Gland Pharma Limited – Walk-In Interview on March 1st, 2024

Gland Pharma Limited – Walk-In Interview on March 1st, 2024

Gland Pharma is the worlds leading player in Injectables Formulation and Manufacturing. It is also into API and Intermediates research and manufacturing. Gland Pharma is present in sterile injectables, oncology and ophthalmic segments, and focus on complex injectables including NCE-1s, First-to-File products and 505b2 filings.

Inviting Formulation R&D (Injectables) Experienced Professionals.

FR&D Department
Qualification / Experience : M.Pharmacy (Pharmaceutics) 1 to 4 Years
Required Skills (Injectables) : • Planning & execution of formulation development activities within timelines.
• Stability study protocol development and stability data evaluation. Evaluation of impurity profiles of drug substance and drug product.
• Hands on experience with development of Injectable solutions, lyophilized drug products and other complex Injectables.

Technology Transfer Department
Qualification / Experience : M.Pharmacy ; 2 to 4 Years
Required Skills (Injectables) : Preparation of documents (BMR, MFR, Technology Transfer & site Transfer Protocols, etc.,). Execution of lab trials and scale-up activities etc..

Job Location : Dundigal, Hyderabad

Walk in Interview
Date : 01 March 2024 (Friday)
Time : 08:30 am – 12:00 pm
Venue : Gland Pharma Ltd. Near Gandimaisamma ‘X’ Road, Dundigal, Qutbullapur Mandal, Hyderabad

Note :Candidates from outstation, kindly share your profiles to Eswarreddy.ravi@glandpharma.com

Job Category: pharma
Job Type: Full Time
Job Location: Hyderabad

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About Pharmaceutical Guidanace

Ms. Abha Maurya is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 18 years of rich experience in pharmaceutical field. During his career, he work in quality assurance department with multinational company’s i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, Nectar life Science Ltd. During his experience, he face may regulatory Audit i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda,Kenya, Tanzania, Zimbabwe. He is currently leading a regulatory pharmaceutical company as a head Quality. You can join him by Email, Facebook, Google+, Twitter and YouTube

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