At a Glance
- Tasks: Lead GxP Quality Assurance strategy and ensure compliance with regulations.
- Company: Join Schrödinger, a leader in drug discovery using innovative computational methods.
- Benefits: Enjoy competitive salary, stock options, flexible work schedule, and over a month of paid vacation.
- Why this job: Be part of a collaborative team making a real impact on human health.
- Qualifications: Requires 12-15 years in Quality Assurance, with leadership experience in pharma or biotech.
- Other info: Schrödinger values diversity and offers a relaxed yet engaged company culture.
The predicted salary is between 138000 - 178000 £ per year.
We are looking to hire a Director, GxP Quality Assurance and Compliance to join us in our mission to discover and develop drugs that improve human health through the use of breakthrough computational methods. We are seeking outstanding individuals to join our drug discovery group and contribute to our rapidly expanding portfolio of drug discovery programs and collaborations. Our drug discovery and early clinical development team includes a cross-functional group of scientists and drug developers with experience working on all common target classes and therapeutic areas. The group is supported by more than 100 software developers and engineers, as well as a large-scale compute infrastructure to apply our proprietary physics-based drug design and optimization platform. Several programs we have worked on have achieved developmental candidate status, and have progressed into clinical development after IND approval. You can view our entire pipeline of wholly-owned programs and collaborations here. Who will love this job:A strategic subject matter expert who’s ready to partner with cross-functional teams as an experienced Quality technical resourceA solutions-oriented and collaborative coach to internal partners An excellent verbal and written communicator with robust project management skills A goal-oriented team player who can bring excellent leadership skills to the oversight of cross-functional teams, including members of our toxicology, bioanalytical, CMC, and clinical teamsWhat you will do:Overall GxP Responsibilities: Design, develop and implement overall GxP Quality Assurance strategy and vision for Schrödinger’s Therapeutics GroupDevelop, implement, and manage the continuous improvement of robust quality management systems, including, e.g., vendor management, deviation management, change control, CAPAs, product label review, risk management, and eQMS (MasterControl) Ensure compliance, in collaboration with relevant SMEs and senior leaders, with all applicable GxP regulations, including GMP, GCP, and GLPEstablish key quality system metrics and process indicators to proactively identify and address quality systems or product issuesOversee the development and implementation of all relevant training programs to ensure staff are knowledgeable about GxP requirements and quality standardsProvide leadership and guidance to teams on inspection readiness, including hosting and participating in regulatory inspections (GMP, BIMO, etc.) Account for appropriate oversight of all vendors, including CDMOs and CROs, to ensure regulatory compliance GMP Responsibilities:Serve as spokesperson and technical subject matter quality expert for all matters governed by GMP-related regulations/guidelines and industry best practices (e.g., FDA, EMA, PMDA, etc.) Perform and manage day-to-day GMP QA activitiesAuthor, review, and approve all relevant GMP quality documentsWhat you should have:Bachelor’s degree in life sciences (Master’s degree in life sciences preferred) Twelve to fifteen years of Quality Assurance experience in the pharmaceutical or biotech industry, with at least five years in a leadership role Technical quality experience preferredExperience in manufacturing operations preferred Expert level knowledge of GMP regulations and FDA requirements, Guidance documents, and industry best practices, with a focus on Analytical/QC testingGood working knowledge of global GxP standards, including USP/Ph., FDA/EMA, and ICHHistory of success with the management of inspections performed by the FDA and other regulatory bodiesExcellent written and oral communication skillsAbility to travel domestically and internationally on occasionPay and perks:Schrödinger understands it’s people that make a company great. Because of this, we’re prepared to offer a competitive salary, stock options, and a wide range of benefits that include healthcare (with dental and vision), a 401k, pre-tax commuter benefits, a flexible work schedule, and a parental leave program. We have regular catered meals in the office, a company culture that is relaxed but engaged, and over a month of paid vacation time. Our Administrative and Human Resources departments also plan a myriad of fun company-wide events. New York is home to our largest office, but we have teams all