Manage multiple projects and ensure timely completion. Education and Experience * Bachelor's, Master's, or PhD in Biochemistry, Chemistry, Biology, Chemical Engineering, Biotechnology, or a related ...
Manage multiple projects and ensure timely completion. Education and Experience * Bachelor's, Master's, or PhD in Biochemistry, Chemistry, Biology, Chemical Engineering, Biotechnology, or a related ...
Associate Clinical Trial Manager - PhD/Post-Doc (Cardiovascular/Renal/Metabolic/Gastrointestinal)
Bristol, ME · On-site
Job Summary Medpace is a leading CRO for Biotech companies and we are currently seeking candidates ... The aCTM will be a part of the Clinical Trial Management team and support Project Coordinators and ...
Associate Clinical Trial Manager - PhD/Post-Doc (Cardiovascular/Renal/Metabolic/Gastrointestinal)
Bristol, ME · On-site
Job Summary Medpace is a leading CRO for Biotech companies and we are currently seeking candidates ... The aCTM will be a part of the Clinical Trial Management team and support Project Coordinators and ...
Job Summary Medpace is a leading CRO for Biotech companies and we are currently seeking candidates ... The aCTM will be a part of the Clinical Trial Management team and support Project Coordinators and ...
Job Summary Medpace is a leading CRO for Biotech companies and we are currently seeking candidates ... The aCTM will be a part of the Clinical Trial Management team and support Project Coordinators and ...
Project Engineer
Berwick, ME · On-site
$100K - $180K/yr
You'll also aid in managing the project itself, helping keep scope, timelines, and priorities on ... Background in energetics, chemicals, process/manufacturing, biotech/pharma, or another regulated ...
Quick apply
Project Engineer
Berwick, ME · On-site
$100K - $180K/yr
You'll also aid in managing the project itself, helping keep scope, timelines, and priorities on ... Background in energetics, chemicals, process/manufacturing, biotech/pharma, or another regulated ...
Experience may include CRA or project management experience; * Possess Regulatory background ... We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and ...
Experience may include CRA or project management experience; * Possess Regulatory background ... We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and ...
Program Manager - Research
Bar Harbor, ME · On-site
$85K - $143K/yr
Interact with patient advocacy groups, rare disease families, academicresearchersand biotech ... Prior experience in project management with a proventrack recordof successful program execution.
Program Manager - Research
Bar Harbor, ME · On-site
$85K - $143K/yr
Interact with patient advocacy groups, rare disease families, academicresearchersand biotech ... Prior experience in project management with a proventrack recordof successful program execution.
Program Manager - Research
Bar Harbor, ME · On-site
$85K - $143K/yr
Interact with patient advocacy groups, rare disease families, academic researchers and biotech ... Prior experience in project management with a proven track record of successful program execution.
Program Manager - Research
Bar Harbor, ME · On-site
$85K - $143K/yr
Interact with patient advocacy groups, rare disease families, academic researchers and biotech ... Prior experience in project management with a proven track record of successful program execution.
Study Director, Rare Disease Translational Center
Bar Harbor, ME · On-site
$85K - $133K/yr
... biotechnology, or contract research organization (CRO) environment, with a track record of successful study management. • Proven leadership and project management skills, with the ability to ...
Study Director, Rare Disease Translational Center
Bar Harbor, ME · On-site
$85K - $133K/yr
... biotechnology, or contract research organization (CRO) environment, with a track record of successful study management. • Proven leadership and project management skills, with the ability to ...
Study Director, Rare Disease Translational Center
Bar Harbor, ME · On-site
$85K - $133K/yr
... biotechnology, or contract research organization (CRO) environment, with a track record of successful study management. Proven leadership and project management skills, with the ability to ...
Study Director, Rare Disease Translational Center
Bar Harbor, ME · On-site
$85K - $133K/yr
... biotechnology, or contract research organization (CRO) environment, with a track record of successful study management. Proven leadership and project management skills, with the ability to ...
Senior Study Director
$98K - $165K/yr
Knowledge, Skills, and Abilities Extensive experience in scientific research, project management, and leadership roles within a pharmaceutical, biotechnology, or contract research organization (CRO ...
Senior Study Director
$98K - $165K/yr
Knowledge, Skills, and Abilities Extensive experience in scientific research, project management, and leadership roles within a pharmaceutical, biotechnology, or contract research organization (CRO ...
Product Management Director - Industrial Manufacturing
Newport, ME · On-site
$210K - $220K/yr
... Biotech, Quantex, Quattroflow, and Wilden. PSG products are manufactured on three continents ... Leader of the product/project plan through the Stage Gate Process * Works closely with sales ...
Product Management Director - Industrial Manufacturing
Newport, ME · On-site
$210K - $220K/yr
... Biotech, Quantex, Quattroflow, and Wilden. PSG products are manufactured on three continents ... Leader of the product/project plan through the Stage Gate Process * Works closely with sales ...
