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YubHub-native raw fields carry `x-` prefix.","jobs":[{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_d9e05746-2aa"},"title":"Associate Director, Bioanalytical Development","description":"<p><strong>Job Title</strong></p>\n<p>Associate Director, Bioanalytical Development</p>\n<p><strong>About Formation Bio</strong></p>\n<p>Formation Bio is a tech and AI-driven pharma company that accelerates all aspects of drug development and clinical trials.</p>\n<p><strong>About the Position</strong></p>\n<p>The Associate Director, Bioanalytical will lead bioanalytical strategy and delivery for assigned programs, working across nonclinical and clinical teams to ensure assays are fit for purpose and support key development decisions.</p>\n<p><strong>Responsibilities</strong></p>\n<ul>\n<li>Lead bioanalytical strategy and delivery for assigned programs across small molecules and biologics, aligned to clinical questions and decision points</li>\n<li>Define assay plans and validation approaches (fit-for-purpose through full validation) for PK/TK, metabolites as applicable, biologics bioanalysis, and immunogenicity</li>\n<li>Manage bioanalytical CROs and specialty labs for assigned workstreams: contribute to partner selection, define scopes, set timelines, and monitor performance, quality, and budget</li>\n<li>Oversee end-to-end bioanalytical execution: protocols, validation reports, sample analysis, data review, and final reports to support program decisions and filings</li>\n<li>Own day-to-day BA operating processes for assigned programs: assay lifecycle tracking, method transfer planning, issue triage, deviation management, and CAPA follow-up with vendors</li>\n<li>Ensure data quality and audit readiness for assigned deliverables through strong documentation practices, traceability, and alignment to regulatory guidance and internal standards</li>\n<li>Partner with Clinical Pharmacology and Clinical Development on study design inputs, sampling strategies, analyte panels, and interpretation of exposure and immunogenicity implications</li>\n<li>Coordinate with Clinical Operations on sample logistics (kits, handling, stability, chain of custody, reconciliation) and resolution of operational issues impacting bioanalysis</li>\n<li>Collaborate with Regulatory Affairs by drafting/reviewing submission components and providing technical input to support IND/CTA and NDA/BLA/MAA activities</li>\n<li>Align with DMPK/Nonclinical on bioanalytical approaches across studies and support translational PK needs</li>\n<li>Work with Biostatistics/Data Science to enable clean data transfers, consistent formats/metadata, and analysis-ready datasets</li>\n<li>Support diligence and asset evaluation by reviewing bioanalytical packages, identifying gaps/risks, and proposing pragmatic remediation plans</li>\n<li>Contribute to Trial Engine scaling by helping standardize templates, workflows, and reporting conventions that improve speed and consistency across programs</li>\n</ul>\n<p><strong>About You</strong></p>\n<ul>\n<li>PhD in a relevant field with 7+ years of bioanalytical experience in biopharma, including clinical-stage support, or a relevant undergraduate degree with 10+ years of experience</li>\n<li>Lead bioanalytical strategy and execution for assigned preclinical and clinical programs across small molecules and biologics</li>\n<li>Deep LC–MS/MS expertise for PK/TK, troubleshooting, and ISR</li>\n<li>Familiar with biologics bioanalysis and immunogenicity (ADA/NAb) approaches and interpretation</li>\n<li>Strong working knowledge of bioanalytical regulatory expectations and submission-quality documentation</li>\n<li>Lead CRO/vendor execution for assigned workstreams; support partner selection and governance as needed</li>\n<li>Comfortable operating in a fast-paced, cross-functional environment with multiple concurrent priorities</li>\n<li>Clear communicator who can translate technical detail into program-relevant recommendations</li>\n<li>Preferred: Experience functioning as part of a clinical study team to integrate tradeoffs between vendor selection, development speed, assay quality and performance, and applicability of method to deliver value to program overall</li>\n<li>Preferred: Familiarity with GCP/GCLP expectations and audit/inspection readiness