time employees can contribute to their 401k upon hire and are eligible for a company contribution. 160 hours of vacation & 40 hours of sick time (both pro-rated base on hire date) and 9 paid holidays. Workplace Type This is a fully onsite position in Waunakee,WI. Application Deadline This position is anticipated to close on Apr 24, 2026. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is embedded into our culture through: • Hiring diverse talent, • Maintaining an inclusive environment through persistent self-reflection, • Building a culture of care, engagement, and recognition with clear outcomes Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. Actalent is an equal opportunity employer. Actalent is a global leader in engineering and sciences services.

Job Description Job Title: Quality Systems Specialist – Auditing and Vendor Management Job Description The Quality Systems Specialist plays a key role in supporting cGMP quality system activities within a biopharmaceutical manufacturing environment. This position focuses on executing and maintaining processes within the MasterControl electronic Quality Management System (eQMS), building and managing a robust supplier and vendor quality program, and ensuring compliance with internal procedures and global regulatory requirements. The specialist reviews validation and qualification documentation, oversees GMP training programs, and supports deviations, investigations, CAPAs, change controls, and Annual Product Review (APR) preparation. This role requires up to 50% domestic and international travel to qualify and audit suppliers and partners. Responsibilities • Execute and maintain cGMP quality system activities using the MasterControl electronic Quality Management System (eQMS)., • Build, implement, and manage a comprehensive supplier and vendor quality program., • Plan, conduct, and document qualification and auditing of suppliers, including up to 50% domestic and international travel., • Support and administer GMP training programs, ensuring accurate and current training records., • Review and approve validation and qualification documentation to ensure compliance with cGMP and internal procedures., • Participate in and support the management of deviations, investigations, and CAPAs, ensuring timely closure and effective corrective and preventive actions., • Manage and oversee change controls, including coordination of change control governance and documentation., • Support and coordinate internal and external audits, including preparation, facilitation, and follow-up activities., • Maintain and oversee document control and batch record review activities within the quality management system., • Ensure compliance with FDA and other global regulatory requirements, as well as internal quality policies and procedures., • Support the preparation and execution of Annual Product Reviews (APRs)., • Collaborate cross-functionally with manufacturing, quality control, supply chain, and other departments to support continuous improvement of quality systems., • Contribute to the development, implementation, and improvement of quality assurance processes, procedures, and work instructions., • Bachelor’s degree or higher in a scientific discipline., • 5+ years of quality experience in the biopharmaceutical or pharmaceutical industry, preferably with a focus on vendor management and auditing., • Strong hands-on experience with quality assurance in a cGMP-regulated environment., • Proficiency in quality auditing and internal audit processes., • Experience managing vendor and supplier qualification and oversight programs., • Demonstrated knowledge of CAPA processes, including investigation, root cause analysis, and implementation of corrective and preventive actions., • Solid understanding of FDA regulations and global regulatory expectations for biopharmaceutical manufacturing., • Experience with quality management systems and document control, including batch record review., • Experience working with MasterControl or similar electronic Quality Management Systems (eQMS)., • Experience in managing and improving quality systems in a biopharmaceutical manufacturing environment., • Familiarity with change control governance and oversight., • Experience supporting Annual Product Review (APR) activities., • Demonstrated ability to support and deliver GMP training programs., • Proven ability to support continuous improvement initiatives within quality systems. This is a first-shift, full-time role, working Monday through Friday with a flexible start time between 7:00 a.m. and 9:00 a.m., for an eight-hour workday. The position is based in a biopharmaceutical manufacturing environment and operates within a collaborative quality organization that includes Quality Management System Specialists and Document Control Technicians. The team works closely together on-site to support production and quality activities. The role involves significant domestic and international travel, up to 