Life Science Job at Lupin Pharma – Apply Now For Drug Safety Associate!
Lupin Pharmaceuticals is actively hiring a Drug Safety Associate for its Somerset, New Jersey location. If you are a detail-oriented healthcare or life sciences professional with a passion for pharmacovigilance and drug safety, this is your chance to join a globally recognized company committed to innovation and patient care. Learn more about the role and apply today!
- Job Position: Drug Safety Associate
- Location: Somerset, NJ
About the Company:
Lupin comprises a fast-growing, innovative, and robust team of manufacturing, research and development, and commercial divisions. Together, these entities make up the generic and branded U.S. business. Lupin has a significant generic pipeline and a branded focus on womenโs health. The company is driven by its first Research and Development facility in the US in Coral Springs, Florida, focusing on generic and branded orally inhaled and nasal drug products. Somerset, New Jersey, is home to one of fifteen commercial manufacturing sites globally and the only commercial manufacturing facility in the United States for Lupin, along with additional Research and Development teams. Lupin prides itself on being people-focused and centered around the impact made on customers rather than financial metrics.
Life Science Job at Lupin Pharma – Job Summary:
Lupin is seeking a Drug Safety Associate to support pharmacovigilance operations in the US and Canada. This position ensures compliance with drug safety regulations by handling adverse event reports, coordinating PV training, supporting SOP development, and assisting with REMS and Risk Management activities.
Life Science Job at Lupin Pharma – Essential Duties And Responsibilities
- Accountable for receipt, acknowledgement, and communication of all adverse event reports received through mail from reporters and other manufacturers, and vice versa.
- Performing triage of mails addressed to the US pharmacovigilance team, including but not limited to Adverse Events, Product Complaints, and Medical Information.
- Maintain and share a log on receipt of all adverse event reports with the reconciliation team.
- Prepare a weekly report on the adverse event reports received through mail and fax from all sources (reporters, manufacturers).
- Accountable for ensuring Pharmacovigilance Trainings are undertaken, conducted, and compliance is achieved.
- Support the North America PV lead in ensuring PV compliance in line with the DSRM SOPs.
Life Science Job at Lupin Pharma – Qualifications:
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Education: Bachelorโs or Masterโs in Life Sciences, Pharmacy (Pharm D), Nursing (R.N), or related field preferred.
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Experience & Skills:
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Solid understanding of PV regulations and post-marketing safety requirements.
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Excellent organizational, verbal, and written communication skills.
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Strong attention to detail with the ability to meet deadlines.
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Experience working in a matrix environment and collaborating with cross-functional teams.
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Proficient in documentation and computer usage for PV systems.
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Work Environment & Physical Requirements:
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Office-based role with regular sitting, walking, and light lifting (up to 15 lbs).
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May require occasional bending or stooping based on administrative needs.
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