ADC Laboratory Analyst Permanent-2 at Merck Sharp & Dohme Corp. /Netherlands

Ballydine, The Municipal District of Carrick-on-Suir, Ireland -

Full Time

Start Date

Immediate

Expiry Date

17 Apr, 26

Salary

0.0

Posted On

17 Jan, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Analytical Chemistry, GMP Compliance, Laboratory Testing, Communication, Data Management, Documentations, Leadership Skills, Analytical Development, Instrument Maintenance, Team Skills, Innovation, Accountability, Technical Lab Skills, Bioanalysis, Chemical Synthesis, Environmental Measurements, High-Performance Liquid Chromatography

Industry

Pharmaceutical Manufacturing

Description

Job Description An amazing opportunity has arisen for a Laboratory Analyst. What you will do: Bring energy, knowledge, innovation and leadership to carry out the following: The Laboratory Analyst has responsibility for Raw Material, Intermediate and Drug Substance testing to meet compliance requirements and customer targets. The Analyst may also take a leadership role in change or improvement projects in ADC or at a site level. The Laboratory Analyst is responsible for ensuring all testing activities comply with cGMP. The Laboratory Analyst assures compliance with all safety and environmental requirements. Compliance with other regulated areas such as HR policies are also responsibilities of the role. To test Raw Materials, Intermediates, Drug Substance and Drug products in accordance with Analytical Standard and/or other approved protocols. To complete routine and non routine testing and review as assigned. To comply with all GMP and analytical procedures relevant to area of work. To adhere and comply with department High Performance Analytical Behaviours. To document all testing activities and to input results into computerised lab systems in accordance with department and our Manufacturing Division standards. To provide analytical support to product quality investigations and new product demonstrations under the supervision of the Laboratory Leader or designate. Complete the investigation of laboratory OOSs in line with site and divisional procedures. Complete checks (e.g. Change control, Deviations) as required for the Drug Substance/Drug Product test package prior to release. To complete testing as required on samples to support process changes. Accountable for own laboratory safety practices. To provide lead analytical support to product quality investigations and new product demonstrations using own initiative and with minimum supervision. Provide leadership in the laboratory aspects of OOS investigations. To identify and aid resolution of analytical issues within the IPT laboratory. To be a resource for analytical testing for the site as required. Execute specific assignments (e.g. stability programme, instrument management and other systems) in a comprehensive manner and under minimum supervision. What skills you will need: In order to excel in this role, you will more than likely have: Minimum of BSc in Chemistry or related discipline. Have knowledge of GMP standards. Have knowledge Laboratory safety standards. Must have good communication skills, both written and verbal. Strong documentation skills are required. Must be motivated, focused and technically strong. To perform analytical testing with a high degree of precision and accuracy. To perform instrument maintenance and troubleshooting. To maintain accurate records in compliance with GMP expectations. To understand and internalise procedures relevant to GMP operations. To communicate clearly and concisely on technical issues. On assignment, to deliver project goals on time. Analytical chemistry – demonstrated ability in all technical elements relevant to ADC IPT operation. Technical lab skills (precision, etc). Strong aptitude for handling analytical instruments. Mechanical and computer. Communication - written, oral. Team and interpersonal skills. Leadership skills. 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. We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. So, if you are ready to: Invent solutions to meet unmet healthcare needs, Impact the future by driving one of the world’s leading healthcare companies, and inspire your team to reach their full potential and push the boundaries of science and technology, please apply today. Required Skills: Accountability, Accountability, Analytical Chemistry, Analytical Development, Analytical Testing, Bioanalysis, Bioanalytical Analysis, Chemical Synthesis, Chemistry, Communication, Data Analysis, Data Management, Documentations, Dosage Forms, Environmental Measurements, GMP Compliance, Good Manufacturing Practices (GMP), High-Performance Liquid Chromatography (HPLC), Improvement Projects, Innovation, Interdisciplinary Collaboration, Laboratory Analysis, Laboratory Safety, Laboratory Services, Laboratory Testing {+ 4 more} Preferred Skills: Current Employees apply HERE Current Contingent Workers apply HERE 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: Regular Relocation: VISA Sponsorship: Travel Requirements: Flexible Work Arrangements: Not Applicable Shift: Valid Driving License: Hazardous Material(s): Job Posting End Date: 01/23/2026 *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. Requisition ID:R380337

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Responsibilities

The Laboratory Analyst is responsible for testing Raw Materials, Intermediates, and Drug Substances to ensure compliance with cGMP and safety standards. They also lead analytical support for product quality investigations and contribute to improvement projects.