<p><strong>Senior P& L Analyst: Nat Gas & Power - Hedge Fund</strong></p><p><br></p><p>Our client a Greenwich based Hedge Fund continues to build out their physical energy trading business. This role offers an opportunity to work in a dynamic environment, supporting risk management activities within the energy sector. The ideal candidate will bring a strong understanding of commodities trading and market risk principles.</p><p><br></p><p><strong>Responsibilities:</strong></p><p>• Analyze daily profit and loss (P& L) reports and provide detailed insights to stakeholders.</p><p>• Monitor trading risk exposure and ensure compliance with established risk limits.</p><p>• Evaluate pricing mechanisms and position-keeping strategies to optimize portfolio performance.</p><p>• Collaborate with traders and product control teams to ensure accurate data flow and reporting.</p><p>• Perform risk assessments on derivatives and hedging strategies related to natural gas and power.</p><p>• Assist in implementing effective risk mitigation strategies.</p><p>• Provide recommendations to improve trading processes and risk management frameworks.</p>
The salary for this position is 77,000 - 87,000. <br> Benefits: The opportunity to work in a growing, innovative environment within the pharmaceutical industry. detail oriented growth and development in a compliance-focused team. Competitive compensation and benefits package <br> We are looking for a dedicated Associate to play a key role in ensuring compliance with quality and regulatory standards within the pharmaceutical industry. Based in Basking Ridge, New Jersey, this position offers an exciting opportunity to contribute to the delivery of high-quality generic pharmaceutical products. The role is ideal for individuals passionate about maintaining regulatory excellence and driving quality management initiatives. <br> Responsibilities: • Ensure adherence to FDA Good Manufacturing Practices (GMP) and other regulatory standards within the pharmaceutical manufacturing process. • Collaborate with cross-functional teams to implement and maintain quality management systems. • Conduct regular audits and inspections to monitor compliance with established protocols and industry regulations. • Provide support in the preparation and submission of regulatory documentation to relevant authorities. • Identify areas for improvement in quality processes and recommend actionable solutions. • Work closely with internal stakeholders to address compliance issues and implement corrective actions. • Stay updated on changes in regulatory requirements and ensure policies and procedures reflect the latest standards. • Assist in training team members on quality and compliance-related topics to promote awareness and adherence. • Contribute to the development and review of quality assurance documentation, including SOPs and guidelines. • Support the resolution of quality-related challenges to maintain product integrity and customer satisfaction.
<p>We are looking for a detail-oriented Regulatory Affairs Labeling Associate to join a dynamic team in Bridgewater, NJ. This long-term contract position offers an excellent opportunity to contribute to regulatory compliance and process improvement within the health and pharmaceutical industry. The ideal candidate will support labeling projects, facilitate cross-functional collaboration, and ensure timely project completion.</p><p><br></p><p>Responsibilities:</p><p>• Coordinate labeling projects to ensure compliance with regulatory standards and guidelines.</p><p>• Offer expert guidance to team members regarding labeling regulations and procedural requirements.</p><p>• Execute project deliverables, including initiating, reviewing, and implementing label updates with a high level of precision.</p><p>• Communicate project progress and updates to cross-functional teams to align efforts and meet deadlines.</p><p>• Build strong relationships with departmental leaders to enhance understanding of process needs and objectives.</p><p>• Represent Clinical Development Operations in project management meetings to provide insights and updates.</p><p>• Develop pharmaceutical labeling drafts and final versions for submission, ensuring adherence to regulatory and client requirements.</p><p>• Collaborate with external vendors to create accurate labeling proofs and oversee final approvals.</p><p>• Manage and track the review process for labeling pieces to ensure timely submissions.</p><p>• Identify and implement necessary changes to approved labeling based on regulatory updates and reference drug modifications.</p>
