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Senior Life Sciences Associate with hybrid working - Derby, Derbyshire, United Kingdom - Getinge
Description
Getinge is a leading Medtech company and global provider of products and systems that contribute to saving lives through quality enhancement and cost efficiency within healthcare and life sciences.
We employ more than 10,000 people globally and we focus every talent and resource towards helping our customers save as many lives as possible.
Senior Quality & Regulatory Associate - Derby, HybridGetinge's Global Centre of Excellence for Chemistry are looking for a Senior Quality & Regulatory Associate to support the Quality and Regulatory Department in the establishment, maintenance, and implementation of the local quality management system in order to comply with applicable regulatory requirements and established standards including ISO 13485, MDR/MDD, 21 CFR 820, REACH.
Quality Assurance:
Design, build and implement new quality processes into the organisation. Drive continuous improvement in all aspects of the existing quality operation. Set high standards and lead others to maintain a quality culture across the business.
Champion the quality management system to the wider business to engage compliance within departmental functions. Document control across all tiers of the document hierarchy from the Quality Manual to records.
Non-conformance and complaint processing including risk assessment, root cause analysis, CAPA implementation, and data trending.
Implementation of effective supplier evaluation and controls in coordination with the procurement team.
Oversee the implementation of an effective local training procedure.
Review of batch related documentation including Goods-In, Quality control and DHR.
Ensure adherence to management system planning and that changes are effectively implemented across the local organisation.
Ensure validation activities for process, equipment, and software are in compliance with local procedures.
Lead, participate in, and ensure adherence to local procedures in:
Risk Management according to ISO 14971
Ensure implementation of labelling compliance activities, updates, and version controls
Regulatory:
Maintenance of medical device registrations with MHRA and EUDAMED
Implementation and maintenance of distributor quality agreements
Management of global regulatory submission records, communicating with global partners to ensure timely submissions/registrations. Working with internal sales to implement appropriate product sale controls based on regulatory status.
At Getinge, we are looking for passionate individuals, who are agile, resilient, take responsibility for their development and focus on achieving excellence.
They never compromise on quality and always act responsibly remembering that our customers always come first. Relevant scientific degree or equivalent in a related disciplineMinimum 5 years' experience in a regulated industry within quality and/or regulatory function having effectively used QMS processes such as change control, failure investigation, CAPA.
Knowledge of medical device quality related frameworks such as ISO 13485, Medical Device Regulation, 21 CFR part 820 is desirable although consideration would be given to candidates with similar experience in chemical, pharmaceutical, food, cosmetic, automotive industries with translatable skills.
Personal qualities:
Takes pride in generating detailed, high-quality documentation that is engaging and audit ready.
Accountability - provide clear and accurate data regarding product and process measurables.
Enthusiasm to drive continuous improvement within quality.
We offer a competitive compensation & benefits package, including private health insurance, hybrid working, pension contributions, attractive family-friendly policies, wellness and training programs, to ensure we support your wellbeing and success.
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Senior Life Sciences Associate with hybrid working professionals in Derby
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Abdulghani Elazreg
Teaching Electronics, wireless communication