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 Concord Biotech Limited Unit – II Valthera

Production
Post : Manager / Asst Manager / Sr. Executive
Qualification : B.Pharm / M.Pharm
Experience : 10 to 15 years
Job Responsibility : Experienced Shift In Charge to Manage daily manufacturing Operations, ensuring strict cGMP, Safety and regulatory Compliance. Key duties include production planning & ensuring execution as per plan, preparing batch records and qualification documents (IQ/OQ/PQ) and coordinating with QC/ Warehouse for uninterrupted workflow. Responsible for equipment maintenance, calibration tracking and leading team training to ensure minimal downtime and high – quality output.

Analytical Development Laboratory – OSD
Chemist / Officer / Sr.Officer
Qualification : MSc / M.Pharm
Experience : 2 to 4 years
Job Responsibility : Perform analysis of finished product/raw material /excipient/drug product accordingly pharmacopeia. Perform analysis of raw material/excipient/drug product accordingly pharmacopeia. Lab batch stability studies and support to formulation development team. Knowledge of conducting calibration of laboratory equipment’s. Should have experience to perform the analysis of UV, Dissolution, HPLC.GC, Particle size, ICP-MS/OES. Knowledge of GDP/GLP in the laboratory.

Executive / Sr. Executive
Qualification : MSc / M.Pharm
Experience : 5 to 10 years
Job Responsibility : Experience to handle the Topical semisolid product. Perform analytical method development, partial validation, validation and routine testing. Dissolution development, Comparative dissolution profile and multimedia dissolution study. Should have experience to perform the analysis of UV, Dissolution, HPLC.GC, Particle size, ICP-OES. Support stability studies, method transfer and impurity profile. Prepare the analytical method and method development report. Maintain accurate documentation and ensure adherence to regulatory and quality systems. Knowledge of GDP/GLP in the laboratory and audit.

Analytical Development Laboratory injectable 
Officer / Senior Officer 
Qualification : M.Pharm, B.Pharm, M.Sc, B.Sc
Experience : 04 to 06 years
Job Responsibility : To perform analysis of samples allocated by the rection head as per routine work allocation for Vendor Qualification samples, R & D batches stability samples, other study samples, Validation samples ete.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 samplesJo Prepare Specification and Standard test Procedure, method validations Protocols/Reports. To maintain all relevant documentation, including analytical reports, logbooks, and data, to ensure complience with GIP, cGMP and other regulatory standards like USFDA

Executive / Sr. Executive
Qualification : M.Pharm, B.Pharm, M.Sc, B.Sc
Experience : 6 to 8 years
Job Responsibility : To opesiaan and execute analytical method validation and method Transfer activity for information products. To Prepare/review of analytical method validation/Transfer protocol and report. To Mentor and guide (umor 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.

Regulatory Affairs
Post : Executive/ Sr. Executive/ Asst. Manager/ Deputy manager/ Manager/ Sr. Manager
Qualification : M.Pharm, B.Pharm, M.Sc
Experience : 5 to 10 years
Job Responsibility : To plan, prepare and review of high-quality dossier with support and guidance, assuring technical congruency and regulatory compliance, meeting agread upon timeline. Review guideline for first time dossier preparation. Lead a team (NMT 5) of regulatory. GAP Analysis for new products Professionals. Query Responses. Launch of the product & life cycle management for global Regulatory.
To plan, prepare and review of high-quality dossier with support and guidance, assuring technical congruency and regulatory compliance, testing agreed upon timeline, 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 she lay out, FDA, CDSCO Related activity along with SUGAM, ONDIS Portal

Walk in Interview
Date & Time : 09th May 2026 from 10:00 Hrs to 14:00 Hrs 
Venue : B1601-1602, B-Wing, Mondeal Heights, Iscon Cross Road, S.G Highway, and Ahmedabad.

Interested Candidate can appear with updated CVs and Current salary Proof with Passport size Photo.
Those who are unable to attend can apply on [email protected] with clearly mentioned position applied for in subject line.