Welcome to Jobfind4u.anekjob.com We provide job seekers with information gathered from various publicly available job posting websites, including but not limited to Google, Indeed, LinkedIn, and other well-known job platforms. Our mission is to help individuals find employment opportunities by offering up-to-date job listings and career-related resources. We do not charge any fees for accessing or using our website, and all job information is provided free of charge.
Jobfind4u.anekjob.com does not directly offer, manage, or engage in the hiring process for any of the job listings featured on our website. All listings are sourced from third-party job posting platforms such as Indeed, LinkedIn, and other recognized job websites.
By using our website, you acknowledge and accept the above terms and conditions. Thank you for visiting Jobfind4u.anekjob.com, and we wish you success in your job search.
Associate Director/Director, Technical Operations and Development - REMOTE East Coast Based
Other Jobs To Apply
No other job posts for this day.
<h3>Who We Are</h3>If you're passionate about gene therapy and its ability to enhance the lives of patients, then Beacon is a great team to join.<br><br>We're a diverse, multi-national team of talented people all working together at our sites in the US and the UK, or as a remote contributor.<br><br>Everyone here, whatever their role or location, plays a genuine part in bringing our treatments to patients. Everyone has a voice, and every contribution makes a difference.<h3>Scope of the Role</h3>As Associate Director/Director, Technical Operations and Development, you will steer late-stage CMC execution for gene therapy programs, ensuring development and manufacturing activities are aligned with global regulatory expectations from Phase III through validation, submission, approval, and launch.<br><br>Key responsibilities include:<br>- Lead cross-functional CMC planning across DP/DS, analytics, and MSAT, with clear milestones and progress reporting<br>- Define and implement analytical and manufacturing control strategies, including CQAs, CPPs, and specification/range setting<br>- Provide technical leadership to resolve complex testing, processing, and manufacturing challenges in regulated environments<br>- Partner with internal and external stakeholders to maintain alignment between program strategy and CMC deliverables<br><br>Required qualifications/skills:<br>- Proven late-stage biotherapeutic CMC leadership through process validation, regulatory submission/approval, and market launch<br>- Strong GMP knowledge and experience supporting GMP biomanufacturing execution<br>- Highly desirable: HSV and AAV gene therapy production experience<br><br>If you’re ready to drive rigorous, approval-focused CMC outcomes, we welcome your application.<h3>How Your Days Flow</h3>Working fully remote on an Eastern schedule, you’ll move between focused technical reviews and collaborative decision-making. Your day may start by aligning on late-stage priorities with CMC peers, then shift to reviewing control strategy elements and data packages that support readiness for validation and filing. You’ll spend time translating emerging risks into practical options, clarifying what “good” looks like for documentation and traceability, and keeping stakeholders synchronized across time zones. As the day progresses, you’ll track progress against interim milestones, prepare concise updates for governance forums, and close out by confirming next steps with partners so teams can execute efficiently and compliantly.<h3>Benefits at a Glance</h3>Medical, dental, and vision coverage; 401(k); life insurance; Health Savings Account (HSA) and Flexible Spending Account (FSA) options; paid time off; employee discounts; and employer-paid short-term and long-term disability (STD & LTD). Competitive salary range: $158,000–$220,000 per year.
