Cohance walk-in Qa, Qc, Production

BSc MPharm Vacancies at Cohance Hyderabad

BSc, MSc, BPharm, MPharm vacancies (2–6 yrs) at Cohance CDMO, Hyderabad walk-in on March 1, 2026.

Cohance Lifesciences is conducting a walk-in interview for experienced professionals at its CDMO plants across Telangana and Andhra Pradesh. This hiring drive is focused on Production, Quality Control, and Quality Assurance functions within regulated pharmaceutical manufacturing environments. Candidates with 2 to 6 years of experience in cGMP-compliant facilities are invited to attend the walk-in scheduled in Hyderabad.

If you are working in API manufacturing, analytical quality control, regulatory compliance, or pharmaceutical production operations and looking for career growth within a Contract Development and Manufacturing Organization (CDMO), this opportunity deserves serious consideration.

Company Overview

Cohance Lifesciences operates as a growing CDMO partner supporting global pharmaceutical companies with development, scale-up, and commercial manufacturing solutions. CDMOs play a critical role in the pharmaceutical supply chain by providing specialized expertise in bulk drug production, process optimization, analytical development, and regulatory-compliant manufacturing.

Cohance focuses on quality-driven manufacturing aligned with current Good Manufacturing Practices (cGMP). The company emphasizes documentation accuracy, data integrity, regulatory compliance, and operational excellence. Its facilities support complex chemical synthesis and analytical testing required for domestic and export markets.

Working in a CDMO environment offers broader technical exposure compared to conventional manufacturing setups. Professionals gain hands-on experience in:

• API and bulk drug manufacturing operations
• Analytical method execution using advanced chromatography systems
• Quality Management Systems (QMS)
• Cleaning validation and documentation compliance
• Regulatory audit preparation for global clients

Cohance’s stated philosophy, “Collaborate. Enhance. Deliver.” reflects its integrated approach toward pharmaceutical development and commercial manufacturing excellence.

Job Role & Responsibilities

Cohance is hiring across three major functional areas: Production, Quality Control, and Quality Assurance.

Production – cGMP Manufacturing Operations

Position Titles: Operators, Chemists
Qualification: B.Sc, M.Sc
Experience: 2–6 Years

Production professionals will be responsible for executing pharmaceutical manufacturing activities in accordance with cGMP standards and internal SOPs.

Key Responsibilities:

• Execution of batch manufacturing processes in API plants
• Handling GLR (General Laboratory Record) and SSR documentation
• Maintaining compliance with Quality Management Systems (QMS)
• Performing Cleaning Validation documentation and verification
• Monitoring critical process parameters during manufacturing
• Ensuring adherence to safety and environmental standards
• Coordinating with QA and QC teams for smooth batch release

This role directly contributes to large-scale pharmaceutical production, making it essential within the CDMO business model. Candidates must demonstrate strong documentation discipline and understanding of GMP compliance.

Professionals with exposure to regulated manufacturing environments will be prioritized.

Quality Control – Analytical Laboratory Operations

Position Titles: Analyst, Senior Analyst, Executive
Qualification: B.Sc, M.Sc, B.Pharm, M.Pharm
Experience: 2–6 Years

Quality Control professionals will perform analytical testing to ensure product quality, regulatory compliance, and batch consistency.

Key Responsibilities:

• Performing chromatographic analysis using HPLC and GC
• Working with Empower 3 software for data processing
• Conducting wet analysis and raw material testing
• Managing stability studies and sample tracking
• Operating and updating LIMS systems
• Ensuring compliance with GLP and data integrity guidelines
• Preparing analytical documentation for regulatory audits

Candidates must possess hands-on experience in pharmaceutical analytical testing. Familiarity with Empower 3 software and LIMS platforms is critical.

QC roles are among the highest demand pharmaceutical positions due to increasing global regulatory scrutiny. Skilled analysts with strong compliance knowledge command competitive salary growth in the pharma sector.

Quality Assurance – In-Process Compliance & QMS

Position Titles: Executive, Senior Executive
Qualification: B.Sc, M.Sc, B.Pharm, M.Pharm
Experience: 2–6 Years

Quality Assurance professionals are responsible for ensuring that manufacturing and analytical activities align with cGMP and regulatory standards.

Key Responsibilities:

• Real-time in-process quality checks (IPQA)
• Monitoring critical manufacturing parameters
• Reviewing batch manufacturing records
• Ensuring adherence to SOPs and QMS protocols
• Supporting internal and external audits
• Handling deviations, CAPA, and change control documentation

QA roles are central to pharmaceutical regulatory compliance. Experience in documentation review, audit readiness, and batch release procedures significantly enhances long-term career prospects.

