Marketing Specialist (Mid)
Planet Pharma · Creve Coeur, MO · 1 wk ago
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Regulatory Affairs Manager
- About the role: Oversee regulatory compliance for pharmaceutical products.
- Responsibilities: Develop and implement regulatory strategies, manage regulatory submissions, and ensure compliance with FDA and EMA guidelines.
- Requirements: Bachelor's degree in a related field, 5+ years of regulatory affairs experience, and strong knowledge of FDA and EU regulations.
- Qualifications: Excellent communication skills, ability to work independently and collaboratively, and proficiency in Microsoft Office.
- Skills: Strong understanding of regulatory processes, excellent organizational and project management skills, and experience with regulatory submission software.
- Benefits: Competitive salary, comprehensive benefits package, professional development opportunities.
- Pay: Negotiable based on experience and qualifications.
- Schedule: Full-time, Monday to Friday, 9 AM to 5 PM.
Process Development Senior Associate
- About the role: Lead process development activities for new product formulations.
- Responsibilities: Design and optimize manufacturing processes, conduct process validation, and support commercialization efforts.
- Requirements: Bachelor's degree in Chemical Engineering or related field, 7+ years of process development experience, and hands-on experience in formulation science.
- Qualifications: Strong problem-solving skills, ability to work in a team environment, and proficiency in process analytical technologies (PAT).
- Skills: Proficient in process design software, excellent communication and presentation skills, and experience with cGMP regulations.
- Benefits: Competitive salary, comprehensive benefits package, professional development opportunities.
- Pay: Negotiable based on experience and qualifications.
- Schedule: Full-time, Monday to Friday, 8 AM to 4:30 PM.
Senior Research Associate, Medicinal Chemistry
- About the role: Conduct medicinal chemistry research to discover and develop novel drug candidates.
- Responsibilities: Design and execute synthesis experiments, analyze data, and contribute to the discovery of new chemical entities.
- Requirements: PhD in Medicinal Chemistry or related field, 6+ years of relevant experience, and expertise in organic synthesis and medicinal chemistry techniques.
- Qualifications: Strong analytical and problem-solving skills, ability to work independently and collaboratively, and proficiency in laboratory safety protocols.
- Skills: Proficient in organic synthesis techniques, excellent communication and collaboration skills, and experience with medicinal chemistry databases.
- Benefits: Competitive salary, comprehensive benefits package, professional development opportunities.
- Pay: Negotiable based on experience and qualifications.
- Schedule: Full-time, Monday to Friday, 9 AM to 5 PM.