over the world. Schrödinger is honored to have been selected as one of Crain’s New York Best Places to Work for the past three years running.Estimated base salary range: $185,000 – $235,000. Actual compensation package is dependent on a number of factors, including, for example, experience, education, degrees held, market data, and business needs. If you have any questions regarding the compensation for this role, do not hesitate to reach out to a member of our Strategic Growth team. Sound exciting? Apply today and join us!As an equal opportunity employer, Schrödinger hires outstanding individuals into every position in the company. People who work with us have a high degree of engagement, a commitment to working effectively in teams, and a passion for the company’s mission. We place the highest value on creating a safe environment where our employees can grow and contribute, and refuse to discriminate on the basis of race, color, religious belief, sex, age, disability, national origin, alienage or citizenship status, marital status, partnership status, caregiver status, sexual and reproductive health decisions, gender identity or expression, sexual orientation, or any other protected characteristic. To us, “diversity” isn’t just a buzzword, but an important element of our core principles and key business practices. We believe that diverse companies innovate better and think more creatively than homogenous ones because they take into account a wide range of viewpoints. For us, greater diversity doesn’t mean better headlines or public images – it means increased adaptability and profitability.
Director, GxP Quality Assurance and Compliance employer: Schrödinger
Contact Detail:
Schrödinger Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Director, GxP Quality Assurance and Compliance
✨Tip Number 1
Familiarize yourself with the latest GxP regulations and industry best practices. Being well-versed in GMP, GCP, and GLP will not only boost your confidence but also demonstrate your commitment to quality assurance.
✨Tip Number 2
Network with professionals in the pharmaceutical and biotech industries. Attend relevant conferences or webinars where you can meet potential colleagues and learn about the latest trends in quality assurance.
✨Tip Number 3
Showcase your leadership skills by discussing past experiences where you successfully led cross-functional teams. Highlight how you managed inspections and ensured compliance, as this aligns perfectly with the responsibilities of the role.
✨Tip Number 4
Prepare for potential interviews by practicing your communication skills. As an excellent verbal communicator, you should be ready to articulate your vision for GxP quality assurance and how you can contribute to our mission at Schrödinger.
We think you need these skills to ace Director, GxP Quality Assurance and Compliance
Some tips for your application 🫡
Tailor Your Resume: Make sure to customize your resume to highlight your experience in GxP Quality Assurance and Compliance. Emphasize your leadership roles and specific achievements in the pharmaceutical or biotech industry.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for drug discovery and your strategic vision for GxP Quality Assurance. Mention how your background aligns with the company's mission and values.
Highlight Relevant Experience: In your application, focus on your twelve to fifteen years of Quality Assurance experience, particularly any leadership roles. Include examples of your success in managing inspections and ensuring compliance with GxP regulations.
Showcase Communication Skills: Since excellent written and oral communication skills are crucial for this role, ensure your application reflects your ability to communicate complex information clearly and effectively. Consider including examples of presentations or reports you've authored.
How to prepare for a job interview at Schrödinger
✨Showcase Your GxP Expertise
Be prepared to discuss your extensive knowledge of GxP regulations, particularly GMP, GCP, and GLP. Highlight specific experiences where you successfully navigated compliance challenges or led quality assurance initiatives.
✨Demonstrate Leadership Skills
As a Director, you'll need to exhibit strong leadership capabilities. Share examples of how you've effectively managed cross-functional teams, mentored colleagues, and driven quality improvements in previous roles.
✨Communicate Clearly and Effectively
Excellent communication is key for this role. Practice articulating complex quality assurance concepts in a clear and concise manner. Be ready to explain how you would ensure that all team members understand GxP requirements.
✨Prepare for Regulatory Scenarios
Expect questions about your experience with regulatory inspections. Prepare to discuss specific instances where you led inspection readiness efforts and how you handled interactions with regulatory bodies like the FDA or EMA.