Concord Biotech has announced a walk-in interview drive for experienced pharmaceutical professionals across Regulatory Affairs, Analytical Development Laboratory (OSD), and Quality Assurance departments. Candidates possessing M.Sc, M.Pharm, or B.Pharm qualifications with relevant industry experience can attend the interview scheduled on 13 June 2026 in Ahmedabad, Gujarat.
This recruitment drive offers opportunities for professionals looking to build their careers with a leading biotech organization working towards innovative healthcare solutions.
Job Overview
Company Name: Concord Biotech
Job Type: Walk-In Interview
Walk-In Date: 13 June 2026
Time: 10:00 AM to 2:00 PM
Location:
297-298/2P, At: Valthera, Taluka Dholka, Dist. Ahmedabad – 382225, Gujarat, India
Available Positions
1. Regulatory Affairs
Positions
- Executive
- Sr. Executive
- Asst. Manager
- Deputy Manager
- Manager
- Sr. Manager
Qualification
- M.Sc
- B.Pharm
- M.Pharm
Experience
- 06 to 12 Years
Roles & Responsibilities
- Plan, prepare and review high-quality regulatory dossiers.
- Ensure technical compliance and regulatory standards.
- Review timelines for dossier preparation.
- Lead regulatory teams for GAP analysis and new product activities.
- Handle regulatory queries and product lifecycle management.
- Review domestic licensing documents.
- Manage product permission, COPP, loan license and CDSCO-related activities.
- Coordinate site approvals, FDA and Sugam/ONDLS portal activities.
Analytical Development Laboratory (OSD)
Chemist / Officer / Sr. Officer
Qualification
- M.Sc
- M.Pharm
Experience
- 02 to 04 Years
Roles & Responsibilities
- Perform analysis of raw materials, excipients and drug products as per pharmacopoeia.
- Support formulation development studies.
- Conduct calibration of laboratory equipment.
- Perform UV, Dissolution, HPLC, GC and Particle Size analysis.
- Follow GDP/GLP practices in the laboratory.
Executive / Sr. Executive
Qualification
- M.Sc
- M.Pharm
Experience
- 05 to 10 Years
Roles & Responsibilities
- Perform analytical method development and validation.
- Execute routine testing and comparative dissolution studies.
- Operate UV, Dissolution, HPLC, GC and Particle Size instruments.
- Support stability studies and impurity profiling.
- Prepare analytical method reports and maintain documentation.
- Ensure compliance with regulatory quality systems and GDP/GLP requirements.
Quality Assurance (QA)
Officer / Sr. Officer
Qualification
- B.Pharm
- M.Pharm
Experience
- 05 to 08 Years
Roles & Responsibilities
- Perform stability sample charging and withdrawals.
- Handle additional sample-related activities.
- Prepare stability master schedules and protocols.
- Manage monthly planning and stability sample inventories.
- Handle raw material, packing material and drug product retain samples.
- Maintain retain/control sample room records.
Required Qualifications
Candidates should possess one of the following qualifications depending on the role:
- M.Sc
- B.Pharm
- M.Pharm
Relevant pharmaceutical industry experience as specified for each position is mandatory.
Salary & Benefits
The official notification does not mention salary details. Based on industry standards and required experience, the expected annual CTC may range between:
- Analytical Development (2–4 years): ₹4.5 – ₹7.5 LPA
- QA Officer/Sr. Officer (5–8 years): ₹6 – ₹10 LPA
- Regulatory Affairs (6–12 years): ₹8 – ₹18 LPA
Additional benefits may include professional growth opportunities, exposure to regulatory projects and a collaborative work environment.
Documents Required
Candidates attending the walk-in interview should carry:
- Updated CV
- Current Salary Proof
- Passport Size Photograph
How to Apply
Eligible candidates can directly attend the walk-in interview at the specified venue on 13 June 2026 between 10:00 AM and 2:00 PM.
Candidates who are unable to attend the interview can send their application to:
Email: careerfdf@concordbiotech.com
Applicants should clearly mention the position applied for in the email subject line.
