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Pv Scientist Jobs (NOW HIRING)

Fladger Associates

Pharmacovigilance (PV)

Boston, MA · On-site

We are looking for a Pharmacovigilance Scientist (approximately 25 hours per week) who can support ... Review the contract and see if relevant PV language is needed or is already covered. * Coordinate ...

Qcells

PV Solutions Engineer

San Francisco, CA · On-site

$115K - $135K/yr

D. in Engineering or Physical Sciences (Electrical, Mechanical, Physics, etc.) with 2-3 years (or 1-2 years with MS/Ph.D.) of relevant experience in the PV solar or renewable energy industry.

Qcells

PV Solutions Manager

Santa Clara, CA

$125K - $160K/yr

D. in Engineering or Physical Sciences (Electrical, Mechanical, Physics, etc.) with 3-4 years (or 2-3 years with MS/Ph.D.) of relevant experience in the PV solar or renewable energy industry.

Qcells

PV Solutions Manager

Irvine, CA

$125K - $160K/yr

D. in Engineering or Physical Sciences (Electrical, Mechanical, Physics, etc.) with 3-4 years (or 2-3 years with MS/Ph.D.) of relevant experience in the PV solar or renewable energy industry.

Qcells

PV Solutions Engineer

Santa Clara, CA · On-site

$115K - $135K/yr

D. in Engineering or Physical Sciences (Electrical, Mechanical, Physics, etc.) with 2-3 years (or 1-2 years with MS/Ph.D.) of relevant experience in the PV solar or renewable energy industry.

Collabera

PV&V Engineer

Waterloo, IA · On-site

... Application PV&V and Application Engineering to ensure the latest hardware and software is ... Science degree or technical degree or equivalent experience required. Requirements and Skills:

Qcells

PV Solutions Manager

San Francisco, CA

$125K - $160K/yr

D. in Engineering or Physical Sciences (Electrical, Mechanical, Physics, etc.) with 3-4 years (or 2-3 years with MS/Ph.D.) of relevant experience in the PV solar or renewable energy industry.

Qcells

PV Solutions Manager

Irvine, CA · On-site

$125K - $160K/yr

D. in Engineering or Physical Sciences (Electrical, Mechanical, Physics, etc.) with 3-4 years (or 2-3 years with MS/Ph.D.) of relevant experience in the PV solar or renewable energy industry.

Qcells

PV Solutions Manager

San Francisco, CA · On-site

$125K - $160K/yr

D. in Engineering or Physical Sciences (Electrical, Mechanical, Physics, etc.) with 3-4 years (or 2-3 years with MS/Ph.D.) of relevant experience in the PV solar or renewable energy industry.

SystImmune, Inc

PV Operations Specialist

Princeton, NJ · On-site

$85K - $115K/yr

The PV Operations Specialist supports the Senior Director of Pharmacovigilance (PV) Operations in ... Bachelor's degree in life sciences, pharmacy, nursing, or related field. * 3-5+ years of experience ...

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Pv Scientist information

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How much do pv scientist jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for pv scientist in the United States is $61.42, according to ZipRecruiter salary data. Most workers in this role earn between $42.55 and $73.80 per hour, depending on experience, location, and employer.

What does a typical day look like for a PV Scientist?

A typical day for a PV Scientist involves reviewing and analyzing individual case safety reports, assessing potential safety signals, and preparing regulatory safety documents and risk management plans. You may participate in team meetings with cross-functional partners such as clinical, regulatory, and medical affairs teams to discuss ongoing safety concerns or emerging issues. Additionally, you’ll interact with global health authorities, respond to their inquiries, and ensure compliance with evolving drug safety regulations. The work is detail-oriented and deadline-driven, but it also offers valuable opportunities for professional growth and meaningful contributions to patient safety.

What are the key skills and qualifications needed to thrive in the Pv Scientist position, and why are they important?

To thrive as a PV (Pharmacovigilance) Scientist, you need an academic background in life sciences or pharmacy, in-depth knowledge of drug safety regulations, and strong analytical skills. Familiarity with pharmacovigilance databases (like Oracle Argus or ARISg), signal detection tools, and regulatory reporting systems is crucial, and certifications such as DSci or PV certifications are advantageous. Excellent written communication, critical thinking, and collaboration skills help you effectively interpret safety data and work cross-functionally. These competencies are essential for ensuring patient safety, regulatory compliance, and effective risk management in pharmaceutical environments.

