Sr Research Associate, Technical Services

Posted 5 Days Ago
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Pudupakkam, Marakkanam, Viluppuram, Tamil Nadu, IND
In-Office
Senior level
Healthtech • Pharmaceutical • Telehealth
The Role
Coordinates pharmaceutical technology transfer, site transfer, validation, submission, and product lifecycle activities. Responsibilities include preparing and reviewing engineering and validation batch documentation, coordinating cross-functional teams, conducting risk and gap assessments, monitoring project timelines, supporting regulatory filings and CMC queries, managing investigations, and providing commercial lifecycle support. Ensures cGMP, audit compliance, environmental procedures, and quality documentation standards while supporting product approvals and launches.
Summary Generated by Built In

Job Description Summary

Senior Technical Services associate for handling of technology transfer activities of execution, documentation, filing support and other activities as responsible.

Job Description

Primary Responsibilities: 
Co-ordination, Communication and Smooth Execution for Technology Transfer Activities:
a)    Co-ordination, Communication for the Technology Transfer of Submission, 
       Site transfer, Validation and lifecycle management of products.
b)    Evaluation, preparation, optimization and finalizing the documents & process for 
       successful execution and implementation at site.
c)    Aligning the team members and CFT’s to achieve organizational goals through 
       discussion to meet the timelines.
d)    Participating in updating the project details in daily, weekly and monthly meetings.
e)    Risk evaluation and gap analysis of projects & finalizing the batch sizes to initiate the
       procurement of prerequisites before commencement of project at site.

f)     Preparation, review and approval of engineering, submission and validation batch  
       documents and preparation and participating in gate meeting and project discussions.
g)    Monitoring of engineering, submission and validation batches as per the timelines 
       and market requirement.
h)    Preparation of placebo and submitting the same to QC for testing as per project         
       requirement.
i)     Support for regulatory filings for the required documentation.
j)     Handling of investigations to make quality documentation and to suggest the way
       forward .
k)    Handling of CMC queries to get the product approval on time and to make readiness 
       for on time launch.
l)     Commercial support throughout the product lifecycle management.

Other Activities.

a)    Audit compliance.
b)    Ensuring cGMP at site level.
c)    Risk evaluation for Nitrosamine impurities.
d)    Following and implementing the organization values during day-to-day activities.

Secondary Responsibilities: 

a) Awareness of EHS policy, significant environment aspect & impacts associated with workplace and contribution to environment management system.
b)Supporting to the cross functional team during Audit and performing internal Audits (Qualified auditor).
c)Responsible to follow and ensure the procedures pertaining to the environmental management system.
d)Responsible to keep the workplace neat and clean.

Endo Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Endo and has not been reviewed or approved by Endo.

  • Fair & Transparent Compensation Pay is considered competitive to good across many roles, with total compensation in commercial positions strengthened by sizable bonus/OTE when targets are met. Subsidiary experiences within the group also point to good compensation, reinforcing a generally positive pay story.
  • Healthcare Strength Core medical, dental, and vision coverage is strong, complemented by virtual care, disease‑management programs, and a health advocate service. Health coverage is described as good, adding perceived value beyond base pay.
  • Retirement Support A 401(k) plan provides a company match up to 4%, supporting employees’ long‑term savings. Current materials outline the matching formula clearly for prospective comparisons.

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The Company
HQ: İzmir
1,722 Employees
Year Founded: 1997

What We Do

At Endo, our far-reaching vision is simple: to help everyone we serve live their best life. As a specialty pharmaceutical company, we’re motivated by a strong sense of purpose to find better ways to meet unique medical needs. Our global team of passionate employees understands the importance of their work. We’re dedicated to supporting one another as we connect with communities and foster partnerships that elevate quality-of-life and bring the best treatments forward. Our uncompromising commitment results in the delivery of life-enhancing therapies. From intelligent product selection to commercialization, we strive to make a meaningful, tangible impact to help everyone live their best life. Endo has global headquarters in Malvern, Pennsylvania. Community Guidelines: 1. Be respectful. Everyone who visits our page should feel comfortable and respected. 2. If we see a comment that violates anything in the following list, it may be removed. • Comments that use profanity; personally attack or bully another individual; or are off-topic, misleading, factually inaccurate, political, spam, defamatory, discriminatory or promotional. • Comments that are excessively repetitive and/or disruptive to the community. • Comments that promote illegal activity, use copyrights or trademarks or are related to an ongoing legal matter. • Comments that appear to be medical advice. We reserve the right to remove a reply for any reason at any time. 3. Adverse Event Reporting: If we see a post about an adverse event, an Endo representative will need to contact you to find out more information to comply with regulatory guidelines. If you experience a side effect while using an Endo product, please consult your physician or pharmacist immediately. You may also report to the FDA at fda.gov/medwatch or 800-FDA-1088. Replies from other users do not necessarily reflect the views of Endo. We do not endorse content added by other users.

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