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Are you looking to join a globally known Accounting firm in downtown Boston? Are you looking for a flexible hybrid schedule? Do you have 5+ years of Accounting experience? If interested, please apply now for immediate consideration
Are you looking for a Cost Accountant role with a rapidly growing manufacturing company? Do you have 3-8 years of experience in cost accounting within the manufacturing sector?
Our client is a family owned multi-billion dollar manufacturer with a downtown office located in Chicago. They have been in business for over 100 years and serve a variety of industries including Consumer Goods, Health & Wellness and Pharmaceuticals. They seek an experienced Quality Manager to assist in building out their Supplier program for a newly launched Value Stream. This role will report to their Director of Supplier Quality.
Responsible for the success of Contract Development and Manufacturing Programs by managing and monitoring the programs' overall portfolio and execution of project plans to ensure timelines and expectations are mutually-defined and adhered to all while providing excellent client service, both internally and externally. The position is a contributing member of the project team and responsible for ensuring timely completion of assigned project deliverables.
Manage pharmaceutical customer relationships in the US and operations. Coordinate with third party logistics distribution partner "3PL", screen and approve daily orders from customers, manage returns process through 3PL, reconcile customer accounts, manage contracts with end customers, manage patient assistance programs, track results to report back to management, oversee compliance to government price reporting and transparency reporting requirements.
Responsible for preparing quarterly provisions: work papers and supporting calculationsPerform tax compliance and prepare reporting packages for corporate group
This individual will be responsible for creating orders for Phase 1 clinical trials (FIH, SAD/MAD, Food Effect, TQT, DDI, Asian Ethnobridging, 14C hAD). They will conduct market research to identify new clients in the biotechnology and pharmaceutical industries who are working on new treatments, and establish new connections with these companies that are relevant to the Clinical Pharmacology Center Phase 1 service portfolio.
You will work with preclinical project teams and scientific leadership, helping to develop, drive and coordinate project strategy and execution. Having a strong scientific background, obtained in a biotech or pharma setting, will help you draw on successful project management experience.
Support chemistry projects, characterizing Starting Materials, Intermediates and APIs and collaborates effectively with Analytical Chemistry colleagues. Assist clients with advanced analytical solutions that help deliver our programs and ultimately progress products to market.
The Sr. Project Engineer provides Process and Project engineering services in support of the Active Pharmaceutical Development and Manufacturing Site. The Sr. Project Engineer will act to ensure the safest and most efficient use of resources in the planning and execution of capital and expense projects.
Design and develop novel synthetic routes to pharmaceutical APIs in the laboratory and implementing the processes at kilogram-scale in internal facilities. Maintain clear and accurate records of experiments in laboratory notebooks in accordance with company policy.
The Process Engineer must apply a broad range of safety, environmental, GMP, engineering, leadership and technical skills across a broad range of issues. Critical to the success of this position is adherence to cGMP and OSHA Process Safety Management regulations, development of robust, reliable production processes, and cost-effective installation of durable, multi-purpose (flexible) chemical and solids processing equipment.
Working as Associate Director of Statistics for Virology and Paediatrics, reporting into the Senior Director of Statistics. Your role will be to support regulatory submission, working collaboratively with internal teams to meet project deliverables and time lines. You will be responsible for all statistics activities across multiple compounds within paediatrics, leading internal and external teams.
This individual will be responsible for finding, developing, and implementing commercial prospects in the pharmaceutical and biotech sectors on a global scale in order to strategically expand the company. This person will create and develop the company's growth plans, such as new niche concepts and service pipeline differentiation, in close cooperation with the company's senior management team.
The Field Applications Scientist (FAS) will be in charge of representing and promoting the scientific benefits and value we offer to our customers. The FAS will assist our sales team by participating in sales calls as the subject matter expert, going to speeches, and utilizing their network for new business prospects.
As the VP, Global Quality Assurance, you will lead global QA strategy and be responsible to developing, maintaining and communicating all quality programs throughout the organization. You will install and maintain a culture of excellence across all divisions of the group and ensure all international regulations and industry standards are adhered to.
Are you looking for your next role with a top tier client? Do you have 3+ years of progressive accounting or public audit experience with a public life science company?
Responsible for identifying, developing and executing business opportunities in the pharmaceutical and biotech industries to strategically grow the business. This will include developing and retaining scientific relationships with leading pharmaceutical/biotech industry leaders.
Responsible for supporting business development activities for company's US-based API manufacturing activities. Organize client interactions and visits to US facilities and negotiate terms and conditions directly.
The Manufacturing Process Engineer will understand the design of scientific products and explain how that translates into manufacturing, assembly, and the packaging processes. The Manufacturing Process Engineer is responsible for providing product and process support for all manufacturing processes, component identification, database documentation, quality criteria.
The Product Development Team develops new & revises existing product formulations to deliver positive patient outcomes. You'll contribute to the ideation/exploration for uses of new-to-ACI ingredients & new-to-ACI business ventures in additional disease-states reliant on specialized medical nutrition.
Drive out-licensing efforts for preclinical assets and partnering strategy on AI platform technologies as well as discovery collaboration with external companies. Responsible for scouting, due diligence, negotiation, and execution of BD deals by working closely with our CBO, management, business development, R&D, AI, legal, and finance teams, as well as external parties.
Our client is an established manufacturer that serves the healthcare, medical device and pharmaceutical industry. They have recently launched a new product that has led to increased sales and business across the globe. They seek a Validation Engineer that will assist in developing processes, documentation and project management.
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