Concord Biotech Limited is a R&D driven biopharma Company that manufactures Active Pharmaceutical Ingredients (API) through fermentation & semi-synthetic process and finished formulations. Concord, founded in the year 2000 has transformed from a single-product company to a broad-spectrum solution provider, offering products across diversified therapeutic segments.
WALK IN INTERVIEW
Production Department
Supervisor / Officer
Qualification : M.Sc / B.Pharm / M.Pharm
Experience : 03 to 05 Years
Job Responsibility : Experience into Manufacturing process, Granulation, Coating, Capsule filling Machine
Packaging Executive / Sr. Executive
Qualification : B.Sc/M.Sc
Experience : 06 to 08 Years
Job Responsibility : Experience in Blister Line, Bottle Line, QMS, Documentations. Can able to Manage shift operation Independently
RA Department
Post : Officer / Executive / Sr. Executive / Asst. Manager
Qualification : M.Sc / B.Pharm / M.Pharm
Experience : 02 to 10 Years
Job Responsibility : GLOBAL Regulatory activities :
• To plan, prepare and review of high-quality dossier with support and guidance, assuring technical congruency and regulatory compliance, meeting agreed upon time line. Review guideline for first time dossier preparation. Lead a team (NMT 5) of regulatory wherever required. GAP Analysis for new products, Query Responses, Launch of the product & life cycle management for global Regulatory work.
Domestic Regulatory activities :
• To plan, prepare and review of high-quality dossier with support and guidance, assuring technical congruency and regulatory compliance, meeting agreed upon time line. Including review & approval of documents related to domestic / India along with artwork.
• Having exposure of Product permission, COPP, Loan License, CDSCO related activity, approval of site lay out, FDA, CDSCO Related activity along with SUGAM, ONDLS Portal usage.
ADL Injectable Analyst
Post : Officer / Sr. Officer
Qualification : B.Sc. / M.Sc. / B.Pharm. / M.Pharm
Experience : 04 to 06 Years
• To perform analysis of samples allocated by the section head as per routine work allocation for Vendor Qualification samples, R & D batches stability samples, Other study samples, Validation samples etc.
• To perform online documentation, report preparation & result reporting.
• To develop, validate and transfer new methods for Injectable and complex Injectable products.
• To manage the stability samples.
• To Prepare Specification and Standard test Procedure, method validations Protocols/Reports
• To maintain all relevant documentation, including analytical reports, logbooks, and data, to ensure compliance with GLP, cGMP and other regulatory standards like USFDA
ADL Injectable Analyst
Post : Executive / Sr. Executive
Qualification : B.Sc. / M.Sc. / B.Pharm. / M.Pharm
Experience : 06 to 08 Years
Job Responsibility : • Plan, design and execute analytical method validation and method Transfer activity for Injectable products.
• To Prepare/review of analytical method validation / Transfer protocol and report.
• To Mentor and guide junior analysts/scientists In Method development and validation with different instruments like GC, ICP, HPLC etc.
• To support in investigations, change control, deviations and other quality notifications.
• To Collaborate with cross Functional teams for quality improvements.
• To have Strong knowledge of regulatory requirements. Should be able to handle GLP section independently in Analytical development Laboratory
Walk in Interview
Date :
ADL : 20th December 2025
Production & RA : 21st December 2025
Time : 09:00 am to 04:00 pm
Venue : Concord Biotech Limited
Unit - II, No.297-298/2P, At : Valthera, Taluka: Dholka,
Dist: Ahmedabad - 382225. Gujarat, India
Interested candidate can appear with updated Cvs, Appointment Letter, Increment Letter and Salary break-up with Passport Size Photo.
Those who are unable to attend can apply on hrinj@concordbiotech.com with clearly mentioned Position Applied for in Subject Line.
Who appeared before 3 months need not to reappear.
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