Pharma Jobs – Concord Biotech Limited is conducting a walk-in interview on 24th March 2026 for experienced professionals in Quality Assurance (IPQA & Analytical Reviewer), Quality Control – Microbiology, and IT (Sr. Officer/Executive) at its Valthera facility near Ahmedabad, Gujarat.
Excellent opportunity for candidates with USFDA/WHO-compliant experience in oral solid dosage forms, microbial testing, and GxP/IT infrastructure to join a leading biotech-pharma organization in India.
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About the Company
Concord Biotech Limited is a prominent Indian pharmaceutical and biotechnology company specializing in fermentation-based APIs, biopharmaceuticals, and formulations with a strong global presence.
The company operates multiple USFDA, WHO-GMP, and other regulated facilities, including the Valthera Unit-II in Ahmedabad, focusing on high-quality production of APIs, microbial-derived products, and finished dosage forms.
Concord is recognized for its innovation in fermentation technology, regulatory excellence, commitment to quality, and a progressive work environment that supports professional growth and scientific advancement.
Job Details
- Company Name: Concord Biotech Limited (Unit-II, Valthera)
- Experience: Varies by role (2–8 years)
- Qualification: B.Pharm / M.Pharm (QA/QC); B.Sc / M.Sc (Microbiology); BCA / MCA / Any Graduate or Diploma in Hardware & Networking (IT)
- Location: Valthera, Taluka Dholka, Dist. Ahmedabad, Gujarat – 382225
- Work Type: On-site
Job Description
Concord Biotech is strengthening its quality, microbiology, and IT functions at the Valthera facility to support regulated manufacturing and compliance. The walk-in targets experienced candidates for IPQA, analytical review, microbial testing, and IT infrastructure roles in a GMP/GxP environment.
IPQA – Officer / Executive
- Department: Quality Assurance
- Market: Pharmaceuticals – Oral Solid Dosage Forms
- Role: IPQA Officer / Executive
- Experience: 4–8 Years
- Education/Qualification: B.Pharm / M.Pharm
Analytical Reviewer – Quality Assurance
- Department: Quality Assurance
- Market: Pharmaceuticals – Oral Solid Dosage Forms
- Role: Analytical Reviewer
- Experience: 2–8 Years
- Education/Qualification: B.Pharm / M.Pharm
Officer – QC Microbiology
- Department: Quality Control – Microbiology
- Market: Pharmaceuticals – Oral Solid Dosage Forms
- Role: Officer – QC Microbiology
- Experience: 3–8 Years
- Education/Qualification: B.Sc / M.Sc (Microbiology / Biotechnology)
Sr. Officer / Executive – IT
- Department: IT
- Market: Pharmaceuticals – Regulated Manufacturing
- Role: Sr. Officer / Executive – IT
- Experience: 3–8 Years
- Education/Qualification: BCA / MCA / Any Graduate or Diploma in Hardware & Networking
Skills/Qualifications
- IPQA: Experience in in-process QA activities for tablets, capsules, dry syrups in OSD
- Analytical Reviewer: Expertise in reviewing analytical documents, master documents, specifications, test methods, and work records
- QC Microbiology: Hands-on microbial limit testing, environmental monitoring, water/product analysis, media preparation
- IT: Proficiency in Windows Server, Active Directory, Hyper-V, backup/restore, IT asset management, CSV (URS/IQ/OQ/PQ), data integrity (ALCOA+), GxP, 21 CFR Part 11
- Strong documentation, audit support, and compliance mindset
- Willingness to work in a regulated, shift-based environment
Key Responsibilities
- Perform IPQA checks, line clearance, and in-process monitoring for OSD
- Review analytical documents, specifications, test methods, and work records
- Conduct microbial limit tests, environmental monitoring, and water analysis
- Manage IT infrastructure (hardware, network, servers, storage, firewall, NAS)
- Administer Windows Server, Active Directory, backup/restore, and CSV documentation
- Ensure data integrity, GxP compliance, and support internal/external audits
- Prepare/review SOPs, change controls, and QMS documents
Benefits/Perks
- Career growth in a USFDA/WHO-GMP compliant biotech-pharma company
- Exposure to advanced OSD formulation, microbiology, and IT systems
- Opportunities for skill enhancement in regulatory and quality domains
- Competitive compensation and performance-based rewards
- Supportive work culture focused on quality and innovation
How to Apply
Walk-in interview is open on 24th March 2026 from 10:00 AM to 02:00 PM. Bring an updated CV, salary proof, passport-size photograph, academic & experience certificates.
Candidates unable to attend can email CV to careerfdf@concordbiotech.com (clearly mention position in subject line). For more pharma jobs, QA/QC openings, microbiology roles, IT pharma jobs, and walk-in interviews in Gujarat, visit Pharma Recruiter.
Walk in prepared on 24th March 2026 and build your career with Concord Biotech!
Walk-in Interview Details
- Date: 24th March 2026
- Time: 10:00 AM – 02:00 PM
- Venue: 297-298/2P, At: Valthera, Taluka Dholka, Dist. Ahmedabad – 382225, Gujarat, India
- Contact/Email: careerfdf@concordbiotech.com
Why You Should Join
Concord Biotech Limited offers a stable, high-compliance environment in a USFDA/WHO-GMP approved facility with a strong focus on quality and innovation.
Employees benefit from hands-on exposure to OSD manufacturing, microbiology, and IT infrastructure in regulated settings, continuous learning, career progression from officer to managerial levels, and long-term job security.
Joining Concord means contributing to high-quality pharmaceutical products while growing professionally in a respected organization committed to excellence and patient health.
FAQs
What experience is required for IPQA and QC Microbiology roles at Concord Biotech?
IPQA: 4–8 years in OSD; QC Microbiology: 3–8 years in microbial limit testing, environmental monitoring, and water analysis.
Is prior experience mandatory for all positions?
Yes—most roles require 2–8 years; freshers are not mentioned in this drive.
Where is the walk-in venue located?
Valthera, Taluka Dholka, Dist. Ahmedabad – 382225, Gujarat (Concord Biotech Unit-II facility).
What growth opportunities exist at Concord Biotech?
Strong potential for advancement in a USFDA/WHO-compliant setup with exposure to OSD formulations, microbiology, and IT in a quality-focused biotech-pharma organization.
