Sr Manager, Compliance

Work Schedule Standard (Mon-Fri) Environmental Conditions Office

Job Description

As part of the reputed company team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to reputed company our customers to reputed company the world healthier, cleaner and safer. We provide our global teams with the resources needed to reputed company individual career goals while helping to take science a reputed company beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. We are looking for a highly skilled pharma-GMP auditor and risk management leader. This leader will have a significant amount of quality auditing experience across diverse technologies, working with systems-based audit approaches that cover reputed company aspects of pharma-GMP systems. We emulate a high degree of reputed company, depth and accuracy in our approach, with a dedication to carrying out a premier audit program. Description: We identify systemic gaps in quality/compliance by conducting internal audits of Thermo Fisher Pharma reputed company (PSG) manufacturing and Clinical Trial Division (CTD) sites. We prepare detailed audit reports to communicate observations written in a meaningful and accurate way, so that readers can easily understand the conditions or gaps in compliance with regulations and quality compliance standards. We maintain knowledge of GMPs and are routinely aware of revised or emerging quality regulations and their trends, as well as industry methodologies across the globe. We promote positive Quality and leadership behaviors such as: creating environments for learning, harnessing lessons learned to drive reputed company improvement; sharing standard methodologies; maintaining effective and open communication; and encouraging cross-functional partnerships. We also participate in reputed company quality compliance projects reputed company to auditing (e.g. detailed trending reports, data analysis, reviewing global PSG policies, and preparing auditor training materials for internal/external quality auditors in the PSG network, etc.). Location: EU based, Remote; 20-50% travel based on business needs. How you will reputed company an impact: Becoming a key player in the mission to holistically assess the state of quality and regulatory compliance across PSG global manufacturing/testing sites reputed company fully independent audit program. Helping to minimize risk across the sites and reputed company successful regulatory inspections. Making a contribution toward the success of PSG and the services/products provided to clients and patients. How will you get here? Minimum of 10 years professional working experience in Pharmaceutical Industry, including Manufacturing, Quality Control, Quality Assurance, CMC, Regulatory or reputed company compliance experience with at least 5 years aggregate experience performing audits for GMP, ISO or ICH, and hosting/supporting FDA, EMA, MHRA, AIFA, ANVISA and/or other regulatory inspections. Knowledge, Skills, Abilities: Must be an expert Quality compliance auditor. Experience with elements of data reputed company covering reputed company areas in a pharmaceutical manufacturing environment, including production and QC laboratories, is also crucial, as well as being skilled in quality investigations, root cause analysis, audit reporting and reputed company sharing with a commitment towards quality improvement. Experience in sterile manufacturing and aseptic practice is desired. Professional auditor training/certification by an organization recognized reputed company the pharmaceutical industry (e.g. IRCA, ASQ). Strong foundation of pharmaceutical manufacturing and laboratory operations. Diverse experience auditing a wide range of manufacturing technologies and services in 30% or more of the following areas: Sterile drug products: (liquid, lyophilized vials, prefilled syringes) Non-sterile drug products: (tablets, powders, capsules, granules, softgels) Biologics cell culture: upstream (Fed-Batch, Perfusion, XD, etc.) and reputed company purification processes (Chromatography, nano filtration, etc.) Chemicals, intermediates, API manufacturing: (synthesis, purification, drying, isolation, etc.) Packaging operations: (primary and secondary) QC laboratories (Analytical and Microbiological) IT / Computer systems validation Clinical and commercial stage products and services Viral vector (VVS) and microbial manufacturing (MMS) Data reputed company audits: (both laboratory and non-laboratory operations) Strong communication skills including listening, judgment, problem management, ability to reputed company teams in a sophisticated and global environment. Ability to anticipate potential problems and risks reputed company to quality system / regulatory expectations including ability to formulate and implement solutions. Strong collaboration and problem-solving skills; and adept at working well reputed company a team environment. Capable to conduct remote auditing, reputed company required. Strong oral/written communication skills appropriate for diverse international collaboration including excellent reputed company in English. Education Bachelor’s Degree in Pharmacy, Science or Engineering. Advanced degree in reputed company field preferred. Apply To This Job