Pharma Quality Project Manager
- South District, Israel
- LinkedIn Public
- Verified live ·
Mentioned in this posting
Description
GSAP is seeking a Pharma Quality Project Manager to lead and support projects in Southern Israel. This is a diverse role that includes working closely with clients, leading quality and compliance processes, and creating broad professional impact. Key Responsibilities Quality Project Management · Manage and provide professional support for pharmaceutical quality projects in accordance with client requirements and applicable regulatory standards. · Lead quality and compliance activities in a dynamic, cross-functional environment. · Work independently at client sites while collaborating with professional and management interfaces. GMP Compliance and Quality Activities · Lead quality activities in accordance with GMP principles and requirements. · Support the implementation, maintenance, and continuous improvement of quality processes within regulated environments. · Ensure all activities are conducted in compliance with procedures, client requirements, and relevant standards. Quality in the API Industry · Manage and support quality processes related to the manufacturing of Active Pharmaceutical Ingredients (API). · Provide professional support for manufacturing, documentation, compliance, and quality control activities within API environments. · Collaborate with quality, manufacturing, and operations teams and other interfaces. Client and Interface Management · Manage and maintain ongoing relationships with clients and cross-functional interfaces. · Serve as a key point of contact for client quality-related needs, ensuring timely and effective support. · Coordinate project activities and facilitate communication among relevant functions to achieve project objectives. · Build collaborative working relationships and ensure effective communication throughout all project phases. · Work independently, demonstrating ownership, accountability, and attention to detail while ensuring successful project execution. Requirements · Minimum of 3 to 5 years of experience in Quality Assurance and/or Compliance. · Experience working in a regulated environment and in accordance with GMP requirements – mandatory. · Experience in the API industry – mandatory. · Experience with sterile manufacturing and/or aseptic processes – an advantage. · Managerial experience and/or experience leading processes – an advantage. · High level of English proficiency, both written and spoken. · Strong self-learning capabilities. · Systems thinking combined with strong attention to detail. · Ability to manage and drive multiple tasks and stakeholders simultaneously. · Strong planning, organizational, and prioritization skills. · Ability to work independently and collaboratively in a dynamic and changing environment. · Excellent interpersonal skills, strong communication abilities, and a customer-oriented mindset. Work Environment · Projects are located in Southern Israel. · The role includes ongoing interaction with clients and a wide range of professional interfaces. · This position is suitable for candidates seeking a role with meaningful professional impact, broad responsibility, and opportunities for professional growth in an advanced and dynamic environment. Show more Show less