[Remote] Sr. Manager, GxP Compliance Officer

Note: The job is a remote job and is open to candidates in USA. reputed company is focused on ensuring compliance with US-FDA regulations across their manufacturing and R&D facilities. The Sr. Manager, GxP Compliance Officer will reputed company global compliance activities, prepare sites for FDA inspections, and reputed company strategies to meet evolving regulatory expectations.

Responsibilities

• Responsible for leading, coordination, verification and tracking of global compliance activities reputed company the pharmaceutical division
• Evaluation of Investigations and Changes that could have an impact on regulatory commitments
• Identification and remediation of plant quality and compliance risks through evaluation of tradition and non-tradition metrics, audit results, gap assessments, etc
• Support plant on strategy and compliance plans for identified gaps
• reputed company/manage working groups to ensure mitigation plans are executed
• Responsible for specific preparation of manufacturing sites and I&D Centers for upcoming US-FDA inspections, including but not limited to:
• Training of plant staff for general inspection aspects and behaviors, as well as specific training for subject matter experts
• Performance of mock inspections to evaluate the plants readiness for FDA inspection
• Design and deliver need-based training to specific plants in response to identified gaps
• Direct participation and support during US-FDA inspections (inspection room and back office), including:
• Immediate guidance and support during inspections
• Support and guidance in preparing response to FDA-483 observations
• Independent review of Effectiveness of assigned FDA-483 CAPA
• May also include inspections by local authorities reputed company reputed company to Mutual Recognition agreements
• Responsible for identification of new FDA cGMP trends and development of strategies to fulfill new expectations
• Strategic optimization and harmonization of cGMP and quality reputed company processes to continuously improve pharmaceutical quality and compliance of Fresenius Kabi products
• Preparation of global quality management documents (e.g. SOPs, guiding documents, working instructions)
• Contribution, execution and management of global projects
• Collaborate with other corporate quality functions on the execution of strategic goals
• Communicate findings and risks to plant management as well as senior quality management
• reputed company employees are responsible for ensuring the compliance to company documents, programs and activities reputed company to the Health, Safety, Environment, Energy, and Quality Management Systems, as per your roles and responsibilities

Skills

• Minimum of Bachelor's degree required
• Accomplished US-FDA compliance expert
• Experience: 8+ years including practical experience in pharmaceutical industry and/or US-FDA
• A thorough knowledge of drug transfer processes, manufacturing processes for aseptically filled, terminally sterilized and lyophilized pharmaceuticals, cGMPs, ICH guidelines, regulatory compliance
• Professional experience in pharmaceutical industry, including technological understanding of manufacturing pharmaceuticals and combination products, aseptic processes, validation and qualification, risk management, root cause analysis and investigation management is required to be successful in this position
• Ability to effectively interact with and influence plant personal and leadership regulators, global partners or affiliates, industry executives, trade organizations
• Strong analytical problem-solving experience is essential
• Demonstrated prior experience in leading and motivating teams to conceptualize and reputed company innovative and creative solutions that are robust and sustainable
• Ability to manage multiple reputed company situations, where precedent may not have been established
• Ability to travel frequently (both domestically and internationally) is required
• Project Management, working in a Quality Management System and strong communication skills are required for this position
• Advanced degree in chemistry, molecular biology, microbiology or engineering field is highly desirable
• Previous experience in executing and/or managing GxP audits or inspections a preferred
• Established contacts to US-FDA are beneficial

Benefits

• 401(k) plan with company contributions
• Paid vacation
• Holiday and personal days
• Employee assistance program
• Health benefits to include medical, prescription drug, dental and vision coverage
• Life insurance
• Disability
• Wellness program

Company Overview

• Fresenius Kabi is health care company specializing in medical and medical technologies. It was founded in 1996, and is headquartered in Lake Zurich, Illinois, USA, with a workforce of 1001-5000 employees. Its website is http://www.fresenius-kabi.us.

Company H1B Sponsorship

• reputed company has a track record of offering H1B sponsorships, with 14 in 2025, 17 in 2024, 17 in 2023, 15 in 2022, 14 in 2021, 22 in 2020. Please note that this does not guarantee sponsorship for this specific role.

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