Gland Pharma- interview for Production (Injectables) Professionals on July 19, 2024

Gland Pharma- interview for Production (Injectables) Professionals on July 19, 2024

Gland Pharma- interview

Gland Pharma walk in interview for Production (Injectables) Experienced Professionals on July 19, 2024 (Friday)

Inviting Production (Injectables) Experienced Professionals

Department: Production

Qualification/ Experience: B.Sc./
B. Pharmacy /M.Sc./ M. Pharmacy With 3-6 Years of experience

Required Skills
(Injectables, Lyophilization, Bag line operators) :

– Expertise in compounding, aseptic operations, and troubleshooting equipment, with a focus on solution-oriented approaches.

– Autoclave operators/ Vial sealing/Line chemist/ Compounding.

– Compounding and filtration of the product as per batch manufacturing record & ensuring cleanliness of compounding area, personal entry and material pass of component area and APA & online documentation and effective coordination within Cross-Functional Teams (CFT), etc.

Date: July 19, 2024 (Friday)

Time: 09:30AM – 12:30 PM

Venue: Gland Pharma Limited, Unit-2 Plot no:42-52, Phase III, TSIIC, Pashamylaram.

Job Location:Unit-2, Pashamylaram Plant, Hyderabad.

Note:Candidates from outstation, kindly share your profiles to Suryateja.velaga@qlandpharma.com/ Hrd.pmy@qlandpharma.com

Disclaimer: Gland Pharma does not seek payment of any kind from prospective candidates for employment with Gland Pharma or authorize any agency or any individual to collect or charge any fees or charges for recruitment.

Job Category: pharma
Job Type: Full Time
Job Location: Pashamylaram Plant Unit 2

Apply for this position

Allowed Type(s): .rtf

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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