The pharmaceuticals sector in the United States presents diverse opportunities for professionals seeking roles in research, development, manufacturing, and sales. Job seekers can find positions ranging from entry-level technicians to senior scientists and executive leadership. The industry is driven by innovation and regulatory compliance, making it a dynamic field for career advancement.624 Pharmaceuticals jobs in the United States
Security Guard Pharmaceuticals
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Job Description
Overview
Allied Universal®, North America's leading security and facility services company, offers rewarding careers that provide you a sense of purpose. While working in a dynamic, welcoming, and collaborative workplace, you will be part of a team that contributes to a culture that positively impacts the communities and customers we serve. We offer comprehensive benefits for most full-time positions, including medical, dental, and vision coverage, life insurance, a retirement plan, employee assistance programs, company discounts, perks, and more.
Job DescriptionAs a Security Guard, you will serve and safeguard clients in a range of industries such as Commercial Real Estate, Healthcare, Education, Government and more.
Part Time available at a Pharmaceutical Manufacturing Company in East Durham NY
7am - 7pm
Saturday & Sunday
$20.75 - $21.75 per hour with DailyPay available
Responsibilities:
- Provide customer service to our clients by carrying out safety and security procedures, site-specific policies and when appropriate, emergency response activities
- Respond to incidents and critical situations in a calm, problem solving manner
- Conduct regular and random patrols around the business and perimeter. Working environments and conditions may vary by client site.
Minimum Requirements:
- Be at least 18 years of age for unarmed roles; 21+ years of age for armed roles
- Possess a high school diploma or equivalent, or 5 years of verifiable experience
- As a condition of employment, applicants will be subject to a background investigation in accordance with all federal, state, and local laws. Allied Universal will consider qualified applications with criminal histories in a manner consistent with applicable laws.
- As a condition of employment, applicants will be subject to a drug screen to the extent permitted by law.
- Licensing requirements are subject to state and/or local laws and regulations and may be required prior to employment.
*A valid driver's license will be required for driving positions only
Perks and Benefits:
- Health insurance and 401k plans for full-time positions
- Schedules that fit with your personal life goals
- Ongoing paid training programs and career growth opportunities
- Employee discounts through our perks program to your favorite restaurants, entertainment venues and much more…
Allied Universal® is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race/ethnicity, age, color, religion, sex, sexual orientation, gender identity, national origin, genetic information, disability, protected veteran status or relationship/association with a protected veteran, or any other basis or characteristic protected by law. For more information:
If you have any questions regarding Equal Employment Opportunity, have difficulty using the online system and require an alternate method to apply, or require an accommodation at any time during the recruitment and/or employment process, please contact our local Human Resources department. To find an office near you, please visit:
Requisition ID2025-1419432
Consultant (Life Sciences, Pharmaceuticals)
Posted 2 days ago
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Company DescriptionAt EVERSANA, we are proud to be certified as a Great Place to Work across the globe. We're fueled by our vision to create a healthier world. How? Our global team of more than 7,000 employees is committed to creating and delivering next-generation commercialization services to the life sciences industry. We are grounded in our cultural beliefs and serve more than 650 clients ranging from innovative biotech start-ups to established pharmaceutical companies. Our products, services and solutions help bring innovative therapies to market and support the patients who depend on them. Our jobs, skills and talents are unique, but together we make an impact every day. Join us! Across our growing organization, we embrace diversity in backgrounds and experiences. Improving patient lives around the world is a priority, and we need people from all backgrounds and swaths of life to help build the future of the healthcare and the life sciences industry. We believe our people make all the difference in cultivating an inclusive culture that embraces our cultural beliefs. We are deliberate and self-reflective about the kind of team and culture we are building. We look for team members that are not only strong in their own aptitudes but also who care deeply about EVERSANA, our people, clients and most importantly, the patients we serve. We are EVERSANA. Job DescriptionEVERSANA® MANAGEMENT CONSULTING combines deep industry and functional area knowledge with