At ProPharma, we help pharmaceutical, biotechnology, and medical device companies bring life-changing therapies to market. From early development through clinical, regulatory approval, and commercialization, we provide expert guidance to navigate complex challenges and accelerate success. Our mission is simple: improving patient health and safety by delivering the highest-quality regulatory, compliance, clinical research, pharmacovigilance, and medical information services throughout the entire product lifecycle. With over 20 years of expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma partners with clients across the complete product lifecycle through an advise-build-operate model. Our end-to-end suite of consulting solutions de-risks and accelerates high-profile drug and device programs, ultimately improving patient health and safety. Discover how ProPharma can help you inspire the future of science!
Open Positions
Process Engineer (Med Device)
Process engineering experience with 0-3 years of experience
On-Site Research Assistant (PART TIME) - Kanpur, Uttar Pradesh
3 years of experience, Bachelor's degree, Strong communication Skills (verbal and written), Ability to work independently and collaboratively
On-Site Research Assistant (PART TIME) - Belagavi, Karnataka
Bachelor's degree, 3 years of experience, strong communication and organizational skills
French Speaking Medical Information Specialist - Graduate Opportunity
Degree in Life Science, Nursing, or Medicine, Fluency in French and English, Strong communication skills
On-Site Research Assistant (PART TIME) - Nagpur, Maharashtra
3 years of related experience, Bachelor’s degree, critical thinking and communication skills
Pharmacovigilance Intern
Completed a degree in Pharmacy, Life Sciences, Medicine, or a related field. Experience with Argus safety database required
Multilingual Medical Information Specialist - French Speaking
Completed Pharmacy or life science degree, Mother tongue/C1 level in French, Strong translation skills, Excellent phone manner
Medical Information Specialist-Toxicology
RN, RPh, PharmD, DVM or equivalent degree, current license, computer knowledge, and telephone etiquette required
Sterile Compounding/Manufacturing Trainer (Columbus, OH)
Experience in sterile compounding, USP <797> compounding, or aseptic training for 503b or aseptic drug manufacturing
Document Specialist
Minimum 3 years of experience in document publishing and/or formatting, pharmaceutical/biotech industry experience preferred, and fluency in English
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