Catalent is looking to hire a Senior Associate, Regulatory Affairs to join a growing team in Madison, WI.
The Senior Associate, Regulatory Affairs position requires a variety of skills necessary for biotech company operations. The Senior Associate, Regulatory Affairs is expected to possess an understanding of regulations and compliance and can conduct work within cGMP guidelines.
The Senior Associate, Regulatory Affairs will assist in preparation and implementation of company regulatory policies and quality systems. The position is responsible for supporting efforts to ensure the site follows applicable regulations, ICH guidance's and industry expectations, and works in direct collaboration with Manufacturing Operations and Quality Assurance in support of that effort.
In concert with Catalent’s Patient First philosophy, Quality Assurance safeguards all systems, processes and actions to ensure regulatory compliance is met, which is essential in the manufacture of quality products. These products are delivered for use in our customer’s clinical studies, which promote future marketed medicines.
Provides technical support in response to customer’s regulatory filings and requests.
Maintains site registrations at the state and federal level, as necessary.
Drafts, edits and maintains Quality Agreements.
Executes and/or reviews change controls as necessary.
Assists in the creation and revision of Standard Operating Procedures as necessary.
Provides data and reports to customers in support of Annual Product Reviews.
Ensures robust investigation into customer complaints, including root cause determination, and timely closure and reporting.
Master's Degree in technical discipline (e.g. biology, biotechnology, engineering) or related life science; or
Bachelor's Degree in technical discipline (e.g. biology, biotechnology, engineering) or related life science with minimum of 3 years’ of related experience; or
Associate’s Degree in technical discipline (e.g. biology, biotechnology, engineering) or related life science with minimum 4 years’ of related experience.
Catalent’s standard leadership competencies that are used to interview and for Performance & Development:
Leads with Integrity and Respect
Demonstrates Business Acumen
Fosters Collaboration and Teamwork
Engages and Inspires
Coaches and Develops
Potential for career growth within an expanding Quality team
Defined career path and annual performance review & feedback process
Cross functional exposure to other areas of Quality
Medical, Dental, Vision, and 401K are all offered from day one of employment
19 days of paid time off annually + 7 paid holidays
Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
Catalent is an Equal Opportunity / Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status, sexual orientation or gender identity. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email along with the job number and title to Jobs@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be routed to a recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Internal Number: 0027260
Catalent offers rewarding opportunities to further your career – join the global drug development and delivery leader! You will help develop some of the nearly 200 products we launch each year or help supply some of the over 7,000 products for patients around the world. Our highly skilled, dedicated global team of over 9,500 is passionate about improving the health of patients by combining their personal expertise with advanced technologies to advance science and supply innovative new products of the highest quality to patients globally.