BioMed Engineer I
Lewiston, ME · On-site
... coding, project management and more. We provide services to clinically excellent community ... Must possess Bachelor's degree in Biomedical Engineering, Biotechnology, Bioinformatics, or related ...
BioMed Engineer I
Lewiston, ME · On-site
... coding, project management and more. We provide services to clinically excellent community ... Must possess Bachelor's degree in Biomedical Engineering, Biotechnology, Bioinformatics, or related ...
... coding, project management and more. We provide services to clinically excellent community ... Must possess Bachelor's degree in Biomedical Engineering, Biotechnology, Bioinformatics, or related ...
... coding, project management and more. We provide services to clinically excellent community ... Must possess Bachelor's degree in Biomedical Engineering, Biotechnology, Bioinformatics, or related ...
BioMed Engineer I
Lewiston, ME · On-site
... coding, project management and more. We provide services to clinically excellent community ... Must possess Bachelor's degree in Biomedical Engineering, Biotechnology, Bioinformatics, or related ...
BioMed Engineer I
Lewiston, ME · On-site
... coding, project management and more. We provide services to clinically excellent community ... Must possess Bachelor's degree in Biomedical Engineering, Biotechnology, Bioinformatics, or related ...
Senior Study Director
Bar Harbor, ME · On-site
$98K - $165K/yr
Knowledge, Skills, and Abilities • Extensive experience in scientific research, project management, and leadership roles within a pharmaceutical, biotechnology, or contract research organization ...
Senior Study Director
Bar Harbor, ME · On-site
$98K - $165K/yr
Knowledge, Skills, and Abilities • Extensive experience in scientific research, project management, and leadership roles within a pharmaceutical, biotechnology, or contract research organization ...
Senior Salesforce Administrator
Westbrook, ME · On-site +1
$100K - $120K/yr
We partner with Pharma, BioTech, and Academia (the scientific community) to improve animal and ... Project management and business analyst skills required. * Ability to work independently and within ...
Senior Salesforce Administrator
Westbrook, ME · On-site +1
$100K - $120K/yr
We partner with Pharma, BioTech, and Academia (the scientific community) to improve animal and ... Project management and business analyst skills required. * Ability to work independently and within ...
The CTM interacts with sponsors and sites and manages the timeline and project deliverables (minus ... We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and ...
The CTM interacts with sponsors and sites and manages the timeline and project deliverables (minus ... We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and ...
... Biotechnology, or Healthcare). The ideal candidate will manage quality documents, process document ... Participate in quality improvement and documentation projects. * Ensure compliance with Quality ...
Quick apply
... Biotechnology, or Healthcare). The ideal candidate will manage quality documents, process document ... Participate in quality improvement and documentation projects. * Ensure compliance with Quality ...
... biotechnology, and medical device firms. For more information, visit www.ctifacts.com What You'll ... Perform site management activities and provide ongoing updates of site status to Clinical Project ...
... biotechnology, and medical device firms. For more information, visit www.ctifacts.com What You'll ... Perform site management activities and provide ongoing updates of site status to Clinical Project ...
... managing people and or leadership experience leading teams, project, programs or directing the allocation of resources * Clinical/medical research experience * 6 years of experience in a biotech ...
... managing people and or leadership experience leading teams, project, programs or directing the allocation of resources * Clinical/medical research experience * 6 years of experience in a biotech ...
Biotech Project Management information
See Maine salary details
$37.3K - $48.1K
2% of jobs
$48.1K - $59K
6% of jobs
$59K - $69.9K
10% of jobs
$75.8K is the 25th percentile. Wages below this are outliers.
$69.9K - $80.8K
13% of jobs
$80.8K - $91.6K
14% of jobs
The median wage is $95.5K / yr.
$91.6K - $102.5K
15% of jobs
$102.5K - $113.4K
13% of jobs
$115.8K is the 75th percentile. Wages above this are outliers.
$113.4K - $124.2K
12% of jobs
$124.2K - $135.1K
7% of jobs
$135.1K - $146K
5% of jobs
$146K - $156.8K
3% of jobs
$37.3K
$99.4K
$156.8K
How much do biotech project management jobs pay per year?
As of Aug 4, 2026, the average yearly pay for biotech project management in Maine is $99,416.00, according to ZipRecruiter salary data. Most workers in this role earn between $76,000.00 and $119,100.00 per year, depending on experience, location, and employer.
What are the key skills and qualifications needed to thrive in biotech project management?
To thrive in Biotech Project Management, you need a strong background in life sciences, experience in project planning and execution, and ideally a relevant degree (such as biology, biotechnology, or project management certification). Familiarity with project management software (like MS Project or Asana), regulatory compliance systems, and possibly certifications like PMP is often expected. Exceptional communication, leadership, problem-solving, and time management skills will help you stand out in this role. These competencies ensure projects remain on schedule, compliant, and collaborative in the fast-paced, highly regulated biotech industry.
