Job Description
Position Summary: This position is responsible for carrying out tasks and projects related to management of Quality Assurance activities as required by Good Manufacturing Practice (GMP). These activities include Incoming material release, Batch release, Change control, Event management, Supplier qualification, Annual product review and Validation compliance activities. Provides support and direction to all departments in respect of specific quality system elements to ensure business, quality and compliance goals are met. GENERAL SCOPE OF RESPONSIBILITIES: Provides support and direction to all departments in respect of specific quality system elements to ensure business, quality and compliance goals are met following the Standard of Leadership behavior model. Partners with other Departments to ensure that compliance systems are implemented in an efficient manner. Duties Batch Record Review & material release to ensure compliance with GMP requirements. Carries out tasks related to the administration of event management systems including Review & Approval of Event, Deviations, and Customer complaints. Carries out tasks related to the management of batch records design and approval. Carries out administration of the SAP Quality Management Module. Carries out tasks relating to the management of site change control systems. Compiles Annual Product Reviews. Supports all validation activities on site as described in the Site Validation Master Plan. Approves and compiles where appropriate validation protocols and reports (analytical, cleaning, computer, process, equipment, etc.). Supports system qualification and process validation activities. Reviews and approves SOPs/work instructions/forms from other departments on behalf of Quality Assurance Co-ordinates and assists in the preparation for regulatory and customer GMP inspections of the site. Participates in the introduction of new process or modified process steps, as part of a New Product Introduction Team (NPI) Perform GMP audits on-site and vendor facilities as required. Performs on the floor walkdowns regularly to ensure process and facilities are maintained to GMP standards. Carries out tasks related to the administration of site supplier approval process. Key Skills and Competencies required: Excellent interpersonal skills Ability to operate as part of a team is critical. Customer focus Innovative Excellent communication skills both written and verbal Attention to detail Good problem solving skills Results and performance driven Adaptable and flexible Decision making QUALIFICATIONS AND EXPERIENCE: ESSENTIAL- Quality Assurance Specialist-QA Operations: Bachelors Degree in a scientific/technical discipline required A minimum of 3-5 years experience in a quality, validation or compliance role within the biological and/or pharmaceutical industry. Knowledgeable of FDA/EMEA regulatory requirements applicable to biologics and/or pharmaceuticals. Ability to apply GMP regulations and other FDA and international guidelines to all aspects of the position. Demonstrated knowledge and application of industry regulations as they apply to quality, including those of FDA, IMB, EMEA and other authorities. DESIRABLE: Experience in auditing of external suppliers, contractors and vendors. Although it is not possible for us to respond to all applications, we at PE Global will do our upmost to give you feedback on your application. You have sent your Cv into us as a company and even though you have sent your CV to a particular position, we are making the reasonable assumption that you are active on the job market and as part of our normal recruitment service we will discuss other suitable positions with you. You are free to opt out of this so please specify in your application to us if you just want to be contacted in relation to a specific vacancy. Your Cv is sent to a central recruitment inbox which a number of people in the applicable PE Global division have access to and so this means that you might not be contacted by the named person in this advert. Skills: quality assurance validation GMP compliance FDA