Director, Validation & Technical Transfer 503B - East Windsor, Nj

Details of the offer

Company Overview Empower is a visionary healthcare company committed to providing quality, affordable medication to millions of patients across the nation. We hold the distinguished position of being the largest 503A compounding pharmacy and FDA-registered 503B outsourcing facility in the country serving the functional medicine markets.
What sets us apart is our relentless focus on three core values: People, Quality and Service. Our dedicated team of professionals collaboratively works to break new ground in the fields of manufacturing, distribution and quality control, providing a uniquely integrated approach to healthcare. Leveraging our vertical integration of the pharmaceutical supply chain, state-of-the-art technology, and a commitment to excellence, we are constantly pushing the boundaries of what is possible in medication accessibility and affordability.
You're not just starting a job; you're joining a mission. We believe in empowering our team to innovate, grow, and drive real change in the healthcare industry. If you're a forward-thinker who thrives in a fast-paced, transformative environment, Empower is the place for you. Here, you'll be encouraged to share your ideas, expand your skill set, and contribute to projects that genuinely make a difference. We prioritize the well-being of our team members, and we offer a supportive and engaging workplace where your contributions are not just recognized but celebrated.
Let's revolutionize healthcare, together. Join us and be a part of something extraordinary.

Position Summary The Director of Validation and Technical Transfer ensures regulatory compliance by leading validation strategies across departments and overseeing the full validation lifecycle. This role fosters seamless collaboration with Research and Development (R&D), Manufacturing, and partners for smooth tech transfers while driving continuous improvement to advance Empower's mission of delivering innovative, accessible medications.

Duties and Responsibilities Leads the validation team through training, performance management, and fostering collaboration to promote growth and knowledge sharing.Develops and implements validation strategies aligned with regulatory requirements and industry best practices across departments.Oversees the full validation lifecycle, ensuring compliance through rigorous documentation for audits, inspections, and milestones.Drives continuous improvement by leveraging technology and collaborating with R&D, Manufacturing, and partners for seamless tech transfers.Engages with regulatory bodies and industry associations to stay updated on trends and implement proactive risk mitigation strategies.While performing the responsibilities of the job, the employee is required to talk and hear. The employee is often required to remain in a stationary position for a significant amount of the workday and frequently use their hands and fingers to handle or feel in order to access, input, and retrieve information from the computer and other office productivity devices. The employee is regularly required to move about the office and around the corporate campus. The employee is regularly required to stand, walk, reach with arms and hands, climb or balance, and to stoop, kneel, crouch or crawl.