specialized expertise in market assessment, analytics, and strategy development. Our global experts help industry executives address their most pressing business challenges.We are the strategic advisory arm of EVERSANA®, serving a broad range of large and small biopharma, med tech and digital therapeutics companies. As part of EVERSANA®, we integrate our strategic planning with launch excellence and commercial execution to provide end-to-end commercialization support to our clients.We offer strategic solutions across a range of innovative therapy areas - driven by our areas of practice in: Brand Strategy/Marketing, Launch/Complete Commercialization, Product Innovation, Corporate Strategy and Business Development, Pricing & Market Access, and Strategic Data Analytics Coordination - providing a diverse range of project experiences, led by experts in their fields.Our industry leaders bring a mix of diverse backgrounds combining science and commercial specialties from preeminent educational institutions, along with experiences gained at leading consulting firms and life sciences organizations.We are growing rapidly and seek team members who value the opportunity to accelerate their personal development while contributing to winning teams; this includes exposure to thought leaders across EVERSANA and constant interaction with clients and team members at all levels.EVERSANA® MANAGEMENT CONSULTING fosters a collaborative and supportive culture in which we strive to create an environment where people can build fulfilling and prosperous careers. Our consulting staff has a wide range of opportunities to develop their skills as life sciences professionals, from leading high-stakes strategic projects/product launches to coordinating and redesigning high-science product commercialization programs across global markets.KEY RESPONSIBILITIESConsultants play an important role in researching and developing client recommendations as part of project teams; primary responsibilities for the position include the following:Leading targeted secondary research (e.g., desk research, secondary data analysis) and primary research (e.g., interviews with key opinion leaders / insurance payers) with minimal oversightSynthesizing research insights to develop logical and effective client recommendationsIndependently running work streams, meeting deadlines, and assisting junior team members as necessaryDeveloping high-quality client communications and deliverables (e.g., PowerPoint slides, Excel models)Communicating verbal and written information in logical, clear, and concise fashionContributing to the development of the firm's capabilities and infrastructureSupporting the development of a high-performance cultureDemonstrate a commitment to diversity, equity, and inclusion through continuous development, modeling inclusive behaviors, and proactively managing bias.All other duties as assigned.EXPECTATIONS OF THE JOB:Travel: Some travel may be required for meeting with clients, stakeholders, or off-site personnel/managementHours: Monday to Friday, 40 hours per week. Overtime and/or weekend/evening hours may be required to meet project deadlines.The above list reflects the general details necessary to describe the expectations of the position and shall not be construed as the only expectations that may be assigned for the position.An individual in this position must be able to successfully perform the expectations listed above. QualificationsMINIMUM KNOWLEDGE, SKILLS AND ABILITIES:The requirements listed below are representative of the experience, education, knowledge, skill and/or abilities required.Education: Bachelor's Degree in a relevant concentration (e.g., business, economics, life sciences, engineering) and a strong academic recordExperience and/or Training:1+ year of experience at a life science consultancy, with experience working on multiple projects and handling associate / analyst-level responsibilitiesA strong passion for-and understanding of dynamics and issues in-the pharma and biotech industriesStrong analytical, problem-solving, and communication skillsTechnology/Equipment: Proficiency in Microsoft Excel and PowerPointPREFERRED QUALIFICATIONS:Education: Advanced degree from a top-tier institutionReasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position.Additional InformationOUR CULTURAL BELIEFSPatient Minded I act with the patient's best interest in mind.Client Delight I own every client experience and its impact on results.Take Action I am empowered and empower others to act now.Grow Talent I own my development and invest in the development of others. Win TogetherI passionately connect with anyone, anywhere, anytime to achieve results.Communication Matters I speak up to create transparent, thoughtful and timely dialogue.Embrace Diversity I create an environment of awareness and respect.Always Innovate I am bold and creative in everything I do.EVERSANA is committed to providing competitive salaries and benefits for all employees. The anticipated compensation range for this position is $120,000 to $130,000 and is not applicable to locations outside of the U.S. The compensation range represents the low and high