NC · On-site
$111K - $149K/yr
About this role The Sr. Associate III, Compliance - Quality Risk Management (QRM) Lead provides operational leadership for Biogen's RTP drug substance manufacturing site, with a focus on quality risk ...
NC · On-site
$31.25 - $40.87/hr
... Biogen's RTP site. You will support maintenance activities for process equipment and utilities, ensuring reliability, uptime, and compliance with safety, quality, and cGMP standards. This role ...
NC · On-site
$98K - $127K/yr
About This Role The Senior Engineer I, Manufacturing Sciences serves as a key scientific resource supporting cell culture bioprocessing for drug substance manufacturing at Biogen's RTP facility. This ...
NC · On-site
$31.25 - $40.87/hr
... Biogen's RTP site. You will support maintenance activities for process equipment and utilities, ensuring reliability, uptime, and compliance with safety, quality, and cGMP standards. This role ...
NC · On-site
$25.96 - $34.13/hr
... Biogen's RTP site. You will support maintenance activities for process equipment and utilities, ensuring reliability, uptime, and compliance with safety, quality, and cGMP standards. This role ...
NC · On-site
$93K - $121K/yr
About This Role We are seeking an experienced technical contributor to join our Automation Systems Engineering team at the Biogen RTP Bio site. The Senior Automation Engineer I will support Syncade ...
CMC Asset Lead, Nephrology
Cambridge, MA · On-site
$204K - $281K/yr
Your efforts will directly contribute to the advancement of Biogen's portfolio in nephrology ... This is a hybrid role that can be based in any of our US offices (RTP, NC or Cambridge, MA or San ...
CMC Asset Lead, Nephrology
Cambridge, MA · On-site
$204K - $281K/yr
Your efforts will directly contribute to the advancement of Biogen's portfolio in nephrology ... This is a hybrid role that can be based in any of our US offices (RTP, NC or Cambridge, MA or San ...
CMC Asset Lead, Nephrology
Cambridge, MA · Hybrid
$204K - $281K/yr
Your efforts will directly contribute to the advancement of Biogen's portfolio in nephrology ... This is a hybrid role that can be based in any of our US offices (RTP, NC or Cambridge, MA or San ...
CMC Asset Lead, Nephrology
Cambridge, MA · Hybrid
$204K - $281K/yr
Your efforts will directly contribute to the advancement of Biogen's portfolio in nephrology ... This is a hybrid role that can be based in any of our US offices (RTP, NC or Cambridge, MA or San ...
CMC Asset Lead, Nephrology
San Francisco, CA · Hybrid
$204K - $281K/yr
Your efforts will directly contribute to the advancement of Biogen's portfolio in nephrology ... This is a hybrid role that can be based in any of our US offices (RTP, NC or Cambridge, MA or San ...
CMC Asset Lead, Nephrology
San Francisco, CA · Hybrid
$204K - $281K/yr
Your efforts will directly contribute to the advancement of Biogen's portfolio in nephrology ... This is a hybrid role that can be based in any of our US offices (RTP, NC or Cambridge, MA or San ...
NC · On-site
$111K - $149K/yr
Drive a strong culture of compliance and data integrity across the RTP site Who you are You are a ... Biogen is an E-Verify Employer in the United States.
NC · On-site
$93K - $121K/yr
... RTP Drug Substance Manufacturing site maintains a strong state of compliance and inspection ... Biogen is an E-Verify Employer in the United States.
Sr. Principal Biostatistician
$134K - $179K/yr
Although we are open to Remote candidates, the strong preference would be to have a Hybrid presence to a Biogen office (Cambridge, MA or RTP, North Carolina). Job Level: Management Additional ...
Sr. Principal Biostatistician
$134K - $179K/yr
Although we are open to Remote candidates, the strong preference would be to have a Hybrid presence to a Biogen office (Cambridge, MA or RTP, North Carolina). Job Level: Management Additional ...
NC · On-site
$81K - $105K/yr
... Biogen Research Triangle Park (RTP) facility. This individual has advanced understanding of the Quality Management Systems and applies that knowledge by coaching peers and ensuring continuous ...
NC · On-site
$81K - $105K/yr
... Biogen Research Triangle Park (RTP) facility. This individual has advanced understanding of the Quality Management Systems and applies that knowledge by coaching peers and ensuring continuous ...
NC · On-site
$93K - $143K/yr
About This Role A Sr. Engineer I/II in Automation & MES is a key member of the RTP Bio Automation ... Biogen is an E-Verify Employer in the United States.
NC · On-site
$81K - $105K/yr
... RTP drug substance manufacturing facility. The Sr. Associate I is responsible for leading key ... Biogen is an E-Verify Employer in the United States.
NC · On-site
$127K - $170K/yr
Situated in RTP Pharma with matrixed global engagement, this role demands an established expert who ... Biogen is an E-Verify Employer in the United States.
