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(Asso.) Manager, CMC, Regulatory Affairs

EyeBio

EyeBio

Compliance / Regulatory
Beijing, China · Shanghai, China
Posted on Jun 11, 2025

Job Description

Position title: Asociate Manager or Manager, CMC

Department: Regulatory Affairs

Report to: Senior Manager of CMC

Location: Beijing/Shanghai, China

Responsibilities

Take CMC lead for products under clinical development and for marketed drug products. Coordinate various aspects of CMC regulatory activities with internal and external stakeholders. Act as a primary representative internally and externally for CMC issues.

  • Provide CMC expertise to support drug development at various stages including clinical trial application, NDA and post approval variations
  • Lead the communication with HQ CMC and China RA teams to ensure high quality CMC submissions in compliance with China regulations and guidelines
  • Act as a primary contact for CMC query response, lead and coordinate the response process between China and HQ teams, and interact with the agency for project related CMC issues
  • Work with regulatory colleagues on specification, quality control testing and inspection for specific products; provide technical input and facilitate the discussion between China and HQ teams
  • Participate in China project development teams to identify CMC needs by working with regulatory and project leads
  • Develop network with pharmaceutical industrial associations and participate in CMC initiatives and task forces

Requirements

  • BS, 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, 3~5 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;
  • Proactive and teamwork spirits

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:

No relocation

VISA Sponsorship:

No

Travel Requirements:

25%

Flexible Work Arrangements:

Not Applicable

Shift:

Not Indicated

Valid Driving License:

No

Hazardous Material(s):

n/a

Required Skills:

CMC Development, CMC Documentation, CMC Strategy, Communication, Interpersonal Relationships, Regulatory Affairs Compliance, Regulatory CMC, Regulatory Communications, Regulatory Compliance, Regulatory Compliance Audits, Regulatory Strategy Development, Regulatory Submissions, Stakeholder Management

Preferred Skills:

Job Posting End Date:

12/31/2025

*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.