Promea Therapeutics Pvt. Ltd. has announced a Walk-In Recruitment Drive for experienced pharmaceutical professionals in Analytical Research & Development (AR&D), Formulation Development Quality Assurance (FDQA), and Formulation Research & Development (FRD). This is an excellent opportunity for candidates with M.Sc. (Analytical Chemistry) or M.Pharmacy qualifications and relevant pharmaceutical industry experience.

The walk-in interview will be conducted at the company’s state-of-the-art facility located in Medical Devices Park, Sultanpur, Ameenpur, Sangareddy, Telangana.

Promea Walk-In Drive – Overview

Particulars Details

Company

Promea Therapeutics Pvt. Ltd.

Job Type

Walk-In Interview

Interview Date

18th July 2026 (Saturday)

Interview Time

09:00 AM – 04:00 PM

Location

Medical Devices Park, Sultanpur, Ameenpur, Sangareddy, Telangana – 502319

Experience

2–5 Years

Qualification

M.Sc. (Analytical Chemistry) / M.Pharmacy

Employment Type

Full-Time

Department-wise Vacancy Details

1. Analytical Research & Development (AR&D)

Position: Executive / Sr. Executive

Vacancies: 10

Qualification:

M.Sc. (Analytical Chemistry)

M.Pharmacy

Experience: 2–5 Years

Key Responsibilities

Perform analytical method development and validation.

Conduct routine testing of pharmaceutical samples.

Execute release and stability testing of raw materials, in-process samples, and finished products.

Prepare validation protocols, reports, specifications, SOPs, and analytical methods.

Ensure calibration, qualification, and maintenance of laboratory instruments following GLP guidelines.

2. Formulation Development Quality Assurance (FDQA)

Position: Executive / Sr. Executive

Vacancies: 5

Qualification:

M.Sc. (Analytical Chemistry)

M.Pharmacy (Quality Assurance)

Experience: 2–5 Years

Key Responsibilities

Review and approve development protocols and reports.

Handle formulation and analytical stability documentation.

Manage process validation, cleaning validation, and analytical method validation.

Monitor change control, deviation management, CAPA, and risk management systems.

Ensure compliance with ICH Guidelines and regulatory requirements.

3. Formulation Research & Development (FRD)

Position: Executive / Sr. Executive

Vacancies: 5

Qualification:

M.Pharmacy (Pharmaceutics)

Experience: 2–5 Years

Key Responsibilities

Develop Oral Solid Dosage (OSD) formulations.

Perform granulation, compression, coating, and stability studies.

Work according to ICH, QbD, and stability guidelines.

Prepare technical documentation and development reports.

Support formulation optimization and technology transfer activities.

Why Join Promea?

Promea offers a professional work environment with several employee benefits, including:

Growth opportunities

Learning & development programs

Health & wellness initiatives

Collaborative work culture

Healthy work-life balance

Walk-In Interview Details

Interview Date: 18th July 2026 (Saturday)

Time: 09:00 AM to 04:00 PM

Venue: Promea Therapeutics Pvt. Ltd.

Medical Devices Park, Sultanpur, Ameenpur,

Sangareddy, Telangana – 502319

Documents to Carry

Candidates should bring:

Updated Resume

Educational Certificates

Experience Certificates

Latest Salary Slips

Government Photo ID Proof

Passport-size Photographs

Relevant Supporting Documents

Contact Details

Email:

hr@cytobiologics.com

careers@promea.in

Phone:

9100554484

9154694056

Selection Process

The recruitment process may include:

Resume Screening

Technical Interview

HR Discussion

Final Selection

Offer Release (based on company requirements)

5 Technical FAQs

1. What analytical techniques should AR&D candidates be familiar with?

Candidates should have practical knowledge of HPLC, GC, UV-Visible Spectroscopy, Dissolution Testing, FTIR, Method Development, Method Validation, and Stability Studies while following GLP and regulatory guidelines.

2. What is expected from FDQA professionals?

FDQA candidates should understand change control, deviation handling, CAPA, risk assessment, process validation, cleaning validation, analytical method validation, documentation review, and ICH regulatory compliance.

3. What technical skills are required for FRD roles?

FRD professionals should possess hands-on experience in OSD formulation development, granulation, compression, coating, formulation optimization, QbD principles, technology transfer, and stability studies.

4. Which regulatory guidelines are important for these positions?

Candidates should be familiar with ICH Guidelines, GLP (Good Laboratory Practices), GMP (Good Manufacturing Practices), data integrity requirements, validation protocols, and pharmaceutical documentation practices.

5. What documents and experience should candidates highlight during the interview?

Applicants should showcase experience in method validation, stability testing, OOS/OOT investigations, SOP preparation, validation reports, regulatory documentation, analytical instruments, and successful pharmaceutical development projects.