end of the salary range for this position and includes billable hours commission. Compensation will be determined based on relevant experience, other job-related qualifications/skills, and geographic location (to account for comparative cost of living). More information about EVERSANA's benefits package can be found at eversana.com/careers. EVERSANA reserves the right to modify this base salary range and benefits at any time. Our team is aware of recent fraudulent job offers in the market, misrepresenting EVERSANA. Recruitment fraud is a sophisticated scam commonly perpetrated through online services using fake websites, unsolicited e-mails, or even text messages claiming to be a legitimate company. Some of these scams request personal information and even payment for training or job application fees. Please know EVERSANA would never require personal information nor payment of any kind during the employment process. We respect the personal rights of all candidates looking to explore careers at EVERSANA.From EVERSANA's inception, Diversity, Equity & Inclusion have always been key to our success. We are an Equal Opportunity Employer, and our employees are people with different strengths, experiences, and backgrounds who share a passion for improving the lives of patients and leading innovation within the healthcare industry. Diversity not only includes race and gender identity, but also age, disability status, veteran status, sexual orientation, religion, and many other parts of one's identity. All of our employees' points of view are key to our success, and inclusion is everyone's responsibility.Consistent with the Americans with Disabilities Act (ADA) and applicable state and local laws, it is the policy of EVERSANA to provide reasonable accommodation when requested by a qualified applicant or candidate with a disability, unless such accommodation would cause an undue hardship for EVERSANA. The policy regarding requests for reasonable accommodations applies to all aspects of the hiring process. If reasonable accommodation is needed to participate in the interview and hiring process, please contact us at us on LinkedIn / Twitter
Sr. Quality Engineer (Pharmaceuticals)
Posted today
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Job Description
We are seeking a highly experienced and motivated Quality Engineer to join our pharmaceutical manufacturing team. The ideal candidate will have a strong experience in quality assurance within the pharmaceutical industry, with a comprehensive understanding of regulatory requirements, quality systems, and process improvements. This role is critical to ensuring compliance with all relevant regulations and standards, leading quality initiatives, and supporting the manufacturing of pharmaceutical products.
Responsibilities
+ Develop, implement, and maintain Quality Management Systems (QMS) in compliance with FDA, EMA, ICH guidelines, and other regulatory requirements.
+ Ensure all processes and products comply with applicable regulatory standards, including cGMP.
+ Lead continuous improvement initiatives to enhance product quality, efficiency, and compliance.
+ Oversee validation activities, including equipment, process, and cleaning validations, ensuring compliance with industry standards.
+ Conduct thorough investigations into quality issues, perform root cause analysis, and implement corrective and preventive actions (CAPA).
+ Plan and conduct internal audits, support external regulatory inspections, and manage responses to audit findings.
+ Evaluate and qualify suppliers, conduct supplier audits, and ensure supplier compliance with quality standards.
+ Maintain accurate and comprehensive quality documentation, including SOPs, batch records, and validation protocols.
+ Mentor and develop junior quality engineers and quality assurance staff, fostering a culture of continuous improvement and quality excellence.
+ Perform risk assessments and implement risk mitigation strategies related to product quality and regulatory compliance.
+ Work closely with cross-functional teams, including R&D, manufacturing, and regulatory affairs, to ensure quality considerations are integrated into all phases of product development and production.
Essential Skills
+ 7-10 years of experience in Quality Assurance within a FDA/GMP environment (pharmaceutical or medical device industry required).
+ Bachelor's degree in a scientific field (Life Sciences, Biotechnology, or equivalent) is required.
+ Proficiency in quality management software, statistical analysis tools, and methodologies such as Six Sigma and Lean.
+ Strong understanding of Quality Management Systems.
+ Experience with Quality Systems including change control, root cause analysis, deviations, documentation management, and training systems.
+ Experience with electronic Quality and Training Management Systems.
+ Previous experience with hosting client audits and/or regulatory inspections required with excellent communication skills.
Additional Skills & Qualifications
+ Certified Quality Engineer (CQE) or Certified Quality Auditor certification preferred.
+ Knowledge of FDA, EMA, ICH guidelines, and cGMP regulations.