What is a PV Scientist job?

A PV (Pharmacovigilance) Scientist is responsible for monitoring, assessing, and preventing adverse drug reactions to ensure patient safety. They analyze safety data, contribute to risk management plans, and prepare regulatory reports. PV Scientists collaborate with medical, regulatory, and clinical teams to ensure compliance with global safety regulations. Their role is critical in ensuring drug safety throughout a product’s lifecycle.

What is a PV scientist?

A PV scientist specializes in photovoltaic technology, focusing on the research, development, and testing of solar energy materials and devices. They often work in laboratories or research facilities, utilizing tools like solar simulators and spectrometers, and may require knowledge of materials science, physics, and relevant certifications. Their goal is to improve solar cell efficiency and performance for renewable energy applications.
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Pv Scientist jobs near you
Head of PV & Drug Safety, West Coast Hub

Head of PV & Drug Safety, West Coast Hub

Biogen

San Francisco, CA • On-site

$326K - $460K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 18 days ago

Biogen rating

9.2

Company rating: 9.2 out of 10

Based on 18 frontline employees who took The Breakroom Quiz

3rd of 71 rated pharmaceutical

Job description

About This Role:
As the Head of Drug Safety & Pharmacovigilance (PV) for the West Coast Hub, you will be at the forefront of ensuring the safety and efficacy of our therapies focused on immune-mediated diseases. This pivotal position requires strategic oversight and scientific leadership tomaintainthe integrity of our global safety surveillance activities. Your role is essential in safeguarding patient well-being andoptimizingthe benefit-risk profile of our therapies throughout their lifecycle. Reporting directly to the Head of Regulatory & PV, you will spearhead safety science, clinical and post-marketing surveillance, and regulatory safety engagement. You will collaborate closely with teams across Medical Safety, Clinical Development, and Regulatory Affairs to drive strategic decisions thatexpeditethe delivery of impactful medicines.

WhatYou'llDo:

  • Define and implement the long-term pharmacovigilance strategy for the West Coast Hub portfolio.

  • Execute PV scientific and operational goals to enable rapid and compliant development of therapies.

  • Develop and oversee policies and processes for safety science, benefit-risk assessment, and signal detection.

  • Serve as a senior representative in global health authority interactions, including regulatory meetings and submissions.

  • Oversee medical evaluation of safety data for signal detection and interpretation across products.

  • Lead the development and execution of Risk Management Plans (RMPs) and REMS programs.

  • Drive innovative safety surveillance activities aligned with global regulatory requirements.

  • Build and mentor a high-performing team of PV professionals, fostering a culture of accountability and innovation.

  • Partner with cross-functional teams to influence product strategy and drive integrated execution.

Who You Are:
You are a strategic thinker with a deep passion for patient safety and drug efficacy. Your extensive experience in pharmacovigilance and drug safety equips you to lead with confidence and precision in a dynamic environment. You excel in fostering collaboration and innovation, guiding high-performing teams to achieve excellence. Your exceptional communication skills and executive presence enable you to influence decisions at all organizational levels, ensuring that safetyremainsa top priority.

Required Skills:

  • MD/PhD with post-graduate clinical training.

  • 12+ years of progressive experience in pharmacovigilance/drug safety in the biotech/pharma industry.

  • Demonstrated success in global safety surveillance and regulatory engagements.

  • Expert knowledge of global PV regulations, FDA/EMA requirements, and clinical safety reporting.

  • Strong analytical and scientific reasoning skills.

  • Outstanding communication and executive presence.

  • Proficiencywith safety databases and analytics platforms.

  • Domestic and international travel may berequired.

Preferred Skills:

  • Advanced training in pharmacoepidemiology or MPH.

  • Experience supporting immune-mediated or rare diseases.

#LI-TD1


Job Level: Management


Additional Information

The base compensation range for this role is: $326,000.00-$460,000.00


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 onto learn more about our DE&I efforts.

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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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

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