Live opening · Posted 19 hours ago

Investigator I / II

Biogen · Research Triangle Park, NC
Workday
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At a glance

The key details from the original listing.

Posted 19 hours ago
CompanyBiogen
LocationResearch Triangle Park, NC
SourceWorkday
ListedPosted 19 hours ago

About the role

Description supplied by the original job listing.

Job Description
As an Investigator within Human Performance & Investigations, you will play a critical role in strengthening operational excellence by leading investigations into quality and safety events across our manufacturing organization. You will apply structured root cause analysis methodologies and Human & Organizational Performance (HOP) principles to identify opportunities for improvement, reduce recurrence risk, and enhance operational reliability. This role offers the opportunity to partner across manufacturing, quality, engineering, environmental health & safety, and site leadership teams to drive meaningful organizational learning and performance improvements.
Shift details: Monday-Friday. There is flexibility to work from 8 am to 5 pm or 7 am to 4 pm. There may be an occasional need for weekend and after-hours support.
What You'll Do
Lead investigations for quality deviations, safety incidents, alert actions, and remedial action requests across manufacturing operations
Conduct interviews, gather and analyze data, facilitate investigation meetings, and apply systematic cause analysis methodologies to identify root and contributing causes
Author clear, concise, and compliant investigation reports within designated quality and safety systems
Partner with cross-functional stakeholders to develop effective corrective and preventive actions (CAPAs) that reduce recurrence risk
Ensure investigations are completed in alignment with Quality Management System (QMS) requirements, regulatory expectations, and established timelines
Share investigative findings and lessons learned across the organization to drive continuous improvement and operational excellence
Support complex and high-impact investigations as needed
Present investigation outcomes and supporting documentation during internal and external audits
Who You Are
You are a curious problem solver who enjoys uncovering the underlying causes of complex operational events. You are skilled at facilitating discussions, gathering insights from multiple stakeholders, and translating technical information into actionable recommendations. You thrive in a collaborative environment and are motivated by improving systems, processes, and organizational performance.
Required Skills for an Investigator I: Pay Range $69,000 - $90,000
The following combination of academic and/or relevant experience may be considered:
Bachelor’s degree from an accredited college or university, STEM preferred
Associate's degree, STEM preferred and at minimum 2 years of direct experience
A High School Diploma (or equivalent) and at minimum of 4 years of direct experience
Experience conducting investigations, root cause analyses, or operational problem-solving activities within regulated environments
Strong analytical and critical thinking skills with the ability to evaluate complex information and develop practical solutions
Excellent technical writing and documentation abilities
Strong facilitation, communication, and stakeholder management skills
Ability to effectively collaborate across multiple functions and levels of the organization
Working knowledge of quality systems, safety programs, and compliance requirements within manufacturing, laboratory, industrial, or regulated environments
Demonstrated ability to manage multiple priorities and meet critical deadlines
Required Skills for an Investigator II: Pay Range $85,000 - $111,000
The following combination of academic and/or relevant experience may be considered:
Bachelor’s degree from an accredited college or university, STEM preferred and at minimum 2 years of direct experience
Associate's degree, STEM preferred and at minimum 4 years of direct experience
A High School Diploma (or equivalent) and at minimum of 6 years of direct experience
Experience conducting investigations, root cause analyses, or operational problem-solving activities within regulated environments
Strong analytical and critical thinking skills with the ability to evaluate complex information and develop practical solutions
Excellent technical writing and documentation abilities
Strong facilitation, communication, and stakeholder management skills
Ability to effectively collaborate across multiple functions and levels of the organization
Working knowledge of quality systems, safety programs, and compliance requirements within manufacturing, laboratory, industrial, or regulated environments
Demonstrated ability to manage multiple priorities and meet critical deadlines
Preferred Skills
Experience with Human & Organizational Performance (HOP) principles
Knowledge of systematic cause analysis methodologies such as Event & Causal Factor Charting, Logic Fault Tree Analysis, or similar techniques
Experience supporting manufacturing, pharmaceutical, biotechnology, chemical, industrial, or other highly regulated operations
Knowledge of cGMP, cGLP, OSHA, EMA, FDA, or similar regulatory requirementsExperience participating in regulatory inspections or audits
Experience participating in regulatory inspections or audits
Job Level: Professional
Additional Information
The base compensation range for this role is: $85,000.00-$110,500.00
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.

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