50% of the time, to conduct supplier and vendor audits and qualifications. Work is primarily office-based within a GMP manufacturing campus, using electronic quality systems and standard office and laboratory documentation tools Job Type & Location This is a Permanent position based out of Madison, WI. Pay and Benefits The pay range for this position is $62000.00 - $90000.00/yr. Competitive compensation; excellent benefits package - including Medical, Dental and Vision on Day 1; Life and AD&D Insurance, and Short and Long-term Disability; Health and Flexible Saving Account options; Employee Assistance Program, generous vacation; paid Holidays; 401k Workplace Type This is a fully onsite position in Madison,WI. Application Deadline This position is anticipated to close on Apr 27, 2026. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is embedded into our culture through: • Hiring diverse talent, • Maintaining an inclusive environment through persistent self-reflection, • Building a culture of care, engagement, and recognition with clear outcomes Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Job Description Job Title: Quality Control Scientist Job Description The Quality Control Scientist will support an in-house Quality Control team responsible for release, characterization, and stability testing of internally manufactured materials. This role involves performing molecular biology and biochemical assays, including DNA and RNA pipetting, PCR, qPCR, gel electrophoresis, sequencing, and related sample preparation. The position also requires conducting high-running assays such as endo- and exonuclease testing and gDNA contamination analysis. Additional responsibilities include solution and buffer preparation, fragment analyzer and HPLC testing using Chromeleon software, and maintaining reagent, consumables, and method-specific inventory to support subject matter experts and QC scientists. The individual will assist with daily laboratory setup, follow established SOPs and written procedures, maintain accurate documentation, and complete all required GMP documentation in compliance with regulatory standards. Responsibilities • Perform molecular biology and biochemical assays involving DNA and RNA., • Conduct pipetting, PCR, qPCR, gel electrophoresis, sequencing, and related sample preparation., • Execute endo- and exonuclease testing and gDNA contamination analysis., • Prepare solutions and buffers, and conduct fragment analyzer and HPLC testing using Chromeleon software., • Maintain reagent, consumables, and method-specific inventory., • Assist with daily laboratory setup and follow established SOPs and written procedures., • Basic molecular biology laboratory skills such as pipetting, PCR, and gel electrophoresis., • Experience with DNA or RNA sample preparation, sequencing, and qPCR., • Ability to perform biochemical and molecular biology assays to support release, characterization, and stability testing., • Bachelor’s degree in Molecular Biology, Biochemistry, Biology, or a related scientific discipline., • 1-4 years of hands-on laboratory experience in a QC, analytical, or regulated laboratory environment working with DNA and RNA sequencing and sample preparation, as well as pipetting, PCR, and gel electrophoresis. The work schedule is Monday to Friday from 8 am to 4:30 pm. The role operates within a laboratory and office environment, alongside small team of biochemists. Job Type & Location This is a Contract position based out of Madison, WI. Pay and Benefits The pay range for this position is $26.00 - $32.00/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 • Hiring diverse talent, • Maintaining an inclusive environment through persistent self-reflection, • Building a culture of care, engagement, and recognition with clear outcomes Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Job Description ENTRY LEVEL-Seeking B.S. in Chemistry, Biochemistry, Biology, Microbiology graduates Job Title: Chemist Job Description We are seeking a dedicated Chemist to join our dynamic team. This role involves testing raw materials before they are used in manufacturing processes, ensuring compliance with USP and EP standards. You will conduct wet chemistry tests such as pH, IR, moisture, and identification tests, while also working on documentation. As you grow in this position, you will gain experience with HPLC and GC methodologies. Responsibilities • Perform quality control testing on incoming raw materials in compliance with USP and EP standards., • Conduct wet chemistry tests including pH, IR, moisture, and identification tests., • Prepare and maintain accurate documentation of all testing procedures and results., • Collaborate with the team to develop and refine testing protocols., • Cross-train with the Finished Product team to perform particle size testing and dissolution studies., • Bachelor's degree in Chemistry, Biochemistry, Biology, or a related life science field., • Experience in a GMP environment, with 