for clinical bioanalysis</li>\n<li>Preferred: Experience shaping sample logistics (kits, stability, chain of custody) and data flow into filings</li>\n</ul>\n<p><strong>Total Compensation Range</strong></p>\n<p>$177,500 - $232,000</p>\n<p><strong>Compensation</strong></p>\n<p>Individual compensation is determined by several factors, including role scope, geographic location, and skills &amp; experience. Your offer will reflect where you fall within the range based on these considerations. In addition to base salary, we offer equity, comprehensive benefits, and generous perks. If the posted range doesn&#39;t match your expectations, we still encourage you to apply!</p>\n<p><strong>Where We Hire</strong></p>\n<p>Formation Bio is prioritizing hiring in key hubs, primarily the New York City and Boston metro areas, with a hybrid model requiring 3 days per week in office. Applicants from the Research Triangle (NC) and San Francisco Bay Area may also be considered. Please apply only if you reside in these locations or are willing to relocate.</p>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a href=\"https://yubhub.co\">YubHub</a></p>","url":"https://yubhub.co/jobs/job_d9e05746-2aa","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Formation Bio","sameAs":"https://www.formation.bio/","logo":"https://logos.yubhub.co/formation.bio.png"},"x-apply-url":"https://job-boards.greenhouse.io/formationbio/jobs/7530453","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":"$177,500 - $232,000","x-skills-required":["PhD in a relevant field","Bioanalytical experience in biopharma","LC–MS/MS expertise","Biologics bioanalysis and immunogenicity","Bioanalytical regulatory expectations"],"x-skills-preferred":["Experience functioning as part of a clinical study team","Familiarity with GCP/GCLP expectations","Experience shaping sample logistics and data flow"],"datePosted":"2026-04-18T15:58:11.388Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"New York, NY; Boston, MA"}},"employmentType":"FULL_TIME","occupationalCategory":"Engineering","industry":"Technology","skills":"PhD in a relevant field, Bioanalytical experience in biopharma, LC–MS/MS expertise, Biologics bioanalysis and immunogenicity, Bioanalytical regulatory expectations, Experience functioning as part of a clinical study team, Familiarity with GCP/GCLP expectations, Experience shaping sample logistics and data flow","baseSalary":{"@type":"MonetaryAmount","currency":"USD","value":{"@type":"QuantitativeValue","minValue":177500,"maxValue":232000,"unitText":"YEAR"}}},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_44d992c5-1cf"},"title":"Associate Director, Drug Product Development","description":"<p><strong>About the Position</strong></p>\n<p>The Associate Director, Drug Product, will provide strategic and hands-on operational leadership for all CMC activities related to drug product development and manufacturing, with a primary focus on sterile injectables (lyophilized and liquid) at all stages of development (IND-enabling to commercialization).</p>\n<p><strong>Responsibilities</strong></p>\n<p><strong>Development and Manufacturing Strategy, Operations and Oversight</strong></p>\n<ul>\n<li>Lead drug product manufacturing strategy and execution for programs from preclinical through commercial stages, ensuring alignment with program objectives, timelines, and budget constraints.</li>\n</ul>\n<ul>\n<li>Serve as the primary technical interface with CDMOs and contract manufacturing organizations for drug product manufacturing activities. Establish and maintain strong partnerships, lead technical discussions, and ensure manufacturing excellence across external manufacturing networks.</li>\n</ul>\n<ul>\n<li>Oversee formulation, aseptic fill-finish, lyophilization (if applicable), visual inspection, labeling, and packaging operations for drug products. Ensure manufacturing processes are robust, scalable, and compliant with cGMP requirements.</li>\n</ul>\n<ul>\n<li>Provide technical guidance and oversight for manufacturing campaigns including batch record review and approval, deviation investigations, change control assessments, and resolution of manufacturing issues</li>\n</ul>\n<ul>\n<li>Support scale-up activities from clinical to commercial manufacturing, including process optimization and validation. Identify and implement continuous improvement opportunities.