Job Description
Win in Life Academy
Business Development Associate - Life science / Technology Fresher Business Development Associate- Life science / Technology Fresher
Win in Life Academy • Bengaluru, Karnataka • via LinkedIn
24 hours ago
Full–time
Apply on LinkedIn
Job description
Company Description
Win in Life Academy is a pioneering institute dedicated to bridging the gap between fresh graduates and industry needs by providing specialized training through experienced industrial faculty. The academy offers a practical, simulation-based learning environment to prepare students for their professional careers. With a strong focus on quality, the academy designs short and long courses in collaboration with industry partners. Committed to student success, the academy provides placement assistance until students achieve their desired job placements.
Role Description
This is a full-time, on-site role for a Business Development Associate – Life Science/Technology Fresher, located in Bengaluru. The associate will identify and generate new business opportunities through lead generation and market research. Responsibilities include building client relationships, delivering presentations, and contributing to the development of business strategies. The role requires regular collaboration with teams and stakeholders to meet business objectives.
Qualifications
• Strong Presentation and Communication skills
• Experience or aptitude in Lead Generation and Market Research
• Proficiency in delivering impactful Presentations
• Ability to work in a collaborative, on-site environment
• Proactive approach, problem-solving mindset, and willingness to learn
• Bachelor’s degree in Science, Engineering, Business, or a related field
Industry
• Education
Employment Type
Full-time
Report this listing
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Fresher Pharmacovigilance Hiring – Elanco Analyst – GDPS (PV Case Processing)
Fresher Pharmacovigilance Hiring – Elanco Analyst – GDPS (PV Case Processing)
Fresher Pharmacovigilance Hiring – Elanco Analyst – GDPS (PV Case Processing) • Bengaluru, Karnataka • via Pharma Stuff
20 hours ago
Full–time
Apply directly on Pharma Stuff
Job description
Elanco Hiring Analyst – GDPS (PV Case Processing) | Life Sciences | Bangalore
Elanco is hiring for the position of Analyst – GDPS (Global Drug Product Safety) in Bangalore, India. This is a full-time opportunity within the Pharmacovigilance and Drug Safety department, focused on adverse event case processing, regulatory compliance, and safety data management. The role is open to Veterinarians (equivalent to US DVM) with or without pharmacovigilance experience, as well as Life Sciences graduates with 0–2 years of PV experience.
If you are looking to build a career in pharmacovigilance, adverse event reporting, regulatory submissions, and global drug safety operations, this role offers structured exposure within a multinational animal health organization.
Company Overview
entity[“organization”,”Elanco”,”animal health company”] is a global leader in animal health, dedicated to innovation in preventing and treating diseases in farm animals and companion animals. Listed on the NYSE (ELAN), Elanco operates across international markets with a strong focus on regulatory compliance, product safety, and scientific excellence.
The company’s mission centers on improving animal well-being while supporting food safety, sustainability, and veterinary healthcare advancement. With a culture rooted in diversity, collaboration, and continuous learning, Elanco empowers professionals to contribute meaningfully to global pharmacovigilance and product safety systems.
Working at Elanco provides exposure to global safety databases, regulatory frameworks, and structured pharmacovigilance processes aligned with international standards.
Job Role & Responsibilities
The Analyst – GDPS will manage adverse event case processing activities, ensuring data accuracy, regulatory compliance, and timely safety reporting. The role requires precision in documentation, understanding of global PV regulations, and the ability to manage case workflows efficiently.
Adverse Event Case Processing
• Perform data entry of adverse event reports into the pharmacovigilance database.
• Assess seriousness, causality, and regulatory reportability of adverse event cases.
• Validate data entries against source documents and call notes.
• Conduct self-review to ensure case completeness, accuracy, and quality.
• Determine follow-up requirements for incomplete or unclear cases.
• Ensure cases are submission-ready for appropriate regulatory authorities.
• Meet defined productivity and quality benchmarks.
• Identify potential delays in submission timelines and escalate appropriately.
• Participate actively in team meetings and contribute to process improvements.
Regulatory Compliance & Safety Management
• Develop understanding of global pharmacovigilance regulations and reporting requirements.
• Comply with internal SOPs and external regulatory timelines.
• Support product complaint case processing activities.
• Maintain adherence to global, local, and regional safety regulations.
• Manage multiple safety cases across different products simultaneously.
The position requires structured thinking, strong documentation skills, and the ability to operate in a compliance-driven environment.
Eligibility & Qualifications
Educational Background
Eligible qualifications include:
Veterinarian (equivalent to US DVM degree), B.V.Sc & AH, B.Pharm, M.Pharm, BSc Life Sciences, MSc Life Sciences, Biotechnology, Microbiology, Biochemistry, Pharmacology, or related Life Sciences disciplines.
Experience Requirements
• 0–2 years of pharmacovigilance or drug safety experience for Life Sciences graduates.
• Veterinarians may apply with or without prior PV experience.
Preferred Skills
• Basic knowledge of medical terminology and adverse event reporting concepts.
• Understanding of global pharmacovigilance regulations.
• Strong verbal and written communication skills.
