Planet Pharma
https://cdn.haleymarketing.com/templates/63514/logos/square.png
https://www.propharmagroup.com
https://www.propharmagroup.com
true
JOB OBJECTIVE: This leadership role requires an individual to specifically have the education and experience to plan, direct, and coordinate regulatory activities to support our drug development programs. This position provides expertise to ensure compliance with federal and state regulations across all functional areas of drug development. Strong knowledge of FDA regulations and submissions is required, as well as established experience interfacing with global regulatory agencies.
CORE DUTIES:
1. Apply strategic knowledge to small molecule drug development across all stages of a product’s lifecycle (pre-IND through post-licensure) and across functional disciplines (e.g., clinical, nonclinical pharmacology/toxicology, clinical pharmacology, CMC).
2. Skillfully lead communications with FDA and other global regulatory agencies (e.g., formal meetings, emails, etc.) to facilitate review and approval of submissions (including INDs and NDAs).
3. Develop, review, submit and follow all regulatory agency submission materials (e.g., initial IND applications, annual reports, clinical study reports, protocols, and amendments, MedWatch reports, etc.).
4. Proactively identify and address regulatory compliance issues. Formulate or implement regulatory affairs policies and procedures to ensure that regulatory compliance is maintained or enhanced.
5. Lead, develop, and implement CMC regulatory strategies to ensure on-time and high-quality submissions for Drug Master Files (DMFs), marketing applications (NDA/ANDA), and post-approval lifecycle submissions. Serve as main contact with regulatory agencies (e.g., FDA, DEA, EMA health authorities, state authorities, etc.) when needed for drug product development.
6. Manage a team of regulatory affairs staff to ensure the team delivers consistent and high-quality work products in a timely manner.
7. Communicate regulatory information to team members, partners, and other stakeholders and ensure that the information is interpreted and relayed correctly.
8. Attend meetings and engage with designated working teams and provide regulatory input and guidance to project teams, including quality control practices.
9. Demonstrates inclusion through their own words and actions and is accountable for a safe workspace. Acts with kindness, curiosity, and respect for others.
10. Embracing and being open to incorporating our 6 Emotional & Social Intelligence (ESI) core principles in daily work.
11. Understands and complies with ethical, legal, and regulatory requirements applicable to our business.
KEY QUALIFICATIONS:
1. Bachelor’s degree required, preferably in Regulatory Science or a health sciences field.
2. A minimum of fifteen years of experience in the pharmaceutical industry (small molecule) or a related area. (Proven 5 years in a senior leadership role with strong management skills).
3. Strong scientific or clinical research background required.
4. Demonstrated knowledge of regulatory affairs, such as 21 CFR 210/211/310/312/314, FDA guidance documents, and ICH guidelines for both development projects and commercial projects, with evidence of successful submissions to FDA, EMA, MHRA, or other health authorities
5. Demonstrated track record of preparing original INDs, NDAs, and amendments in compliance with applicable FDA regulations.
6. Demonstrated CMC regulatory experience with drug substance and/or drug product and API production.
7. Familiar with a variety of the field's concepts, practices, and procedures, including FDA guidance documents and ICH guidelines and GCP.
8. Ability to work in a cross-functional team environment with dynamic timelines and priorities.
9. Experience with DEA-regulated substances and clinical trials.
10. Strong knowledge of eCTD elements and format and submissions process and procedures.
11. Critical thinking/problem-solving, writing, oral communication and organizing skills and presentation skills.
12. Ability to rely on experience and judgment to plan and accomplish goals.
13. Ability to perform a variety of tasks, including conducting primary work as well as leading and directing the work of others. A wide degree of creativity and latitude is expected.
14. Experience working with all levels of management and key business stakeholders.
PREFERRED QUALIFICATIONS:
1. Master's degree in management of Drug Development, Regulatory Affairs, or similar field.
2. Professional certification in regulatory affairs (e.g., RAC or similar credential).
PHYSICAL DEMANDS:
1. Ability to use a computer/Microsoft Office applications.
2. Ability to remain stationary for several hours at a time.
Â
Diversity is important to us. We are proud to be an Equal Opportunity Employer, and make employment decisions without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, disability, or any other protected class.
Salary range: $200-$260k. Salary will be commensurate with experience.Â
Director, Regulatory Affairs
2800 Woods Hollow Rd Fitchburg, WI 53711 US
Posted: 10/06/2023
2023-10-06
2023-12-26
Employment Type:
Direct Hire/Perm
Job Category: Regulatory Sciences and Medical Writing
Job Number: 576796
Is job remote?: No
Country: United States
Job Description
JOB OBJECTIVE: This leadership role requires an individual to specifically have the education and experience to plan, direct, and coordinate regulatory activities to support our drug development programs. This position provides expertise to ensure compliance with federal and state regulations across all functional areas of drug development. Strong knowledge of FDA regulations and submissions is required, as well as established experience interfacing with global regulatory agencies.