0-3 years preferred., • Competency in HPLC and GC techniques is advantageous., • Undergraduate research experience or summer internship experience is highly valued., • Self-driven with the ability to take initiative and find work independently. You will work primarily in a quality control laboratory setting as part of the Raw Material team, consisting of four chemists. The lab environment is modern, with shared workspaces and laptops provided for each chemist. The team collaborates closely with the Finished Product and Analytical Development teams, which consist of approximately five chemists each. This role will initially involve 90% lab work, with potential to transition to 70% lab work after 2-3 years. The company promotes from within, offering opportunities for advancement into lead or supervisory roles Job Type & Location This is a Contract to Hire position based out of Verona, WI. Pay and Benefits The pay range for this position is $22.00 - $25.00/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 • Hiring diverse talent, • Maintaining an inclusive environment through persistent self-reflection, • Building a culture of care, engagement, and recognition with clear outcomes Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Job Description Description The Cleaning Validation Specialist is responsible for the execution and documentation of cleaning validation activities for laboratory equipment within a GMP-regulated contract development and manufacturing organization (CDMO). This role supports established cleaning validation programs by performing sampling, data collection, and protocol adherence to ensure equipment cleanliness and regulatory compliance. Key Responsibilities: Execute approved cleaning validation protocols, including swab and rinse sampling activities Collect, review, and accurately document validation data in compliance with GMP and data integrity requirements Perform visual inspections and verify equipment readiness following cleaning activities Support equipment changeovers, routine revalidation, and continued process verification activities Assist with deviation investigations related to cleaning execution and support CAPA implementation Maintain validation records and support document updates as needed Additional Skills & Qualifications Bachelor’s degree in a scientific or technical discipline 3+ years experience performing HPLC cleaning validation activities in a GMP manufacturing environment Familiarity with swab/rinse sampling techniques and GMP documentation practices Job Type & Location This is a Contract position based out of Verona, WI. Pay and Benefits The pay range for this position is $30.00 - $32.00/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 • Hiring diverse talent, • Maintaining an inclusive environment through persistent self-reflection, • Building a culture of care, engagement, and recognition with clear outcomes Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Job Description Description The Cleaning Validation Specialist is responsible for the execution and documentation of cleaning validation activities for laboratory equipment within a GMP-regulated contract development and manufacturing organization (CDMO). This role supports established cleaning validation programs by performing sampling, data collection, and protocol adherence to ensure equipment cleanliness and regulatory compliance. Key Responsibilities: Execute approved cleaning validation protocols, including swab and rinse sampling activities Collect, review, and accurately document validation data in compliance with GMP and data integrity requirements Perform visual inspections and verify equipment readiness following cleaning activities Support equipment changeovers, routine revalidation, and continued process verification activities Assist with deviation investigations related to cleaning execution and support CAPA implementation Maintain validation records and support document updates as needed Skills hplc instrumentation Top Skills Details hplc instrumentation Additional Skills & Qualifications Bachelor’s degree in a scientific or technical discipline 3+ years experience performing cleaning validation activities in a GMP manufacturing environment Familiarity with swab/rinse sampling techniques and GMP documentation practices Strong attention to detail and ability to follow approved procedures and protocols Experience Level Intermediate Level Job Type & Location This is a Contract position based out of Verona, WI. Pay and Benefits The pay range for this position is $30.00 - $32.00/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 • Hiring diverse talent, • Maintaining an inclusive environment through persistent self-reflection, • Building a culture of care, engagement, and recognition with clear outcomes Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Job Description ENTRY LEVEL-Seeking new B.S. in Chemistry, Biology graduates Job Title: QC Analytical Chemist Job Description We