NC · On-site
$31.25 - $40.87/hr
... Park (RTP). These teams are the backbone of our operations - each playing a critical role in ... Biogen is an E-Verify Employer in the United States.
NC · On-site
$33.17 - $43.27/hr
... Park (RTP). These teams are the backbone of our operations - each playing a critical role in ... Biogen is an E-Verify Employer in the United States.
NC · On-site
$25.96 - $34.13/hr
... Park (RTP). These teams are the backbone of our operations - each playing a critical role in ... Biogen is an E-Verify Employer in the United States.
Biogen Rtp information
See salary details
$16.59 - $18.16
2% of jobs
$18.16 - $19.73
5% of jobs
$19.73 - $21.31
9% of jobs
$22.23 is the 25th percentile. Wages below this are outliers.
$21.31 - $22.88
15% of jobs
$22.88 - $24.45
17% of jobs
The median wage is $24.58 / hr.
$24.45 - $26.03
19% of jobs
$26.91 is the 75th percentile. Wages above this are outliers.
$26.03 - $27.60
13% of jobs
$27.60 - $29.17
9% of jobs
$29.17 - $30.75
4% of jobs
$30.75 - $32.32
3% of jobs
$32.32 - $33.89
3% of jobs
$16
$25
$33
How much do biogen rtp jobs pay per hour?
As of Jul 28, 2026, the average hourly pay for biogen rtp in the United States is $25.28, according to ZipRecruiter salary data. Most workers in this role earn between $22.12 and $27.16 per hour, depending on experience, location, and employer.
What is Biogen RTP?
Biogen RTP refers to Biogen's facility located in Research Triangle Park (RTP), North Carolina. This site is a significant hub for Biogen's manufacturing, research, and development operations, focusing on producing and advancing therapies for neurological and neurodegenerative diseases. The RTP campus is known for its innovative work environment and plays a crucial role in supporting Biogen's global mission to improve the lives of patients. Employees at Biogen RTP are engaged in a variety of roles, including biotechnology research, pharmaceutical manufacturing, quality assurance, and support functions.
Does Biogen allow remote work?
Biogen offers remote work options for some roles, depending on the position and team needs. Many positions may require in-office presence or hybrid arrangements, and remote work policies can vary by department and location. Candidates should review specific job postings for remote work eligibility and requirements.
What is the PTO policy for Biogen?
For a Biogen Rtp role, the PTO policy typically includes paid time off that accrues based on length of service and company policies. Employees generally receive vacation and sick leave benefits, with specific details outlined in the employee handbook or HR resources. PTO policies may vary by location and employment status, so it is advisable to consult the company's official policies or HR for precise information.
What does a typical day look like for someone working at Biogen’s RTP (Research Triangle Park) facility?
A typical day at Biogen’s RTP facility often involves working within specialized teams focused on biopharmaceutical manufacturing or research. Employees may spend their time operating advanced equipment, monitoring production processes, analyzing samples, or collaborating on cross-functional projects to ensure product quality and innovation. The environment emphasizes teamwork, safety, and adherence to strict regulatory standards. Additionally, there are regular meetings to align on project goals and discuss process improvements, offering opportunities to learn from colleagues across different disciplines.
What is the salary range at Biogen?
The salary range for a Biogen Rtp position varies depending on experience, role, and location, but generally falls between $70,000 and $120,000 annually. Entry-level roles may start lower, while experienced professionals or specialized positions can earn higher salaries. Compensation often includes benefits such as health insurance and bonuses.
Is Biogen a good place to work?
Biogen Rtp offers a professional environment focused on biotechnology and pharmaceutical research, with opportunities for skill development in areas like bioprocessing and regulatory compliance. Employee reviews often cite competitive benefits and a collaborative workplace, though experiences can vary by role and department.
What are the key skills and qualifications needed to thrive as a Biogen RTP (Research Triangle Park) employee, and why are they important?
To thrive as a Biogen RTP employee, you generally need a background in life sciences, biotechnology, or pharmaceuticals, often supported by a relevant degree and industry experience. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practice (GMP), and regulatory compliance tools is typically required. Strong analytical thinking, teamwork, and effective communication are vital soft skills for excelling in this collaborative and innovation-driven environment. These skills and qualifications are essential to ensure high-quality research, regulatory adherence, and successful product development in a leading biopharmaceutical company.
