Bioconjugation GMP Manufacturing Supervisor at Veranova L P

Discover Veranova:At Veranova we believe people are our most important asset and we are dedicated to building the most talented workforce in our industry. Our commitment to uncompromising focus on quality compliance safety and excellence in delivery shapes everything we do. We are not just looking for skills; we are seeking innovative individuals who have a mindset open to learning and growth and a desire to make a difference.Veranova is a global leader in the development and manufacturing of complex active pharmaceutical ingredients (APIs) for pharma and biotech customers. With deep technical expertise and impressive flexibility we develop solutions and processes that support and accelerate innovation.Join us on our mission to enable current and next-generation therapeutics to improve and save the lives of patients.Role Overview:Veranova is seeking a highly motivated adaptable and experienced Supervisor to support its new state-of-the-art single-use DS biologics manufacturing facility in Devens MA and to integrate this operation with existing cGMP manufacturing this role you will oversee the systems teams and processes required to enable clinical manufacturing and future commercial launches. This is a unique opportunity to help shape the future of the Devens site as it expands into bioconjugate manufacturing building on its strong foundation in process development and in clinical and commercial production of linker-payloads for global pharmaceutical partners.Core Responsibilities: Distribution of responsibilities across multiple workstreams within the GMP manufacturing asset. Drive prioritization and sequencing of workstreams within a client process to achieve results consistent with process design. Align operational and project timelines deliverables and resourcesEvaluate industrys best practices and select an appropriate program and project delivery that supports the dynamic nature of a new facility startup and integrates with existing governance and delivery frameworksManage the tools standards business processes documentation metrics and communication associated with operational GMP facilityOrganize prioritize sequence and track contract manufacturing projects in cGMP facilityManage staff of operations personnel assure training and batch record execution to achieve successful project executionAdditional assignments/ duties to support team objective and contribute to the Veranova mission may evolve based on business needsQualifications:Bachelors degree in engineering life sciences or related field and 7-10 years of experience in biotech/pharma manufacturing or process development with a minimum of 2 years direct people leadership experienceMasters degree in engineering life sciences or related field and 5 years of experience in biotech/pharma manufacturing or process development with a minimum of 2 years of direct people leadership experienceStrong understanding of cGMP complianceProven experience managing project timelines for delivery of client drug substanceDemonstrated ability to thrive in a dynamic environment and collaborate across diverse technical areasPreferredExperience with biological drug substance manufacturing equipment and processes single-use equipment technologies and cGMP facility qualification and startupSalary Range: $105000 - $125000 annual base salaryOur Commitment:Health & Wellness: Comprehensive health & wellness benefits. Access to mental health resources and wellness programs. Generous PTO and holiday pay policies.Financial Wellness: Veranova is committed to fair and transparent compensation practices. This includes a competitive base salary eligibility for performance-based bonuses and an attractive 401(k) Plan with company match. Salary ranges reflect the scope and expectations of the role and are based on market data internal equity and role-specific factors. Final compensation may vary depending on experience skills education and business needs.Professional Development: Opportunities for continuous learning through LinkedIn Learning workshops conferences and mentorship. Tuition Assistance for Undergraduate and Graduate degree programs.Inclusive Culture: At Veranova an inclusive culture is integral to our values. We welcome people with diverse experiences and perspectives who share our mission to improve and save lives. Even if you dont meet every qualification we encourage you to apply. Veterans first responders and those transitioning from military to civilian life bring valuable skills that strengthen our team.Additional Information:Applicants for this role must be authorized to work in the United States without further employer sponsorship. Agency and Search Firm Representatives: Veranova does not accept unsolicited resumes from agencies and/or search firms for this job posting.All your information will be kept confidential according to EEO guidelines.Veranova is an Equal Opportunity Employer. It is the policy of Veranova to provide equal employment access and opportunity to all persons regardless of age race color national origin religion sex sexual orientation gender identity and/or expression physical or mental disability genetic information citizenship marital status veteran status or any other characteristic protected by federal state or local law.All applications are carefully considered and your details will be stored on our secure Application Management System. This is used throughout Veranova for the selection of suitable candidates for our vacancies as they arise. Veranova respects your privacy and is committed to protecting your personal information. For more information about how your personal data is used please view ourprivacy notice.#LI-OnsiteRequired Experience:Manager Key Skills Lean Manufacturing,Six Sigma,Continuous Improvement,FDA Regulations,Lean,Packaging,Production Planning,cGMP,Cell Culture,Leadership Experience,Supervising Experience,Manufacturing Employment Type : Full-Time Experience: years Vacancy: 1 Yearly Salary Salary: 105000 - 125000