are seeking a dedicated QC Analytical Chemist to join our dynamic team. This role involves testing raw materials before they are used in manufacturing processes, ensuring compliance with USP and EP standards. You will conduct wet chemistry tests such as pH, IR, moisture, and identification tests, while also working on documentation. As you grow in this position, you will gain experience with HPLC and GC methodologies. Responsibilities • Perform quality control testing on incoming raw materials in compliance with USP and EP standards., • Conduct wet chemistry tests including pH, IR, moisture, and identification tests., • Prepare and maintain accurate documentation of all testing procedures and results., • Collaborate with the team to develop and refine testing protocols., • Cross-train with the Finished Product team to perform particle size testing and dissolution studies., • Bachelor's degree in Chemistry, Biochemistry, Biology, or a related life science field., • Experience in a GMP environment, with 0-3 years preferred., • Competency in HPLC and GC techniques is advantageous., • Undergraduate research experience or summer internship experience is highly valued., • Self-driven with the ability to take initiative and find work independently. You will work primarily in a quality control laboratory setting as part of the Raw Material team, consisting of four chemists. The lab environment is modern, with shared workspaces and laptops provided for each chemist. The team collaborates closely with the Finished Product and Analytical Development teams, which consist of approximately five chemists each. This role will initially involve 90% lab work, with potential to transition to 70% lab work after 2-3 years. The company promotes from within, offering opportunities for advancement into lead or supervisory roles. Job Type & Location This is a Contract to Hire position based out of Verona, WI. Pay and Benefits The pay range for this position is $22.00 - $25.00/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 • Hiring diverse talent, • Maintaining an inclusive environment through persistent self-reflection, • Building a culture of care, engagement, and recognition with clear outcomes Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Job Description Job Description: Mechanical Designer Join a dynamic team of three individuals as a Mechanical Designer, where you will have the opportunity to design components such as strainers, spray balls, and baskets. You may also assist with designing components of the full cleaning system. Utilize your expertise in 2D and 3D design using SolidWorks and AutoCAD. Responsibilities • Design various mechanical components including strainers, spray balls, and baskets., • Assist in designing components of the full cleaning system., • Utilize SolidWorks and AutoCAD for 2D and 3D design work., • Proficiency in SolidWorks and AutoCAD for mechanical design., • Experience in mechanical drafting and machine design., • Strong understanding of material properties and sheet metal design., • Associate's degree in Engineering or Mechanical Engineering., • Minimum of 2 years of experience working with SolidWorks and/or AutoCAD., • At least 2 years of experience as a mechanical designer. 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 • Hiring diverse talent, • Maintaining an inclusive environment through persistent self-reflection, • Building a culture of care, engagement, and recognition with clear outcomes Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Job Description Job Description: Mechanical Design Engineer Join a dynamic team as a Mechanical Design Engineer, where you will have the opportunity to design components such as strainers, spray balls, and baskets. You may also assist with designing components of the full cleaning system. Utilize your expertise in 2D and 3D design using SolidWorks and AutoCAD. Responsibilities • Design various mechanical components including strainers, spray balls, and baskets., • Assist in designing components of the full cleaning system., • Utilize SolidWorks and AutoCAD for 2D and 3D design work., • Proficiency in SolidWorks and AutoCAD for mechanical design., • Experience in mechanical drafting and machine design., • Strong understanding of material properties and sheet metal design., • Associate's degree in Engineering or Mechanical Engineering., • Minimum of 2 years of experience working with SolidWorks and/or AutoCAD., • At least 2 years of experience as a mechanical designer. 