Regulatory Affairs Associate at Phibro

Job Description:

Latest job information from Phibro for the position of Regulatory Affairs Associate. If the Regulatory Affairs Associate vacancy in Sligo matches your qualifications, please submit your latest application or CV directly through the updated Jobkos job portal.

Please note that applying for a job may not always be easy, as new candidates must meet certain qualifications and requirements set by the company. We hope the career opportunity at Phibro for the position of Regulatory Affairs Associate below matches your qualifications.

About Phibro Animal Health Corporation

Phibro Animal Health Corporation is a publicly traded, global organization with a rich history in animal health and nutrition as a manufacturer and marketer of medicated feed additives, vaccines, nutritional specialty products, and mineral nutrition. We strive to be a trusted partner with livestock producers, farmers, veterinarians, and consumers who raise or care for farm and companion animals by providing solutions to help them maintain and enhance the health of their animals.

Phibro is a diversified company in manufacturing and marketing products for ethanol performance, microbials for plants, home and industrial applications, and specialty chemicals for various industrial markets. In addition to, Phibro's revenues are in excess of $1 billion and are supported by over 2,300 employees worldwide.

At Phibro, people are our greatest asset. We strive to develop a diverse workforce that fosters an environment where people feel supported in openly sharing their creativity and skills that allows them to be the most successful that they can be.

If you are interested in working for Phibro and feel that you do not meet all qualifications, we encourage you to apply as you might be the right candidate for this role or other positions.

The Regulatory Affairs Associate is an integral part of our Regulatory Affairs team based out of our Ireland - Sligo site.

Key requirements:

    Understanding of the international and European Veterinary Medicines regulatory framework and guidelines.    Understanding of the Regulatory Submission procedures in EU and the international area.     Understanding of the Labelling and artwork management     Technical knowledge about Veterinary Medicines quality/safety/efficacy requirements.

Responsibilities:    Provide regulatory support for the company's veterinary vaccine portfolio.    Support all regulatory aspects of assigned projects in accordance with the business strategy, priorities and timelines.     Establish and maintain effective working relationships with other PAHC business units (Manufacturing, Quality and Marketing) to ensure regulatory perspectives are incorporated into business plans.    Supports all types of product lifecycle activities     Supports writing responses to questions raised by regulatory authorities.    Prepare and organize the regulatory package submission to the different countries (international area)     Cross functions support: o    Supports quality in implementing Regulatory authorities approvals, o    Supports Supply chain with regulatory information on the productso    Supports CCP process by assessing impact of the changes on existing registrations and implement the variation processo    Ensures the Artwork management process is under control, approved artworks are communicated to the right stakeholders on time, 

Education & Experience:Minimum of a bachelor's degree in a relevant scientific or veterinary discipline, At least 3-5 years' experience in international pharmaceutical industry, including experience in regulatory. Ideally experience with veterinary vaccines and/or products derived using rDNA technology. Proficient in scientific written and spoken English. Additional language skills are a plus.

Personal attributes:Self-starter takes initiative.Team player essential,Ability to handle several projects simultaneously.Good organizational, prioritization and time management skills. Can work effectively under pressure.Excellent attention to detail.Proactive: identify regulatory risks and propose solutions.Demonstrate integrity.

To learn more about Phibro Animal Health's competitive benefits package, please click here: Phibro Benefits. 

Phibro is an Equal Opportunity Employer

All qualified applicants will receive consideration for employment without regard to race, national origin, gender, age, religion, disability, sexual orientation, gender identity, veteran status, marital status or any other characteristics protected by law.

Business Unit: Animal Health & Mineral Nutrition   Division: Animal Health & Nutrition Department: Regulatory Affairs Location: Ireland - Sligo Work Schedule: Monday - Friday (40 Hours) 

Job Info:

• Company: Phibro
• Position: Regulatory Affairs Associate
• Work Location: Sligo
• Country: IE

How to Submit an Application:

After reading and understanding the criteria and minimum qualification requirements explained in the job information Regulatory Affairs Associate at the office Sligo above, immediately complete the job application files such as a job application letter, CV, photocopy of diploma, transcript, and other supplements as explained above. Submit via the Next Page link below.