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Associate Director, CMC

Merck

Associate Director, CMC

full-timePosted: Aug 25, 2026Updated: Sep 1, 2026CHN - Beijing - Beijing (Wangjing Park)

Job Description

Job DescriptionJob ResponsibilitiesLeadership and Team Management: Manage a team within China RA CMC, including performance management, training, workload oversight, and support for a healthy work-life balance. Ensure team activities are delivered effectively, efficiently, and in compliance with external regulatory requirements and internal quality procedures.Cross-functional Collaboration and Risk Management: Collaborate with departmental and cross-functional partners to share technical and regulatory knowledge, align expectations, coordinate planning and monitoring activities, and mitigate risks.CMC Regulatory Submissions: Deliver timely and efficient CMC regulatory submissions across drug development and the lifecycle management.Technical Regulatory Support: Partner with regulatory colleagues on product specifications, quality control testing, and inspection-related matters; provide technical input and facilitate discussions between China and HQ teams.Project Team Engagement: Participate in China project development teams and work with regulatory and project leads to identify and address CMC needs.External Engagement: Build networks with pharmaceutical industry associations and participate in CMC initiatives and task forces.RequirementsBS, MS or PhD degree in chemistry, biology, or related scientific disciplines; advanced degree is preferred;Expertise in CMC areas such as chemistry, formulation and analytical, at least 5 years of R&D and/or regulatory experience;Knowledge in CMC regulatory requirements and ICH guidelines;Good oral and written communication skills in both English and Chinese;Proven ability in cross-functional cooperation, alignment and ownership in problem solving;Experience in managing and coaching a high performing team.Required Skills: CMC Development, CMC Strategy, Policy Implementation, Regulatory Compliance, Regulatory Labeling, Regulatory Operations, Regulatory Submissions, Strategic Thinking, Team Management, Vendor ManagementPreferred Skills: Current Employees apply HERECurrent Contingent Workers apply HERESearch 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:No relocationVISA Sponsorship:NoTravel Requirements:10%Flexible Work Arrangements:Not ApplicableShift:Not IndicatedValid Driving License:NoHazardous Material(s):n/aJob Posting End Date:12/31/2026*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.

Locations

  • CHN - Beijing - Beijing (Wangjing Park)
  • CHN - Shanghai - Shanghai (Tower A)

Skills Required

  • CMC areas such as chemistryintermediate
  • managingintermediate

Required Qualifications

  • BS, MS or PhD degree in chemistry, biology, or related scientific disciplines; advanced degree is preferred; (degree in phd degree in chemistry)
  • Expertise in CMC areas such as chemistry, formulation and analytical, at least 5 years of R&D and/or regulatory experience; (experience, 5 years)
  • Knowledge in CMC regulatory requirements and ICH guidelines; (experience)
  • Good oral and written communication skills in both English and Chinese; (experience)
  • Proven ability in cross-functional cooperation, alignment and ownership in problem solving; (experience)
  • Experience in managing and coaching a high performing team. (experience)

Preferred Qualifications

  • Current Employees apply HERE (experience)
  • Current Contingent Workers apply HERE (experience)

Responsibilities

  • Leadership and Team Management: Manage a team within China RA CMC, including performance management, training, workload oversight, and support for a healthy work-life balance. Ensure team activities are delivered effectively, efficiently, and in compliance with external regulatory requirements and internal quality procedures.
  • Cross-functional Collaboration and Risk Management: Collaborate with departmental and cross-functional partners to share technical and regulatory knowledge, align expectations, coordinate planning and monitoring activities, and mitigate risks.
  • CMC Regulatory Submissions: Deliver timely and efficient CMC regulatory submissions across drug development and the lifecycle management.
  • Technical Regulatory Support: Partner with regulatory colleagues on product specifications, quality control testing, and inspection-related matters; provide technical input and facilitate discussions between China and HQ teams.
  • Project Team Engagement: Participate in China project development teams and work with regulatory and project leads to identify and address CMC needs.
  • External Engagement: Build networks with pharmaceutical industry associations and participate in CMC initiatives and task forces.

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