This position is hybrid to our Cambridge MA facility and require frequent on-site presence About This Role As a Specialist in Product Complaints, you will play a critical role in ensuring the timely and compliant processing of product complaints and associated sample evaluations across Biogen's global markets. You will support the complaint intake process, coordinate sample receipt and evaluation activities, and help drive investigations that support product quality and patient safety. Working closely with cross-functional teams, you will analyze complaint data, identify trends, and contribute to continuous improvement initiatives within the Quality organization. This role serves as a key link between affiliates, laboratories, and quality stakeholders to ensure consistent complaint handling and regulatory compliance. What You’ll Do Respond to complaint-related inquiries and support team email management Process incoming product complaint cases and sample ship-kit requests. Coordinate complaint sample shipments, receipt, storage, and laboratory evaluations Analyze complaint data, identify trends, and communicate findings to management and stakeholders Review and approve customer inputs for accuracy, consistency, and compliance Conduct complaint investigations utilizing structured investigative methodologies and root cause analysis tools to determine complaint cause and product impact. Support the development, maintenance, and execution of sample investigation methods Evaluate complaint samples and document results in accordance with cGMP requirements. Assess complaint criticality and risk, identify appropriate escalation pathways, and determine next steps based on available evidence and quality requirements Collaborate cross-functionally with Manufacturing, Quality Assurance, Quality Control, Engineering, Regulatory Affairs, Medical Safety, and Supply Chain partners to support investigations and resolution activities Write and revise SOPs concerning the Technical Product Complaint Quality System with minimal guidance Track, verify, and support implementation of corrective and preventive actions (CAPAs) Support laboratory safety, training, and equipment readiness activities Manage multiple priorities and projects simultaneously while ensuring timely completion of deliverables Who You Are You are a detail-oriented quality professional who is passionate about product quality and patient safety. You enjoy investigating complex issues, evaluating risk, solving problems, and collaborating across teams in a highly regulated environment. You can think critically through ambiguous situations, assess issue significance, identify appropriate actions, and drive investigations to effective conclusions. You are comfortable leading discussions, influencing stakeholders, and balancing compliance with business needs. Required Skills Bachelor's Degree in Life Sciences, Engineering, Quality, or related discipline plus 2+ years of experience in a quality or product complaints cGMP environment
Experience
supporting or conducting investigations, including root cause analysis and problem-solving activities, including knowledge of investigative methodologies and quality system processes Strong critical thinking with the ability to assess issue criticality and determine appropriate next steps Demonstrated ability to manage multiple priorities, projects, and deadlines in a fast-paced environment Strong cross-functional collaboration and stakeholder management skills Strong written and verbal communication abilities Preferred Skills Knowledge of Product Complaint systems/operations and cGMP requirements for biologics, oral-dose products, medical devices, drug delivery devices, and combination products Knowledge of Product Complaint regulations and standards (e.g., FDA, EMA, ISO 13485, ISO 14971) Medical device and/or combination product complaint handling experience
Experience
handling deviations, investigations, CAPAs, and effectiveness verification activities
Experience
with risk management principles and risk-based decision making
Experience
leading or participating in cross-functional improvement initiatives or projects Working knowledge of quality tools such as 5 Whys, Fishbone Analysis, Fault Tree Analysis, trending, and statistical analysis methods Job Level: Professional Additional Information The base compensation range for this role is: $73,000.00-$95,000.00 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 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. Not ready to apply? Submit your resume to our Talent Community and we’ll contact you if any applicable jobs become available. 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. Scam Advisory: Please be cautious of scam recruitment offers claiming to be from Biogen. All legitimate correspondence from a Biogen employee will come from a "@biogen.com" email account. Learn more about scams and fraudulent job postings here.