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 • Hiring diverse talent, • Maintaining an inclusive environment through persistent self-reflection, • Building a culture of care, engagement, and recognition with clear outcomes Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Job Description Job Description: Mechanical Design Engineer Join a dynamic team as a Mechanical Design Engineer, where you will have the opportunity to design components such as strainers, spray balls, and baskets. You may also assist with designing components of the full cleaning system. Utilize your expertise in 2D and 3D design using SolidWorks and AutoCAD. Responsibilities • Design various mechanical components including strainers, spray balls, and baskets., • Assist in designing components of the full cleaning system., • Utilize SolidWorks and AutoCAD for 2D and 3D design work., • Proficiency in SolidWorks and AutoCAD for mechanical design., • Experience in mechanical drafting and machine design., • Strong understanding of material properties and sheet metal design., • Associate's degree in Engineering or Mechanical Engineering., • Minimum of 2 years of experience working with SolidWorks and/or AutoCAD., • At least 2 years of experience as a mechanical designer. 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 • Hiring diverse talent, • Maintaining an inclusive environment through persistent self-reflection, • Building a culture of care, engagement, and recognition with clear outcomes Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Job Description Description Regulatory Strategy & Leadership Develop and execute global regulatory strategies that support product development, commercialization, and business objectives. Lead the planning, preparation, and submission of regulatory filings across multiple markets, including the United States, European Union, and other international regions. Oversee regulatory submissions such as FDA 510(k), PMA, and IND/IDE applications, as well as EU MDR Technical Documentation and CE Mark activities. Act as the primary regulatory interface with health authorities, notified bodies, and international regulatory agencies. Provide regulatory guidance throughout the product lifecycle, supporting R&D, clinical activities, labeling strategy, manufacturing, and post-market activities. Monitor changes in global regulatory requirements and standards, assess regulatory risk, and proactively communicate potential impacts to stakeholders. Quality System Leadership Design, implement, and maintain a robust Quality Management System. Ensure compliance with applicable regulations and standards, including: FDA 21 CFR Part 820 (including transition to QMSR) ISO 13485 EU MDR quality system requirements MDSAP, as applicable Maintain continuous inspection readiness and lead preparation for FDA inspections and notified body audits. Oversee and improve core quality processes, including: Corrective and Preventive Actions (CAPA) Complaint handling and post-market surveillance, including vigilance reporting Nonconformance and deviation management Document control and training systems Lead risk management activities in accordance with ISO 14971. Establish and manage supplier qualification and supplier quality oversight programs. Develop and deliver quality and regulatory training programs to promote organizational understanding and compliance. EU MDR / CE Mark Oversight Own the strategy and execution for EU MDR compliance, including notified body engagement and audit readiness. Ensure continued CE Mark compliance as products evolve and regulations change. Skills Regulatory affairs, Regulatory, Medical device, Regulatory submission, Fda, Quality assurance, Iso 13485, Supplier quality, Regulatory compliance, Regulatory documents, Gmp Top Skills Details Regulatory affairs,Regulatory,Medical device,Regulatory submission,Fda,Quality assurance,Iso 13485,Supplier quality,Regulatory compliance,Regulatory documents,Gmp Additional Skills & Qualifications Bachelor’s degree in Life Sciences, Engineering, or related technical field 7+ years of progressive Regulatory Affairs and/or Quality Assurance experience in medical devices, biotech, wound care, or combination products 3+ years in a formal leadership role Demonstrated success leading multiple U.S. and EU regulatory submissions, including FDA (510(k), De Novo, PMA, and/or combination products) and CE Marking under EU MDR (2017/745) Experience supporting products from development through commercialization Expertise in FDA regulations (21 CFR Parts 210, 211, 820), EU MDR, ISO 13485, ISO 14971, design controls, risk management, and clinical and post‑market regulatory requirements, including hands-on interaction with FDA and Notified Bodies Preferred Advanced degree: Masters or PhD RAC and/or ASQ certifications (CQA, CQE). Prior experience with biomaterials, wound care, antimicrobial technologies, or combination products. Experience Level Expert Level Job Type & Location This is a Permanent position based out of Middleton, WI. Pay and Benefits The pay range for this position is $100000.00 - $150000.00/yr. Medical, Dental, Vision 401K Match Competitive benefits and PTO Workplace Type This is a fully onsite position in Middleton,WI. Application Deadline This position is anticipated to close on Apr 22, 2026. