Research and Development Pharmacist at AP MAX INC

Houston, Texas, United States -

Full Time

Start Date

Immediate

Expiry Date

13 May, 26

Salary

135000.0

Posted On

12 Feb, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Formulation Development, Stability Testing, Analytical Methods, Problem-Solving, Attention to Detail, Documentation Skills, Collaboration, Regulatory Compliance, Research, Product Development, Quality Assurance, Technical Guidance, Continuous Improvement, Innovation, Project Management, Compounding Pharmacy

Industry

Retail Pharmacies

Description

Company Overview At Allia Health, the umbrella organization for Southend Pharmacy, Brello Health, and Woven, we don’t just follow industry trends—we redefine them. Our mission is to commoditize anti-aging solutions, making them affordable and accessible to the average consumer—not just the wealthy. By offering customized and cost-effective wellness products that follow cost-containment models, we aim to improve people’s quality of life and meet them wherever they are on their health journey. About Southend Pharmacy At Southend Pharmacy, we are dedicated to delivering exceptional pharmacy services that uphold the highest standards of compliance, safety, and patient care. As a growing organization, we are seeking a detail-oriented and skilled Research and Development Pharmacist to support the Research and Development Manager with the development of new compounded products in alignment with business goals and regulatory requirements. Job Summary The Research & Development (R&D) Pharmacist is responsible for the development, optimization, and validation of pharmaceutical formulations and processes. This role partners closely with pharmacy operations, quality, regulatory, and leadership teams to design safe, compliant, and scalable formulations that meet clinical, business, and regulatory requirements. Key Responsibilities Formulation & Product Development * Design, develop, and optimize new and existing pharmaceutical formulations (sterile and/or non-sterile). * Conduct formulation trials, stability studies, compatibility testing, and feasibility assessments. * Select appropriate APIs, excipients, delivery systems, and packaging components. * Troubleshoot formulation, process, or stability challenges and recommend improvements. Research & Testing * Research and identify potential future product opportunities. * Design and execute bench-scale and pilot-scale experiments. * Analyze and interpret data from formulation and stability studies. * Maintain thorough documentation of experiments, results, and conclusions. * Stay current with scientific literature, compounding trends, and emerging technologies. Regulatory & Compliance * Ensure all R&D activities comply with USP , , , FDA guidance, and applicable state regulations. * Develop and review SOPs, master formulation records (MFRs), and validation documentation. * Support regulatory submissions, internal audits, and inspections as needed. Cross-Functional Collaboration * Collaborate with operations to transfer formulations into production. * Partner with Quality Assurance on investigations, deviations, and CAPAs related to formulations. * Provide technical guidance and training to pharmacists and technicians. * Support clinical, sales, or customer-facing teams with product knowledge when needed. Continuous Improvement & Innovation * Identify opportunities to improve product quality, efficiency, and scalability. * Evaluate new ingredients, technologies, and equipment. * Participate in strategic planning for product pipelines and innovation initiatives. Qualifications Required * Doctor of Pharmacy (PharmD) or Bachelor of Science in Pharmacy required. * 2–5+ years of experience in pharmaceutical R&D, compounding pharmacy, or formulation development preferred. * Working knowledge of USP , , and * Demonstrated expertise in formulation development, stability testing, formulation troubleshooting, and analytical methods. Preferred * Board Certification in Sterile Compounding (BCSCP) or equivalent preferred. * Experience with peptides, hormones, injectables, or complex dosage forms. * Hands-on experience with sterile and/or non-sterile compounding strongly preferred. Knowledge and Skills * Strong analytical and problem-solving ability * Ability to manage multiple projects and meet deadlines. * Meticulous attention to detail * Excellent documentation skills Physical Requirements * Ability to sit for extended periods of time at a desk and working on a computer. * Ability to communicate effectively in person, over the phone, or via virtual meeting. * Ability to maintain focus in a typical office environment with moderate noise levels. * Ability to perform repetitive motions with hands and arms, such as typing. Benefits * Salary Range: $125,000 - $135,000 annually. * Work Arrangement: Onsite * Comprehensive benefits package including medical, dental, paid time off. * 401(k) retirement savings plan. * Eligible for quarterly bonus based on performance and departmental goals. Allia Health Group is unable to offer visa sponsorship at this time. Candidates must be legally authorized to work in the United States without current or future sponsorship. Equal Opportunity Employer Statement Allia Health Group is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status. If you have any questions or require accommodations during the application process, please contact hr@alliahealth.co [hr@alliahealth.co]. Standard hours 8-5

Responsibilities

The R&D Pharmacist is responsible for the development, optimization, and validation of pharmaceutical formulations and processes. This role involves collaborating with various teams to ensure formulations meet clinical, business, and regulatory requirements.