Job Description The Associate Director for Drug Product Quality Assurance (DP-QA) role will involve establishing the Quality structure, ensuring the processes conform to our Company policies and comply with cGMPs, Health Agency regulations and all other applicable governing regulations, with the mission and ambition to manufacture breakthrough medicines from Delaware for patients around the world. Close collaboration with high-performance talent from our Company global team and the biotechnology industry to develop and execute multiple Quality Assurance systems and processes will be key, and the successful candidate will inspire his/her team to build the future of our Company antibody drug conjugates and high potent compounds through a Quality culture that delivers unconstrained supply, that is Right First Time to patients worldwide. Providing training and guidance on the interpretation and implementation of our Company policies and regulatory requirements will also be key priorities. Throughout the development of the new facility, the successful candidate will focus on commissioning, qualification, and/or validation of the facility, equipment, and process. Position Responsibilities: Acting in the role of leading the sterile Drug Product (DP) Quality Assurance team. Responsible for ensuring that the processes for the manufacture of biologics DP have been conducted in compliance with GMP, the registered marketing authorisation and the associated regulatory requirements. In-depth knowledge of US and European GMP guidelines, ICH and other international regulatory requirements, as applicable to the site. Drive compliance direction for the site by ensuring adherence to divisional policies and guidelines as well as regulatory requirements. Responsible for reviewing and approving GMP documentation to support corporate compliance/regulatory expectations for manufacturing operations. Assisting in, and facilitating investigations, ensuring effective Root Cause Analysis and CAPAs. Identify and facilitate major compliance initiatives to improve compliance status and overall operational efficiency of the site. Be an advocate of continuous improvement in the Quality Management Systems. Provide Quality oversight to the qualification/validation, technical transfers, regulatory approvals and commercial operations for sterile DP at the facility. Responsible for the management of batch record review, discrepancy reporting, investigations and CAPAs associated with Drug Product Release. Drives opportunities for continuous improvement. Provide audit support and participate in response team for audits and inspections by Health Authorities. Provide support and expertise for the preparation of regulatory submissions, inspection readiness activities, during health authority inspections including interaction with inspectors, responses to inspection observations, and monitoring of follow up actions. Manage team of shift specialists within the Drug Product QA Operations organization. Qualifications and skills required: General This role requires a seasoned Associate Director with a minimum of 10 years’ experience in Quality Control, Quality Assurance or Pharmaceutical, Vaccine or Biological Operations, or Technical Operations. A self-starter and results-focussed, the successful candidate will have strong contemporary knowledge of relevant cGMPs, regulations and current industry trends. Technical Must have at least 5 years of operational experience in a regulated environment. Must have experience in supporting tech transfer or process validation either internally or externally. Must have experience in drug product quality operations and batch record review. Demonstrated knowledge of Cleaning in Place, Cleaning out of Place, Sanitize in Place. Demonstrated understanding of continuous quality / process improvement tools (As defined by the site, e.g. DMAIC, Lean QA, 5S etc). Exceptional analytical, problem solving & root-cause analysis skills. Ability to multi-task and handle tasks with competing priorities effectively. Strong technical aptitude (i.e. able to read & comprehend technical documentation & execute procedures), global regulatory experience & experience interfacing with regulators is preferred. Strong operations support background ensuring value added and effective quality oversight. People A great communicator with proven ability to deliver excellence Knowledge of relevant cGMPs, regulations and current industry trends related to Antibody Drug Conjugate drug product Manufacturing. Experience with new product introductions and/or process qualification/technology transfer Demonstrated expertise to effectively communicate within all levels of the organization around concepts of design controls, design verification and validation activities; production & process controls; Corrective & Preventive Action (CAPA), complaints & risk management; & product quality improvement using tools such as six sigma, DFR, etc. Excellent communication skills (written and oral). Required to work on his/her own initiative in addition to working as part of and guiding a team. Must be able to work across a team matrix to meet accelerated timelines. Desire to continuously learn, improve and develop. Ability to facilitate groups with perspectives and bring teams to consensus and alignment. Effective communication, presentation and interpersonal skills, to interface effectively with all levels of colleagues and with external customers in a team orientated manner. Able to demonstrate good judgment in collecting and synthesizing relevant data and information to enable timely decisions; communicates and escalates issues and decisions as needed. Planning and scheduling skills, Proven organizational skills, Flexible approach. Goal/results orientated, Starter/Finisher. Education Bachelor’s degree (or higher) in Chemistry, Biology, Microbiology, Automation, Engineering or in a relevant discipline, the successful candidate will also ideally have a proven track record in delivering excellence. Direct experience in manufacture of antibody drug conjugates manufacturing preferred. #ADC #ADC2026 Required Skills: Adaptability, Adaptability, Analytical Thinking, Change Management, Commercial Operations Management, Communication, Competency Management, Compliance Reporting, Cross-Cultural Awareness, Cross-Functional Teamwork, Evaluate Information, GMP Training, Good Distribution Practice (GDP), Government Regulation, Inspection Readiness, Legal Compliance, Manufacturing Quality Control, Multitasking, Operations Support, Policy Compliance, Prioritization, Procedure Adherence, Quality Auditing, Quality Management Standards, Quality Metrics {+ 8 more} Preferred Skills: Current Employees apply HERE Current Contingent Workers apply HERE US and Puerto Rico Residents Only: Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights EEOC GINA Supplement We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State Acts The primary location for this posting is: USA - Delaware - Wilmington (Biotech) Where required by law, the compensation range for this role is provided below. The salary range for the primary location of this role is: $142,400.00 - $224,100.00 This range reflects the Company's reasonable expectation of the base salary applicable to this role at the time of posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs. The successful candidate will be eligible for annual bonus and long-term incentive, if applicable. We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits. Additional location(s): Please note the salary range above applies to the Primary Location of the position. Where a role has other listed locations, different compensation guidelines may apply. You may find the salary ranges for additional locations below. If the salary range is not listed for the location you are applying to, our Talent Acquisition team will provide further information to you relevant to your location. Additional location(s) Compensation Information: San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance 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: No relocation VISA Sponsorship: No Travel Requirements: 10% Flexible Work Arrangements: Hybrid Shift: 1st - Day Valid Driving License: No Hazardous Material(s): n/a Job Posting End Date: 10/29/2026 *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. Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where we have codified our legacy for over a century. Our success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.

Associate Director, Drug Product, Quality Assurance.

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