Job DescriptionJob Description About This Role The Associate Director HEOR/Access Value Lead role is a part of the HEOR/Access Leadership Team in US Medical, a strategic partner within Biogen. * Operationalize the USM Insight evaluation process (i360) together with the MADs to advance actionable insights and learnings to advance value proposition strategies for Biogen assets for engagement with both internal and external customers. The individual in this role will work closely with cross functional partners in HEOR/Access, the Medical Account Directors (MADs) and with other functional areas within Biogen such as Market Access & Reimbursement (MA&R), Value & Access, and TA and HEOR Medical Directors to develop the value propositions and content. Biogen's priority is to continue to foster and enable a diverse and inclusive workforce - representing age, gender, sexual identity, race, ethnicity, Veterans, and people with disabilities - that reflects the communities where we operate and the patients who we serve.$148k-193k yearly est.12d ago
Central Divisional General Manager
This is a key commercial leadership role with significant opportunity for succession to more senior roles within the broader Biogen organization. The Divisional General Manager will strengthen both the building and the operational readiness of the field teams. This person will also develop relationships across the entire Biogen organization in order to facilitate support and success in identifying and pursuing broader business opportunities. What You'll Do This person will be fully accountable for the Biogen field teams in the Division and will be partnering closely with the West and East Divisional General Managers and Sage to ensure strategic, operational, and executional alignment. Job DescriptionJob Description About This Role In this highly visible and key leadership role, the Central Divisional General Manager of the US Neuropsychiatry Franchise will be responsible for the sales strategy and launch for treatment of major depressive disorder and postpartum depression.$171k-295k yearly est.28d ago
Distinguished Scientist, Drug Metabolism and Pharmacokinetics
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Chemist - II (Associate)
Location: Wilson, NC 27893 Job Title: Chemist - II (Associate)$60k-77k yearly est.2d ago
Deviation Specialist I
Job Details:
Position: Deviation Specialist I
Location: West Point, PA (Hybrid - 3 Days Onsite and 2 Days Remote)
Duration: 12+ Months
Job Description:
Roles and Responsibilities:
· Primary responsibilities include day-to-day technical support to manufacturing operations, including resolution and reduction of process deviations, development and implementation of corrective/preventative actions, and leading manufacturing and laboratory investigations
· This individual will be responsible for providing scientific support for manufacturing areas within the Client's Manufacturing Division (MMD)
· This Individual will also develop working relationships with counterparts in other areas supporting aseptic manufacturing, testing, planning, and release and is required to utilize sound scientific and engineering principles to investigate process deviations.
· Real-time troubleshooting and root cause analysis of laboratory test failures and manufacturing atypical events, with the goal of fully understanding root cause and product impact and development of corrective/preventative actions is required
· Analysis of complex problems through critical analytical thinking and the design/execution of laboratory/pilot scale experiments is required
· Off-shift work may be required.
Education Requirement:
· B.S./M.S. in Mechanical or Chemical Engineering degree or other science degree.
Top 3 Skills:
· Top skillsets: previous DM experience, root cause analysis experience, Time management (deadlines/deliverables), Investigation Writing experience.
· For those that interview... manager may ask candidates for writing samples to their see technical ability.
· Personality type- someone cool, calm, collected (not easily excitable) Suggested possible backgrounds- chemical engineering or science background
Required Skills:
· 0-3+ years of relevant work experience in a cGMP environment (e.g. Production, Development, Process Engineering, Technical Services or related field) in pharmaceutical/ biotech industry.
· Support of vaccine operations or technical services support.
· Support of deviation investigations and/or project work.
· Previous experience in writing investigations for atypical events in a manufacturing environment.
· Experience with troubleshooting biotech equipment, barrier technology, and closed system processing.
· Experience with, MIDAS, SAP
· Ability to read Piping and Instrumentation Diagrams
· Familiar with Lean Six Sigma Methodologies and proven analytical/ problem solving capabilities
· Demonstrated ability to work both independently and as a part of a cross-functional team
· Excellent written and verbal communication skills
Comments/Special Instructions:
Work site:-
West Point/Hybrid (minimum 3 days on-site/2 days remote).
Typical day-
· Tier/DM Huddle meetings in the morning.
· Review errors that didn't go well.
· Have smaller meetings to determine which events require further investigation, etc.
· Will also include some research, some writing, about 60/40 Desk/floor time.
