QA GMP-GDP Auditor and Project Manager - 6626 ASH
QA GMP-GDP Auditor and Project Manager - 6626 ASH
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Our client, an innovative and dynamic bio-pharmaceutical company headquartered in Switzerland, covering multiple therapeutic areas, committed into delivering products on the market over the next 5 years, is looking a QA GMP-GDP Auditor and Project Manager for a 12 months contract based in Basel.
QA GMP-GDP Auditor and Project Manager
Main Responsibilities:
* Ensure GDP compliance of facilities.
* Manage, review and approve change controls, deviations and CAPAs related to the internal pharmaceutical operations facilities (not project specific)
* Write, review, and/or approve internal quality system SOPs and other GMP/GDP and regulatory related documentation
* Evaluate, develop, establish, and maintain internal processes and procedures for compliance with GMP / GDP standards and for process improvement (QS document including Quality agreements with third parties
* Administer systems to monitor (KPIs), track, and trend regulatory compliance (e.g. deviations, CAPA, investigations, complain, change control etc.)
* Manage filing process and system for all quality documents
* Support processes and procedures for document management in the EDMS
* Establish External QA Audit and internal self-inspection frequency based on Risk Assessment, as appropriate. Prepare and/or participate to the annual audit plan
* Establish and maintain an approved supplier list for GMP/GDP suppliers/service providers
* Coordinate and conduct GMP / GDP audits and self-inspections; write corresponding audit reports
* Promptly report critical self-inspection findings to the Responsible Person and management, as perSI procedure
* Coordinate, plan and manage Regulatory Agency Inspections
* Support preparation of Regulatory Agency Inspections
* Notify management of potential quality and regulatory issues
* Monitor changes in quality regulations and initiate required activities to keep the quality system aligned and compliant
* Support optimization of Viatris' pharmaceutical quality system by preparing for the review of relevant Key Performance Indicators
* Pro-actively participate to the optimization of the quality system by proposing new procedures, tools or modification of existing ones
* Provide coaching and advise to Junior QA GMP/GDP Auditor and Project Manager when required
Qualifications and Experience:
* Relevant Swiss working/residency permit and/or Swiss/EU-Citizenship required;
* University degree in Pharmacy, Chemistry or alternative technical/science university degree: master level minimum.
* 3-6 years of experience in different positions like pharmaceutical product development/ quality control/ analytical development/ chemical production or similar operational positions in the pharmaceutical industry
* Knowledge and understanding of drug substance and/or Drug Product development, manufacturing process, quality control, packaging and distribution
* Experience in quality assurance of drug substance and/or drug product
* Excellent knowledge of relevant GMP/GDP and international quality regulations: ICH, ISO, WHO, PIC, FDA, EU GMP Guide (EudraLex Vol. 4), EU GDP
* Ability to interpret and implement Quality standards
* Ability to manage complex projects and prioritize workload according to the project importance
* Ability to pro-actively initiate and lead quality compliance activities
* Ability to manage multiple tasks with competing priorities
* Good interpersonal and influencing skills
* Self-confident, assertiveness and autonomy to deal with complex stakeholders/situations
* Ability to communicate clearly and professionally both verbally and in writing
* Fluent in English and at least basic knowledge of an additional European language, German or French advantageous
Seniority level
* Seniority level
Mid-Senior level
Employment type
* Employment type
Contract
Job function
* Job function
Quality Assurance
* Industries
Pharmaceutical Manufacturing and Biotechnology Research
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