What cities are hiring for Biogen Rtp jobs? Cities with the most Biogen Rtp job openings:
What states have the most Biogen Rtp jobs? States with the most job openings for Biogen Rtp jobs include:
What job categories do people searching Biogen Rtp jobs look for? The top searched job categories for Biogen Rtp jobs are:
$111K - $149K/yr
Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Posted 17 days ago
Biogen rating
9.3
Based on 20 frontline employees who took The Breakroom Quiz
3rd of 86 rated pharmaceutical
Job description
About this role
The Sr. Associate III, Compliance - Quality Risk Management (QRM) Lead provides operational leadership for Biogen's RTP drug substance manufacturing site, with a focus on quality risk management (QRM), inspection readiness, data integrity, and compliance systems. This role is responsible for ensuring the site always remains in a state of control and inspection-ready, supporting both domestic and international regulatory expectations. As a key member supporting site leadership, this individual will drive continuous improvement across quality systems while promoting a strong compliance culture aligned with cGMP and Biogen Quality Management System standards.
What you'll do
Who you are
You are a quality and compliance leader with strong expertise in risk management and a passion for driving continuous improvement in regulated manufacturing environments. You thrive in cross-functional settings, influence stakeholders effectively, and bring a proactive, inspection-ready mindset to all aspects of your work.
Required skills
Preferred skills
Job Level: Management
Additional Information
The base compensation range for this role is: $111,000.00-$149,000.00
Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity.
Regular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance.
In addition to compensation, Biogen offers a full and highly competitive range of benefits designed to support our employees' and their families physical, financial, emotional, and social well-being; including, but not limited to:
Why Biogen?
We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.
At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our Biogen.
All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.
The Sr. Associate III, Compliance - Quality Risk Management (QRM) Lead provides operational leadership for Biogen's RTP drug substance manufacturing site, with a focus on quality risk management (QRM), inspection readiness, data integrity, and compliance systems. This role is responsible for ensuring the site always remains in a state of control and inspection-ready, supporting both domestic and international regulatory expectations. As a key member supporting site leadership, this individual will drive continuous improvement across quality systems while promoting a strong compliance culture aligned with cGMP and Biogen Quality Management System standards.
What you'll do
- Lead and manage the site Quality Risk Management (QRM) program, ensuring alignment with global policies and site procedures
- Maintain and oversee QRM repositories and lifecycle management within the Quality Management System
- Serve as the site Subject Matter Expert (SME) for risk management during audits and regulatory inspections
- Drive inspection management activities including scheduling, execution, response coordination, and regulatory requests
- Lead implementation and continuous improvement of risk management practices across the site
- Collaborate cross-functionally to support compliance, data integrity, and quality initiatives
- Facilitate governance meetings and influence stakeholders to adopt best practices in risk management
- Support development of QRM training and enable risk facilitators across the organization
- Use data and established KPIs to monitor compliance and drive continuous improvement
Who you are
You are a quality and compliance leader with strong expertise in risk management and a passion for driving continuous improvement in regulated manufacturing environments. You thrive in cross-functional settings, influence stakeholders effectively, and bring a proactive, inspection-ready mindset to all aspects of your work.
Required skills
- Bachelor's degree in scientific, technical, or relevant discipline
- At minimum 6 years of Quality Assurance experience in pharmaceutical, biotech, or manufacturing environments
- Strong knowledge of cGMP regulations and global regulatory standards (e.g., FDA 21 CFR 210/211, ICH Q9)
- Experience with quality systems including risk management, change control, deviation management, and inspection readiness
- Ability to analyze complex data, make decisions under pressure, and lead critical initiatives
- Excellent communication, organizational, and stakeholder management skills
Preferred skills
- Master's degree (MBA, MS, or similar) with relevant experience
- Experience leading site-wide or global quality risk management programs
- Strong background supporting regulatory inspections and audit responses
- Demonstrated ability to influence cross-functional teams and drive cultural change in quality and compliance
- Advanced knowledge of quality metrics and data-driven decision making
Job Level: Management
Additional Information
The base compensation range for this role is: $111,000.00-$149,000.00
Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity.
Regular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance.
In addition to compensation, Biogen offers a full and highly competitive range of benefits designed to support our employees' and their families physical, financial, emotional, and social well-being; including, but not limited to:
- Medical, Dental, Vision, & Life insurances
- Fitness & Wellness programs including a fitness reimbursement
- Short- and Long-Term Disability insurance
- A minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31)
- Up to 12 company paid holidays + 3 paid days off for Personal Significance
- 80 hours of sick time per calendar year
- Paid Maternity and Parental Leave benefit
- 401(k) program participation with company matched contributions
- Employee stock purchase plan
- Tuition reimbursement of up to $10,000 per calendar year
- Employee Resource Groups participation
Why Biogen?
We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.
At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our Biogen.
All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.
About Biogen
Sourced by ZipRecruiter
At Biogen, our mission is clear - we are pioneers in neuroscience. Biogen discovers, develops, and delivers worldwide innovative therapies for people living with serious neurological and neurodegenerative diseases. Together, our employees create, commercialize, and manufacture transformative therapies for our patient population.
Industry
Scientific research and development services
Company size
5,001 - 10,000 Employees
Headquarters location
Cambridge, MA, US
Year founded
1978