What are the responsibilities and job description for the Quality Assurance Manager position at SciPro?
Quality Assurance Manager
We are seeking an experienced Quality Assurance Manager to join our Radiopharmaceutical clients team. This role is ideal for a dynamic professional with a strong background in the pharmaceutical, biotech, or CDMO industries. The successful candidate will play a critical role in ensuring compliance with regulatory standards and fostering a culture of quality excellence.
Great opportunity to work in Radiopharmaceuticals and develop your career working with some of the most advanced technologies in the industry!
Key Responsibilities:
- Lead and support onsite FDA inspections and client audits, leveraging prior experience with FDA audits.
- Collaborate with cross-functional teams to develop and implement solutions that address quality challenges proactively.
- Manage and mentor a team of direct reports, providing guidance and support to drive performance and professional growth.
Qualifications:
- A minimum of 5 years of industry experience in Quality Assurance within the pharmaceutical, biotech, or CDMO sectors. Candidates with QA experience outside these industries will not be considered.
- Strong understanding of 21 CFR 211 and other relevant regulatory requirements.
- Proven ability to confidently represent the organization during FDA inspections and audits.
- Demonstrated leadership experience, including managing direct reports.
Ideal Candidate Attributes:
- A solution-oriented mindset with the ability to think on their feet and act decisively.
- Strong communication skills, confidence, and the ability to inspire trust and credibility.
- Proactive and self-driven, capable of working independently without requiring extensive guidance.
This is an excellent opportunity for a confident, proactive professional to make a significant impact in a high-stakes environment. If you are looking for a chance to excel in your career, we would love to hear from you!
j.muratore@sciproglobal.com
