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Open nowFirst seen 4 days ago

R&D Director – Pharmaceutical Manufacturing

PM Consulting1,477 open roles

Where
Philippines, Laguna, Philippines
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Your applicationOpen nowR&D Director – Pharmaceutical ManufacturingPM Consulting · Philippines, Laguna, Philippines

  1. YouYes, apply to this one.

  2. CV RocketCV written for this posting.

  3. 25 readersRecruiter, hiring manager, skeptic. Round after round.

  4. CV RocketApplied on PM Consulting's own form.

The reply lands in your private mailbox

3×more interviews than doing it yourself with ChatGPT.

The clock on this job

Early applications get read.

12.3% of postings close within 7 days. Measured by our own scanner across the market. PM Consulting postings stay open a median of 1 days.

Share of postings closed within
  1. 2.1%1 day
  2. 4.5%3 days
  3. 12.3%7 days
  4. 19.3%14 days
  5. 35.6%30 days
  6. 57.8%60 days
This job: first seen 4 days ago

PM Consulting median: 1 days open

The posting

Key Responsibilities:

Strategy & Leadership

  • Shape and execute the overall R&D direction in line with business growth goals and client needs
  • Oversee the full product development lifecycle, from formulation through to process optimization
  • Spearhead innovation efforts to broaden the organization's capabilities across different product forms such as tablets, liquids, and creams
  • Recruit, develop, and lead a high-performing R&D team

Product Development & Technology Transfer

  • Lead the development of new product formulations based on client specifications
  • Manage pilot batch production, scale-up activities, and the handover of developed products to the manufacturing floor
  • Ensure smooth collaboration between R&D, Production, Quality Assurance, and Regulatory teams throughout the process
  • Provide technical support for troubleshooting issues with existing commercial products

Regulatory & Compliance

  • Ensure all R&D activities meet local and international regulatory requirements including FDA, ASEAN, and PIC/S standards
  • Review and approve key technical documents such as product dossiers, validation protocols, and study reports
  • Support the preparation of regulatory submissions and address technical inquiries from clients and regulatory authorities

Client & Stakeholder Management

  • Serve as the main technical point of contact for toll manufacturing clients
  • Provide scientific expertise and guidance during product development discussions
  • Ensure R&D deliverables are completed on schedule and in line with client expectations
  • Quality & Continuous Improvement
  • Uphold strict adherence to GMP, GLP, and internal quality standards across all R&D activities
  • Identify and implement improvements that enhance efficiency, reduce costs, and shorten turnaround times
  • Establish and promote best practices in formulation and analytical development

Qualifications & Requirements:

  • Bachelor's degree in Pharmacy, Chemistry, Chemical Engineering, or a related field; Master's or PhD is preferred
  • Licensed Pharmacist is highly preferred
  • At least 12–15 years of experience in pharmaceutical R&D, with a minimum of 5 years in a leadership capacity
  • Strong background in a toll manufacturing or CDMO (Contract Development and Manufacturing Organization) setting is highly preferred
  • Proven track record in formulation development, scale-up, and technology transfer
  • Deep knowledge of regulatory frameworks including FDA, ASEAN, PIC/S, and GMP
  • Demonstrated ability to manage multiple client accounts and projects simultaneously
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