
11 - 50 employees
Founded 2013
🧬 Biotechnology
💊 Pharmaceuticals
⚕️ Healthcare Insurance
Biotechnology • Pharmaceuticals • Healthcare Insurance
Pharmavise Corporation is the first Continuous Compliance Organization (CCO) dedicated to maintaining the highest standards of quality and regulatory compliance in the life sciences industry. Our esteemed client base includes Fortune 500 companies in pharmaceuticals, medical devices, and biotechnology. We offer bespoke solutions tailored to meet the specific compliance needs of our clients, supporting them from development through commercialization and ensuring they exceed their compliance goals while enhancing patient health and safety.
🕒 June 3
Consultant with 15+ years of experience in GxP operations and regulatory compliance. Leading consulting engagements with pharmaceutical and biotech clients on quality systems and compliance issues.
🕒 May 21
Gene Therapy Experts needed for leading gene therapy projects at Pharmavise Corporation. Engaging in research and development to advance gene therapy programs and mentor junior staff.
🕒 May 20
Medical Science Liaison responsible for providing scientific expertise and fostering relationships with healthcare professionals and researchers in the pharmaceutical industry.
🕒 May 19
Project Manager for life sciences consulting supporting GxP and FDA-regulated projects remotely. Leading cross-functional teams and ensuring compliance across pharmaceutical, biotechnology, and medical device organizations.
🕒 April 21
Pharmaceutical Manufacturing Specialist focusing on engineering support in pharmaceutical operations. Collaborate with teams to ensure compliance and optimize manufacturing processes for patient safety.
🕒 March 18
Regulatory CMC Expert providing guidance for biologics compliance at Pharmavise. Leading regulatory strategies for biologic products while ensuring compliance with global regulations.
🕒 March 18
Consultant offering expert consultation on homeopathic treatments, developing personalized treatment plans and collaborating with healthcare professionals.
🕒 March 18
Lead and contribute to cell therapy research and development projects at Pharmavise Corporation. Collaborate cross-functionally with teams to enhance efficacy and compliance in cell therapy programs.
🕒 March 18
Remote Bioequivalence Expert providing expert consultation and study support for pharmaceutical clients. Collaborating with cross-functional teams to ensure compliance in bioequivalence programs and studies.
🕒 March 18
Provide expert consultation in drug safety and pharmacovigilance to pharmaceutical companies. Collaborate on compliance issues and develop risk management strategies for drug products.
🕒 March 17
Medical Device Quality and Compliance Expert overseeing QMS activities for medical devices. Ensuring adherence to regulatory standards and leading cross-functional collaboration.
🕒 March 17
Regulatory Affairs Consultant providing expert guidance on biosimilars development projects for pharmaceutical companies. Collaborating with global teams and ensuring compliance with regulatory standards.
🕒 March 11
Business Development Manager specializing in life sciences consulting to drive growth and client acquisition. Responsible for proposal development and managing client relationships while supporting the company's expansion.
🕒 December 11, 2025
GxP Consultant delivering expert consulting engagements in quality and regulatory compliance for life sciences sectors. Leading GxP-focused quality systems and providing strategic advice on regulatory pathways.
🕒 October 23, 2025
Electrical Engineer designing, testing, and validating medical device components remotely. Collaborating with cross-functional teams in a regulated environment to meet compliance standards.
🕒 October 23, 2025
R&D Engineer role at Pharmavise Corporation, focused on medical device design, development, and regulatory compliance. Collaborating with cross-functional teams to improve patient outcomes through innovative solutions.
🕒 October 23, 2025
Project Manager leading medical device product development from concept through launch. Collaborating across teams to ensure compliance with regulatory and quality standards and adherence to project timelines.
🕒 October 23, 2025
UX/UI Designer creating user-focused digital experiences for regulated medical devices. Collaborating to design compliant interfaces that enhance patient safety and meet business goals.
🕒 October 23, 2025
Quality Engineer ensuring compliance with medical device regulations, collaborating across cross-functional teams. Drive quality excellence and support audits in product lifecycle processes.
🕒 October 23, 2025
Contract Administrator responsible for drafting and managing clinical study agreements in the medical device industry. Collaborating across teams to ensure compliance and efficiency in contract processes.
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