CORE DUTIES:
1. Apply strategic knowledge to small molecule drug development across all stages of a product’s lifecycle (pre-IND through post-licensure) and across functional disciplines (e.g., clinical, nonclinical pharmacology/toxicology, clinical pharmacology, CMC).
2. Skillfully lead communications with FDA and other global regulatory agencies (e.g., formal meetings, emails, etc.) to facilitate review and approval of submissions (including INDs and NDAs).
3. Develop, review, submit and follow all regulatory agency submission materials (e.g., initial IND applications, annual reports, clinical study reports, protocols, and amendments, MedWatch reports, etc.).
4. Proactively identify and address regulatory compliance issues. Formulate or implement regulatory affairs policies and procedures to ensure that regulatory compliance is maintained or enhanced.
5. Lead, develop, and implement CMC regulatory strategies to ensure on-time and high-quality submissions for Drug Master Files (DMFs), marketing applications (NDA/ANDA), and post-approval lifecycle submissions. Serve as main contact with regulatory agencies (e.g., FDA, DEA, EMA health authorities, state authorities, etc.) when needed for drug product development.
6. Manage a team of regulatory affairs staff to ensure the team delivers consistent and high-quality work products in a timely manner.
7. Communicate regulatory information to team members, partners, and other stakeholders and ensure that the information is interpreted and relayed correctly.
8. Attend meetings and engage with designated working teams and provide regulatory input and guidance to project teams, including quality control practices.
9. Demonstrates inclusion through their own words and actions and is accountable for a safe workspace. Acts with kindness, curiosity, and respect for others.
10. Embracing and being open to incorporating our 6 Emotional & Social Intelligence (ESI) core principles in daily work.
11. Understands and complies with ethical, legal, and regulatory requirements applicable to our business.
KEY QUALIFICATIONS:
1. Bachelor’s degree required, preferably in Regulatory Science or a health sciences field.
2. A minimum of fifteen years of experience in the pharmaceutical industry (small molecule) or a related area. (Proven 5 years in a senior leadership role with strong management skills).
3. Strong scientific or clinical research background required.
4. Demonstrated knowledge of regulatory affairs, such as 21 CFR 210/211/310/312/314, FDA guidance documents, and ICH guidelines for both development projects and commercial projects, with evidence of successful submissions to FDA, EMA, MHRA, or other health authorities
5. Demonstrated track record of preparing original INDs, NDAs, and amendments in compliance with applicable FDA regulations.
6. Demonstrated CMC regulatory experience with drug substance and/or drug product and API production.
7. Familiar with a variety of the field's concepts, practices, and procedures, including FDA guidance documents and ICH guidelines and GCP.
8. Ability to work in a cross-functional team environment with dynamic timelines and priorities.
9. Experience with DEA-regulated substances and clinical trials.
10. Strong knowledge of eCTD elements and format and submissions process and procedures.
11. Critical thinking/problem-solving, writing, oral communication and organizing skills and presentation skills.
12. Ability to rely on experience and judgment to plan and accomplish goals.
13. Ability to perform a variety of tasks, including conducting primary work as well as leading and directing the work of others. A wide degree of creativity and latitude is expected.
14. Experience working with all levels of management and key business stakeholders.
PREFERRED QUALIFICATIONS:
1. Master's degree in management of Drug Development, Regulatory Affairs, or similar field.
2. Professional certification in regulatory affairs (e.g., RAC or similar credential).
PHYSICAL DEMANDS:
1. Ability to use a computer/Microsoft Office applications.
2. Ability to remain stationary for several hours at a time.
Â
Diversity is important to us. We are proud to be an Equal Opportunity Employer, and make employment decisions without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, disability, or any other protected class.
Salary range: $200-$260k. Salary will be commensurate with experience.Â
Share This Job:
Related Jobs:
Login to save this search and get notified of similar positions.About Fitchburg, WI
Ready to embark on a new career adventure in the picturesque area around Fitchburg, Wisconsin? This thriving community offers an array of job opportunities amidst stunning natural landscapes, vibrant arts scene, and renowned local eateries. From exploring the University of Wisconsin-Madison Arboretum to catching a show at the Overture Center for the Arts, there's something for everyone here. Consider joining the workforce in this dynamic region and unlock a world of growth and possibilities. Explore our job listings today and set your sights on a fulfilling career in Fitchburg and its surrounding charm.
Although this hasn't been an issue at Planet Pharma, the staffing industry has seen an increase in people falsely representing themselves as recruiters to gather personal information from job seekers. For your safety, do not provide sensitive data to anyone you have not spoken with thoroughly and never provide banking information during the application process. Candidate safety is a top priority at Planet Pharma.
