Ipca Walk-In QA QC Production

B.Pharm QA QC Production Jobs Silvassa

B.Pharm, B.Sc, ITI, Diploma candidates apply for Ipca QA, QC, Production jobs in Silvassa. 1–12 yrs experience.

Ipca Laboratories Ltd. is conducting a major recruitment drive for its Athal Plant Silvassa Formulation (OSD) Unit for multiple departments including Quality Control, Quality Assurance, Production, Packing, and Maintenance. This opportunity is ideal for professionals searching for pharma manufacturing jobs, QC analyst careers, pharmaceutical production vacancies, GMP compliance roles, and regulatory pharmaceutical jobs in India.

Candidates with expertise in HPLC analysis, IPQA, QMS documentation, granulation, compression, coating, packing operations, and engineering maintenance can secure excellent long-term growth opportunities in one of India’s most established pharmaceutical manufacturing companies.

The pharmaceutical industry is rapidly expanding due to rising global healthcare demand, making skilled professionals in regulated manufacturing environments highly valuable. Professionals with experience in USFDA and MHRA-approved facilities are especially in demand for pharmaceutical compliance management, analytical quality systems, and regulated OSD manufacturing operations.

Company Overview

Ipca Laboratories Ltd. is a globally recognized pharmaceutical company with a strong presence in more than 120 countries across six continents. Established in 1949, the company manufactures over 350 pharmaceutical formulations and 80 APIs for multiple therapeutic segments.

The company is widely respected for its advanced pharmaceutical manufacturing facilities approved by major global regulatory authorities including UK-MHRA, EDQM-Europe, and WHO-Geneva. Ipca is among the world’s largest manufacturers and suppliers of several Active Pharmaceutical Ingredients (APIs).

The Athal Silvassa formulation unit specializes in OSD manufacturing operations and follows strict pharmaceutical quality systems, data integrity practices, cGMP standards, and regulatory compliance guidelines.

Working with Ipca Laboratories offers professionals strong exposure to pharmaceutical compliance management, regulatory audits, analytical testing systems, quality assurance processes, and modern manufacturing technologies.

Job Role & Responsibilities

Ipca Laboratories is hiring experienced candidates across multiple pharmaceutical departments.

Quality Control (QC)

Designations

• Sr. Officer
• Officer
• Jr. Officer
• Technician

Key Responsibilities

• Handle analytical instruments including HPLC, GC, UV, IR, Dissolution Tester, and KF Autotitrator
• Operate Waters and Shimadzu analytical systems using Empower software
• Conduct raw material, finished product, and stability analysis
• Ensure compliance with cGMP, cGLP, data integrity, and regulatory guidelines
• Prepare and review laboratory documentation and analytical records
• Support OOS, OOT, and analytical investigation activities
• Assist microbiology-related analytical operations where required

Preferred Skills

• HPLC and GC analytical expertise
• Knowledge of GCMS and LCMS systems
• Understanding of pharmaceutical laboratory compliance systems
• Regulatory audit readiness and documentation management

Quality Assurance (QA)

Designations

• Sr. Officer
• Officer
• Jr. Officer

Key Responsibilities

• Handle IPQA activities and in-process quality checks
• Manage QMS documentation and GMP compliance systems
• Review batch manufacturing records and quality documents
• Support change control, deviations, CAPA, and investigation activities
• Ensure manufacturing processes meet regulatory standards
• Coordinate with production and QC teams to maintain product quality

Preferred Skills

• Strong knowledge of pharmaceutical quality systems
• Expertise in IPQA and QMS documentation
• Understanding of regulatory compliance and audit processes

Production Department

Designations

• Sr. Officer
• Officer
• Jr. Officer
• Technician

Key Responsibilities

• Operate and supervise granulation, compression, and coating equipment
• Handle manufacturing systems such as Fette, Glatt, Ganson, and imprinting machines
• Monitor batch manufacturing activities and GMP compliance
• Maintain production records and process documentation
• Ensure manufacturing efficiency and process safety

Preferred Skills

• OSD manufacturing operations
• Granulation and coating expertise
• Tablet and capsule manufacturing exposure

Packing Department

Designations

• Sr. Officer
• Officer
• Jr. Officer
• Technician

Key Responsibilities

• Operate CAM, IMA, Blister, CVC, and Cartonator packing machines
• Handle QMS documentation for packing operations
• Ensure labeling accuracy and packaging quality compliance
• Maintain pharmaceutical packing efficiency and documentation integrity

Maintenance Department

Designations

• Sr. Officer
• Officer
• Jr. Officer

Key Responsibilities

• Perform preventive and corrective maintenance activities
• Troubleshoot mechanical, electrical, and pneumatic systems
• Support equipment installation, calibration, and validation
• Maintain operational reliability of manufacturing equipment

These pharmaceutical roles directly contribute to medicine quality, patient safety, regulatory compliance, and efficient healthcare manufacturing.

Eligibility / Qualifications

Quality Control

• B.Sc
• B.Pharm
• Diploma
• ITI
• HSC / SSC

Quality Assurance

• B.Pharm
• M.Pharm
• Diploma

Production & Packing

• B.Sc
• ITI
• Diploma
• HSC

Maintenance

• B.Tech
• B.E.

