... biotechnology, and medical device roles. I came across your profile and wanted to see if you are ... Design Quality - Lifecycle Management Location: Lake County, IL (Hybrid) Duration: 12+ Month ...
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... biotechnology, and medical device roles. I came across your profile and wanted to see if you are ... Design Quality - Lifecycle Management Location: Lake County, IL (Hybrid) Duration: 12+ Month ...
US Lifecycle Management Lead
Cambridge, MA · On-site
$155K - $214K/yr
About This Role The US Lifecycle Management Lead is a senior individual contributor accountable for ... As a mid-sized biotechnology company, we provide the stability and resources of a well-established ...
US Lifecycle Management Lead
Cambridge, MA · On-site
$155K - $214K/yr
About This Role The US Lifecycle Management Lead is a senior individual contributor accountable for ... As a mid-sized biotechnology company, we provide the stability and resources of a well-established ...
US Lifecycle Management Lead
Cambridge, MA · On-site
$155 - $214/hr
About This Role The US Lifecycle Management Lead is a senior individual contributor accountable for ... As a mid-sized biotechnology company, we provide the stability and resources of a well-established ...
US Lifecycle Management Lead
Cambridge, MA · On-site
$155 - $214/hr
About This Role The US Lifecycle Management Lead is a senior individual contributor accountable for ... As a mid-sized biotechnology company, we provide the stability and resources of a well-established ...
US Lifecycle Management Lead
Cambridge, MA · Hybrid
$155K - $214K/yr
About This Role The US Lifecycle Management Lead is a senior individual contributor accountable for ... As a mid-sized biotechnology company, we provide the stability and resources of a well-established ...
US Lifecycle Management Lead
Cambridge, MA · Hybrid
$155K - $214K/yr
About This Role The US Lifecycle Management Lead is a senior individual contributor accountable for ... As a mid-sized biotechnology company, we provide the stability and resources of a well-established ...
Engineer - Biotech Medical Device (Lifecycle Management, Design Controls, Documentation) - (JP15650)
Thousand Oaks, CA · Hybrid
$40 - $46/hr
Engineer - Biotech Medical Device (Lifecycle Management, Design Controls, Documentation) - (JP15650) Location: Thousand Oaks CA OR Cambridge MA Employment Type: Contract Business Unit: Mechanical ...
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Engineer - Biotech Medical Device (Lifecycle Management, Design Controls, Documentation) - (JP15650)
Thousand Oaks, CA · Hybrid
$40 - $46/hr
Engineer - Biotech Medical Device (Lifecycle Management, Design Controls, Documentation) - (JP15650) Location: Thousand Oaks CA OR Cambridge MA Employment Type: Contract Business Unit: Mechanical ...
Associate Director, US Oncology - Late Lifecycle Strategy
North Wales, PA · On-site
$120 - $180/hr
Minimum 5 years of pharmaceutical, biotechnology, healthcare, or related commercial experience ... Experience in lifecycle management, commercialization strategy, market access, or oncology ...
Associate Director, US Oncology - Late Lifecycle Strategy
North Wales, PA · On-site
$120 - $180/hr
Minimum 5 years of pharmaceutical, biotechnology, healthcare, or related commercial experience ... Experience in lifecycle management, commercialization strategy, market access, or oncology ...
... lifecycle management using the Oracle Agile platform. Responsibilities of this position include ... biotech, clinical trials, forensics, medical device, pharmaceutical, public health and research ...
... lifecycle management using the Oracle Agile platform. Responsibilities of this position include ... biotech, clinical trials, forensics, medical device, pharmaceutical, public health and research ...
Sr. Manager Engineering
Raritan, NJ · On-site
Own the lifecycle management strategy for cell therapy manufacturing equipment, utilities, and ... Legend Biotech Privacy Notice.
Sr. Manager Engineering
Raritan, NJ · On-site
Own the lifecycle management strategy for cell therapy manufacturing equipment, utilities, and ... Legend Biotech Privacy Notice.
Ensure readiness and alignment for INDs, CTAs, BLA/MAA submissions, and lifecycle management ... Legend Biotech Privacy Notice.
Ensure readiness and alignment for INDs, CTAs, BLA/MAA submissions, and lifecycle management ... Legend Biotech Privacy Notice.
Associate Director, AS&T Lifecycle Management (Biological Method Expert)
Gaithersburg, MD · On-site
$146K - $234K/yr
As the Associate Director AS&T Lifecycle Management, you will be making a meaningful contribution ... Pharmacy, Biotechnology, or a related field with 10+ years in a regulated environment in the ...
Associate Director, AS&T Lifecycle Management (Biological Method Expert)
Gaithersburg, MD · On-site
$146K - $234K/yr
As the Associate Director AS&T Lifecycle Management, you will be making a meaningful contribution ... Pharmacy, Biotechnology, or a related field with 10+ years in a regulated environment in the ...
... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas ... Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas ... Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
Own the lifecycle management strategy for cell therapy manufacturing equipment, utilities, and ... Legend Biotech Privacy Notice. Salary: . Date posted: 08/11/2026
Own the lifecycle management strategy for cell therapy manufacturing equipment, utilities, and ... Legend Biotech Privacy Notice. Salary: . Date posted: 08/11/2026
... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas ... Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas ... Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas ... Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
Quick apply
... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas ... Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas ... Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas ... Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas ... Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas ... Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas ... Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas ... Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas ... Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas ... Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas ... Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
Quick apply
... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas ... Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas ... Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas ... Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
Lifecycle Management Biotech information
See salary details
$69.5K - $78.8K
2% of jobs
$78.8K - $88K
7% of jobs
$88K - $97.3K
13% of jobs
$99.9K is the 25th percentile. Wages below this are outliers.
$97.3K - $106.6K
11% of jobs
$106.6K - $115.9K
12% of jobs
$115.9K - $125.1K
5% of jobs
The median wage is $125.4K / yr.
$125.1K - $134.4K
20% of jobs
$142.5K is the 75th percentile. Wages above this are outliers.
$134.4K - $143.7K
6% of jobs
$143.7K - $153K
3% of jobs
$153K - $162.2K
18% of jobs
$162.2K - $171.5K
3% of jobs
$69.5K
$124.8K
$171.5K
How much do lifecycle management biotech jobs pay per year?
As of Aug 26, 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 is lifecycle management in biotech?
Lifecycle management in biotech refers to the strategic process of overseeing a biotechnology product from its initial development through commercialization and eventually to its discontinuation. This includes optimizing product performance, ensuring regulatory compliance, managing intellectual property, and implementing strategies to extend product value and market presence. Effective lifecycle management helps maximize a product's market potential while minimizing risks and costs throughout its entire lifespan.
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.
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 is the difference between Lifecycle Management Biotech vs Process Development Scientist?
| Aspect | Lifecycle Management Biotech | Process Development Scientist |
|---|---|---|
| Required Credentials | Bachelor's or Master's in Biotechnology, Life Sciences, or related fields; often certifications in project management | Bachelor's or Master's in Chemical Engineering, Biotech, or related fields; sometimes advanced degrees |
| Work Environment | Pharmaceutical or biotech companies, focusing on product lifecycle from development to commercialization | Laboratories and manufacturing facilities, focusing on process design and optimization |
| Employer & Industry Usage | Used in biotech and pharma industries for product lifecycle management | Common 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.
Contractor
Re-posted 8 days ago
Job description
Hi,
My name is Karthik Mutyala and I’m a Recruitment Manager with Stark Pharma, specializing in pharmaceutical, biotechnology, and medical device roles. I came across your profile and wanted to see if you are open to new opportunities.
If interested, please send me your updated resume along with the best number and time to reach you.
Job Title: Manager, Design Quality – Lifecycle Management
Location: Lake County, IL (Hybrid)
Duration: 12+ Month Contract
Job Summary
We are seeking an experienced Manager, Design Quality – Lifecycle Management to support quality assurance and compliance activities for medical devices and combination products throughout product lifecycle management. This role will serve as the Quality representative on cross-functional teams, ensuring successful product transfers, design changes, validation activities, and ongoing compliance with global regulatory requirements.
The ideal candidate will have deep expertise in Design Controls, Change Management, Risk Management, and lifecycle quality support for medical devices and combination products such as infusion pumps, pre-filled syringes, autoinjectors, and on-body injectors.
Key Responsibilities
- Lead quality and compliance activities related to product transfer, commercialization, and on-market lifecycle management
- Serve as the primary Quality lead for design transfer activities supporting internal and external manufacturing sites
- Lead and support validation activities including IQ/OQ/PQ/PPQ and Test Method Validation (TMV)
- Drive lifecycle design change projects in accordance with Design Control and Change Control requirements
- Own change management plans, impact assessments, execution strategies, and closure activities for on-market product changes
- Ensure Design History File (DHF), traceability, and risk management documentation remain compliant and inspection-ready
- Identify and drive remediation of gaps within design control, risk management, and quality system processes
- Support supplier and contract manufacturing quality activities during design and process changes
- Participate in regulatory inspections, audits, CAPA investigations, NCR reviews, and quality review boards as a Subject Matter Expert (SME)
- Collaborate cross-functionally with Engineering, Manufacturing, Regulatory, Supply Chain, and external partners to ensure product quality and compliance
- Contribute to continuous improvement initiatives and development of quality procedures, policies, and best practices
Required Qualifications
- Bachelor’s degree in Engineering, Science, or related technical discipline
- 8+ years of experience within Medical Device or Combination Product industries
- 5+ years of Quality Assurance experience supporting regulated products
Strong expertise in:
- Design Controls
- Change Control
- Risk Management
- Product Lifecycle Management
- Validation activities (IQ/OQ/PQ/PPQ)
Experience supporting medical devices and combination products such as:
- Infusion Pumps
- Pre-filled Syringes (PFS)
- Autoinjectors
- On-Body Injectors
Working knowledge of:
- FDA 21 CFR Part 820
- FDA 21 CFR Part 4
- ISO 13485
- ISO 14971
- EU MDR (2017/745) and MDD requirements
- Strong project management, communication, and cross-functional leadership skills