Zenara walk-in QC, QA IPQA & Production

Zenara Hiring QC QA Production Jobs | MPharm

Zenara Biophore hiring for QC, QA IPQA & Production roles. B.Pharm, M.Pharm candidates with 3-5 years experience can apply.

Zenara, a Biophore Company, has announced a walk-in interview drive for experienced pharmaceutical professionals in Quality Control, Quality Assurance IPQA, and Production Packing departments. The company is hiring candidates with formulation manufacturing experience for Executive and Junior Executive positions.

This latest pharma recruitment opportunity is suitable for candidates searching for Quality Control jobs, IPQA jobs in pharma, packing executive jobs, formulation manufacturing careers, pharmaceutical QA jobs, and regulated pharma company vacancies.

Candidates with 3 to 5 years of experience in formulation pharmaceutical manufacturing and qualifications such as B.Pharm and M.Pharm are eligible to attend the walk-in interview.

The company is specifically looking for professionals with expertise in HPLC, chromatographic techniques, IPQA operations, BMR/BPR review, control sample handling, and pharmaceutical packing activities.

Candidates seeking career growth in regulated pharmaceutical manufacturing environments with exposure to cGMP systems, regulatory compliance, and formulation operations should explore this opportunity.

Company Overview

Zenara, a Biophore Company, operates in the pharmaceutical manufacturing sector with a focus on quality-driven formulation manufacturing and regulated pharmaceutical operations.

Biophore is recognized in the pharmaceutical industry for its focus on research-driven manufacturing, regulatory compliance systems, and pharmaceutical quality management practices.

Zenara’s manufacturing and quality operations are aligned with pharmaceutical regulatory standards and cGMP-based manufacturing systems.

Professionals working at Zenara may gain exposure to:

• Pharmaceutical quality systems
• Formulation manufacturing operations
• IPQA and compliance systems
• Chromatographic analytical techniques
• Packing operations and process monitoring
• Regulatory documentation practices
• cGMP manufacturing environments

The company is currently expanding its team for Quality Control, Quality Assurance, and Production Packing operations.

Job Role & Responsibilities

1. Quality Control – Executive

Candidates selected for the Quality Control department will handle analytical and quality monitoring activities related to pharmaceutical formulation products.

Key Responsibilities

• Handling HPLC and chromatographic analysis
• Maintaining cGLP compliance systems
• Supporting 21 CFR Part 11 compliance activities
• Performing analytical testing and documentation
• Supporting quality investigations and reporting
• Ensuring compliance with pharmaceutical quality standards
• Reviewing laboratory records and analytical documentation
• Coordinating with quality and manufacturing teams

Required Skills

• Knowledge of HPLC
• Chromatographic techniques
• cGLP compliance
• 21 CFR Part 11 understanding

2. Quality Assurance (IPQA) – Jr. Executive / Executive

The IPQA team will manage in-process quality activities and support pharmaceutical quality systems.

Key Responsibilities

• Conducting in-process quality checks
• Reviewing BMR and BPR documents
• Monitoring manufacturing compliance
• Handling control samples
• Supporting APR and CPV review activities
• Managing vendor qualification documentation
• Supporting audit readiness and compliance systems
• Ensuring GMP adherence during production operations

Required Skills

• BMR & BPR review
• Vendor qualification exposure
• Control sample handling
• APR & CPV report review
• IPQA process monitoring

3. Production (Packing Executive)

Candidates selected for Production Packing roles will handle primary and secondary packing activities in formulation manufacturing.

Key Responsibilities

• Planning packing operations
• Monitoring packing equipment performance
• Handling preventive maintenance coordination
• Managing primary and secondary packing activities
• Performing balance calibration
• Maintaining packing documentation records
• Monitoring cleaning activities and operational compliance
• Ensuring smooth packaging line operations

Required Skills

• Packing operations management
• Equipment monitoring
• Preventive maintenance coordination
• Documentation and record updation
• Primary and secondary packaging operations

Eligibility / Qualifications

Candidates with the following qualifications are eligible to apply:

• B.Pharm
• M.Pharm

Relevant Courses

Pharmaceutical Sciences, Pharmaceutics, Pharmaceutical Analysis, Industrial Pharmacy, Quality Assurance, Pharmaceutical Chemistry, Regulatory Affairs, Pharmaceutical Manufacturing, Formulation Development

Experience Required

• 3 to 5 years

Important Eligibility Note

• Only formulation background candidates will be considered

Candidates with experience in regulated formulation manufacturing facilities may receive preference.

Why Candidates Should Apply

The pharmaceutical formulation sector continues to offer strong career opportunities in Quality Control, Quality Assurance, and Production operations due to increasing global demand for regulated pharmaceutical products.

Joining Zenara can provide valuable experience in:

• Pharmaceutical quality systems
• Formulation manufacturing operations
• Regulatory compliance management
• HPLC and analytical systems
• Packaging process operations
• IPQA monitoring systems
• Pharmaceutical documentation and audit systems

Professionals aiming to strengthen their pharmaceutical manufacturing careers in regulated environments can benefit from this opportunity.

Skills That Can Improve Selection Chances

Candidates with the following expertise may have an advantage during selection:

• Exposure to regulated formulation plants
• Experience in cGMP environments
• Strong analytical and documentation skills
• HPLC operational knowledge
• Experience in audit support activities
• Knowledge of pharmaceutical compliance systems
• Packing process management skills
• IPQA and quality systems exposure

Work Environment & Career Growth

Zenara offers opportunities to work in structured pharmaceutical manufacturing systems with exposure to:

• Regulatory pharmaceutical operations
• Quality assurance systems
• Pharmaceutical analytical techniques
• GMP documentation practices
• Process validation systems
• Packaging and production operations

Candidates may also develop expertise in pharmaceutical compliance, audit preparation, and regulated manufacturing systems.

Location & Salary

Job Location

Location details will be shared during the walk-in process.

Salary

Salary will be offered based on candidate experience, formulation exposure, technical skills, and interview performance.

Application Process

Interested candidates can attend the walk-in interview directly with the required documents.

Walk-In Interview Date

16 May 2026 (Saturday)

Interview Timing

10:00 AM to 3:00 PM

Documents Required

Candidates should carry the following documents:

• Updated Resume
• Last 3 Months Payslips
• CTC Details
• Educational Certificate Xerox Copies
• Aadhaar Card Copy
• PAN Card Copy

Contact Details

• Email ID: hrd@zenara.com
• Contact Number: +91-7337363325

Important Note

The company has clarified that it is not associated with any manpower consultancy for recruitment activities. Candidates are advised to apply directly through official channels only.

FAQs

1. Which departments are hiring at Zenara?

Zenara is hiring for Quality Control, Quality Assurance (IPQA), and Production Packing departments.

2. What qualifications are eligible?

Candidates with B.Pharm and M.Pharm qualifications are eligible.

3. How much experience is required?

Candidates with 3 to 5 years of formulation pharmaceutical experience can apply.

4. Is formulation experience mandatory?

Yes. Only candidates from formulation manufacturing backgrounds will be considered.

5. What skills are preferred for QC roles?

HPLC knowledge, chromatographic techniques, cGLP compliance, and 21 CFR Part 11 exposure are preferred.

6. What documents should candidates carry?

Candidates should bring resume, payslips, educational certificates, Aadhaar copy, and PAN card copy.

Summary Table

Company	Zenara (A Biophore Company)
Department Vacancies	Quality Control, QA IPQA, Production Packing
Qualification	B.Pharm, M.Pharm
Experience	3 to 5 Years
Location	Hyderabad