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Hikma Pharmaceuticals PLC

Sr. Scientist

Cherry Hill, NJ · On-site

$56.95K - $95K/yr

As a developer, manufacturer, and supplier of essential medicines, Hikma Pharmaceuticals USA Inc. and its affiliates' purpose is to put better health within reach, every day for millions of patients ...

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What are the key skills and qualifications needed to thrive as a professional at Hikma Pharmaceuticals, and why are they important?

To thrive at Hikma Pharmaceuticals, you generally need a background in pharmaceutical sciences, chemistry, or a related field, often supported by relevant degrees or industry experience. Familiarity with Good Manufacturing Practices (GMP), quality control systems, and regulatory compliance tools is typically required. Strong analytical thinking, attention to detail, and effective teamwork are valued soft skills in this environment. These skills and qualities are important to ensure product quality, regulatory adherence, and successful collaboration within the pharmaceutical industry.

What are some common challenges faced by professionals working at Hikma Pharmaceuticals, and how can new hires best navigate them?

Professionals at Hikma Pharmaceuticals often work in a fast-paced, highly regulated environment where adapting to evolving compliance standards and strict deadlines is essential. New hires may encounter challenges in keeping up with regulatory requirements and collaborating across diverse, cross-functional teams. To navigate these challenges, it's important to proactively seek guidance from experienced colleagues, stay updated on industry regulations, and develop strong communication skills to foster effective teamwork. Embracing a culture of continuous learning and being open to feedback can also help new employees succeed and grow within the company.

What are Hikma jobs?

Hikma jobs refer to employment opportunities at Hikma Pharmaceuticals, a global pharmaceutical company specializing in the development, manufacture, and marketing of generic, branded, and injectable medicines. Positions at Hikma span various fields including research and development, manufacturing, quality assurance, regulatory affairs, sales, and corporate roles. Employees at Hikma work to ensure the delivery of high-quality medications to patients worldwide. The company offers opportunities for career growth, training, and working in a diverse, international environment.

What is the difference between Hikma vs Pharmacist?

AspectHikmaPharmacist
Required CredentialsTypically requires a degree in pharmacy or related field, licensing varies by countryRequires a pharmacy degree and licensure to practice
Work EnvironmentPharmaceutical manufacturing, quality control, or research settingsCommunity pharmacies, hospitals, clinics
Employer & Industry UsagePharmaceutical companies, research labs, manufacturing plantsHealthcare facilities, retail pharmacies
Common Search & Comparison IntentUnderstanding roles in pharmaceutical industry, career optionsPatient care, medication dispensing, healthcare services

Hikma generally refers to a pharmaceutical company involved in drug manufacturing and research, whereas a Pharmacist is a healthcare professional responsible for dispensing medications and advising patients. While both are connected to the pharmaceutical industry, Hikma focuses on production and development, and Pharmacists on patient care and medication management.

What cities are hiring for Hikma jobs? Cities with the most Hikma job openings:
What states have the most Hikma jobs? States with the most job openings for Hikma jobs include:
What job categories do people searching Hikma jobs look for? The top searched job categories for Hikma jobs are:
Hikma jobs near you
Infographic showing various Hikma job openings in the United States as of May 2026, with employment types broken down into 3% Internship, 92% Full Time, 3% Part Time, and 2% Nights. Highlights an 100% Physical job distribution.
Director, Formulation Development (Respiratory, Nasal & Semi-Solid Liquids)

Director, Formulation Development (Respiratory, Nasal & Semi-Solid Liquids)

Hikma Pharmaceuticals PLC

Columbus, OH • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 14 days ago

Hikma Pharmaceuticals rating

7.8

Company rating: 7.8 out of 10

Based on 27 frontline employees who took The Breakroom Quiz

39th of 70 rated pharmaceutical

Job description

Job Title: Director, Formulation Development (Respiratory, Nasal & Semi-Solid Liquids)
Location: Columbus, OH
Job Type: Full time
Req ID: 11461
About Us:
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, eight 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.
Description:
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 Director, Formulation Development (Respiratory, Nasal & Semi-Solid Liquids) to join our team.
In this role, you will be responsible for scientific and strategic leadership for the formulation development of complex drug products, with a primary focus on respiratory, nasal, semi-solid, and liquid dosage forms. This role is accountable for formulation strategy from early development through commercialization and serves as a key technical authority across CMC programs. This is a significant opportunity to directly impact the development of safe, cost-effective medicines that will make better health within reach every day.
Key Responsibilities:
  • Regular and predictable onsite attendance and punctuality.
  • Lead formulation development for multiple inhalation (MDIs, DPIs, nebulized products), intranasal sprays and drops, semi-solids (topicals, gels, creams, ointments) plus liquid oral and topical products.
  • Define and execute formulation strategies aligned with product quality, manufacturability, and regulatory expectations.
  • Provide technical leadership on QbD, risk assessments, and control strategies.
  • Partner closely with Analytical, Device Development, Process Development, Clinical, Quality, and Regulatory Affairs.
  • Support preparation and review of CMC sections for INDs, NDAs/ANDAs, and global regulatory submissions.
  • Lead troubleshooting and scientific root-cause analysis for formulation and stability issues.
  • Build, mentor, and develop high-performing formulation teams.
  • Evaluate new technologies and approaches to enhance complex product differentiation.
  • Own the formulation department budget, ensuring optimal allocation of resources to strategic initiatives.
  • Monitor financial performance and ensure efficient use of funds across programs and scientific operations.

Qualifications:
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:
  • Bachelors Degree with relevant experience in Pharmaceutics, Pharmaceutical Sciences, Chemical Engineering, or related discipline.
  • Masters Degree with relevant experience in Pharmaceutics, Pharmaceutical Sciences, Chemical Engineering, or related discipline.
  • 12+ years of progressive experience in formulation development.
  • 2 years of experience with hands on expertise in respiratory and/or nasal drug delivery, strong experience with semi solid and liquid formulations.
  • Proven track record supporting CMC development through regulatory approval.
  • Prior experience leading scientific teams in a matrix environment.
  • Communication must be appropriate, timely, and accurate.
  • Strong planning and organizing skills & adaptable to changing priorities.
  • Expert in working to cGMP standards is essential.

Preferred Qualifications:
  • PhD with relevant experience in Pharmaceutics, Pharmaceutical Sciences, Chemical Engineering, or related discipline.

What We Offer*:
  • 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.
Recruiters:
Please note that Hikma has a set roster of approved recruiters for specific roles agreed to in advance and does not accept unsolicited resumes or calls from third-party recruiters or employment agencies regarding open positions. In the absence of a signed agreement and approval from Hikma's Human Resources department to submit resumes for a specific position, Hikma will not approve, nor will be under an obligation to make, any payment to such non-approved third-parties in the event a candidate they refer is hired by Hikma.
Equal Opportunity Employer:
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.
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