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Our Business
Adare Pharma Solutions is a global Contract Development and Manufacturing Organization (CDMO) with locations across North America and Italy.
We offer a wide range of manufacturing, packaging, and research and development services.
Our clients range from growing biotech firms advancing groundbreaking clinical trials to established pharmaceutical companies producing high volumes of approved, widely used medicines.
By combining top talent from the life sciences industry with modern research and manufacturing technologies, Adare enables clients to deliver potentially lifesaving medicines in more easily consumable formats - particularly for patients such as infants or the elderly.
This is the meaning behind “Transforming Drug Delivery – Transforming Lives.”
Our Culture
When it comes to being an employee of Adare, although we are located across multiple countries and come from diverse backgrounds, we work together toward a common purpose.
Supported by leadership that is experienced and highly regarded in the industry, we are paving the way for a brighter and better future by attracting top talent from both within and beyond the CDMO space.
In addition to delivering high-quality results for our external clients, we foster a collaborative, client-centric culture internally - one where employees support one another, share knowledge, and encourage each other to bring their best selves to work each day.
Why Come to Adare?
Adare is Private Equity owned and poised for growth.
Employees are provided with internal development opportunities to progress within the organization, enhancing their professional skills and industry knowledge through Adare’s investment in their growth.
We offer a variety of fields to embark in, including manufacturing, engineering, quality, chemistry, formulations, analytical research and development, finance, supply chain, sales, marketing, project management, human resources, and environmental health and safety.
Our benefits package is highly competitive, offering medical, dental, and vision coverage; a retirement plan with company match, paid time off and company holidays, tuition reimbursement with no waiting period, life insurance, pet insurance, Flexible Spending Accounts (medical and dependent care), and disability coverage.
Position
Formulations Technical Specialist
Location
Vandalia, OH
Summary
The Formulations Technical Specialist is responsible for supporting projects by developing and maintaining the necessary documentation and tasks required to fulfil project needs.
This person will work alongside project teams to drive activities, accelerate timelines, offer ideas to implement future enhancements/work efficiencies, and provide adequate quality oversight and expertise for the creation and review of internal quality documents.
Responsibilities
* Managing Clinical and Registration Batch Preparation and execution. Responsibilities include:
* Initiate and retain stability samp...
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Type: Permanent Location: Vandalia, US-OH
Salary / Rate: Not Specified
Posted: 2026-07-21 08:50:47
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Global Director, Digital Enablement
Baltimore Aircoil Company (BAC) is the global leader in sustainable solutions for evaporative cooling, thermal storage, and heat transfer equipment, headquartered in Jessup, Maryland.
We are seeking a strategic, results-driven Global Director, Digital Enablement to own and evolve our enterprise-wide SAP landscape, drive digital transformation, and ensure global process excellence across all business functions.
POSITION PURPOSE
The Global Director, Digital Enablement is a senior leader responsible for defining and executing the SAP strategy, optimizing business processes, and ensuring operational excellence across BAC’s global footprint.
This role balances leadership, technical depth, and business partnership, driving successful SAP transformation programs, modernizing enterprise applications, and enabling world-class customer experiences.
PRINCIPAL ACCOUNTABILITIES
* Define and execute the global SAP roadmap aligned with business strategy and digital transformation goals, including leading S/4HANA transformation programs and evaluating emerging SAP capabilities (AI, automation, cloud ERP).
* Drive standardization, simplification, and modernization of business processes across regions, ensuring seamless integration of SAP with non-SAP systems and enterprise architecture.
* Establish application governance, architecture standards, and data integrity practices for SAP platforms including ERP, S/4HANA, analytics, and integrated enterprise applications.
* Lead global SAP programs, managing budgets, resources, and risk to ensure on-time, on-budget delivery and continuous improvement initiatives, utilizing Agile/DevOps methodologies as appropriate.
* Act as a trusted advisor to senior leaders and stakeholders, translating business needs into scalable SAP-enabled solutions and driving cross-functional alignment -.
* Lead, mentor, and develop a global team, including SAP functional leads, technical architects, program managers, and contractors, fostering a collaborative, high-performance culture.
* Partner with the global infrastructure lead to manage system integrators and strategic vendors, negotiate and oversee SAP and partner contracts, and optimize total cost of ownership while improving service quality.