Knowledge and Skills Expertise in GMP, Food and Drug Administration regulations, and validation software, with proficiency in Microsoft Office, Quality Management, and Maintenance Systems.Strong leadership, communication, and interpersonal skills, with the ability to manage projects and foster cross-functional collaboration.Key Competencies Customer Focus: Ability to build strong customer relationships and deliver customer centric solutions.Optimizes Work Processes: Know the most effective and efficient processes to get things done, with a focus on continuous improvement.Collaborates: Builds partnerships and works collaboratively with others to meet shared objectives.Resourcefulness: Secures and deploys resources effectively and efficiently.Manages Complexity: Makes sense of complex, high quality, and sometimes contradictory information to effectively solve problems.Ensures Accountability: Holds self and others accountable to meet commitments and objectives.Situational Adaptability: Adapts approach and demeanor in real time to match shifting demands of different situations.Communicates Effectively: Develops and delivers multi-mode communications that convey a clear understanding of the unique needs of different audiences.Values People: Our people define who we are as a company, and we believe that understanding and addressing the needs of our team, clients, and community is fundamental to fostering a culture of support and growth.Quality: Quality stands at the core of our mission, reflecting our commitment to excellence in every medication we produce.Service: We are here to serve others. Every interaction with our patients, providers, employees and other stakeholders comes from a place of service.Innovation: By continuously exploring new methodologies and embracing technology, we ensure that every solution we offer is at the forefront of pharmaceutical care. Experience and Qualifications Bachelor's degree in pharmaceutical science, life science, instructional design, engineering, or a related field required.Minimum of 12 years in a Good Manufacturing Practice (GMP)-regulated pharmaceutical environment, including 10 years in validation and 8 years of independent decision-making.Certified Quality Engineer Preferred. Employee Benefits, Health, and Wellness No-Cost Medication: Get your prescribed compounded medications at no cost, ensuring your health without the financial burden.Onsite Health & Wellness – IV Therapy Drips: Rejuvenate with complimentary onsite IV Therapy drips, enhancing your well-being and energy levels.Comprehensive Medical, Dental, and Vision Options: Choose from three medical plans tailored to your needs, plus options for dental and vision coverage for you and your family.Telehealth visits: Access board-certified Doctors anytime, anywhere for you and your family.Paid & Volunteer Time Off: Enjoy paid time off for personal pursuits and contribute to causes you care about with volunteer time off.Paid Holidays (8 scheduled; 2 floating): Celebrate with eight scheduled holidays and two floating holidays, giving you flexibility and time for personal traditions.Life & AD&D Coverage: Secure your and your family's financial future with life and accidental death and dismemberment (AD&D) insurance.FSA (Flexible Spending Account): Manage healthcare expenses smartly with pre-tax dollars in a Flexible Spending Account (FSA).401K Dollar-for-Dollar Up to 4%: Invest in your future with our 401K plan, featuring a dollar-for-dollar match up to 4%.Company Paid Long-Term Disability: Provided at no cost, which replaces 60% of your income if you become disabled for a long period of time.Flexible Schedules: Balance work and life seamlessly with our flexible scheduling options.Rewards & Recognition Program: Your hard work doesn't go unnoticed – enjoy rewards and recognition beyond your paycheck.Additional Voluntary Benefits Accident Insurance: Pays a lump sum benefit to help cover expenses following an accidental injury.Hospital Indemnity Insurance: Enhance your peace of mind with supplemental hospital insurance for unexpected stays.Critical Illness: Protect your finances from the expenses of a serious health issue.Short-Term Disability: Protect your income during illness or injury with short-term disability coverage.Supplemental Life & AD&D: Add an extra layer of financial protection for you and your loved ones with supplemental life and AD&D coverage.Legal Services: Access professional legal assistance to address concerns confidently.Identity Theft Protection: Safeguard your identity and finances with our identity theft protection benefit.Pet Insurance: Care for your furry family members with our pet insurance coverage.Employee Assistance Program: Confidential counseling and support services for a holistic approach to your well-being.
#J-18808-Ljbffr


Nominal Salary: To be agreed

Source: Grabsjobs_Co

Job Function:

Requirements

Ux Researcher

Job Title: UX Researcher Onsite/Hybrid: 50% onsite at Princeton, NJ Work Schedule: Monday-Friday, office hours 12 Months Contract with high possibilities of ...


Aequor - New Jersey

Published 7 days ago

Summer 2025 Internship Program - Materials Planning - Plainsboro, Nj

Summer2025 Internship Program – Materials Planning Plainsboro, NJ, US On-Site If you're looking to grow your network and gain new skills within a global com...


Dsm - New Jersey

Published 6 days ago

Summer 2025 Internship Program - Strategic Transformation, Taste Texture & Health - Plainsboro, Nj

2025 Internship Program – Trainee Strategic Transformation, TTH NA Plainsboro, NJ, US Hybrid / On-Site – (1 day remote / 4  days on-site) If you're looking ...


Dsm - New Jersey

Published 5 days ago

Professional/Research/Manager Casual

Below you will find the details for the position including any supplementary documentation and questions you should review before applying for the opening. T...


Rutgers University - New Jersey

Published 7 days ago

Built at: 2024-11-23T15:40:32.885Z