Formulation Development Cmc Jobs (NOW HIRING)

Job Title: Sr. Scientist, Formulation Development

Location: Columbus, OH

Job Type: Full time

Req ID: 11881

As a developer, manufacturer, and supplier of essential medicines, Hikma Pharmaceuticals USA Inc. and its affiliates’ mission is to bring Better Health. Within Reach. Every Day.® for millions of patients around the world. We are a trusted, reliable partner and dependable source of over 800 high-quality generic, specialty and branded pharmaceutical products that hospitals, physicians and pharmacists need to treat their patients across North America, the Middle East, North Africa and Europe. Through our 32 manufacturing plants, three R&D centers, and 9,500+ employees worldwide, we are always hard at work creating high-quality medicines and making them accessible to the people who need them.

We are committed to building a diverse and inclusive team and encourage applications from candidates of all backgrounds. We are seeking a talented and motivated Sr. Scientist, Formulation Development to join our team.

Hikma is expanding its orally inhaled and nasal drug product (OINDP) capability, and we're looking for a formulation scientist who wants to work on technically demanding, high-impact programs from early development through to regulatory submission and launch. This role sits within our growing OINDP formulation team and will be pitched at level depending on your experience. What matters most is depth of knowledge, scientific rigor, and the ability to work at pace across a commercially oriented pipeline.

• Design and execute formulation development studies for OINDPs, applying QbD principles throughout
• Lead or contribute to CMC sections of regulatory dossiers (ANDA, NDA, 505(b)(2) — formulation development reports, excipient justifications, comparability studies. Draft controlled correspondence and responses to project specific deficiency letters as needed.
• Characterize formulations using methods relevant to OINDP: particle size, aerodynamic performance (NGI/ACI), spray geometry, viscosity, osmolality, and related physical chemistry
• Support Bioequivalence strategy development, including, IVIVC, biowaiver arguments, and Q1/Q2/Q3 sameness justifications
• Analyze and interpret experimental data using relevant tools (e.g. JMP, Minitab, Python, or Excel) to draw clear scientific conclusions, identify trends, and define the next cycle of formulation or process development with confidence
• Collaborate with device/engineering teams on product–device compatibility and human factors considerations
• Drive tech transfer and scale-up activities, including work with CDMOs
• Author and review protocols, batch records, and CMC documentation to GMP/GLP standards. Manufacture developmental and clinical (pilot / registration) batches.

We value the skills and experiences candidates bring to the table. While we have listed some qualifications below, we encourage candidates to apply even if they do not meet all of them:

• Bachelor’s Degree (Pharmaceutical Sciences, Chemistry, Chemical Engineering) plus a minimum 4 yrs experience with the following:
  • Hands-on OINDP formulation development experience or drug-device formulation is particularly valued. Experience in formulation development of pharmaceutical dosage forms is valued. OR
• Master’s degree (Pharmaceutical Sciences, Chemistry, Chemical Engineering) plus a minimum 2 years of experience with the following:
  • Hands‑on OINDP formulation development experience or drug‑device formulation is particularly valued. Experience in formulation development of pharmaceutical dosage forms is valued. OR
• PhD (Pharmaceutical Sciences, Chemistry, Chemical Engineering) plus minimum 1 years of experience with the following:
  • Hands‑on OINDP formulation development experience or drug‑device formulation is particularly valued. Experience in formulation development of pharmaceutical dosage forms is valued.
• Working knowledge of ICH guidelines and FDA/EMA expectations for OINDP
• Experience in working to cGMP and compliance requirements is desirable but not essential.
• Experience with excipient selection and justification (preservative systems, antioxidants, tonicity agents).
• Ability to work effectively across formulation, analytical, clinical, QA, operations, IP, and regulatory functions.

• Experience with scale up in GMP environment
• Experience with regulatory submissions (ANDA / NDA)
• Knowledge (understanding and interpretation) of analytical characterization techniques
• Experience with good documentation practices for GMP batches
• Experience with use of statistical tools in data analysisKnowledge of in‑vitro in‑vivo correlation

• Annual performance bonus, commission, and share potential
• Auto enrollment in a Hikma-sponsored 401(k) program at a pre‑tax contribution rate of 4% of eligible pay. Hikma will match 100% of the first 6% of eligible pay that you contribute
• A generous paid time off (PTO) bank starting with 20 days (prorated based on hire date). Additional days granted upon reaching work milestone anniversaries
• 3 personal days (prorated based on hire date)
• 11 company paid holidays
• Comprehensive benefits including health, dental, vision, mental health, disability, life insurance, prescription drug coverage, and a variety of voluntary benefits
• Employee discount program
• Wellbeing rewards program
• Safety and Quality is a top organizational priority
• Career advancement and growth opportunities
• Tuition reimbursement
• Paid maternity and parental leave
• Eligibility requirements apply to some benefits and depend on the job classification, role, and length of employment. Benefits are subject to change as well as specific plan or program terms.

Hikma Pharmaceuticals USA Inc. is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status, or other characteristics protected by law.