* Ensure SAP systems comply with global regulatory and audit requirements, maintaining strong controls (SOX, GDPR, etc.), including data governance, cybersecurity, and system reliability.
* Oversee the prioritization of enhancements and change requests, including business case preparation, cost-benefit analysis, and negotiation of prioritization with functional directors and VPs.
* Establish process approaches within all business functions, ensuring clear understanding of process inputs, outputs, and KPIs, and lead the definition and creation of KPIs to measure achievement of goals.
* Lead and manage master data management and data governance initiat...
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Type: Permanent Location: Jessup, US-MD
Salary / Rate: Not Specified
Posted: 2026-07-21 08:45:32
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Get to know us: NOVO Health Services offers linen management solutions to the healthcare industry.
NOVO Health keenly focuses on safety and infection control and provides its partner hospitals with a value-driven linen management control system that measures and monitors linen utilization by department to eliminate excess internal costs.
NOVO's wide range of service programs offer a variety of options to provide a seamless, single source distribution system.
NOVO's regional healthcare linen facilities are HLAC accredited and operate with state-of-the-art processing equipment and processes.
* The Quality Technician supports the site-level Quality and Compliance Systems for the hygienic processing of healthcare textiles.
This role ensures daily compliance with HLAC, TRSA Hygienically Clean, and ISO 9001:2015 standards while serving as the plant’s key contact for infection prevention, product quality, and document control.
* This will be completed via:
+ Perform infection prevention (IP) and product audits, ensuring compliance with HLAC and TRSA standards.
+ Conduct process and work-construction audits to confirm hygienic, appearance, and order accuracy requirements are maintained.
+ Manage local document control, including removal of obsolete procedures, posting of new documents, and verifying operator training on updates.
+ Maintain training matrices and records in coordination with Human Resources; ensure ongoing training compliance beyond initial onboarding.
+ Support customer complaint investigations, collect data, assist root cause analysis, and issue or implement quality alerts as needed.
+ Execute incoming product and linen inspections, monitor supplier performance, and support vendor quality verification.
+ Track and report defect rates (stains, holes, wash loss, packaging, etc.) to support continuous improvement and trend analysis.
+ Verify critical-to-quality (CTQ) process parameters such as wash temperatures, drying cycles, ironer settings, and hygiene validation steps.
+ Conduct or coordinate scale verification and equipment calibration checks as part of internal audit readiness.
+ Participate in product or customer introduction reviews (APQP-style) to verify product quality, packaging, and performance before rollout.
+ Support corrective and preventive action (CAPA) activities in collaboration with the Regional Quality Manager.
+ Provide feedback and recommendations for continuous improvement, particularly where quality, hygiene, and appearance impact customer satisfaction.
+ Serve as the on-site liaison for internal audits, regional quality visits, and accreditation reviews.
Education/Training:
* High School diploma or GED required.
* Associate degree or equivalent industry experience in quality, healthcare, or manufacturing preferred but not required.
* ISO 9001:2015 int...
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Type: Permanent Location: Louisville, US-KY
Salary / Rate: Not Specified
Posted: 2026-07-21 08:44:28
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Your Job
Georgia-Pacific is seeking a Test Fixture Designer with more of a mechanical design focus to help us maintain our market leadership in our devices test lab at our Technical Center in Neenah, Wisconsin.
As a test fixture designer, you will have a great opportunity to shape the operation of our lab in an environment that fosters innovation and creativity and rewards you for value created.
enMotion®, Compact®, and SmartStock® are all market-leading brands of away from home GP PRO products by Georgia-Pacific.
Our dispensers for each of those brands are examples of the innovative devices we develop, manufacture, and market.
If you're excited by an opportunity to continuously learn and grow while supporting those brands, we'd like to talk with you.
At Georgia-Pacific, we share your enthusiasm for pushing boundaries and embracing creative solutions.
We constantly challenge the status quo, take calculated risks, and strive to improve the products we make.
Our Team
The Georgia-Pacific Devices Test Lab team represents the people who use our dispensers and products every day and the maintainers who service them.
We are entrepreneurs who innovate and collaborate cross-functionally to design, develop, test, and execute projects that create value for our consumers, customers, communities, as well as GP.
We value lifelong learners who want to contribute and grow with us.
