Role Description The Contract Compliance Administrator (Recycling Division) is responsible for managing company agreements, contracts, insurance certifications, UCC filings, baler equipment, equipment leases, and other compliance-related issues. You will also be held responsible for liaising negotiations between the company, Pratt Corporate, and its business partners, ensuring that the prompt document closure for all areas is compliant and complete. Contract Compliance Administration entails oversight on all legal documentation signed by the business unit to ensure that each stipulation and annex is within the acceptable bounds of the law and is duly followed by internal and external clients. The CCA will monitor the performance and efficiency of contracts, agreements, and equipment usage with suppliers. - The CCA works as part of the Accounting department, upholding the internal policies and processes regarding contract management. - Responsible for managing client-specific contracts and providing counsel for maintaining the quality of contracts within the unit. - Review and provide oversight for all existing contracts by inspecting the contract database. - Provide technical services in developing a standard and appropriate use of language for each document. - Work in coordination with managers to analyze sourcing and contracts strategies. - Identify new trends and make recommendations for beneficial sourcing and procedures. - Ensure smooth internal and external client relations regarding contract drafts and negotiations. - Resolve conflicts or infringements arising from existing contracts. - Expected to be an outstanding leader in the field of contracts administration. - Knowledge and expertise on law governing contract drafting and management is necessary. - Excellent management and interpersonal skills with the ability to work as an individual contributor and team member. - Review and advise Controller of unusual or out-of-scope items/issues. - Follow up to ensure final copies of contracts are filed electronically. - Capex processing and recording, working with Recycling personnel to obtain full information when requesting CAPEX. - Liaison with corporate purchasing to coordinate paperwork and obtain proper approvals. - Maintain good control of all Division assets and conduct random audits at each plant. - Liaison for Insurance requests/requirements. - Track and record baler movement to/from fiber suppliers. - Record appropriate UCC filings with each jurisdiction as needed. - Follow all company policies per Employee Handbook & Code of Conduct. - Follow all company safety guidelines. - Perform other job-related duties as assigned. Qualifications - Prefer college degree with 5 years of experience. - Strong, demonstrated experience in contract administration. - Proficiency using MS Office, Adobe Acrobat, and SAP. - Ability to coordinate with teams while needing little supervision or direction. - Capable of working on multiple projects with varying deadlines. - Professional demeanor and clear communication skills. - Ability to work remotely. - Limited travel required. - Professional attitude & conduct to co-workers, supervisors, and the general public at all times. - Multi-tasking, interpersonal communication, problem-solving, and time management skills are needed. - High degree of safety awareness and safety discipline. Benefits - Paid Holidays from DAY ONE. - Insurance benefits and wellness reimbursement program within ONE MONTH of hire. - 3 Months: 401(k) with match. - 12 months: FULL tuition reimbursement and PAID childbearing/parenting leave. Company Description Why choose Pratt? - Growth/Development – we believe strongly in investing in our talented people as we know that their success means our collective success. - Family – we view each of our fellow coworkers as extended family and are proud to welcome each of you. - Entrepreneurial Spirit - each of our facilities operates independently, allowing the local leadership and team to propose and implement site-specific changes.

• Assist in maintaining Centene Corporation’s Compliance Program • Provide regulatory interpretation, perform compliance reporting, lead special projects • Develop and implement compliance auditing and monitoring strategies • Respond to external requests for information required by the organization for its regulatory filings • Manage compliance reporting responsibilities and respond to inquiries from state and federal regulatory agencies • Manage ethics and compliance projects or implementations • Review and synthesize regulatory requirements and create policy and/or position statements • Assist in managing annual code of conduct attestation and remediation • Communicate state and federal requirements to internal and external clients • Provide development guidance and assist in the identification, implementation, and maintenance of compliance policies, procedures and work instructions • Assist in the identification, analysis, and resolution of compliance issues • Maintain and review regulatory documentation necessary to maintain corporate standards • Assist in developing, producing and conducting compliance training programs • Perform periodic compliance audits, risk assessments and conducts related to ongoing compliance monitoring activities • Assist health plans in managing relationships with regulatory agencies and seek to resolve policy issues which may negatively impact service to members • Assist management with interim health plan compliance officer responsibilities • Plan, direct and coordinate the implementation of Compliance Committee policy to ensure decisions are properly executed • Serve as a company-wide resource and liaison on policies, contract issues and provisions, communications, workflow, and quality improvements initiatives

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Job Description In this role you will be a pivotal team member with regulatory affairs responsibilities, leading discussions, and coordinating regulatory strategies globally on assigned (Phase 1 to 4) clinical trials, studies and projects. You will be part of a global team providing innovative solutions and global regulatory expertise, being client interfacing to provide strategic regulatory intelligence and guidance. You will feel confident providing regulatory advice and carry out projects in the provision of regulatory affairs services whilst acting as liaison with internal and external clients. You will act as a representative of the regulatory department with other departments, supporting business development, working on initiatives, and contributing to quality improvement. You will also arrange, lead, and report on client and regulatory agency meetings. The following skills are required to be successful in this position: - preparation and assembly of global regulatory submissions - interacting with sponsors, - review and assess clinical trial regulatory documents, - review and assess scientific literature. - manages project teams and preparation - participate in launch meetings, review meetings and project team meetings. Optional skills: - Experience with bid defense meetings Qualifications - External What the role requires you to have: - Bachelor's degree or advanced degree preferred, or equivalent and relevant formal academic / vocational qualification - Previous experience that provides the knowledge, skills, and abilities to perform the job - Knowledge of the global clinical trials landscape Knowledge, Skills and Abilities: - Excellent command of the English language (written and oral) as well as local language where applicable - Excellent attention to detail and quality as well as excellent editorial/proofreading skills - Exceptional interpersonal skills to work effectively in a team environment and act as a liaison with other departments - Advanced computer skills including the use of Microsoft Word, Excel, Power Point; capable of learning new technologies - Strong organizational, time management, and planning skills to create and follow timelines, conduct long-range planning, adapt to changing priorities and handle multiple projects - Capable of working independently and exercising independent judgment to assess sponsor regulatory needs and work with project team members to producing compliant deliverables - Excellent understanding of global/regional/national country requirements/regulatory affairs procedures for clinical trial authorization; expert knowledge of ICH and other global regulatory guidelines - Excellent analytical, investigative and problem-solving skills

• Support clients in meeting complex global environmental regulations with a focus on EPR requirements • Produce high-quality compliance reports and provide expert guidance to clients • Conduct in-depth research into evolving environmental legislation worldwide • Liaise with national enforcement agencies across EU Member States and internationally • Manage client registrations and submissions of product, battery, and packaging data to regulators and recycling schemes • Work with Sphera’s EC4P platform to help clients minimize environmental impacts at end-of-life