Cohance Walk-in Drive for Production, QA, and QC Roles on 21st Dec 2025 | B.Sc, M.Sc, B.Pharma, Diploma, or ITI Candidates are Eligible

Discover top pharma jobs at Cohance with walk-in interviews for QA jobs, QC jobs, and production jobs. Join pharmaceutical careers in India at our innovative CDMO and Formulation plants.

About the Company

Cohance Lifesciences stands as a global leader in contract development and manufacturing organization (CDMO) services, specializing in advanced drug conjugates (ADCs), nucleic acid chemistry, and small molecules.

Formed through strategic integrations, the company boasts state-of-the-art facilities across India, the U.S., and Japan, ensuring seamless innovation from API to finished dosage forms (FDF).

With a commitment to regulatory excellence—evidenced by 22 successful US FDA audits—and a focus on sustainability, Cohance drives purposeful partnerships that advance health sciences worldwide. Our growth trajectory targets a $1B milestone by 2030, fostering a culture of compliance, technical depth, and customer-centric solutions.

Job Details

• Company Name: Cohance Lifesciences
• Experience: 2-6 Years (varies by role)
• Qualification: B.Sc, M.Sc, B.Pharma, Diploma, or ITI
• Location: Pashamylaram and Nacharam, Telangana, India
• Work Type: On-site

Job Description

Cohance Lifesciences is expanding its operations with immediate openings in production, quality control, and quality assurance at our CDMO and Formulation plants.

These roles support our mission to deliver high-quality pharmaceutical products while adhering to global standards. We’re seeking dedicated professionals for walk-in interviews to drive manufacturing excellence and compliance.

Production – Primary and Secondary Packing, Capsule Filling, and Check Weigher

• Department: Production
• Role: Handle primary/secondary packing, capsule filling, and check weigher operations
• Experience: 2-6 Years
• Education/Qualification: B.Sc/M.Sc/Diploma/ITI

Production – Manufacturing Operations, Production Activities, BPR, cGMP Compliance, and Line Clearance

• Department: Production
• Role: Oversee manufacturing operations, BPR execution, cGMP compliance, and line clearance
• Experience: 2-5 Years
• Education/Qualification: B.Sc/M.Sc/Diploma/ITI

Quality Control – HPLC and GC Analysis, EMPOWER3

• Department: Quality Control
• Role: Perform HPLC/GC analysis using EMPOWER3 software
• Experience: 2-6 Years
• Education/Qualification: B.Sc/M.Sc/B.Pharma

Quality Assurance – Line Clearance, Batch Record Review, Deviation Handling, CAPA, and GMP/cGMP Compliance

• Department: Quality Assurance
• Role: Manage line clearance, batch reviews, deviations, CAPA, and GMP/cGMP adherence
• Experience: 2-6 Years
• Education/Qualification: B.Sc/M.Sc/B.Pharma

Skills/Qualifications

• Proficiency in HPLC, GC analysis, and EMPOWER3 for quality testing
• Expertise in primary/secondary packing, capsule filling, and check weigher systems
• Strong knowledge of manufacturing operations, BPR, and line clearance protocols
• In-depth understanding of GMP/cGMP compliance, deviation handling, and CAPA processes
• Technical skills in formulation and CDMO production activities
• Excellent attention to detail and regulatory awareness
• Ability to collaborate in fast-paced, compliance-driven environments

Key Responsibilities

• Execute packing and filling operations with precision
• Conduct HPLC/GC tests for product quality assurance
• Review batch records for accuracy and compliance
• Handle deviations and implement CAPA effectively
• Ensure line clearance and cGMP adherence daily
• Monitor production activities for efficiency
• Support manufacturing in CDMO and formulation units

Benefits/Perks

• Robust career growth in a global CDMO leader
• Continuous learning via training in advanced pharma tech
• Competitive salary with performance incentives
• Inclusive work culture promoting equal opportunities
• Exposure to international projects and innovation hubs

How to Apply

To apply for these pharma jobs, visit our careers page at cohance.com/careers or email your resume to careers@cohance.com.

For personalized guidance, connect with Pharma Recruiter at pharmarecruiter.in. Prepare your documents and join our walk-in—your next pharmaceutical career in India starts here!

Walk-in Interview Details

• Date: December 21, 2025
• Time: 9:00 AM to 2:30 PM
• Venue: 1st Floor, A Maisaiah Yadav Estates, Above G Pullareddy Sweet Shop, Mythri Nagar, NH 65, Madeenaguda, Miyapur, Telangana, 500049
• Contact/Email: 9966795443 or careers@cohance.com
• Documents Required: Resume, photocopies of educational certificates, 3 months’ pay slips, and CTC structure

Why You Should Join

At Cohance, you’ll thrive in a collaborative culture recognized for innovation and excellence, where diverse teams drive breakthroughs in drug development. Enjoy long-term career stability amid our $1B growth vision, with ample learning opportunities in cutting-edge modalities like ADCs and oligonucleotides.

Our compliance-focused environment ensures professional growth while contributing to global health advancements—empowering you to collaborate, enhance, and deliver impactful solutions daily.

FAQs

Who is eligible for these QA jobs and QC jobs at Cohance?

Candidates with 2-6 years of experience and qualifications like B.Sc, M.Sc, B.Pharma, Diploma, or ITI in pharma-related fields are ideal for production jobs and quality roles.

What is the application process for pharmaceutical careers in India at Cohance?

Submit your resume via cohance.com/careers or attend the walk-in interview. For expert tips, visit pharmarecruiter.in.

How does the walk-in interview for pharma jobs work?

Arrive between 9 AM and 2:30 PM on December 21, 2025, at the Miyapur venue with required documents. Expect on-site screening and discussions.

What are the salary and growth opportunities in these production jobs?

Competitive salaries align with industry standards, plus pathways for advancement in CDMO innovation. Explore more at pharmarecruiter.in for insights.