Sr. Manager, GxP Compliance Officer

The Sr. Manager, GxP Compliance Officer (GCO) assures that all manufacturing sites and R&D Centers having activities with US-FDA are in compliance with US-FDA regulations, including but not limited to, cGMPs, cGLPs, and electronic records. This includes global facilities within Fresenius Kabi for importation of API or finished products to the US market. This position organizes and promotes company-wide US-FDA quality and compliance improvement and compliance improvement efforts.

Salary Range: $140,000-$165,000

• Position is eligible to participate in a bonus plan with a target of 14% of the base salary (include only if applicable to the grade level)

• Final pay determinations will depend on various factors, including, but not limited to experience level, education, knowledge, skills, and abilities.

• Our benefits and programs are comprehensive and thoughtfully crafted to ensure our colleagues live healthy lives and have support when it matters most. Benefits offered include a 401(k) plan with company contributions, paid vacation, holiday and personal days, employee assistance program, and health benefits to include medical, prescription drug, dental and vision coverage.

Responsibilities

• Responsible for leading, coordination, verification and tracking of global compliance activities within 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
• Lead/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 when related 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 related 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
• All employees are responsible for ensuring the compliance to company documents, programs and activities related to the Health, Safety, Environment, Energy, and Quality Management Systems, as per your roles and responsibilities

Requirements

• Minimum of Bachelor’s degree required. Advanced degree in chemistry, molecular biology, microbiology or engineering field is highly desirable.
• 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.
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