We are aware of a global phishing scam with employees from companies impersonated across email, WhatsApp, and Telegram.We are confident that no PageGroup system has been breached. Find out how to protect yourself and the signs to look out for
Browse our jobs and apply for your next role.
Reach out to us or discover some great insights that could help you fill your next vacancy.
PageGroup changes lives for people through creating opportunity to reach potential.
We find the best talent for our clients and match candidates to their ideal jobs.
Identify, cultivate, and maintain relationships with new and current clients. Spearhead the development of business at a quickly growing, impactful CDMO in the pharmaceutical industry.
Play a crucial role on the clinical development team, providing strategic medical leadership in the development of novel drugs and therapies. Responsible for US Clinical development and will offer medical guidance to discovery projects, ensuring the highest standards of clinical research.
Play a crucial role in our clinical development team, providing strategic medical leadership in the development of novel drugs and therapies. Responsible for US Clinical development and will offer medical guidance to discovery projects, ensuring the highest standards of clinical research.
Senior Project Manager for the Healthcare division of a reputable full-service general contracting firm, headquartered in St. Louis. Responsible for all project phases from lead-generation to close. Communicates effectively and establishes relationships with clients, architects, engineers, and subcontractors to ensure project success.
My client is seeking a Director of Quality located near Chicago, IL. The Director of Quality Control will develop, implement, and periodically evaluate a program to ensure the organization's production operations, from raw materials to finished products, meet the quality, integrity, and efficiency standards set by the organization.
Collaborate with cross-functional teams to gather and synthesize information. Translate complex scientific data into clear and compelling content for various audiences.
The Senior Quality Engineer role is a highly visible and dynamic role with exponential growth opportunity. You will be hands on across multiple departments improving quality processes and programs, tackling quality issues and leading the quality focus in product launches.
Lead the development of the Bioprocess Filtration Portfolio, leveraging both new and existing assets to meet market demands and industry trends. Serve as the subject matter expert on bioprocess filtration, providing technical support and guidance to internal teams and external stakeholders.
Responsible for developing new and existing businesses within their territory. Meet sales objectives and satisfy customer needs by educating and selling the company product lines and services to research facilities.
This IT Business Partner/SME for Finance will act as a liasion between IT and Finance Business functions prioritizing ERP and IT solutions. This is a hybrid role in Andover, MA. Full time, direct hire opportunity.
This person will be primarily responsible for orchestrating the company's involvement in tradeshows and industry events. This includes planning and coordination, overseeing the tradeshow calendar, managing booth design and logistics, and handling staff accommodations.
The Divisional Chief Financial Officer role plays a pivotal role in optimizing financial performance, advancing strategic planning, and fostering the growth of 2/3 of their overall business.
Uncover and secure new business opportunities in your designated territory. Thrive as an independent contributor in the dynamic large molecule bioanalytical domain, specializing in early-phase clinical services.
Lead key partnerships, boost revenue through new deals with Big Pharma. Join a dynamic, fast-paced company as the 2nd BD hire, with rapid career growth and uncapped earning potential.
Managing high level partnerships with Big Pharma and help increase overall revenue by establishing new deals. Join fast paced, highly dynamic company as 2nd BD hire with opportunity to rapidly grow your career with uncapped earning potential.
Provide regulatory expertise through all stages of the product lifecycle, including development of CMC strategy. Perform regulatory assessments for manufacturing changes, provides guidance on regulatory expectations for the site, oversees the TSE/BSE program, and provides compliance documents to support Health Authority submissions
As a Engineering Manager, you will lead the design, development, and commercialization of our novel combination devices. In this role, you will be responsible for managing and executing all aspects of device development, from concept generation and prototyping to validation and manufacturing transfer.
Identify and pursue new business opportunities in the pharmaceutical and biotechnology sectors related to preclinical discovery and development. Leverage a strong technical background in preclinical research, with a focus on immuno-oncology, oncology, degenerative disorders, or related areas to effectively communicate with clients and internal teams.
Take the helm as the main liaison for vital pharmaceutical clients, managing every facet of alliance management. Cultivate lasting relationships, working collaboratively to ensure shared success.
Elevate the company's prominence by fostering beneficial collaborations, advocating our integrated services to potential partners. This role bridges science and business, building enduring relationships while aligning drug discovery and CMC capabilities.
Drive pioneering clinical development initiatives in the small molecule space, advancing novel therapeutics and shaping the future of healthcare. Lead groundbreaking research and contribute to transformative treatments in the dynamic biotech landscape.
Take charge of hardware design and specification for biologics manufacturing control systems, ensuring compliance with industry norms and regulations. Collaborate effectively with cross-functional teams to decipher automation requirements and transform them into resilient hardware solutions.
Take the lead in establishing and optimizing Antibody Drug Conjugate (ADC) manufacturing processes from inception to full-scale operation. Lead a dedicated team to drive efficient downstream operations in ADC production, ensuring successful project delivery.
Lead regulatory affairs in our small molecule pharmaceutical company, spearheading FDA interactions and medical writing to ensure compliance and successful product development. Your expertise will drive regulatory strategies, ensuring the approval and commercial success of small molecule therapies.
Create Job alert to receive Healthcare Pharmaceutical jobs via email the minute they become available
Submit your resume to register with us and we will contact you if a suitable role becomes available
If you’re interested in Healthcare Pharmaceutical jobs such as Pharmaceutical Engineering jobs, Pharmaceutical Scientist jobs, Healthcare Science jobs, Biomedical Scientist jobs, here are some basics to keep in mind. In these roles, you’ll take on the very important and crucial responsibility of determining what technological devices are appropriate for use when it comes to the process of manufacturing a drug. You will give input on how the drug should be labeled, as well as how it should ultimately be offered to consumers when it is ready for market. In addition, you will be responsible for all of the safety issues associated with the drug you’re working to produce, and potentially, take on the task of developing drugs in laboratories for research and testing.
Healthcare Pharmaceutical Roles and Responsibilities
Healthcare Pharmaceutical Skills and Qualifications
This website has app functionality. Add it to your home screen for fast access and offline features.