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Liquid Manufacturing Chemist

Job in Uppal Kalan, Telangana, India
Listing for: SAIN MEDICAMENTS PVT. LTD
Full Time position
Listed on 2026-03-06
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Validation Engineer
Job Description & How to Apply Below
Location: Uppal Kalan

Job Title:

Liquid Manufacturing Chemist
Department:
Manufacturing / Production

Location:

Hyderabad
Reporting To:
Production Manager / Plant Head

Job Summary:

We are seeking an experienced and detail-oriented Liquid Manufacturing Chemist with at least 5 years of experience in pharmaceutical formulation. The ideal candidate will be responsible for overseeing the manufacturing process of liquid dosage forms (syrups, suspensions, solutions), ensuring strict compliance with cGMP, quality, and safety standards.

Key Responsibilities:

Plan and execute manufacturing batches of liquid formulations as per approved Batch Manufacturing Records (BMRs).
Supervise and monitor the manufacturing process of syrups, suspensions, and solutions to ensure consistency and quality.
Ensure compliance with GMP, SOPs, safety standards, and regulatory guidelines at all stages of production.
Perform in-process checks and ensure accurate documentation of all manufacturing processes.
Troubleshoot issues in formulation, mixing, or filling processes, and coordinate with QA/QC, R&D, and maintenance teams.
Maintain cleanliness and calibration of manufacturing equipment (reactors, tanks, filtration units, filling lines, etc.).
Train and supervise junior staff or operators to maintain high productivity and safety standards.
Manage raw material usage and coordinate with the stores/warehouse for timely availability.
Participate in internal audits, validation activities, and CAPA implementation.
Ensure proper documentation for all production activities, deviations, and incident reports.
Qualifications and

Experience:

Education:

B.Pharm / M.Pharm /

B.Sc / M.Sc in Chemistry, Pharmaceutical Sciences, or related field.

Experience:

Minimum 5 years of hands-on experience in the manufacturing of liquid dosage forms in a pharmaceutical formulation company.
Good knowledge of cGMP, WHO, and regulatory requirements (USFDA, MHRA, etc.).
Proficient in handling manufacturing equipment and understanding technical aspects of liquid formulation processes.
Strong communication, documentation, and team management skills.
Preferred

Skills:

Experience in regulatory audits and compliance.
Knowledge of ERP systems and electronic documentation.
Familiarity with QMS tools (Change Control, Deviation, CAPA).
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