Work Environment
This position involves office/desk work in a Monday-Friday role with normal day hours. Flexibility is offered as long as core hours are met. You will have the opportunity to work with large-scale biological and chemistry pharma operations, contributing to impactful work that supports making biologics used for pharmaceutical products.
Pay and Benefits
The pay range for this position is $42.00 - $72.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Saint Louis,MO.
Application Deadline
This position is anticipated to close on Aug 28, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.
Sr. Quality Engineer (Pharmaceuticals)
Posted 3 days ago
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Job Description
Job Description
We are seeking a highly experienced and motivated Quality Engineer to join our pharmaceutical manufacturing team. The ideal candidate will have a strong experience in quality assurance within the pharmaceutical industry, with a comprehensive understanding of regulatory requirements, quality systems, and process improvements. This role is critical to ensuring compliance with all relevant regulations and standards, leading quality initiatives, and supporting the manufacturing of pharmaceutical products.
Responsibilities
+ Develop, implement, and maintain Quality Management Systems (QMS) in compliance with FDA, EMA, ICH guidelines, and other regulatory requirements.
+ Ensure all processes and products comply with applicable regulatory standards, including cGMP.
+ Lead continuous improvement initiatives to enhance product quality, efficiency, and compliance.
+ Oversee validation activities, including equipment, process, and cleaning validations, ensuring compliance with industry standards.
+ Conduct thorough investigations into quality issues, perform root cause analysis, and implement corrective and preventive actions (CAPA).
+ Plan and conduct internal audits, support external regulatory inspections, and manage responses to audit findings.
+ Evaluate and qualify suppliers, conduct supplier audits, and ensure supplier compliance with quality standards.
+ Maintain accurate and comprehensive quality documentation, including SOPs, batch records, and validation protocols.
+ Mentor and develop junior quality engineers and quality assurance staff, fostering a culture of continuous improvement and quality excellence.
+ Perform risk assessments and implement risk mitigation strategies related to product quality and regulatory compliance.
+ Work closely with cross-functional teams, including R&D, manufacturing, and regulatory affairs, to ensure quality considerations are integrated into all phases of product development and production.
Essential Skills
+ 7-10 years of experience in Quality Assurance within a FDA/GMP environment (pharmaceutical or medical device industry required).
+ Bachelor's degree in a scientific field (Life Sciences, Biotechnology, or equivalent) is required.
+ Proficiency in quality management software, statistical analysis tools, and methodologies such as Six Sigma and Lean.
+ Strong understanding of Quality Management Systems.
+ Experience with Quality Systems including change control, root cause analysis, deviations, documentation management, and training systems.
+ Experience with electronic Quality and Training Management Systems.
+ Previous experience with hosting client audits and/or regulatory inspections required with excellent communication skills.
Additional Skills & Qualifications
+ Certified Quality Engineer (CQE) or Certified Quality Auditor certification preferred.
+ Knowledge of FDA, EMA, ICH guidelines, and cGMP regulations.
Work Environment
This position involves office/desk work in a Monday-Friday role with normal day hours. Flexibility is offered as long as core hours are met. You will have the opportunity to work with large-scale biological and chemistry pharma operations, contributing to impactful work that supports making biologics used for pharmaceutical products.
Pay and Benefits
The pay range for this position is $42.00 - $72.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Saint Louis,MO.
Application Deadline
This position is anticipated to close on Aug 25, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.
Security GSOC Operator Pharmaceuticals
Posted 8 days ago
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Allied Universal is Currently Hiring a Full Time GSOC Operator for a Pharma Company in Boston MA
Sunday - Thursday 11 PM - 7 AM
Starting Pay is $24.00 Per Hour / Paid Orientation / Paid Training / Opportunity For Advancement
Candidate is Required to Have 2+ Years of Previous Security Experience
As a GSOC Operator, you will serve and safeguard clients in a range of industries such as Commercial Real Estate, Healthcare, Education, Government and more. The Global Security Operations Center (GSOC) Operator, under guidance of GSOC Supervisor, is responsible for assisting company personnel in all concerns that pertain to safety and security for corporate locations around the globe. The individual will work in a GSOC environment, monitoring several screens. The Operator will use a variety of tools that range from access control and alarm monitoring systems to various business intelligence sources, open-source media, Internet, and in-house tools. The Operator is required to detect, analyze, and alert others of any incidents which may impact the client's people, products, property, or brand image. These may range from extreme weather conditions, political instability, crime, terror, to technical failures.