• Ability to manage multiple products and prioritize workloads effectively.
• Proficiency in working with multiple databases and Microsoft Office tools.
• Flexibility to handle high case volumes when required.
• Self-motivated and adaptable to process changes.
Candidates demonstrating strong attention to detail and regulatory awareness will perform well in this role.
Location & Employment Details
• Location: Bangalore, India
• Employment Type: Full-Time
• Department: Global Drug Product Safety (GDPS)
• Job Requisition ID: R0024602
• Travel Requirement: 0%
[caption id="attachment_156069" align="aligncenter" width="1200"] Analyst – Pharmacovigilance Hiring at Elanco – BPharm, MPharm, MBBS, BDS, MSc Life Scienceso[/caption]
Application Process
Interested candidates can apply directly through Elanco’s official careers portal using the link below:
Apply Here: https://elanco.wd5.myworkdayjobs.com/en-US/External_Career/job/Analyst—GDPS_R0024602?locationCountry=c4f78be1a8f14da0ab49ce1162348a5e
Career Growth Opportunities
With experience, professionals can advance into roles such as:
• Senior Pharmacovigilance Associate
• Drug Safety Specialist
• Safety Data Management Lead
• Global Safety Reporting Analyst
• Pharmacovigilance Quality Reviewer
The expanding global animal health and pharmaceutical safety landscape ensures strong career stability in this domain.
Frequently Asked Questions (FAQs)
1. Is this role open to freshers?
Yes, Life Sciences graduates with 0–2 years of experience are eligible.
2. Are veterinarians eligible?
Yes, veterinarians (equivalent to US DVM) can apply with or without prior PV experience.
3. Is prior pharmacovigilance experience mandatory?
It is preferred but not mandatory for eligible candidates.
4. What type of cases will be handled?
The role involves adverse event case processing and product complaint case management.
5. Is this a remote position?
No, this is an on-site role based in Bangalore.
Summary Table
Company
Elanco
Vacancies
Analyst – GDPS (PV Case Processing)
Required Education
DVM, B.V.Sc & AH, B.Pharm, M.Pharm, BSc/MSc Life Sciences, Biotechnology, Microbiology, Biochemistry
Experience
0–2 years pharmacovigilance experience; veterinarians may apply with or without PV experience
Tagged as: Pharma Jobs in Bangalore
Business Development Associate - Life science / Technology Fresher Business Development Associate- Life science / Technology Fresher
Win in Life Academy • Bengaluru, Karnataka • via LinkedIn
24 hours ago
Full–time
Apply on LinkedIn
Job description
Company Description
Win in Life Academy is a pioneering institute dedicated to bridging the gap between fresh graduates and industry needs by providing specialized training through experienced industrial faculty. The academy offers a practical, simulation-based learning environment to prepare students for their professional careers. With a strong focus on quality, the academy designs short and long courses in collaboration with industry partners. Committed to student success, the academy provides placement assistance until students achieve their desired job placements.
Role Description
This is a full-time, on-site role for a Business Development Associate – Life Science/Technology Fresher, located in Bengaluru. The associate will identify and generate new business opportunities through lead generation and market research. Responsibilities include building client relationships, delivering presentations, and contributing to the development of business strategies. The role requires regular collaboration with teams and stakeholders to meet business objectives.
Qualifications
• Strong Presentation and Communication skills
• Experience or aptitude in Lead Generation and Market Research
• Proficiency in delivering impactful Presentations
• Ability to work in a collaborative, on-site environment
• Proactive approach, problem-solving mindset, and willingness to learn
• Bachelor’s degree in Science, Engineering, Business, or a related field
Industry
• Education
Employment Type
Full-time
Report this listing
More jobs at Win in Life Academy
See web results for Win in Life Academy
F
Fresher Pharmacovigilance Hiring – Elanco Analyst – GDPS (PV Case Processing)
Fresher Pharmacovigilance Hiring – Elanco Analyst – GDPS (PV Case Processing)
Fresher Pharmacovigilance Hiring – Elanco Analyst – GDPS (PV Case Processing) • Bengaluru, Karnataka • via Pharma Stuff
20 hours ago
Full–time
Apply directly on Pharma Stuff
Job description
Elanco Hiring Analyst – GDPS (PV Case Processing) | Life Sciences | Bangalore
Elanco is hiring for the position of Analyst – GDPS (Global Drug Product Safety) in Bangalore, India. This is a full-time opportunity within the Pharmacovigilance and Drug Safety department, focused on adverse event case processing, regulatory compliance, and safety data management. The role is open to Veterinarians (equivalent to US DVM) with or without pharmacovigilance experience, as well as Life Sciences graduates with 0–2 years of PV experience.
If you are looking to build a career in pharmacovigilance, adverse event reporting, regulatory submissions, and global drug safety operations, this role offers structured exposure within a multinational animal health organization.
Company Overview
entity[“organization”,”Elanco”,”animal health company”] is a global leader in animal health, dedicated to innovation in preventing and treating diseases in farm animals and companion animals. Listed on the NYSE (ELAN), Elanco operates across international markets with a strong focus on regulatory compliance, product safety, and scientific excellence.