$86k-113k yearly est.14d ago
Sr. Supervisor, Manufacturing
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Mechanic III, Maintenance
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HR Business Partner (Hybrid PA/NJ)
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Manager, Pharmacy Operations - Zuranolone
This individual will be expected to drive SPP value to Biogen and our patients through the established accountability model by maximizing performance of identified metrics such as: cycle time, conversion, adherence and discontinuation. 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.$115k-151k yearly est.5d ago
Distinguished Scientist, Drug Metabolism and Pharmacokinetics
Genentech requires all new hires to be fully vaccinated against COVID-19 as of their start date. The Drug Metabolism and Pharmacokinetics (DMPK) department at Genentech is seeking a highly motivated scientific leader who will be supporting small molecule/macrocyclic peptide projects in discovery and development as part of the PK-Transport group.$147k-191k yearly est.22h ago
Sr Clinical Trial Manager, Cardiovascular/Renal, Home-Based USA, IQVIA Biotech
IQVIA's Biotech Division is seeking a Sr Clinical Trial Manager for a Home-Based role. Assures clear client and internal team communication, process documentation, and compliance with Good Clinical Practices and procedures set forth by IQVIA Biotech and its clients. Communicate and document all interactions with client as required by SOP.Serve as client advocate within IQVIA Biotech.Develop and implement Clinical Monitoring Plan. Assure that the appropriate IQVIA Biotech and/or sponsor SOPs are followed.Ensure all project documentation is appropriately filed per IQVIA Biotech SOPs.Assist PM in preparation of audit responses, as appropriate.Assist PM with preparation of information for inclusion in monthly report to client.$117.2k-146.5k yearly15h ago
Manager, Medical Affairs (Remote/Home-Based)
$154.6k-193.8k yearly4d ago
Manufacturing Coordinator V (LSM)
$83k-115k yearly est.12d ago
Senior Director, Global Medical Affairs - Neuropsychiatry
* Develop and implement global medical strategy for Biogen's neuropsychiatry programs As the Senior Director, Global Medical Affairs - Neuropsychiatry within the Worldwide Medical organization, you will be responsible for leading the medical strategy of the Neuropsychiatry therapeutic area and ensuring successful regional partnership and medical launch readiness. Biogen's priority is to continue to foster and enable a diverse and inclusive workforce - representing age, gender, sexual identity, race, ethnicity, Veterans, and people with disabilities - that reflects the communities where we operate and the patients who we serve.$186k-252k yearly est.2d ago
Senior Manager, Pharmacovigilance (PV) Vendor Oversight Lead
The Senior Manager, Pharmacovigilance Vendor Oversight Lead is a global position that includes managing teams and collaborating with key stakeholders across several time zones. * Continuously track existing purchase orders to ensure compliance with Biogen financial policies and track active spending against negotiated contract value. The Senior Manager, Pharmacovigilance Vendor Oversight Lead, sits within the Safety Surveillance and Aggregate (SSA) reports team and is accountable for managing and oversight (timely, quality standards) the vendors and team members within the unit.$116.5k-187.8k yearly3d ago
Sr. Director, Specialized Immunology
The current focus is on lupus, a therapeutic area in which Biogen has clinical programs, but we are currently exploring possibilities to broaden this scope. At Biogen, we are pioneers in science and care deeply about making a difference. * Work collaboratively across R&D to create a preclinical pipeline of differentiated programs with strong biologic rationale and clinical feasibility, using the multiple modalities available to Biogen and ranging in stage from exploratory to pre-IND. Specialized Immunology (SI) is a new group in Research at Biogen, located within the Multiple Sclerosis and Immunology Research Unit.$186k-252k yearly est.8d ago
Sr. Director, MS&I Development Unit Liaison, Clinical Pharmacology & Pharmacometrics
* Provides SME insight and input into high profile clinical pharmacology activities including training, CDP and study designs with R&D across drug modalities and Biogen disease areas.$115k-151k yearly est.9d ago
Senior Analyst, R&D Finance
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Research Fellow, ML Application for Molecular Modeling & Design across Discovery Modalities
Beyond Biologics Drug Discovery, and as part of a four-modality company, we partner with colleagues in gene therapy, computational chemistry, and computational biology, supporting Biogen portfolio programs across all therapeutic areas including Alzheimer's disease and dementia, Parkinson's disease, Amyotrophic lateral sclerosis (ALS) and multiple sclerosis. As pioneers in neuroscience, Biogen discovers, develops, and delivers worldwide innovative therapies for people living with serious neurological diseases as well as related therapeutic adjacencies. One of the world's first global biotechnology companies, Biogen was founded in 1978 by Charles Weissmann, Heinz Schaller, Sir Kenneth Murray, and Nobel Prize winners Walter Gilbert and Phillip Sharp. Today, Biogen has a leading portfolio of medicines to treat multiple sclerosis, has introduced the first approved treatment for spinal muscular atrophy, and developed the first and only approved treatment to address a defining pathology of Alzheimer's disease. Biogen is also commercializing biosimilars and focusing on advancing one of the industry's The Research Fellow role at Biogen is an 18-month position designed to provide a unique opportunity for scientists to gain exposure to drug discovery and train in an industry research setting.$59k-74k yearly est.11d ago
Neurodivergent Co-op, Asset Development and Portfolio Management
To participate in the Biogen Internship Program, students must meet the following eligibility criteria: 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. Limitless @ Biogen provides support for managers and interns throughout the 6-month co-op. This internship role is part of the Limitless @ Biogen program; the summer co-op for neurodiverse college students. As an intern or co-op at Biogen, you can expect to be placed on a real project, under the guidance of experience professionals and subject matter experts who are invested in your career and academic growth.$105k-157k yearly est.18d ago
