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Home Flexible Job Board Sr. Director, Business Development (Japan)

$81,000–111,000/yr 103d ago

Sr. Director, Business Development (Japan)

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Avid Bioservices

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Summary

Drive sales and increase market visibility for Avid Bioservices within the biopharmaceutical and biotechnology sectors in Japan. Lead the entire sales cycle from prospecting and proposal development to contract negotiation and execution of service agreements.

Job Description

Looking to join a passionate team dedicated to developing and manufacturing life-saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes.

Your Role:
The Senior Director, Business Development will have a strategic role in driving increased sales and business for Avid amongst biotechnology, biopharmaceutical and pharmaceutical companies, or others as deemed appropriate, and increasing Avid Bioservices’ visibility in the marketplace, while creating mutually beneficial business partnerships.

Key Responsibilities:

  • Grow Avid’s market share and revenue within the biopharmaceutical/biotechnology CDMO industry by identifying and meeting with prospective clients to sell the benefits of partnering with us.
  • Generate and close new biologics development and manufacturing opportunities, assuring revenue, bookings and pipeline targets are met.
  • Lead opportunities from prospecting through contract negotiation and execution.
  • Develop long term relationships with biotech and pharma executives
  • Partner internally with technical, operations, program management, legal and finance teams.
  • Present proposals and negotiate Master Service Agreements, Work Statements and Commercial Supply Agreements.
  • Develop and implement sales strategies
  • Maintain relationships with existing clients to secure follow-on business.
  • Utilize CRM (salesforce.com) to manage opportunities with clients.
  • Solicit and manage requests for proposals, information, and quotations from clients and potential clients.
  • Collaborate with the proposal writer to customize and assemble documentation due to clients and ensure completion and issuance of responses for all forms of requests for information.
  • Collaborate with the proposal writer to develop pricing models, structure, and negotiate manufacturing contracts, and support project scope of work documentation.
  • Represent Avid at industry conferences such as BIO, DCAT, JPM and CPhI. 
  • Coordinate and manage client site visits and audits.
  • Exhibit strong executive presence with the ability to communicate effectively across all levels of the organization.
  • Schedule travel as needed and submit expense reports in a timely manner.
  • Participate in mandatory team meetings and regularly standing internal calls.

Minimum Qualifications:

  • Bachelor’s degree (B.A or B.S.) in biology, chemistry or similar science disciplines from a four-year college or university, with a Master’s in Business Administration preferred.
  • 10+ years of experience in CDMO sales positions demonstrating knowledge, capability and expertise in the biologics/pharmaceuticals industry or equivalent combination of education and experience.
  • 5+ years selling biologics development and manufacturing services specifically is preferred.
  • Demonstrate ability to establish and build professional relationships. Growing and expanding sales and customer base is required.
  • Demonstrated ability to work within a team environment, supporting fellow business operations, marketing, proposal writers and project management professionals.
  • Demonstrated experience within the territories with access to biopharmaceutical accounts.
  • Ability to navigate internal teams to ensure the best support of client needs.
  • Proficient in Microsoft suite of software programs, and others a needed.
  • Strong understanding of:
    • Cell line development
    • Upstream and downstream processing
    • Process development and scale up
    • Tech transfer
    • Analytical development
    • GMP manufacturing
    • PPQ and commercial manufacturing
    • Regulatory requirements for biologics (FDA, EMA, ICH)
    • Modalities such as monoclonal antibodies

 Position Type/Expected Hours of Work: This role is a full-time remote position based in Japan. Days and hours of work are Monday through Friday unless otherwise stated by Supervisor. The employee must also have the ability to work overtime and/or weekends when necessary.Compensation:  We offer competitive compensation packages for this role, including a base salary, performance-based bonuses, and comprehensive benefits such as health, dental, and vision insurance, 401(k) matching, and paid time off. The compensation range for this role is $81,000 - $111,000 annually depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment. Who you are:  

  • You have a "bring it on!" team player approach and an unshakable positive attitude, always ready to tackle anything that comes your way.
  • Your written and verbal skills are out of this world, and you communicate with clarity and confidence.
  • You have exceptional multitasking skills and an unparalleled attention to detail that ensure the smooth running of everything.
  • You are a master at building relationships, capable of establishing connections with anyone, be it team members, clients, vendors, or suppliers.

Physical Demands & Work Environment:  

In this dynamic role, expect a blend of regular activities like sitting, standing, and walking, with occasional physically engaging tasks such as lifting objects up to 25 pounds. The work environment might expose you to electrical shocks, toxic chemicals, vibrations, or loud noise levels occasionally. However, reasonable accommodations are available to enable individuals with different abilities to perform effectively, ensuring a supportive and adaptable work setting. Your visual acuity, including close, distance, and color vision, will be essential in navigating through the diverse day-to-day demands of this position.

About the company

Avid Bioservices

Avid Bioservices is a biologics CDMO and partner focused on delivering quality, speed, and predictability from DNA to CGMP.

We support biotech and pharma companies across the full development lifecycle, with integrated capabilities in cell line development, process development, and CGMP manufacturing for clinical and commercial supply.

Our platforms are intentionally aligned from early development through manufacturing, enabling seamless tech transfer and reducing risk as programs scale.

Our approach is built on predictable delivery. We combine rapid timelines with disciplined execution, giving our partners confidence in both speed and outcomes.

With transparent communication and strong program management, our teams operate as an extension of our clients - ensuring clarity, accountability, and momentum at every stage.

Quality underpins everything we do. We have a strong regulatory track record and a commitment to operational excellence that enables consistent, reliable results from early-phase programs through commercial production.

Our U.S.-based facilities provide a trusted, scalable manufacturing environment.

At Avid, our services are designed to solve a single problem: how to move biologics programs forward quickly and reliably without compromising quality. By aligning our capabilities, platforms, and teams around that goal, we help our partners accelerate development and deliver therapies to patients with confidence.

Founded

2002

Company size

201-500 employees

Industry

Pharmaceutical Manufacturing

Org type

Public Company

Headquarters

Tustin, California

Apply Now

About the company

Avid Bioservices

Avid Bioservices is a biologics CDMO and partner focused on delivering quality, speed, and predictability from DNA to CGMP.

We support biotech and pharma companies across the full development lifecycle, with integrated capabilities in cell line development, process development, and CGMP manufacturing for clinical and commercial supply.

Our platforms are intentionally aligned from early development through manufacturing, enabling seamless tech transfer and reducing risk as programs scale.

Our approach is built on predictable delivery. We combine rapid timelines with disciplined execution, giving our partners confidence in both speed and outcomes.

With transparent communication and strong program management, our teams operate as an extension of our clients - ensuring clarity, accountability, and momentum at every stage.

Quality underpins everything we do. We have a strong regulatory track record and a commitment to operational excellence that enables consistent, reliable results from early-phase programs through commercial production.

Our U.S.-based facilities provide a trusted, scalable manufacturing environment.

At Avid, our services are designed to solve a single problem: how to move biologics programs forward quickly and reliably without compromising quality. By aligning our capabilities, platforms, and teams around that goal, we help our partners accelerate development and deliver therapies to patients with confidence.

Founded

2002

Company size

201-500 employees

Industry

Pharmaceutical Manufacturing

Org type

Public Company

Headquarters

Tustin, California

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