Medley Pharmaceuticals Hiring QC,ADL,QA Officers

Medley Pharmaceuticals Hiring QC, ADL, QA Officers | Daman

Medley Pharmaceuticals recruiting QC, ADL, QA Officers for OSD units in Daman. Apply now with B.Pharm/M.Pharm/M.Sc qualifications.

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Medley Pharmaceuticals Ltd., a renowned name in the Indian pharmaceutical sector, is inviting talented professionals to join its OSD (Tablets, Capsules & Liquids) manufacturing facility in Daman. This opportunity is ideal for candidates seeking long-term growth in Quality Control (QC), Analytical Development Laboratory (ADL), and Quality Assurance (QA) departments within a globally reputed organization known for its commitment to excellence and innovation.

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Company Overview

Medley Pharmaceuticals Ltd. is one of India’s most trusted pharmaceutical companies with a strong domestic and international presence. Established with the vision of delivering quality healthcare at affordable prices, Medley operates in multiple therapeutic areas including cardiology, gastroenterology, anti-infectives, and nutraceuticals.

The company’s manufacturing facilities are WHO-GMP, ISO, and regulatory authority compliant, ensuring that all products meet stringent international quality standards. Medley is committed to innovation, continuous improvement, and maintaining the highest levels of quality and safety across its operations.

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Job Roles & Responsibilities

Quality Control (QC) – RM & FG (Officer)

Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm
Experience: 2–5 Years

Key Responsibilities:

• Testing of Raw Materials (RM) and Finished Goods (FG) samples.
• Hands-on experience in operating HPLC, GC, UV, IR, KF, and Dissolution apparatus.
• Ensure documentation and data integrity as per Good Manufacturing Practices (GMP).
• Maintain cGMP and safety compliance in all testing procedures.
• Perform analytical method verification and calibration checks.

Preferred Skills: Analytical reasoning, technical troubleshooting, and sound knowledge of regulatory compliance in QC.

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Analytical Development Laboratory (ADL) – Validation (Officer)

Qualification: M.Sc / B.Pharm / M.Pharm
Experience: 2–6 Years

Key Responsibilities:

• Conduct method validation, verification, and transfer as per regulatory guidelines.
• Preparation and review of validation protocols, reports, and SOPs.
• Operation of HPLC, GC, UV, IR, KF, and Dissolution instruments.
• Ensure data accuracy, traceability, and adherence to GLP (Good Laboratory Practices).
• Support regulatory submissions and respond to analytical queries.

Preferred Skills: Strong analytical background, hands-on experience with modern analytical techniques, and familiarity with ICH guidelines.

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Quality Assurance (QA) – IPQA (Officer)

Department: QA – In-Process Quality Assurance (OSD)
Qualification: B.Pharm / M.Pharm / M.Sc
Experience: 2–6 Years

Key Responsibilities:

• Perform in-process checks for granulation, compression, and packing operations.
• Execute line clearance activities for manufacturing and packing areas.
• Review and ensure compliance of Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR).
• Conduct IPQA activities during batch manufacturing and packaging processes.
• Maintain quality assurance logs, deviation reports, and CAPA documentation.

Preferred Skills: Thorough understanding of cGMP, documentation control, and process validation principles.

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Eligibility / Qualifications

Educational Backgrounds Accepted:
B.Pharm, M.Pharm, M.Sc, B.Sc
(Courses may include: Pharmaceutical Sciences, Analytical Chemistry, Organic Chemistry, Industrial Chemistry, Pharmacology)

Experience Range: 2–6 years (based on position)

Required Skills:

• Excellent knowledge of cGMP and regulatory guidelines.
• Experience handling advanced analytical instruments.
• Strong documentation and data integrity awareness.
• Effective communication and teamwork skills.

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Location & Salary

Location: Daman, Kachigam
Department: OSD Manufacturing (Tablets, Capsules, and Liquids)
Salary: Competitive and commensurate with industry standards.
Work Environment: Modern, GMP-certified facility offering strong career growth and training opportunities.

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Application Process

Interested candidates can apply by sending their updated CV to the email address below:
Email: keval@medleylab.com
Subject Line: Department & Designation

Ensure your resume includes detailed experience, current CTC, and notice period. Candidates meeting the eligibility criteria will be contacted for further selection rounds.

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Why Join Medley Pharmaceuticals?

• Opportunity to work with one of the top WHO-GMP-certified pharmaceutical companies in India.
• Exposure to state-of-the-art equipment and global quality systems.
• Excellent career growth prospects in a structured, learning-oriented environment.
• Strong focus on employee development, training, and quality excellence.
• Be part of a company that’s expanding rapidly across domestic and international markets.

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Frequently Asked Questions (FAQs)

Q1. Who can apply for Medley Pharmaceuticals Daman vacancies?
Candidates with B.Pharm, M.Pharm, B.Sc, or M.Sc degrees and 2–6 years of experience in QC, ADL, or QA can apply.

Q2. What is the work location for these positions?
All openings are based at Daman, Kachigam (OSD – Tablets, Capsules & Liquids).

Q3. How can I apply for the Medley Pharmaceuticals walk-in or direct recruitment?
Email your updated CV to keval@medleylab.com with the subject line mentioning Department & Designation.

Q4. What instruments should I have experience in for QC and ADL roles?
Candidates should have hands-on experience with HPLC, GC, UV, IR, KF, and Dissolution systems.

Q5. Is experience mandatory for QA-IPQA positions?
Yes, candidates should have 2–6 years of relevant experience in IPQA for OSD manufacturing operations.

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Category	Details
Company	Medley Pharmaceuticals Ltd.
Vacancies	QC (RM & FG), ADL (Validation), QA (IPQA)
Required Education	B.Pharm, M.Pharm, B.Sc, M.Sc
Experience	2–6 years
Location	Daman, Kachigam

Tagged as: Pharma Jobs in Daman