</li>\n</ul>\n<ul>\n<li>Develop comprehensive manufacturing plans and schedules in collaboration with Project Management, Clinical Supply, and Commercial teams. Track manufacturing timelines and proactively manage risks to ensure on-time delivery of drug product for clinical trials and commercial supply.</li>\n</ul>\n<ul>\n<li>Lead technical assessments and qualification of new CDMOs for drug product manufacturing. Conduct site audits and ongoing performance monitoring. Manage relationships with multiple manufacturing partners across different geographic regions</li>\n</ul>\n<p><strong>Additional Core CMC Responsibilities (Quality, Regulatory &amp; Cross-Functional)</strong></p>\n<ul>\n<li>Ensure all manufacturing activities comply with cGMP regulations, ICH guidelines, and internal quality standards. Support regulatory inspections and audits at manufacturing sites. Review and approve batch records, protocols, and manufacturing-related documentation.</li>\n</ul>\n<ul>\n<li>Author and review CMC sections of regulatory submissions (INDs, BLAs, CTAs) related to drug product manufacturing, process validation, and manufacturing site changes. Support responses to health authority questions.</li>\n</ul>\n<ul>\n<li>Partner closely with Drug Substance Manufacturing, Analytical Development, Quality Assurance, Regulatory Affairs, Clinical Supply, and Project Management leads to ensure seamless integration of manufacturing activities into overall program execution.</li>\n</ul>\n<ul>\n<li>Collaborate with procurement to ensure timely contracting for drug product manufacturing.</li>\n</ul>\n<p><strong>About You</strong></p>\n<ul>\n<li>MS or Ph.D. in Chemical Engineering, Pharmaceutical Sciences, Biochemistry, Biotechnology, or related discipline.</li>\n</ul>\n<ul>\n<li>6+ years of experience in the biopharmaceutical industry with hands-on experience in biologics drug product manufacturing, formulation development, and fill-finish operations.</li>\n</ul>\n<ul>\n<li>Demonstrated track record of successfully managing drug product manufacturing campaigns for biologics (proteins, monoclonal antibodies, antibody-drug conjugates, or other large molecules) from preclinical through late-stage clinical or commercial manufacturing.</li>\n</ul>\n<ul>\n<li>Technical expertise in aseptic fill-finish operations, lyophilization processes, formulation development, stability programs, and drug product characterization for biologics.</li>\n</ul>\n<ul>\n<li>Extensive experience working with CDMOs and contract manufacturing organizations, including site selection, technology transfers, manufacturing oversight, and performance management. Proven ability to troubleshoot complex manufacturing issues and drive continuous improvement initiatives.</li>\n</ul>\n<ul>\n<li>Strong knowledge of cGMP regulations, FDA and EMA guidelines, ICH quality guidelines, and regulatory expectations for drug product manufacturing.</li>\n</ul>\n<ul>\n<li>Experience authoring and reviewing CMC sections of regulatory submissions (INDs, BLAs, CTAs) related to drug product manufacturing and validation activities.</li>\n</ul>\n<ul>\n<li>Strong project management skills with demonstrated ability to manage multiple manufacturing programs simultaneously, meet aggressive timelines, and navigate competing priorities.</li>\n</ul>\n<ul>\n<li>Excellent communication and interpersonal skills with ability to influence and build strong relationships with internal stakeholders and external manufacturing partners.</li>\n</ul>\n<ul>\n<li>Willingness to travel domestically and internationally (approximately 20-30%) to manufacturing sites for audits, manufacturing oversight, and technical meetings.</li>\n</ul>\n<p><strong>Total Compensation Range</strong></p>\n<p>$177,000 - $235,000</p>\n<p><strong>Where We Hire</strong></p>\n<p>Formation Bio is prioritizing hiring in key hubs, primarily the New York City and Boston metro areas, with a hybrid model requiring 3 days per week in office. Applicants from the Research Triangle (NC) and San Francisco Bay Area may also be considered. 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This role ensures all requests and tasks related to service line installation and meter sets are handled promptly and proactively, creating a smooth transition for customers using natural gas.