Experience Requirement

• 1 to 12 years depending on role and department

Relevant Courses

B.Pharm, M.Pharm Quality Assurance, B.Sc Chemistry, B.Sc Pharmaceutical Science, Diploma in Chemical Engineering, Diploma in Mechanical Engineering, ITI Fitter, ITI Technician, B.Tech Mechanical Engineering, B.E Electrical Engineering

Required Skills

• Pharmaceutical compliance management
• GMP and cGLP documentation
• OSD manufacturing operations
• HPLC and GC analytical testing
• IPQA and QMS systems
• Regulatory audit readiness
• Pharmaceutical production and packing operations
• Equipment troubleshooting and validation

Location & Salary

Work Location: Ipca Athal Plant, Silvassa, Dadra and Nagar Haveli and Daman and Diu

Salary: Competitive pharmaceutical industry salary package based on department, technical skills, and experience level

Professionals with expertise in regulated pharmaceutical manufacturing, analytical quality control, and GMP production systems are among the highest-demand talent categories in the pharmaceutical sector.

Application Process

Walk-In Interview Details

Date: 09 May 2026 (Saturday)
Time: 09:00 AM to 04:00 PM

Venue:
Ipca Athal Site
Plot No. 255/1,
Village Athal,
Silvassa,
Dadra and Nagar Haveli and Daman and Diu – 396235

Documents Required

• Updated Resume
• Passport-size photograph
• 10th, 12th, ITI, Diploma, Graduation, and Post Graduation certificates
• Experience and joining letters
• Current company appointment letter
• Salary slips and CTC breakup

Important Notes

• Candidates with tablet and capsule manufacturing exposure will be preferred
• Candidates from syrup, injectables, API, and soft gelatin backgrounds may not be considered for QA and QC departments
• M.Sc freshers are not eligible for QC fresher roles
• Candidates interviewed within the last six months at Ipca Athal should not apply
• Shift duty flexibility is mandatory
• Experience in regulated plants like USFDA and MHRA facilities is preferred

Apply Now

Interested and eligible candidates should attend the walk-in interview early to secure their opportunity. High competition is expected for QA, QC, and production roles.

Apply before the reporting time to improve your interview chances and avoid delays.

Disclaimer:
Ipca Laboratories Ltd. does not charge any recruitment fees directly or indirectly.

Why This Opportunity Matters

Pharmaceutical Quality Assurance, Quality Control, Production, and Packing are among the most critical operational functions in regulated pharmaceutical manufacturing. Professionals skilled in analytical testing, GMP manufacturing systems, pharmaceutical documentation, and compliance management are highly valued across global healthcare organizations.

Working at Ipca Laboratories helps professionals strengthen expertise in regulatory pharmaceutical operations, quality systems, analytical instrumentation, and manufacturing excellence.

Professionals with experience in HPLC systems, OSD manufacturing, IPQA, QMS documentation, and regulated plant operations have strong long-term career growth opportunities in multinational pharmaceutical companies, CROs, CDMOs, and regulated healthcare manufacturing facilities.

SEO Keywords Included Naturally

• Pharma QA jobs
• QC analyst jobs
• Pharmaceutical manufacturing jobs
• GMP compliance careers
• Regulatory pharmaceutical jobs
• HPLC analyst jobs
• OSD manufacturing jobs
• Pharmaceutical quality systems
• Pharma production operator jobs
• Data integrity pharma jobs
• Pharmaceutical compliance management
• Regulatory affairs and quality assurance

Key Highlights

• Company: Ipca Laboratories Ltd.
• Departments: QA, QC, Production, Packing, Maintenance
• Roles: Sr. Officer, Officer, Jr. Officer, Technician
• Qualification: B.Pharm, M.Pharm, B.Sc, ITI, Diploma, B.Tech
• Experience: 1–12 Years
• Industry: OSD Formulation Manufacturing
• Location: Silvassa
• Walk-In Date: 09 May 2026

FAQs

Who can apply for Ipca Laboratories recruitment drive?

Candidates with B.Pharm, M.Pharm, B.Sc, ITI, Diploma, or engineering qualifications and relevant pharma experience can apply.

What departments are hiring?

Quality Control, Quality Assurance, Production, Packing, and Maintenance departments.

What technical skills are preferred?

HPLC, GC, IPQA, QMS, GMP documentation, granulation, coating, compression, and pharmaceutical packing operations.

Is regulated plant experience preferred?

Yes, candidates with USFDA or MHRA-regulated plant exposure are highly preferred.

How can I apply?

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

Are freshers eligible?

Some technician-level roles may consider limited experience candidates, but relevant pharmaceutical exposure is preferred.

Summary Table

|———————————-|———————————-|
| Company | Ipca Laboratories Ltd. |
| Vacancies | QA, QC, Production, Packing, Maintenance Roles |
| Required Education | B.Pharm, M.Pharm, B.Sc, ITI, Diploma, B.Tech |

Experience	1–12 Years