Hikma Pharmaceuticals
Manager, Regulatory Affairs - U.S. Animal Health
Hikma Pharmaceuticals, Berkeley Heights, New Jersey, us, 07922
Manager, Regulatory Affairs - U.S. Animal Health
Location:
Berkeley Heights, NJ or Columbus, OH
Job Type:
Full Time
About Us 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 around the world. We are a trusted, reliable partner and dependable source of over 760 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 global footprint of 30+ manufacturing plants, 8+ R&D centers, and 9,000+ empowered employees, we are committed to making high‑quality medicines accessible to the people who need them.
Position Overview 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 Manager, Regulatory Affairs – U.S. Animal Health to join our team. In this role, you will lead regulatory strategy and execution for Hikma’s veterinary pharmaceutical portfolio, including injectables and oral solids. The role ensures compliance with applicable regulations, supports product development, registration and lifecycle management, and serves as liaison between the company and regulatory authorities. The ideal candidate will bring deep animal health regulatory expertise, strong project leadership, and a collaborative mindset to drive successful regulatory outcomes. This role will start as an individual contributor with the aim of supporting the build‑out of the animal health function at Hikma. Occasional travel to regulatory meetings or manufacturing sites will be required.
Key Responsibilities
Develop and implement regulatory strategies for new and existing animal health pharmaceutical products
Prepare and manage regulatory submissions (e.g., JINAD, NADA, ANADA, supplements) to FDA‑CVM authorities
Oversee the maintenance and accuracy of technical regulatory information to ensure high‑quality, compliant submissions
Ensure ongoing compliance throughout the product lifecycle
Serve as animal health subject matter expert on cross‑functional project teams and connect with other Hikma global regulatory experts, providing animal health‑specific guidance from early development through lifecycle, offering strategic leadership and counsel across Clinical, Quality, and Business Development functions
Provide regulatory insight by, in coordination with the Legal function, interpreting legislation and translating it into clear, actionable guidance to improve project outcomes and predictability
Facilitate scientific advice and pre‑submission consultations
Prepare and lead meetings with regulatory authorities
Monitor emerging regulatory changes and assess impact on Hikma’s animal health portfolio
Manage regulatory documentation and ensure accuracy and completeness
Mentor other regulatory staff and contribute to team development
Prepare risk assessments and regulatory evaluations for complex issues
Maintain relationships with all regulatory bodies for animal health
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:
Bachelor’s or Master’s degree in life sciences, veterinary medicine, or related field.
Minimum 5 years of regulatory affairs experience in the animal health pharmaceutical industry
Strong knowledge of FDA‑CVM regulations and submission pathways
Experience with pharmaceutical product development and lifecycle management
Excellent communication, organizational, and project management skills
Experience with clinical trial requirements is a plus
Preferred Qualifications
Some experience with global regulatory submissions (e.g., EU, Canada)
Familiarity with eCTD and electronic submission platforms
Ability to interpret complex regulatory requirements and translate them into actionable strategies
Fluent in English; additional languages are a plus for global roles
Compensation Base Salary:
$120,000 to $180,000 annually. The compensation for this position will be determined during the interview process and will vary based on multiple factors, including, but not limited to, work location, prior experience and job‑related knowledge, relevant skills and expertise, current business needs, and market factors. The Talent Acquisition team can provide more details about the specific salary range for the job location during the hiring process.
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 3% 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 HumanResources 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.
#J-18808-Ljbffr
Berkeley Heights, NJ or Columbus, OH
Job Type:
Full Time
About Us 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 around the world. We are a trusted, reliable partner and dependable source of over 760 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 global footprint of 30+ manufacturing plants, 8+ R&D centers, and 9,000+ empowered employees, we are committed to making high‑quality medicines accessible to the people who need them.
Position Overview 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 Manager, Regulatory Affairs – U.S. Animal Health to join our team. In this role, you will lead regulatory strategy and execution for Hikma’s veterinary pharmaceutical portfolio, including injectables and oral solids. The role ensures compliance with applicable regulations, supports product development, registration and lifecycle management, and serves as liaison between the company and regulatory authorities. The ideal candidate will bring deep animal health regulatory expertise, strong project leadership, and a collaborative mindset to drive successful regulatory outcomes. This role will start as an individual contributor with the aim of supporting the build‑out of the animal health function at Hikma. Occasional travel to regulatory meetings or manufacturing sites will be required.
Key Responsibilities
Develop and implement regulatory strategies for new and existing animal health pharmaceutical products
Prepare and manage regulatory submissions (e.g., JINAD, NADA, ANADA, supplements) to FDA‑CVM authorities
Oversee the maintenance and accuracy of technical regulatory information to ensure high‑quality, compliant submissions
Ensure ongoing compliance throughout the product lifecycle
Serve as animal health subject matter expert on cross‑functional project teams and connect with other Hikma global regulatory experts, providing animal health‑specific guidance from early development through lifecycle, offering strategic leadership and counsel across Clinical, Quality, and Business Development functions
Provide regulatory insight by, in coordination with the Legal function, interpreting legislation and translating it into clear, actionable guidance to improve project outcomes and predictability
Facilitate scientific advice and pre‑submission consultations
Prepare and lead meetings with regulatory authorities
Monitor emerging regulatory changes and assess impact on Hikma’s animal health portfolio
Manage regulatory documentation and ensure accuracy and completeness
Mentor other regulatory staff and contribute to team development
Prepare risk assessments and regulatory evaluations for complex issues
Maintain relationships with all regulatory bodies for animal health
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:
Bachelor’s or Master’s degree in life sciences, veterinary medicine, or related field.
Minimum 5 years of regulatory affairs experience in the animal health pharmaceutical industry
Strong knowledge of FDA‑CVM regulations and submission pathways
Experience with pharmaceutical product development and lifecycle management
Excellent communication, organizational, and project management skills
Experience with clinical trial requirements is a plus
Preferred Qualifications
Some experience with global regulatory submissions (e.g., EU, Canada)
Familiarity with eCTD and electronic submission platforms
Ability to interpret complex regulatory requirements and translate them into actionable strategies
Fluent in English; additional languages are a plus for global roles
Compensation Base Salary:
$120,000 to $180,000 annually. The compensation for this position will be determined during the interview process and will vary based on multiple factors, including, but not limited to, work location, prior experience and job‑related knowledge, relevant skills and expertise, current business needs, and market factors. The Talent Acquisition team can provide more details about the specific salary range for the job location during the hiring process.
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 3% 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 HumanResources 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.
#J-18808-Ljbffr