**RESPONSIBILITIES:**
+ Provide customer service to our clients by carrying out safety and security procedures, site-specific policies and when appropriate, emergency response activities
+ Respond to incidents and critical situations in a calm, problem solving manner
+ Investigate alarms and respond by sending security patrol, or alerting Fire services or Police as needed
+ Assist company employees in all concerns that pertain to safety and security
+ Monitor travel safety and security of company's employees
**QUALIFICATIONS:**
+ Be at least 18 years of age for unarmed roles; 21+ years of age for armed roles
+ Possess a high school diploma or equivalent, or five (5) years of verifiable experience
+ Minimum of two (2) years of military, law enforcement, government, or security experience
+ As a condition of employment, applicants will be subject to a background investigation in accordance with all federal, state, and local laws. Allied Universal will consider qualified applications with criminal histories in a manner consistent with applicable laws.
+ Licensing requirements are subject to state and/or local laws and regulations and may be required prior to employment.*A valid driver's license will be required for driving positions only
**BENEFITS:**
+ Medical, dental, vision, basic life, AD&D, and disability insurance
+ Enrollment in our company's 401 (k) or Supplemental Income Plan, subject to eligibility requirements
+ Eight paid holidays annually, five sick days, and four personal day
+ 40 hours of vacation after one year of employment at eligible work assignments. Unused vacation is only paid out where required by law.
Allied Universal® is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race/ethnicity, age, color, religion, sex, sexual orientation, gender identity, national origin, genetic information, disability, protected veteran status or relationship/association with a protected veteran, or any other basis or characteristic protected by law. For more information: you have any questions regarding Equal Employment Opportunity, have difficulty using the online system and require an alternate method to apply, or require an accommodation at any time during the recruitment and/or employment process, please contact our local Human Resources department. To find an office near you, please visit: Universal® is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race/ethnicity, age, color, religion, sex, sexual orientation, gender identity, national origin, genetic information, disability, protected veteran status or relationship/association with a protected veteran, or any other basis or characteristic protected by law. For more information: you have any questions regarding Equal Employment Opportunity, have difficulty using the online system and require an alternate method to apply, or require an accommodation at any time during the recruitment and/or employment process, please contact our local Human Resources department. To find an office near you, please visit: ID:** 2025-1414388
**Location:** United States-Massachusetts-Boston
**Job Category:** Security Officer
Principal Scientist, Bio-Pharmaceuticals
Posted today
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Senior Research Scientist - Pharmaceuticals
Posted today
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Job Description
Key responsibilities include designing and conducting experiments to identify and validate drug targets, synthesizing and characterizing potential drug candidates, and performing in vitro and in vivo studies to assess efficacy and safety. You will be adept at analyzing complex biological and chemical data, utilizing sophisticated analytical techniques and instrumentation. The ideal candidate will possess a Ph.D. in Pharmacology, Medicinal Chemistry, or a related life sciences discipline, with a strong publication record and significant experience in pharmaceutical R&D. Essential skills include expertise in drug discovery methodologies, understanding of regulatory requirements, and a proven ability to manage research projects independently. You will collaborate closely with chemists, biologists, and clinical researchers to advance drug development programs. This position offers a challenging and rewarding opportunity to contribute to the development of life-saving medicines within a dynamic research environment in Jacksonville, Florida, US .
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Senior Research Scientist - Pharmaceuticals
Posted today
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Qualifications:
- Ph.D. in Pharmacology, Biochemistry, Molecular Biology, or a related life science discipline.
- 5+ years of postdoctoral or industry research experience in pharmaceutical R&D.
- Proven expertise in drug discovery and development processes.
