Pharmaceutical jobs in Colorado Springs, ColoradoCrear alertas

Kelly® Science & Clinical is seeking a Pharmaceutical Principal Investigator for a direct hire opportunity with one of our clients, a leading small molecule CDMO at their Colorado Springs, CO facility. If you’re passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts. Workplace: Onsite in Colorado Springs, CO Salary: $125,000-140,000 Are you ready to drive innovation and success in pharmaceutical manufacturing? We are seeking a dynamic Principal Investigator to serve as a technical authority in process development, scale-up, and technology transfer. If you thrive in collaborative, fast-paced environments and are passionate about advancing life-changing therapies, this is your opportunity to make a significant impact. Responsibilities Strategic Process Development & Scale-Up • Spearhead the development and scale-up of robust, scalable manufacturing processes across a wide spectrum of drug products, • Design and lead process characterization and optimization studies, defining critical process parameters and proven acceptable ranges, • Champion Quality by Design (QbD) strategies and advanced statistical methodologies, ensuring seamless progression from laboratory concepts to pilot-scale execution Technology Transfer Leadership • Serve as the technical lead for all technology transfer activities, bridging R&D, global manufacturing sites, and client partners, • Develop and implement comprehensive transfer protocols and process equivalence strategies to ensure flawless execution, • Lead high-performing, cross-functional teams through knowledge transfer, process mapping, and documentation best practices Pilot Plant & cGMP Operations Management • Oversee cGMP-compliant pilot plant operations, supporting clinical and commercial production, validation, and process improvement, • Drive continuous improvement projects—maximizing efficiency, quality, and yield, • Provide expert troubleshooting and manage deviations, ensuring on-time project delivery Capital Projects & Facility Optimization • Lead equipment qualification and validation for cutting-edge process installations, • Direct facility expansion and modification projects to support innovation and new technology implementation, • Optimize facility workflows to enhance operational excellence and scalability Quality Assurance & Regulatory Compliance • Ensure strict adherence to cGMP (21 CFR 210/211) and data integrity (21 CFR 11) regulations, • Develop and execute robust process validation strategies in accordance with global regulatory standards, • Lead investigations, implement corrective/preventive actions, and maintain perpetual audit readiness Project Management & Client Engagement • Manage multiple, high-profile client technology transfer programs—delivering on time and within budget, • Serve as the primary technical liaison for clients, providing strategic insight and technical guidance, • Develop detailed project plans, risk assessments, and contingency strategies to de-risk tech transfer activities, • Mentor cross-functional teams, fostering a culture of excellence and innovation Qualifications Education: • Bachelor’s degree in Engineering, Pharmaceutical Sciences, or related field; advanced degree (MS/PhD) preferred Experience: • 8+ years’ experience (Bachelor’s), 5+ years (MS), or 3+ years (PhD) in pharmaceutical process development, technology transfer, and scale-up within a CDMO or CRO environment, • Demonstrated success managing complex, cross-functional projects in a regulated setting Technical Mastery • Deep expertise in pharmaceutical process engineering, manufacturing technologies, process validation, and equipment qualification, • Comprehensive understanding of cGMP, quality systems, and regulatory compliance, • Proven skills in process automation, risk management, and project execution Leadership & Collaboration • Recognized leadership in guiding technical teams and cross-functional project groups, • Outstanding client relationship management and communication abilities, • Strategic thinker with a results-driven mentality, adept at navigating complex challenges and inspiring teams Why Join Us? • Work alongside industry leaders and innovators, • Participate in high-impact projects accelerating life-saving therapies to market, • Competitive salary, comprehensive benefits, and opportunities for continued professional growth What happens next: Once you apply, you’ll proceed to the next steps if your skills and experience look like a good fit. But don’t worry – even if this position doesn’t work out, you’re still in our network. That means our team of expert Science & Clinical recruiters will have access to your profile, making your opportunities limitless.