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is embedded into our culture through: • Hiring diverse talent, • Maintaining an inclusive environment through persistent self-reflection, • Building a culture of care, engagement, and recognition with clear outcomes Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Job Description Job Title: Quality Systems Specialist - CAPAs and Deviations Job Description The Quality Systems Specialist plays a crucial role in supporting cGMP quality system activities within a biopharmaceutical manufacturing environment. The position involves executing and maintaining quality processes such as GMP training programs, validation and qualification document review, investigations, deviations, change controls, and CAPAs. A significant portion of the role focuses on overseeing the CAPA system, tracking progress, ensuring timely closure of CAPAs, managing extensions, and assisting with deviations. The specialist collaborates cross-functionally to ensure adherence to quality system procedures, supports continuous improvement initiatives, coordinates internal and external audits, manages training documentation, and oversees activities like APR preparation and change control governance to ensure regulatory compliance and product quality. Responsibilities • Oversee the CAPA system, ensuring CAPAs are tracked and closed out timely., • Assist with managing deviations and implementing necessary changes., • Execute and maintain GMP training programs and quality processes., • Review validation and qualification documents., • Collaborate cross-functionally to ensure compliance with quality system procedures., • Support continuous improvement initiatives., • Coordinate internal and external audits., • Manage training documentation., • Quality assurance expertise., • Experience in quality auditing and document control., • Familiarity with compliance and FDA regulations., • Proficiency in managing quality management systems and internal audits., • Bachelor’s degree or above in a scientific discipline., • Minimum 2 years of Quality Assurance or Quality Systems experience in the biopharma/pharmaceutical industry. The role is based in a dynamic team environment with QMS Specialists and Document Control Technicians. The team is expanding with plans to add 2 more members. The work schedule is the first shift, Monday to Friday, with start times between 7-9 am for an 8-hour workday. The team works closely together, although space is currently limited. The office is located in building 1. Job Type & Location This is a Permanent position based out of Madison, WI. Pay and Benefits The pay range for this position is $52000.00 - $80000.00/yr. Competitive compensation; excellent benefits package - including Medical, Dental and Vision on Day 1; Life and AD&D Insurance, and Short and Long-term Disability; Health and Flexible Saving Account options; Employee Assistance Program, generous vacation; paid Holidays; 401k Workplace Type This is a fully onsite position in Madison,WI. Application Deadline This position is anticipated to close on Apr 27, 2026. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is embedded into our culture through: • Hiring diverse talent, • Maintaining an inclusive environment through persistent self-reflection, • Building a culture of care, engagement, and recognition with clear outcomes Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Job Description Description The Quality Specialist supports Quality Control testing activities through routine and non-routine biochemical and molecular biology assays. This person will perform analytical testing to support release, characterization, and stability testing of raw materials, production intermediates, and final products in a GMP-regulated environment. Perform routine and non-routine analytical biochemical and molecular biology assays in support of raw material, in-process, and final product testing. Execute testing in accordance with approved protocols, SOPs, and GMP requirements. Conduct daily laboratory activities following written procedures with accuracy and attention to detail. Test raw materials and components to determine QC acceptability. Perform visual and measurement inspections; identify, reject, and return nonconforming materials. Support incoming inspection activities, including sample analysis, batch record review, historical trend review, and documentation of findings. Approve in-process production by confirming specifications and communicating required adjustments to the supervisor. Generate and support Nonconformance Reports (NCRs) and Change Orders as required. Maintain testing reagent inventory and assist with routine laboratory and instrument upkeep. Manage retention samples, including filing, inventory accuracy, and general organization. Troubleshoot assay or instrument issues as needed and escalate appropriately. Ensure complete, accurate, and compliant documentation of all laboratory activities in accordance with GMP standards. Demonstrate flexibility to support shifting priorities and variable schedules as needed. Additional Skills & Qualifications Bachelor’s degree in Molecular Biology, Biochemistry, Biology, or a related scientific discipline. 