Eligibility / Qualifications

Candidates applying for this walk-in drive must meet the specified education and experience criteria.

Eligible Courses (comma-separated):

B.Sc Chemistry, B.Sc Industrial Chemistry, B.Sc Life Sciences, M.Sc Chemistry, M.Sc Organic Chemistry, M.Sc Analytical Chemistry, B.Pharm, M.Pharm

Experience Requirement:

• 2 to 6 years of experience in pharmaceutical manufacturing or analytical laboratories
• Hands-on exposure to cGMP environments
• Strong knowledge of documentation practices and regulatory compliance

Preferred Skills:

• Experience with Empower 3 chromatography software
• Working knowledge of LIMS systems
• Understanding of Cleaning Validation protocols
• Familiarity with QMS and audit processes

Candidates without relevant pharmaceutical industry exposure may not meet the eligibility criteria for this drive.

Location & Salary Insights

Cohance CDMO plants operate across Telangana and Andhra Pradesh. The walk-in interview will be conducted in Hyderabad.

While specific salary figures are not disclosed, compensation is typically aligned with:

• Technical expertise in API manufacturing
• Experience with analytical instrumentation (HPLC, GC)
• QMS and regulatory audit exposure
• Years of relevant pharmaceutical experience

Hyderabad continues to be a major pharmaceutical and bulk drug manufacturing hub in India. Professionals working in this region benefit from exposure to export-driven manufacturing and USFDA-compliant systems, strengthening their long-term earning potential.

Walk-In Interview Details

Interview Date: March 01, 2026
Timing: 9:00 AM to 2:30 PM

Interview Location:
Hotel Kinara Grand
Ramakrishna Nagar
Hafeezpet, Madeenaguda
Hyderabad – 500049

Candidates are advised to arrive early to complete registration smoothly.

Documents Required

Applicants must carry the following documents:

• Updated Resume
• Photocopies of all educational certificates
• Last 3 months’ pay slips
• Current CTC structure details

Incomplete documentation may impact the interview evaluation process.

Application Process

This recruitment drive follows a direct walk-in interview format.

Steps to Apply:

1. Prepare updated resume highlighting relevant pharmaceutical experience.
2. Arrange all required documents.
3. Attend the walk-in interview at the specified venue on March 01, 2026.
4. Complete technical and HR discussion rounds.

For additional details, candidates may contact:
9154293301 / 9966795443

Official website: https://cohance.com

Cohance is committed to equal employment opportunities and does not discriminate based on age, gender, race, religion, disability, or any legally protected characteristic.

Why This Opportunity Matters for Pharma Professionals

The CDMO sector represents one of the fastest-growing segments within the pharmaceutical industry. Global pharmaceutical companies increasingly rely on specialized contract manufacturers for scalability and compliance-driven production.

Working in a CDMO like Cohance provides exposure to:

• Multi-client regulatory requirements
• High documentation standards
• Advanced analytical systems
• Cross-functional collaboration
• Global compliance benchmarks

These experiences significantly enhance professional credibility and open pathways toward senior regulatory, quality, and production leadership roles.

Career Growth Pathways

Professionals selected through this walk-in drive may progress toward roles such as:

• Senior Production Executive
• QC Senior Analyst / QC Manager
• QA Compliance Officer
• Validation Specialist
• Regulatory Affairs Executive
• Plant Operations Lead

Consistent performance in cGMP environments directly influences long-term salary progression and leadership opportunities.

Frequently Asked Questions (FAQs)

1. What experience level is required?

Candidates must have 2–6 years of relevant pharmaceutical manufacturing or analytical experience.

2. Is Empower 3 knowledge mandatory for QC?

Yes. Hands-on experience with Empower 3 and chromatographic systems is expected.

3. Are freshers eligible?

No. This drive requires experienced professionals.

4. What departments are hiring?

Production, Quality Control, and Quality Assurance.

5. Is this opportunity suitable for regulated market exposure?

Yes. CDMO environments offer strong regulatory and compliance exposure.

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Walk-In Drive Summary

Company	Cohance Lifesciences
Vacancies	Production – Operator / Chemist; Quality Control – Analyst / Senior Analyst / Executive; Quality Assurance – Executive / Senior Executive
Required Education	B.Sc, M.Sc, B.Pharm, M.Pharm
Experience	2–6 Years