Job Description Whether you are working in a Pharmacy looking for additional income, an established healthcare sales professional, or looking to break into Medical Sales, Healthcare Marketing Group, LLC is a great opportunity for you. As a Pharmacy Relationship Manager, you will help drive the growth of our company through building and retaining customer relationships. You can even change the way healthcare is delivered to Americans. Our Pharmacy Savings Card works like GoodRx and SingleCare. With savings of up to 80% off prescriptions, we provide the highest discounts in the industry! We are now seekingPharmacy Relationship Managers in your area!* What does a Pharmacy Relationship Manager do? • Educate Pharmacy Staff about how their customers can save up to 80% on prescriptions, • Provide Savings Cards by engaging with medical offices and educating Office Staff about how their patients can save up to 80% on medications What you need to qualify: • Pharmaceutical/medical sales experience is preferred but not required, • Sales skills with a proven track record, • Exceptional interpersonal skills (building strong relationships), • Excellent verbal and written communication skills, • Ability to work independently to oversee accounts and increase revenue, • Reliable transportation (this position is partially remote and you will be visiting medical professionals in your area) *We are currently hiring Pharmacy Relationship Managers in the San Antonio metropolitan area. Please only apply to one city; your desired territories will be discussed during the interview. Benefits Training and compensation: • We include comprehensive training and ongoing coaching, • Monthly Bonuses, • Great Commission!

Job DescriptionRESPONSIBILITIES: Process Development & Scale-Up: • Lead process development activities to establish robust, scalable manufacturing processes for diverse drug products, • Design and execute process characterization studies to identify critical process parameters (CPPs) and proven acceptable ranges (PARs), • Develop and optimize unit operations for various dosage forms, ensuring seamless transition from laboratory to pilot scale, • Serve as technical lead for end-to-end technology transfer activities between R&D, manufacturing sites, and client facilities, • Develop and execute comprehensive tech transfer protocols, including process comparability and equivalence studies, • Lead cross-functional tech transfer teams to ensure successful knowledge transfer and process implementation, • Oversee cGMP pilot plant operations for process validation, clinical, and commercial batch production, • Develop and optimize manufacturing processes to enhance efficiency, yield, and quality, • Implement continuous improvement initiatives for pilot plant operations and equipment utilization, • Lead equipment qualification and validation activities for new process equipment installations, • Manage facility modification projects to support process improvements and technology implementation, • Develop and execute capital project plans for process equipment upgrades and expansions, • Ensure compliance with cGMP standards (21 CFR 210/211) and data integrity requirements (21 CFR 11), • Develop and implement process validation strategies in accordance with regulatory requirements, • Lead process-related investigations and implement corrective/preventive actions, • Manage multiple client tech transfer projects simultaneously, ensuring adherence to timelines and budgets, • Serve as primary technical contact for client process-related discussions and strategy development, • Develop project plans, risk assessments, and contingency strategies for tech transfer activities Education & Experience: • Bachelor’s degree in chemical engineering, Mechanical Engineering, or related field with 8+ years' experience, • Advanced degree (M.S. with 5+ years or Ph.D. with 3+ years) in Engineering or Pharmaceutical Sciences preferred, • Extensive experience in pharmaceutical process development and technology transfer within CDMO/CRO environment, • Strong background in pharmaceutical process engineering and manufacturing technology, • Hands-on experience with process validation and equipment qualification, • Extensive knowledge of cGMP requirements and quality systems, • Demonstrated expertise in tech transfer methodologies and best practices, • Proven experience managing capital projects and process improvement initiatives, • Excellent organizational and time management skills, • Ability to manage multiple complex projects simultaneously, • Excellent technical leadership and team management skills, • Strong client relationship management and communication abilities, • Ability to work effectively in cross-functional team environments, • Demonstrated problem-solving and decision-making capabilities, • Strong documentation and technical writing skills At LGM Pharma, we always take pride in putting our people first. We are an equal opportunity employer. We offer medical, dental, vision and company matching 401K. All suitably qualified candidates will receive consideration for employment based on objective work-related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws.

