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The Engineering Manager blends hands-on technical work with team leadership. The role focuses on maintaining product compliance across Class I-III devices through updated test protocols, documentation, and design changes. You'll work closely with internal partners to ensure standards are kept current, gaps are identified early, and products continue to meet regulatory and customer expectations.
Lead and inspire a team of Product Life Cycle Engineers while driving cutting‑edge testing, compliance, and design improvements that keep advanced Class I-III medical devices at the forefront of global standards. As a cross‑functional force‑multiplier, you'll shape product strategy, elevate quality, fuel innovation, and ensure every device delivers exceptional performance and unmistakable customer value.
The Plant General Manager will be leading a flagship manufacturing facility and will be responsible for running the entire plant operations owning the P&L and driving cultural change and transformation.
This Senior Quality Engineer will own key quality systems, audits, and customer-facing problem resolution while ensuring ongoing compliance with AS9100D and ISO9001:2015. You'll be a trusted technical leader driving corrective actions, new product quality plans, and continuous improvement initiatives.
This Senior Quality Engineer role strengthens and advances the company's AS9100‑aligned Quality Management System while driving continuous improvement, audit readiness, and defect‑reduction initiatives. The position partners closely with Operations, Engineering, and QC to execute data‑driven root cause analysis and elevate quality performance across multiple manufacturing sites.
The Senior Project Manager - Healthcare focused will oversee construction projects within the healthcare sector, ensuring they are completed on time, within scope, and to the highest standards. This role is ideal for a detail-oriented professional with experience managing complex projects in the construction industry.
This Director-level role oversees all Regulatory Affairs and Quality Assurance activities, ensuring the company meets global medical device standards while expanding its product portfolio. You will shape regulatory strategy, strengthen the QMS, and drive compliance across a highly innovative environment.
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