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Salary
≈ $16k – $36k per year (Estimated)
Location
In office (Pudupākkam)
Seniority
Senior
Employment
Full-Time

Confirmed on the employer's own hiring board on Oct 19, 2026. First seen by Alion on Sep 4, 2026. Par Health scores B on the Alion truth index.

Overview
Company
Impact
Profile match
Par Health is a US pharmaceutical company based in Saint Louis, Missouri, that makes generic and essential medicines, including sterile injectables, controlled substances, active pharmaceutical ingredients and oral products for hospitals, pharmacies and distributors. It was formed from the generics businesses of Endo and Mallinckrodt after the two companies combined in 2025, and it runs manufacturing and research sites in Missouri, Indiana, Illinois, North Carolina, Pennsylvania and India. Par Health hires production and packaging operators, quality control technicians, research associates, compliance specialists, supply chain and EHS managers and sales staff.

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.

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