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Lifecycle Management Biotech Jobs (NOW HIRING)

PSC Biotech

CQV Engineer

Columbus, OH · On-site

PSC Biotech providesthelife sciences with essential services to ensure thathealth careproducts are ... Experience withvalidation lifecycle management and risk-basedapproaches. * Excellentanalyticaland ...

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Lifecycle Management Biotech information

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$171.5K

How much do lifecycle management biotech jobs pay per year?

As of Jun 25, 2026, the average yearly pay for lifecycle management biotech in the United States is $124,832.00, according to ZipRecruiter salary data. Most workers in this role earn between $99,000.00 and $151,500.00 per year, depending on experience, location, and employer.

What are some typical challenges faced by professionals in Lifecycle Management within the biotech industry?

Professionals in Lifecycle Management Biotech often navigate the complexities of maintaining product compliance as regulations evolve, coordinating cross-functional teams (such as R&D, regulatory, and manufacturing), and managing product updates post-launch. Balancing ongoing improvements with cost-effectiveness, while ensuring uninterrupted supply to patients, can be particularly challenging. Additionally, these roles frequently require adapting strategies to align with shifting market demands and technological advancements.

How much does a buyer planner make at Legend biotech?

A buyer planner in the biotech industry typically earns between $60,000 and $85,000 annually, depending on experience and location. The role involves procurement, inventory management, and supply chain coordination, often requiring familiarity with ERP systems and strong negotiation skills.

What are the key skills and qualifications needed to thrive as a Lifecycle Management Biotech professional, and why are they important?

To thrive as a Lifecycle Management Biotech professional, you need a strong background in biotechnology, regulatory affairs, and project management, often supported by a degree in life sciences or related fields. Familiarity with regulatory submission systems, data analytics tools, and quality management software is typically required. Excellent cross-functional communication, problem-solving skills, and attention to detail are vital soft skills for coordinating teams and ensuring compliance. These competencies are crucial for efficiently managing product lifecycles, maintaining regulatory approval, and maximizing product value in a highly regulated industry.

What are LCM projects in pharma?

Lifecycle Management (LCM) projects in pharma involve strategies to extend the value of a drug product after its initial launch, including formulation improvements, new indications, or manufacturing process enhancements. As a biotech professional, managing these projects requires coordination across R&D, regulatory, and manufacturing teams to ensure compliance and timely product updates.

What is the highest paying job in biotech?

In biotech, senior executive roles such as Chief Scientific Officer (CSO) or Vice President of Research typically have the highest salaries, often exceeding $200,000 annually. These positions require extensive experience, advanced degrees, and leadership skills, and they oversee research and development strategies within biotech companies.

What is the difference between Lifecycle Management Biotech vs Process Development Scientist?

AspectLifecycle Management BiotechProcess Development Scientist
Required CredentialsBachelor's or Master's in Biotechnology, Life Sciences, or related fields; often certifications in project managementBachelor's or Master's in Chemical Engineering, Biotech, or related fields; sometimes advanced degrees
Work EnvironmentPharmaceutical or biotech companies, focusing on product lifecycle from development to commercializationLaboratories and manufacturing facilities, focusing on process design and optimization
Employer & Industry UsageUsed in biotech and pharma industries for product lifecycle managementCommon in biotech, pharma, and chemical industries for process innovation

Lifecycle Management Biotech focuses on managing a biotech product throughout its lifecycle, including regulatory and market considerations. Process Development Scientist concentrates on designing and optimizing manufacturing processes. Both roles require strong scientific backgrounds but differ in scope and daily tasks.

What is lifecycle management in biotech?

Lifecycle management in biotech involves overseeing a product from development through commercialization, including stages like research, manufacturing, regulatory approval, and post-market support. It requires coordination across teams, knowledge of regulatory requirements, and often the use of project management tools to ensure product success throughout its lifespan.

Regional Business Development Manager - Biotech & CDMO Services

MatchaTalent

San Francisco, CA • On-site, Remote

Full-time

Posted yesterday

Job description

Open to candidates across the US - Any nationality residing in the US with a US visa
Work From Anywhere (WFA) - Remote basis.


Client Overview:
Our client is a rapidly growing pharmaceutical technology and CDMO company specializing in small molecule drug development, chemical synthesis, process optimization, and GMP manufacturing solutions for the global pharmaceutical and biotechnology industries. Headquartered within one of China's leading national biopharmaceutical industrial zones, the company operates advanced R&D laboratories, synthesis centers, and large-scale GMP production facilities supporting innovative pharma and biotech clients worldwide.

With a strong technical foundation in chemical process development and scalable manufacturing, the organization provides integrated outsourcing solutions for drug discovery, development, and commercial production. As part of its international growth strategy, the company is expanding its commercial footprint across the United States to strengthen partnerships with innovative pharmaceutical companies, biotech startups, and enterprise sourcing organizations.

Job Role:
The International Business Development Manager is a senior-level commercial hunting role responsible for expanding the company's CDMO and pharmaceutical outsourcing business across the United States. Acting as a strategic bridge between US-based pharmaceutical clients and China manufacturing operations, the position focuses on identifying high-value opportunities, securing outsourcing projects, and building long-term enterprise partnerships within the small molecule pharmaceutical ecosystem.

This role requires a highly independent professional with deep pharmaceutical industry exposure, strong commercial instincts, and the ability to communicate complex manufacturing and technical capabilities to executive-level stakeholders. The successful candidate will manage the entire business development lifecycle, from lead generation and RFP acquisition to contract negotiation and strategic account development.

Key Responsibilities:

  • Develop and manage a strong pipeline of pharmaceutical and biotechnology clients across the United States and Europe for CDMO and small molecule outsourcing services.
  • Identify and approach key decision-makers within sourcing, procurement, CMC, external manufacturing, and R&D departments.
  • Lead commercial discussions, negotiations, and execution of agreements including CDA, NDA, MSA, and long-term service contracts.
  • Capture and manage RFP/RFQ opportunities while coordinating closely with technical and manufacturing teams to deliver tailored solutions.
  • Conduct client visits, industry networking, and conference participation to strengthen market visibility and expand strategic relationships.
  • Present technical manufacturing capabilities, process development expertise, and production advantages to enterprise stakeholders.
  • Monitor pharmaceutical outsourcing trends, competitor activities, and regional biotech developments to support commercial strategy.
  • Collaborate with headquarters and technical teams to ensure smooth communication between international clients and manufacturing operations.

Requirements:

  • Bachelor's Degree, Master's Degree, or PhD in Chemistry, Chemical Engineering, Pharmaceutical Sciences, or related disciplines.
  • Minimum 5 years of experience in pharmaceutical business development, technical sales, CDMO services, or biotech outsourcing environments.
  • Strong existing network within pharmaceutical, biotech, or CDMO ecosystems, especially among procurement, sourcing, CMC, or manufacturing stakeholders.
  • Solid understanding of chemical synthesis, process development, GMP manufacturing, scale-up operations, and small molecule production workflows.
  • Proven ability to develop enterprise pipelines, negotiate commercial agreements, and secure outsourcing projects.
  • Strong communication, presentation, and stakeholder management capabilities in highly technical commercial environments.
  • Experience operating independently in high-ownership, client-facing business development roles.
  • Native or fluent Mandarin Chinese and professional English communication skills are mandatory.
  • Must be a Chinese national currently residing in the United States with valid working authorization.

Job code: #677