</p>\n<p>The incumbent initiates and maintains customer relationships and uses strong technical research skills within multi-jurisdictional and multi-functional teams supporting AGL, CG, and VNG. This position interacts with customers by phone, email, and fax, supporting a service population of more than two million.</p>\n<p>Responsibilities include adherence to regulatory standards, compliance with policies and procedures, and supporting training of new employees.</p>\n<p>Key responsibilities include:</p>\n<ul>\n<li>Initiating new residential and commercial projects</li>\n<li>Providing specialized support for account executives across AGL, CG, and VNG</li>\n<li>Gathering and documenting essential project information</li>\n<li>Responding to inquiries regarding natural gas availability</li>\n<li>Maintaining high volumes of documentation for fuel line inspections and pending meter sets</li>\n<li>Preparing field orders and updating customer account information</li>\n<li>Providing problem-solving solutions, including conceptual thinking when required</li>\n<li>Coordinating work requests with internal departments and service centers</li>\n<li>Serving as primary municipal contact for resolving fuel line inspection requirements and updating reference materials</li>\n<li>Researching and verifying service card information</li>\n<li>Troubleshooting missing contract submissions</li>\n<li>Processing high-volume email requests</li>\n<li>Managing NGAD referrals and marketer dashboard orders</li>\n<li>Acting as liaison for multi-family master meter conversions and municipality acquisition projects</li>\n<li>Completing onboarding tasks in the BCA work queue</li>\n<li>Working proactive reports to expedite customer requests</li>\n<li>Addressing electronic notifications to prevent onboarding delays</li>\n<li>Processing all online customer requests across all construction types</li>\n<li>Scheduling residential and commercial meter sets via customer or marketer requests</li>\n<li>Promoting natural gas benefits and additional equipment opportunities</li>\n<li>Overseeing large commercial projects through meter installation</li>\n<li>Promoting energy efficiency programs and rebates</li>\n<li>Determining and maintaining required documentation</li>\n<li>Providing site-related information to contractors</li>\n<li>Assisting employees when leadership is unavailable</li>\n<li>Supporting executive-level escalations</li>\n<li>Training and coaching new employees</li>\n<li>Assisting with system testing for new implementations</li>\n<li>Providing backup call support during peak volume</li>\n<li>Identifying and resolving complex ECC issues</li>\n<li>Reporting service disruptions</li>\n<li>Adhering to policy, procedure, and quality standards</li>\n<li>Tracking work activity for business process reporting</li>\n<li>Redirecting misrouted customer requests as appropriate</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a href=\"https://yubhub.co\">YubHub</a></p>","url":"https://yubhub.co/jobs/job_67c09e3f-d0f","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Atlanta Gas Light (AGL), Chattanooga Gas (CG), and Virginia Natural Gas (VNG)","sameAs":"https://www.atlantagas.com/","logo":"https://logos.yubhub.co/atlantagas.com.png"},"x-apply-url":"https://emje.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/SouthernCompanyJobs/job/18012","x-work-arrangement":"hybrid","x-experience-level":"mid","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Basic MS PowerPoint skills","Intermediate MS Excel and MS Word proficiency","Advanced customer service skills","Strong active listening and oral comprehension skills","Basic computer proficiency; 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Our technology is central to the Era of Pervasive Intelligence, from self-driving cars to learning machines. We lead in chip design, verification, and IP integration, empowering the creation of high-performance silicon chips and software content.</p>\n<p><strong>Job Description</strong></p>\n<p>We are seeking a motivated and detail-oriented audit professional with a strong interest in technology, information security, and risk management. You will be responsible for planning and executing IT and/or Information Security audits in accordance with the annual audit plan. You will also perform IT risk assessments to identify key risks and support the development and refinement of the annual IT audit plan.