What are the most common challenges faced by professionals in biotech project management?
Biotech Project Management professionals often juggle cross-disciplinary teams, tight timelines, and complex regulatory requirements, which can make prioritizing tasks a challenge. Navigating scientific uncertainties and adapting to project scope changes are daily realities given the fast pace of biotech innovation. Having strong organizational and people skills helps to manage competing priorities while keeping all stakeholders aligned. By mastering these challenges, professionals can significantly contribute to the timely advancement of vital scientific initiatives.
What is a biotech project management?
A Biotech Project Management job involves overseeing and coordinating research, development, and commercialization projects in the biotechnology industry. Project managers in this field ensure that scientific, regulatory, and business objectives are met on time and within budget. They work closely with cross-functional teams, including scientists, regulatory experts, and business stakeholders, to drive project success. Strong organizational, problem-solving, and communication skills are essential for managing risks and ensuring compliance with industry regulations.
What are popular job titles related to Biotech Project Management jobs in Maine? For Biotech Project Management jobs in Maine, the most frequently searched job titles are:
What job categories do people searching Biotech Project Management jobs in Maine look for? The top searched job categories for Biotech Project Management jobs in Maine are:
Contractor
Medical, Dental, Vision, Life, Retirement
Re-posted 2 days ago
Abbott rating
7.9
Based on 136 frontline employees who took The Breakroom Quiz
160th of 536 rated manufacturers
Job description
Title: Product Composition Coordinator/Product Safety Specialist
Location: South Portland, ME
Duration: 8 Month Assignment
100% Onsite
Position Summary
The Product Composition Coordinator/Product Safety Specialist ensures compliance with regulations and internal standards related to Product Safety and Safety Data Sheet (SDS) generation. This role coordinates with multiple sites to gather accurate product composition data for SDS creation and develops standardized templates and processes. The position collaborates with Technical Product Support, R&D, Operations, Quality Assurance, Regulatory Affairs, and external suppliers.
Key Responsibilities
Education and Experience
Preferred Qualifications
Key Skills
Product Safety, SDS, EHS, Product Stewardship, Biochemistry, Chemistry, Biotechnology, Quality Assurance, Technical Project Management, Problem Solving, Communication, Attention to Detail.
Consultants Eligible Benefits Upon Waiting Period:
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional and branded generic medicines.
Working together, Abbott and Talent Solutions partner to deliver top talent for contingent roles at Abbott, building better and healthier lives. Abbott believes all employees are essential to creating life-changing breakthroughs, performing key duties to create life-changing breakthroughs.
Location: South Portland, ME
Duration: 8 Month Assignment
100% Onsite
Position Summary
The Product Composition Coordinator/Product Safety Specialist ensures compliance with regulations and internal standards related to Product Safety and Safety Data Sheet (SDS) generation. This role coordinates with multiple sites to gather accurate product composition data for SDS creation and develops standardized templates and processes. The position collaborates with Technical Product Support, R&D, Operations, Quality Assurance, Regulatory Affairs, and external suppliers.
Key Responsibilities
- Maintain and support EHS sections of Safety Data Sheets and SDS inventory.
- Develop and maintain Product Safety systems and programs.
- Partner with Quality and Operations to integrate Product Safety into processes and manufacturing.
- Conduct product assessments related to Product Stewardship regulations.
- Support SDS and Product Composition strategies and coordinate with third-party consultants.
- Manage multiple projects and ensure timely completion.
Education and Experience
- Bachelor's, Master's, or PhD in Biochemistry, Chemistry, Biology, Chemical Engineering, Biotechnology, or a related field.
Preferred Qualifications
- 5+ years in the biotechnology industry with Product Safety or Product Stewardship experience.
- Expertise in Safety Data Sheet (SDS) generation.
- Experience with Product Safety regulations and technical project management.
Key Skills
Product Safety, SDS, EHS, Product Stewardship, Biochemistry, Chemistry, Biotechnology, Quality Assurance, Technical Project Management, Problem Solving, Communication, Attention to Detail.
- Travel: May be required.
Consultants Eligible Benefits Upon Waiting Period:
- Medical and Prescription Drug Plans
- Dental Plan
- Vision Plan
- Health Savings Account (for High Deductible Health Plans)
- Flexible Spending Accounts (Health, Limited Purpose, Dependent Care, Commuter Parking and Commuter Transit)
- Supplemental Life Insurance
- Short Term Disability (coverage varies by state)
- Long Term Disability
- Critical Illness, Hospital coverage, Accident Insurance
- MetLife Legal, MetLife ID Fraud, and MetLife Pet Insurance
- 401(k)
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional and branded generic medicines.
Working together, Abbott and Talent Solutions partner to deliver top talent for contingent roles at Abbott, building better and healthier lives. Abbott believes all employees are essential to creating life-changing breakthroughs, performing key duties to create life-changing breakthroughs.
- Published on 09 Mar 2026, 1:08 PM