The company’s mission centers on improving animal well-being while supporting food safety, sustainability, and veterinary healthcare advancement. With a culture rooted in diversity, collaboration, and continuous learning, Elanco empowers professionals to contribute meaningfully to global pharmacovigilance and product safety systems.
Working at Elanco provides exposure to global safety databases, regulatory frameworks, and structured pharmacovigilance processes aligned with international standards.
Job Role & Responsibilities
The Analyst – GDPS will manage adverse event case processing activities, ensuring data accuracy, regulatory compliance, and timely safety reporting. The role requires precision in documentation, understanding of global PV regulations, and the ability to manage case workflows efficiently.
Adverse Event Case Processing
• Perform data entry of adverse event reports into the pharmacovigilance database.
• Assess seriousness, causality, and regulatory reportability of adverse event cases.
• Validate data entries against source documents and call notes.
• Conduct self-review to ensure case completeness, accuracy, and quality.
• Determine follow-up requirements for incomplete or unclear cases.
• Ensure cases are submission-ready for appropriate regulatory authorities.
• Meet defined productivity and quality benchmarks.
• Identify potential delays in submission timelines and escalate appropriately.
• Participate actively in team meetings and contribute to process improvements.
Regulatory Compliance & Safety Management
• Develop understanding of global pharmacovigilance regulations and reporting requirements.
• Comply with internal SOPs and external regulatory timelines.
• Support product complaint case processing activities.
• Maintain adherence to global, local, and regional safety regulations.
• Manage multiple safety cases across different products simultaneously.
The position requires structured thinking, strong documentation skills, and the ability to operate in a compliance-driven environment.
Eligibility & Qualifications
Educational Background
Eligible qualifications include:
Veterinarian (equivalent to US DVM degree), B.V.Sc & AH, B.Pharm, M.Pharm, BSc Life Sciences, MSc Life Sciences, Biotechnology, Microbiology, Biochemistry, Pharmacology, or related Life Sciences disciplines.
Experience Requirements
• 0–2 years of pharmacovigilance or drug safety experience for Life Sciences graduates.
• Veterinarians may apply with or without prior PV experience.
Preferred Skills
• Basic knowledge of medical terminology and adverse event reporting concepts.
• Understanding of global pharmacovigilance regulations.
• Strong verbal and written communication skills.
• Ability to manage multiple products and prioritize workloads effectively.
• Proficiency in working with multiple databases and Microsoft Office tools.
• Flexibility to handle high case volumes when required.
• Self-motivated and adaptable to process changes.
Candidates demonstrating strong attention to detail and regulatory awareness will perform well in this role.
Location & Employment Details
• Location: Bangalore, India
• Employment Type: Full-Time
• Department: Global Drug Product Safety (GDPS)
• Job Requisition ID: R0024602
• Travel Requirement: 0%
[caption id="attachment_156069" align="aligncenter" width="1200"] Analyst – Pharmacovigilance Hiring at Elanco – BPharm, MPharm, MBBS, BDS, MSc Life Scienceso[/caption]
Application Process
Interested candidates can apply directly through Elanco’s official careers portal using the link below:
Apply Here: https://elanco.wd5.myworkdayjobs.com/en-US/External_Career/job/Analyst—GDPS_R0024602?locationCountry=c4f78be1a8f14da0ab49ce1162348a5e
Career Growth Opportunities
With experience, professionals can advance into roles such as:
• Senior Pharmacovigilance Associate
• Drug Safety Specialist
• Safety Data Management Lead
• Global Safety Reporting Analyst
• Pharmacovigilance Quality Reviewer
The expanding global animal health and pharmaceutical safety landscape ensures strong career stability in this domain.
Frequently Asked Questions (FAQs)
1. Is this role open to freshers?
Yes, Life Sciences graduates with 0–2 years of experience are eligible.
2. Are veterinarians eligible?
Yes, veterinarians (equivalent to US DVM) can apply with or without prior PV experience.
3. Is prior pharmacovigilance experience mandatory?
It is preferred but not mandatory for eligible candidates.
4. What type of cases will be handled?
The role involves adverse event case processing and product complaint case management.
5. Is this a remote position?
No, this is an on-site role based in Bangalore.
Summary Table
Company
Elanco
Vacancies
Analyst – GDPS (PV Case Processing)
Required Education
DVM, B.V.Sc & AH, B.Pharm, M.Pharm, BSc/MSc Life Sciences, Biotechnology, Microbiology, Biochemistry
Experience
0–2 years pharmacovigilance experience; veterinarians may apply with or without PV experience
Tagged as: Pharma Jobs in Bangalore
💡 Quick Summary
Seeking a career-building opportunity? The Fresher Pharmacovigilance Hiring – Elanco Analyst – GDPS (PV Case Processing) position is now open for candidates interested in the Fresher Jobs sector. This role in Bangalore offers a professional environment and growth potential.
Requirement Snapshot: Candidates should possess basic communication skills, a proactive attitude, and the ability to work in a team. Experience in Fresher Jobs is a plus.
