MSD
Job title:
Manager, Quality Assurance – Carlow, Hybrid
Company
MSD
Job description
Job DescriptionAs a part of our dedicated team at our state-of-the-art Carlow site, you will have the opportunity to deliver life-changing medication to patients across the globe. We’re calling for a dynamic and committed Manager, Quality Assurance, who will be instrumental in maintaining our firm commitment to quality and compliance with cGMP and corporate regulations. This role presents an incredible opportunity for you to contribute directly to our purpose – advancing the prevention and treatment to patients.Your Core ResponsibilitiesAs a key member of our team, you will uphold and promote compliance with cGMP and corporate regulations by supporting operational and business areas, and monitoring site cGMP activities.It will be your responsibility to maintain the principles of data integrity (ALCOA) in daily business activities and complete relevant CGMP training.You will be the cornerstone in escalating any potential CGMP violations or issues that could impact the safety, efficacy, quality, or purity of our manufacturing division’s human health products.Your role includes fostering an inclusive culture in Carlow that values safety and compliance, and providing essential training to team members.You will have the opportunity to support the development of enhanced quality reporting measuresand ensure effective communication processes across all company levels.You will actively participate and contribute to continuous improvement initiatives, such as batch record review, discrepancy reporting, investigations, the QMS, CAPA’s, and change control.Your role will empower you to keep job descriptions updated, manage your team within the allocated budget, and promote personal growth and development.Creating team priorities and fostering a high-performing and inclusive culture will be a critical part of your role.Who You AreYou are ready if you have:We are seeking a proactive and detail-oriented professional with a Bachelor’s Degree or higher, preferably in a related Science discipline.You should have a minimum of 5 years of experience in pharmaceutical manufacturing facility operations, ideally with Vial and Syringe experience.You should possess a solid understanding of cGMP and Quality Management Systems.Your experience in people management, including coaching and mentoring, will be critical in this role.We value individuals with demonstrated decision-making abilities.Nice to have, but not essential:Lean implementation experience or continuous improvement experience would be advantageousCurrent Employees applyCurrent Contingent Workers applySecondary Language(s) Job Description:As a company, we are committed to ‘Inventing for Life’ in all that we do. We keep the patient at the very heart of all that we do and strive to find solutions and treatments for some of the world’s most challenging healthcare needs.As an equal opportunity employer, we are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. Please don’t hesitate to contact the Talent Acquisition Advisor assigned to this role should you need any support during our recruitment process.We are committed to flexible working where possible, and this is why our Company has introduced a new hybrid working model for office-based colleagues around the world.Please feel free to speak to us about what flexibility means to you during your application or click on the link to find out more about ourSo, if you are ready to:Invent solutions to meet unmet healthcare needs, please apply today.Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.Employee Status: RegularRelocation:VISA Sponsorship:Travel Requirements:Flexible Work Arrangements: HybridShift:Valid Driving License:Hazardous Material(s):Job Posting End Date: 10/15/2024*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
Expected salary
Location
Carlow
Job date
Sun, 06 Oct 2024 05:48:19 GMT
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