layiq

/la·yiq/adjective

worthy; deserving; fitting; suitable.

A role, opportunity, or path that merits attention, time, and pursuit.

LAYIQ - Sr Manager, GxP Compliance Officer at Fresenius Kabi

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 Recogition 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

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.
Previous experience in executing and/or managing GxP audits or inspections a preferred
Ability to effectively interact with and influence plant personal and leadership regulators, global partners or affiliates, industry executives, trade organizations.
Established contacts to US-FDA are beneficial
Strong analytical problem-solving experience is essential. Demonstrated prior experience in leading and motivating teams to conceptualize and develop innovative and creative solutions that are robust and sustainable.
Ability to manage multiple complex situations, where precedent may not have been established. Ambiguity and uncertainty will often be associated within the framework of decision making facing this individual.
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.
Bilingual English/Spanish preferred
The Company’s primary business language is English. The successful candidate must be able to effectively speak, read, write, and understand English to perform the essential functions of the position, including independently understanding policies, procedures, training materials, and workplace communications written in English due to our heavily regulated work environment.
Additional Information
We offer an excellent salary and benefits package including medical, dental and vision coverage, as well as life insurance, disability, 401K with company contribution, and wellness program.

Sr Manager, GxP Compliance Officer

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