Ritsa Pharma has announced an excellent recruitment opportunity for experienced pharmaceutical professionals at its Genome Valley, Hyderabad facility. The company is inviting applications for multiple departments, including Warehouse, Quality Control (QC), Analytical Quality Assurance (AQA), Regulatory Affairs, and Production (Packing). Candidates with relevant pharmaceutical experience can apply by sending their updated CV via email.

If you are looking for a career with a fast-growing pharmaceutical organization that values quality, innovation, collaboration, integrity, and excellence, this is an excellent opportunity.

Job Overview

Particular Details

Company Name

Ritsa Pharma

Job Type

Full-Time

Job Location

Genome Valley, Hyderabad

Industry

Pharmaceutical

Experience Required

2–8 Years (Post-wise)

Application Mode

Email

Email ID

HR@ritsapharma.com

Available Positions

1. Executive / Sr. Executive – Warehouse

Experience: 2–8 Years

Responsible for warehouse operations, material handling, inventory management, dispensing activities, SAP/ERP documentation, and GDP compliance.

2. Analyst – Quality Control (QC)

Experience: 2–8 Years

Perform analytical testing of raw materials, finished products, stability samples, and documentation as per GMP & GLP guidelines.

3. Analytical Quality Assurance (AQA)

Experience: 2–8 Years

Review analytical documents, laboratory investigations, OOS/OOT handling, audit support, and ensure data integrity compliance.

4. Regulatory Affairs

Experience: 5–8 Years

Prepare regulatory dossiers, manage global submissions, lifecycle management, regulatory documentation, and coordinate with health authorities.

5. Operator – Packing Executive (Production)

Experience: 4–6 Years

Operate packaging equipment, maintain batch records, ensure GMP compliance, perform line clearance, and support production activities.

Eligibility Criteria

B.Pharm / M.Pharm / B.Sc / M.Sc or relevant qualification depending on the role.

Relevant pharmaceutical industry experience.

Strong understanding of GMP, GDP, GLP, SOPs, and pharmaceutical documentation.

Good communication and teamwork skills.

Job Location

Genome Valley, Hyderabad, Telangana

How to Apply

Interested candidates should email their updated resume to:

HR@ritsapharma.com

Important: Mention the position applied for in the email subject line.

Example: Subject: Application for Analyst – QC

Why Join Ritsa Pharma?

Professional work environment

Career growth opportunities

Exposure to regulated pharmaceutical manufacturing

Employee-focused culture

Strong emphasis on Quality, Innovation, Collaboration, Integrity, and Excellence

Required Technical Skills

Good Manufacturing Practices (GMP)

Good Laboratory Practices (GLP)

Good Documentation Practices (GDP)

SOP compliance

Data Integrity (ALCOA+)

HPLC, GC, UV, Dissolution (for QC)

Regulatory dossier preparation

Warehouse inventory management

Batch Manufacturing & Packaging Records

Deviation, CAPA, Change Control, OOS/OOT handling

Selection Process

Resume Screening

Technical Evaluation

HR Interview

Final Selection

Offer & Joining

Documents Required

Updated Resume

Educational Certificates

Experience Certificates

Latest Salary Slip (if applicable)

Government Photo ID

Passport-size Photographs

5 Technical FAQs

1. What analytical instruments should a QC Analyst be proficient in?

QC Analysts should have practical knowledge of HPLC, GC, UV-Visible Spectrophotometer, FTIR, Dissolution Apparatus, pH Meter, and analytical balance, along with instrument calibration and troubleshooting.

2. What is the role of Analytical Quality Assurance (AQA)?

AQA reviews laboratory documentation, verifies analytical data integrity, investigates Out of Specification (OOS) and Out of Trend (OOT) results, ensures compliance with GMP/GLP, and supports regulatory inspections.

3. What responsibilities are involved in Regulatory Affairs?

Regulatory Affairs professionals prepare and maintain CTD/eCTD dossiers, manage product registrations, coordinate regulatory submissions, respond to agency queries, and ensure compliance with country-specific regulations.

4. What are the key responsibilities of a Warehouse Executive in a pharmaceutical company?

Warehouse professionals handle material receipt, quarantine, sampling coordination, storage, dispensing, inventory control, FEFO/FIFO practices, SAP/ERP entries, and GDP-compliant documentation.

5. What GMP practices are important for Packing Executives?

Packing Executives must perform line clearance, batch record documentation, equipment verification, in-process checks, packaging material reconciliation, labeling verification, and adherence to cGMP and safety procedures.