Job Description Work 100% remotely, set your own schedule, and earn additional income while making a real difference in men's health and lives. Hone is one of the fastest-growing health companies in the United States, and we are looking for physicians who have deep knowledge and experience in prescribing for men with hypogonadism. If you are a physician with a strong background in treating hypogonadism and experience prescribing testosterone and other hormone-optimizing pharmaceuticals, this is an opportunity to join a mission-driven team that is reshaping access to care. We treat patients with a combination of pharmaceutical products in accordance with AUA-defined protocols, supplements, and lifestyle changes. We are committed to making care more convenient and affordable for patients. Experience with weight-loss and thyroid medications is a plus, as we have expanded beyond men's hormones into these treatment areas. We have also launched services for women. Experience with women's hormone therapy allows you to see our female patients as well, but is certainly not required. We are looking nationwide and value physicians licensed in multiple states. Who We Are We're a modern health company with a simple mission: help our patients take control of their health and age with confidence. Our platform removes barriers to care through education, technology, and convenience. Our primary focus is hormone optimization for men. We are looking to add to our growing team of 150+ physicians who specialize in treating hormones and are passionate about improving patient outcomes through telemedicine. You'll join a supportive, innovative environment where you'll receive full training on our proprietary telemedicine platform, HIPAA-compliant technology, and technical support. What You'll Do • Conduct video-based consultations from anywhere with an internet connection, • Review labs and create personalized treatment plans, • Prescribe and titrate medications based on clinical findings, • Educate patients on safe and effective hormone optimization, • Provide feedback to help us continuously enhance the patient experienceWhat We're Looking For, • MD or DO with an active license (multi-state licenses preferred), • Minimum 2 years of experience in Endocrinology, Urology, Family Medicine, or Hormone Therapy, • DEA license with authority to prescribe Schedule III medications, • Strong communication skills and a passion for patient-centered care, • Comfort with technology and willingness to learn telemedicine workflows, • Availability for at least 8 hours per week, • A prescribing philosophy that values holistic care and hormone optimization, not just prescribing testosterone to everyone Help men regain their health and confidence - from anywhere. If you are passionate about hormone health, thrive in innovative environments, and want to help men live their best lives, we would love to hear from you.

Job Description RESPONSIBILITIES: R&D Technical Execution: • Conduct hand, laboratory, and pilot-scale trials for new and reformulated products, generating precise and accurate data reports., • Obtain raw materials, perform weighing, and execute product development trials, including pilot and clinical batches., • Perform product development equipment set-up, operation, and clean-up., • Perform visual inspection and physical testing on intermediates and finished trial products., • Play a key role in site expansion and facility build-out projects by providing critical operational and technical input., • Serve as a primary R&D liaison for third-party contractors, vendors, and equipment suppliers to ensure project alignment with technical requirements and timelines., • Support the timely execution of capital projects by coordinating R&D activities with construction and installation schedules., • Support facility management activities for the R&D and pilot plant areas, including coordinating maintenance, calibrations, and repairs., • Assist in managing site services and infrastructure relevant to the R&D operations to ensure minimal downtime., • Identify and implement process improvements to enhance operational efficiency, safety, and compliance within the R&D facilities., • Perform other related duties as required to support the strategic and operational goals of the department and site. QUALIFICATIONS: Education & Experience: • Bachelor’s degree in engineering, Science, or a related field is preferred; equivalent combination of education and significant relevant experience will be considered., • 5+ years of experience in a pharmaceutical manufacturing or R&D environment, with a demonstrated ability to handle increasing responsibility., • Proven experience in supporting facility projects, working effectively with third-party contractors, and managing timelines is highly desired., • Technical & Professional Skills:, • Able to apply concepts of basic algebra and geometry for calculations and layout planning., • Proficient in MS Word, Excel, and Project (or similar project management software)., • Able to read and interpret technical procedures, SOPs, GMPs, construction plans, and equipment manuals., • Strong communication, coordination, and interpersonal skills for effective collaboration with internal teams and external parties., • Strong attention to detail and able to manage multiple complex tasks simultaneously. Physical Requirements: • Able to regularly lift up to 25 pounds and navigate active construction or facility expansion sites as needed. At LGM Pharma, we always take pride in putting our people first. We are an equal opportunity employer. We offer medical, dental, vision and company matching 401K. All suitably qualified candidates will receive consideration for employment based on objective work-related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws.

BioLife Plasma Services is a subsidiary of Takeda Pharmaceutical Company Ltd. At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs.

Are you ready to drive innovation and success in pharmaceutical manufacturing? We are seeking a dynamic Principal Investigator to serve as a technical authority in process development, scale-up, and technology transfer. Bachelor's degree in Engineering, Pharmaceutical Sciences, or related field; adv

Establish reports for reviewing procurement of pharmaceuticals.

Kelly® Science & Clinical is seeking a Pharmaceutical Principal Investigator for a direct hire opportunity with one of our clients, a leading small molecule CDMO at their Colorado Springs, CO facility. Are you ready to drive innovation and success in pharmaceutical manufacturing? We are seeking a d

BioLife Plasma Services is a subsidiary of Takeda Pharmaceutical Company Ltd. At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs.