Lab Analyst - Data Verifier (full-time) Sligo Not disclosed Permanent full-time Updated 02/11/2013 Description AbbVie (NYSE:ABBV) is a global, research-based biopharmaceutical company formed in 2013 following separation from Abbott. AbbVie combines the focus and passion of a leading-edge biotech with the ex... AbbVie (NYSE:ABBV) is a global, research-based biopharmaceutical company formed in 2013 following separation from Abbott. AbbVie combines the focus and passion of a leading-edge biotech with the expertise and capabilities of a long-established pharmaceutical leader to develop and market advanced therapies that address some of the world’s most complex and serious diseases. In 2013, AbbVie will employ approximately 21,000 people worldwide and markets medicines in more than 170 countries. Key responsibilities of our Lab Analyst - Data Verifier: · Responsible for housekeeping duties in the lab. · Responsible for the timely completion of chemical testing of raw material. · Ensure that all test equipment is used and maintained correctly. · Responsible for raising change requests and data verification as assigned. · Ensure all in process sampling and testing is completed in a timely manner. · Maintain up-to-date, complete and precise records of all tests performed. · Adhere to cGMP and GLP requirements. · Assist in the resolution of quality problems as required. · Developing and changing of in-house laboratory procedures as appropriate. · Aid in training of new analyst. · Supports the transfer of new products. · Adheres to and supports all EHS & E standards, procedures and policies Education / Experience requirements: Education: 3rd level qualification in a relevant Science discipline Job/Technical Skills: - Experience operating to cGMP standards utilizing laboratory equipment. - Previous experience in a pharmaceutical manufacturing environment is desirable but not essential. Cognitive/Business Skills: - Requires a high level of attention to detail and mental concentration, to ensure accuracy and total compliance with procedures at all times. - Requires proven problem solving skills and the ability to adapt to new requirements. - Must be results driven striving to meet all targets and metric standards as set by site/department and division leaders - Requires total commitment to quality and maintaining a high standard of work at all times. - Demonstrates the highest levels of integrity and a strong work ethic at all times - Strong communication skills both verbal and written are required for the execution of this role. - Strong interpersonal skills are required. - Supports the principles of Perfect Performance. Ownership/Accountability: - Expected to handle all day-to-day incoming, in-process and final product testing and analysis. If problems occur, can consult their leader. - Shows a high level of tenacity to ensure closure of issues and projects. - Demonstrates an ethos of Right First Time at all times. - Adheres to and follows all procedures policies and guidelines ensuring compliance with cGMP and IMB/FDA regulations and company policies, procedures and guidelines. Influence/Leadership: - Is responsible for ensuring that proper analytical test methods and procedures are adhered to. - May be required to contribute to site teams. Decision Making/Impact: - Expected to handle all day to day analytical issues/queries, however, if a major problem occurs they will confer with relevant personnel or Team Leader. - Decision making within confines of agreed responsibility with Team Leader. Supervision Received ; - Individuals will be self motivated and work with a high level of autonomy. - The position will report directly to the Analytical Chemist/Department Manager - Goals are reviewed on a regular basis and formal performance reviews are carried out once per year.
Posted on: Sat, 02 Nov 2013 15:31:31 +0000
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