1–3 years of hands-on laboratory experience in a QC, analytical, or regulated laboratory environment (entry-level candidates with strong academic lab experience may be considered). 1-3 years of GMP Experience Level Intermediate Level Job Type & Location This is a Contract position based out of Madison, WI. Pay and Benefits The pay range for this position is $26.00 - $32.00/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 • Hiring diverse talent, • Maintaining an inclusive environment through persistent self-reflection, • Building a culture of care, engagement, and recognition with clear outcomes Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Job Description Clinical Research Nurse ALL SHIFTS AVAILABLE (day time, overnight, weekends) Job Description The Clinical Research Nurse is responsible for overseeing study unit activities in Phase 1 clinical trials, with a focus on ensuring the safety and welfare of study participants. Responsibilities • Enroll patients into clinical trials and conduct the Informed Consent (ICF) process by educating, explaining, and informing participants of study procedures., • Utilize skills, knowledge, nursing diagnosis, and clinical judgment to provide high-standard care for participants in clinical trials., • Observe participant general well-being and potential adverse events using nursing assessment skills., • Document adverse events and take appropriate action as needed., • Perform study-related activities such as cannulation, telemetry, holters, vital signs, ECGs, and venipuncture., • Collect and process biological samples according to protocol and Standard Operating Procedures., • Record data obtained in a timely, error-free manner according to protocol and Standard Operating Procedures., • Active Registered Nurse (RN) or Licensed Practical Nurse (LPN) license in good standing in Wisconsin., • Associates Degree or Bachelors Degree in Nursing (ASN or BSN)., • Previous experience with clinical research is preferred. The candidate will work in the Phase I Clinical Research Unit in Madison, WI. This is an excellent opportunity for an RN or LPN to gain experience and training in the clinical research space, with room for advancement in clinical and regulatory areas. The organization provides extensive training in clinical research, as well as study-specific training Job Type & Location This is a Contract to Hire position based out of MADISON, WI. Pay and Benefits The pay range for this position is $30.00 - $39.00/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 • Hiring diverse talent, • Maintaining an inclusive environment through persistent self-reflection, • Building a culture of care, engagement, and recognition with clear outcomes Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Job DescriptionJob Title: Greenhouse Technician Job Description The role involves setting up, maintaining, and cleaning greenhouse areas while caring for plants used in research and development activities. You will use a spray chamber to test products on various plants and weeds, mix chemical formulas for laboratory activities, and prepare media and reagents for microbiological studies. Additionally, you will assist with R&D projects, lab work, and perform necessary administrative tasks. Responsibilities • Set up, maintain, and clean greenhouse areas., • Care for plants used in R&D activities., • Use a spray chamber for product testing on plants and weeds., • Mix chemical formulas for lab activities and testing., • Prepare media and reagents for microbiological studies., • Assist with R&D projects and laboratory work., • Collect and catalog greenhouse and laboratory data.Essential Skills, • Background in plant care, chemistry, or environmental science., • Interest in aligning career goals with the company's work.Additional Skills & Qualifications, • Degree in Biology, Chemistry, or Environmental Science., • Interest in obtaining a pesticide license., • Knowledge in plant science, weed science, soil science, entomology, and microbial science.Work Environment The candidate will work in greenhouse, laboratory, and office areas. This is a 1st shift role, Monday through Friday, from 8 am to 4:30 pm. The role involves collaboration with a team of three, a project manager, and a director. The candidate must be comfortable working with plants, handling chemical products, and conducting microbiological and entomology studies. Job Type & Location This is a Contract to Hire position based out of Madison, WI. Pay and Benefits The pay range for this position is $20.00 - $24.00/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 • Hiring diverse talent, • Maintaining an inclusive environment through persistent self-reflection, • Building a culture of care, engagement, and recognition with clear outcomes Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

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