</p>\n<p><strong>Responsibilities</strong></p>\n<ul>\n<li>Planning and executing IT and/or Information Security audits in accordance with the annual audit plan.</li>\n<li>Performing IT risk assessments to identify key risks and support the development and refinement of the annual IT audit plan.</li>\n<li>Evaluating the design and operating effectiveness of IT General Controls (ITGCs) and, where applicable, IT Application Controls.</li>\n<li>Supporting SOX compliance activities, including walkthroughs, control testing, issue identification, and remediation follow-up.</li>\n<li>Conducting audits over key systems and platforms, including ERP and cloud-based applications (e.g., SAP and/or Salesforce).</li>\n<li>Collaborating with business, IT, and Information Security stakeholders to understand processes, risks, and controls.</li>\n<li>Preparing clear, concise audit documentation, reports, and presentations that communicate findings, risks, and recommendations.</li>\n<li>Tracking and validating remediation of audit findings and control deficiencies.</li>\n<li>Staying current on emerging technology risks, regulatory expectations, and industry best practices related to IT and cybersecurity.</li>\n</ul>\n<p><strong>Benefits</strong></p>\n<p>At Synopsys, innovation is driven by our incredible team around the world. We feel honored to work alongside such talented and passionate individuals who choose to make a difference here every day. We&#39;re proud to provide the comprehensive benefits and rewards that our team truly deserves.</p>\n<ul>\n<li>Health &amp; Wellness: Comprehensive medical and healthcare plans that work for you and your family.</li>\n<li>Time Away: In addition to company holidays, we have ETO and FTO Programs.</li>\n<li>Family Support: Maternity and paternity leave, parenting resources, adoption and surrogacy assistance, and more.</li>\n<li>ESPP: Purchase Synopsys common stock at a 15% discount, with a 24 month look-back.</li>\n<li>Retirement Plans: Save for your future with our retirement plans that vary by region and country.</li>\n<li>Compensation: Competitive salaries.</li>\n</ul>\n<p><strong>Team</strong></p>\n<p>You will join a collaborative and forward-thinking Internal Audit team that partners closely with the business and technology functions. The team values quality, integrity, and open communication, and provides opportunities to work across a broad range of systems, processes, and risks. You&#39;ll gain exposure to senior stakeholders, develop your technical and audit expertise, and play a meaningful role in strengthening the organization&#39;s control environment.</p>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a href=\"https://yubhub.co\">YubHub</a></p>","url":"https://yubhub.co/jobs/job_f7bc3829-4cd","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Synopsys","sameAs":"https://careers.synopsys.com","logo":"https://logos.yubhub.co/careers.synopsys.com.png"},"x-apply-url":"https://careers.synopsys.com/job/bengaluru/it-auditor-sr-associate-staff/44408/92463617200","x-work-arrangement":"onsite","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["IT audit","information security","risk management","SOX compliance","ERP","cloud-based applications","SAP","Salesforce","IT General Controls","IT Application Controls","auditing","risk assessment","control testing","issue identification","remediation follow-up","auditing documentation","reporting","presentation","emerging technology risks","regulatory expectations","industry best practices"],"x-skills-preferred":["CISA","CIA","CISSP","auditing software","risk management software"],"datePosted":"2026-03-08T22:18:27.923Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Bengaluru"}},"employmentType":"FULL_TIME","occupationalCategory":"Finance","industry":"Technology","skills":"IT audit, information security, risk management, SOX compliance, ERP, cloud-based applications, SAP, Salesforce, IT General Controls, IT Application Controls, auditing, risk assessment, control testing, issue identification, remediation follow-up, auditing documentation, reporting, presentation, emerging technology risks, regulatory expectations, industry best practices, CISA, CIA, CISSP, auditing software, risk management software"}]}