This position is located at the Neenah Technical Center (NTC), the central site for research, development, and lab services for Georgia-Pacific's North American Consumer Products business.
What You Will Do
* Device Testing: Assist in the planning, development, and execution of GP PRO device and product validation test plans in support of our product development process.
This would include conducting the testing and recording results.
* Testing Efficiency: Design, develop, and implement custom test equipment, test fixtures, test methods, and instrumentation to streamline device testing through automation and data acquisition.
* Test Protocols: Assist with the investigation, development, and implementation of custom test protocols in support of validation and verification testing.
* Test Fixture Design: Design test fixtures considering factors like reliability, throughput, test coverage, product tolerances, test parameters, and ease of use.
Create and maintain supporting documentation for test fixtures.
* Continuous Improvement: Implement continuous improvement processes to increase lab efficiency.
* Test Lab Capabilities: Proactively recommend and create improvements to test lab technical capabilities as device development needs shift.
Identify validation failures, file observations, and troubleshoot mechanical failures.
Work with cross functional team members to support root-cause analysis.
Recommend lab capability upgrades and procurements to meet evolving validation needs.
Who You Are (Basic Qualifications)
* Associates degree or highe...
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Type: Permanent Location: Neenah, US-WI
Salary / Rate: Not Specified
Posted: 2026-07-21 08:31:06
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At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
Join Roche, where every voice matters.
The Position
Wer wir sind
Du startest bei uns im Bereich Pharma Biotech in Penzberg.
Wir stellen Arzneimittelwirkstoffe in unterschiedlichen Indikationsgebieten, z.
B.
in der Onkologie zur Behandlung von Brustkrebs und Herz-Kreislauf, her.
In der Funktionseinheit mikrobiologische Produkt-Qualitätskontrolle werden die biotechnologisch produzierten Wirkstoffe auf Einhaltung der hohen Qualitätsstandards geprüft.
Aufgabe der Einheit “Quality Control Microbiology, Environmental Monitoring & Cleaning” ist u.
a.
die Durchführung mikrobiologischer Testungen zur Überprüfung der Wirkstoffe und der Prozessanlage.
Deine Aufgaben
* Du bist für die GMP-gerechte Durchführung der Analysen im Rahmen der mikrobiologischen Produkt-Qualitätskontrolle verantwortlich
* Das Testspektrum und Dein Aufgabengebiet umfassen mikrobiologische, biochemische und molekularbiologische Methoden wie z.
B.
Keimzahlbestimmung, Test auf Endotoxine und Identifizierung von Mikroorganismen
* Du dokumentierst Deine Versuche und Ergebnisse entsprechend den behördlichen Anforderungen
* Du arbeitest gemeinsam im Team in der Routine-Analytik
* Du bist an der Entwicklung, Etablierung und Validierung analytischer Methoden beteiligt.
Insbesondere bist du für die Validierung von Methoden für neue Einsatzstoffe zuständig
* Du hältst unsere Vorgaben zur GMP-gerechten Analytik auf dem neuesten Stand
Wer Du bist
* Du hast eine abgeschlossene naturwissenschaftliche Ausbildung in einem der folgenden Bereiche: Biologie- oder Chemielaborant/in, Biologisch-, Chemisch- oder Medizinisch- Technische/r Assistent/in oder Vergleichbares
* Du bringst mindestens drei Jahre praktische Erfahrung im Laborumfeld mit und bist mit den GMP-Vorgaben vertraut
* Du bringst Erfahrung in der Validierung von mikrobiologischen Methoden, insbesondere für die Einsatzstofftestung mit
* Du hast gute Kenntnisse in mikrobiologischen und biochemischen Methoden
* Teamarbeit macht Dir Spaß und Du arbeitest gerne detailgetreu
Diese Position ist auf 2 Jahre befristet.
Bewerbungszeitraum bis mindestens 03.08.2026.
(Bewerbung möglich, solange die Stelle ausgeschrieben ist)
Wir freuen uns auf Deine Bewerbung!
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Zum aktuellen Zeitpunkt benötigen wir keine weiteren Dokumente, wie Motivationsschreiben, Zeugnisse oder Ähnliches.
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Type: Permanent Location: Penzberg, DE-BY
Salary / Rate: Not Specified
Posted: 2026-07-21 08:30:29
