Senior Director Quality Assurance & Regulatory Affairs
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Senior Director Quality Assurance & Regulatory Affairs
$150000 - $220000 per year | Milton, MA | Remote | Permanent
New Senior Director Quality Assurance & Regulatory Affairs Opportunity!
A bit about us:
We are a well established consulting firm that provides solutions to medical device company, pharmaceuticals and biologics. We are looking for a Senior Director of Quality and Regulatory Affairs to join our team!
Why join us?
Opportunity to wear different hats in a small company-lots of growth!
Strong benefits and compensation package
Opportunity to work in multiple therapeutic and diagnostic areas
• Experience in writing PMAs
• Background in both regulatory and QA.
• Must have experience with design controls
• Must have a history with testing devices to universal standards
• While medical device history is the primary requirement, some history with pharmaceuticals or biologics would also be useful
Job Details
Job Details:
We are seeking a Senior Director of Quality Assurance & Regulatory Affairs to join our dynamic team. This is a permanent, full-time position, but we are also open to contract basis, that will play a crucial role in ensuring the quality and safety of our medical devices and aesthetic products, including dermal fillers. The successful candidate will be responsible for overseeing all aspects of quality assurance and regulatory affairs, ensuring compliance with cGMP requirements, SOP, FDA, PMAs, and other relevant regulations.
Responsibilities:
1. Develop and implement quality assurance policies and procedures to ensure compliance with cGMP requirements, SOP, FDA, PMAs, and other applicable regulations.
2. Lead regulatory affairs activities, including the preparation of regulatory submissions and interactions with regulatory authorities.
3. Oversee the validation and verification of medical devices and aesthetic products, including dermal fillers.
4. Conduct internal audits and inspections to ensure adherence to quality standards and regulatory requirements.
5. Coordinate with cross-functional teams to resolve quality and regulatory issues.
6. Keep abreast of changes in regulatory legislation and guidelines, and ensure that these changes are communicated and implemented within the organization.
7. Provide training and guidance to staff on quality assurance and regulatory affairs matters.
8. Lead continuous improvement initiatives to enhance the efficiency and effectiveness of our quality and regulatory processes.
Qualifications:
1. Bachelor's degree in a scientific or related field. An advanced degree will be an added advantage.
2. Minimum of 10 years of experience in quality assurance and regulatory affairs in the medical device industry
3. Strong experience in writing PMAs
4. Must have experience with design controls
5. Must have a history with testing devices to universal standards
6. In-depth knowledge of cGMP requirements, SOP, FDA, PMAs, and other relevant regulations, PMA's is a requirement
7. Proven experience with medical devices and aesthetic products, including dermal fillers.
8. Excellent problem-solving and decision-making abilities.
9. Ability to handle multiple tasks and projects simultaneously.
This is an exciting opportunity for a seasoned Director of Quality Assurance & Regulatory Affairs to make a significant impact on our company's success. If you have the required skills and experience, and you are passionate about ensuring the quality and safety of medical devices, we would love to hear from you.
Jobot is an Equal Opportunity Employer. We provide an inclusive work environment that celebrates diversity and all qualified candidates receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, age (40 and over), disability, military status, genetic information or any other basis protected by applicable federal, state, or local laws. Jobot also prohibits harassment of applicants or employees based on any of these protected categories. It is Jobot’s policy to comply with all applicable federal, state and local laws respecting consideration of unemployment status in making hiring decisions.
Sometimes Jobot is required to perform background checks with your authorization. Jobot will consider qualified candidates with criminal histories in a manner consistent with any applicable federal, state, or local law regarding criminal backgrounds, including but not limited to the Los Angeles Fair Chance Initiative for Hiring and the San Francisco Fair Chance Ordinance.
Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal.
By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from Jobot, and/or its agents and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy here: jobot.com/privacy-policy
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Senior Director Quality Assurance & Regulatory Affairs
$150000 - $220000 per year | Milton, MA | Remote | Permanent
New Senior Director Quality Assurance & Regulatory Affairs Opportunity!
A bit about us:
We are a well established consulting firm that provides solutions to medical device company, pharmaceuticals and biologics. We are looking for a Senior Director of Quality and Regulatory Affairs to join our team!
Why join us?
Opportunity to wear different hats in a small company-lots of growth!
Strong benefits and compensation package
Opportunity to work in multiple therapeutic and diagnostic areas
• Experience in writing PMAs
• Background in both regulatory and QA.
• Must have experience with design controls
• Must have a history with testing devices to universal standards
• While medical device history is the primary requirement, some history with pharmaceuticals or biologics would also be useful
Job Details
Job Details:
We are seeking a Senior Director of Quality Assurance & Regulatory Affairs to join our dynamic team. This is a permanent, full-time position, but we are also open to contract basis, that will play a crucial role in ensuring the quality and safety of our medical devices and aesthetic products, including dermal fillers. The successful candidate will be responsible for overseeing all aspects of quality assurance and regulatory affairs, ensuring compliance with cGMP requirements, SOP, FDA, PMAs, and other relevant regulations.
Responsibilities:
1. Develop and implement quality assurance policies and procedures to ensure compliance with cGMP requirements, SOP, FDA, PMAs, and other applicable regulations.
2. Lead regulatory affairs activities, including the preparation of regulatory submissions and interactions with regulatory authorities.
3. Oversee the validation and verification of medical devices and aesthetic products, including dermal fillers.
4. Conduct internal audits and inspections to ensure adherence to quality standards and regulatory requirements.
5. Coordinate with cross-functional teams to resolve quality and regulatory issues.
6. Keep abreast of changes in regulatory legislation and guidelines, and ensure that these changes are communicated and implemented within the organization.
7. Provide training and guidance to staff on quality assurance and regulatory affairs matters.
8. Lead continuous improvement initiatives to enhance the efficiency and effectiveness of our quality and regulatory processes.
Qualifications:
1. Bachelor's degree in a scientific or related field. An advanced degree will be an added advantage.
2. Minimum of 10 years of experience in quality assurance and regulatory affairs in the medical device industry
3. Strong experience in writing PMAs
4. Must have experience with design controls
5. Must have a history with testing devices to universal standards
6. In-depth knowledge of cGMP requirements, SOP, FDA, PMAs, and other relevant regulations, PMA's is a requirement
7. Proven experience with medical devices and aesthetic products, including dermal fillers.
8. Excellent problem-solving and decision-making abilities.
9. Ability to handle multiple tasks and projects simultaneously.
This is an exciting opportunity for a seasoned Director of Quality Assurance & Regulatory Affairs to make a significant impact on our company's success. If you have the required skills and experience, and you are passionate about ensuring the quality and safety of medical devices, we would love to hear from you.
Jobot is an Equal Opportunity Employer. We provide an inclusive work environment that celebrates diversity and all qualified candidates receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, age (40 and over), disability, military status, genetic information or any other basis protected by applicable federal, state, or local laws. Jobot also prohibits harassment of applicants or employees based on any of these protected categories. It is Jobot’s policy to comply with all applicable federal, state and local laws respecting consideration of unemployment status in making hiring decisions.
Sometimes Jobot is required to perform background checks with your authorization. Jobot will consider qualified candidates with criminal histories in a manner consistent with any applicable federal, state, or local law regarding criminal backgrounds, including but not limited to the Los Angeles Fair Chance Initiative for Hiring and the San Francisco Fair Chance Ordinance.
Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal.
By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from Jobot, and/or its agents and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy here: jobot.com/privacy-policy
Apply tot his job
Apply To this Job