- Strong track record of scientific publications and presentations.
- Proficiency in relevant laboratory techniques and instrumentation.
- Excellent data analysis and interpretation skills.
- Ability to lead research projects and mentor junior scientists.
- Strong collaboration and communication skills.
Senior Formulation Scientist - Pharmaceuticals
Posted today
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Job Description
Responsibilities:
- Lead the design and execution of formulation development studies for new chemical entities (NCEs) and existing products.
- Develop robust and scalable formulations for various dosage forms, with a focus on oral solid dosage forms (tablets, capsules) and potentially extended-release systems.
- Conduct pre-formulation studies, including physicochemical characterization of drug substances and excipients.
- Perform compatibility studies, stability testing, and dissolution profiling for developed formulations.
- Investigate and troubleshoot formulation challenges, proposing creative and scientifically sound solutions.
- Optimize formulations to achieve desired pharmacokinetic profiles, bioavailability, and manufacturability.
- Collaborate closely with analytical development, process development, and regulatory affairs teams.
- Prepare comprehensive formulation development reports, technical documents, and regulatory submission materials.
- Stay current with advances in pharmaceutical sciences, drug delivery technologies, and relevant regulatory guidelines.
- Mentor junior scientists and provide technical guidance on formulation development projects.
- Contribute to the strategic planning of formulation development activities within the R&D organization.
- Ensure all activities comply with GMP, GLP, and relevant safety standards.
Qualifications:
- Ph.D. or Master's degree in Pharmaceutics, Pharmaceutical Sciences, Chemistry, or a related field.
- Minimum of 7 years of experience in pharmaceutical formulation development, with a strong emphasis on solid dosage forms.
- Demonstrated expertise in designing, developing, and optimizing oral dosage forms.
- In-depth knowledge of excipient selection, drug-excipient compatibility, and formulation techniques.
- Experience with analytical techniques used for characterizing drug substances and formulated products (e.g., HPLC, dissolution testing, particle size analysis).
- Familiarity with GMP/GLP regulations and their application in formulation development.
- Excellent problem-solving, analytical, and critical thinking skills.
- Strong communication, presentation, and interpersonal skills.
- Proven ability to manage multiple projects simultaneously and work effectively in a cross-functional team environment.
- Experience with advanced drug delivery systems (e.g., controlled release, nanomedicine) is a plus.
- A proactive approach to learning and staying updated with scientific advancements.
Our client offers a competitive compensation package, excellent benefits, and opportunities for professional growth within a leading pharmaceutical innovator. Shape the future of medicine.
Senior Formulation Scientist - Pharmaceuticals
Posted 1 day ago
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Key responsibilities include designing and executing pre-formulation studies, developing solid oral dosage forms, sterile injectables, or topical formulations, depending on project needs. You will conduct stability studies, compatibility testing, and analytical method development to support formulation characterization. This role involves troubleshooting formulation challenges, optimizing existing formulations, and scaling up processes from laboratory to pilot and commercial scales. You will be responsible for preparing comprehensive development reports, documenting experimental procedures, and ensuring compliance with regulatory guidelines (e.g., FDA, ICH). Collaboration with analytical development, quality assurance, regulatory affairs, and manufacturing departments will be integral to your success. You will also mentor junior scientists and contribute to the scientific strategy of the formulation development group.
Essential qualifications include a Master's or Ph.D. in Pharmaceutical Sciences, Chemistry, Chemical Engineering, or a related field. A minimum of 5-7 years of progressive experience in pharmaceutical formulation development, with a focus on a specific dosage form (e.g., oral solids, injectables), is required. Expertise in a wide range of formulation techniques and analytical methods (HPLC, GC, dissolution testing, particle size analysis) is mandatory. Proven experience with solid state characterization and excipient selection is essential. Knowledge of cGMP principles and regulatory requirements for drug development is critical. Excellent problem-solving skills, strong project management capabilities, and outstanding written and verbal communication skills are paramount. Join our innovative team in Columbus, Ohio, US and contribute to the development of life-changing medicines.