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Lifecycle Management Biotech Jobs (NOW HIRING)

PSC Biotech

CQV Engineer

Columbus, OH · On-site

$45 - $55/hr

... biotech industries. * Strong knowledge of regulatory requirements and industry standards. * Experience with validation lifecycle management and risk-based approaches. * Excellent analytical and ...

PSC Biotech

CQV Engineer

Los Angeles, CA

$85K - $100K/yr

... biotech industries. * Strong knowledge of regulatory requirements and industry standards. * Experience with validation lifecycle management and risk-based approaches. * Excellent analytical and ...

Madrigal Pharmaceuticals

Experience in pharmaceutical / biotech Quality Systems, global standards deployment, lifecycle management across Development QA to Commercial QA, and operating effectively within a virtual biotech ...

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Lifecycle Management Biotech information

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$69.5K

$124.8K

$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.
Packaging Engineer - Biotech Combination Products/Device Operations (JP15206)

Packaging Engineer - Biotech Combination Products/Device Operations (JP15206)

3 Key Consulting

Thousand Oaks, CA • Hybrid

$36 - $41/hr

Full-time

Posted 16 days ago

Job description

Job Title: Packaging Engineer – Biotech Combination Products/Device Operations (JP15206)
Location: Thousand Oaks, CA. 91320
Employment Type: Contract
Business Unit: Packaging Engineering & Labeling 
Duration: 1+ year with likely extensions and/or conversion to permanent.
Posting Date: 04/09/2026
Pay Rate: $36 - $41/hour W2 with Benefits
Notes: Hybrid - 3-4 days onsite - Standard hours
3 Key Consulting is hiring a Packaging Engineer for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
This position reports into the Packaging Engineering group under Combination Products Operations (CPO) in Thousand Oaks, CA. This position will apply engineering principles to execute the proper design, qualification and implementation of Primary and Secondary Packaging components and the associated systems such as documentation, equipment, and processes. Knowledge of primary and secondary packaging systems and material science is essential to the position. The position requires organizational, project management, technical problem solving and communication (written and verbal) skills, and the ability to work in teams and adapt to rapidly changing environments. Day-to-day commercial support, and Lifecycle Management.
This position is responsible and accountable for the following:
  • Support for testing and evaluation leading to recommendation and selection of primary and secondary packaging materials
  • Familiarity with Material Testing standards, requirements and equipment is essential
  • Writing test protocols, perform technical evaluations and testing to support reports used to justify the use of selected materials and packaging components
  • Writing technical specifications, creating engineering drawings, and developing artwork templates
  • Competent with AutoCAD, Illustrator, or similar software application to create, modify and approve engineering drawings
  • Support line trials and packaging validation activities prior to introduction of any new or change in components/processes
  • Collaborate with cross-functional teams (i.e. Quality, Device Engineering, Supply Chain, Artwork, Manufacturing, Regulatory, etc.) in pre-commercial and commercial activities
     
Preferred Qualifications:
  • BS Packaging, Mechanical Engineering, Chemical Engineering or Life Sciences
  • 3+ years general packaging/engineering experience is strongly preferred
  • Knowledge of primary and secondary packaging systems and material science is essential to the position
  • The position requires organizational, project management, technical problem solving and communication (written and verbal) skills, and the ability to work in teams and adapt to rapidly changing environments
  • Independent problem solver with demonstrated skills working in teams or leading project teams
  • Strong Interpersonal and communication skills

Why is the Position Open?
Supplement additional workload on team
Top Must Have Skills:
Organizational, project management, technical problem solving and communication (written and verbal) skills. Medical devices or pharma, biotech experience. Lab based experience.
Day to Day Responsibilities:
Execute the proper design, qualification and implementation of Primary and Secondary Packaging components and the associated systems such as documentation, equipment, and processes. Day-to-day commercial support, and Lifecycle Management.
Basic Qualifications:
Master degree OR Bachelor degree and 2 years of experience OR Associate degree and 6 years of experience 
Red Flags:
Not able to go on-site.
Not able physically move for a majority of the shift. (Walking between different buildings to grab equipment and working with different lab teams)
Interview process:
1-2 rounds of interviews
We invite qualified candidates to send your resume to resumes@3keyconsulting.com.  If you decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our website www.3keyconsulting.com/careers. You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.