GLAND -INTERVIEW on 02 March 2024

GLAND -INTERVIEW on 02 March 2024

GLAND -INTERVIEW

GLAND GLAND PHARMA LTD
WALK IN INTERVIEW Date: 02 March 2024 (Saturday)
Time: 08:30 AM – 11:30 AM
Inviting Engineering & Packing (Injectables) Experienced Professionals.
Engineering
Diploma/B.E/B.Tech
3 to 8 Years

1. Process Mechanical Engineer:
Responsible for line preventive, breakdown maintenance & major activities. Analyzing the breakdowns for various failure modes effects & causes and proposes to corrective action & preventive action. Responsible for cGMP activities.
2. Instrumentation Engineer:
Responsible for Attending the equipment breakdowns and maintenance activities in the respective area. Responsible for cGMP activities.
Packing
ITI/Diploma/ B.Sc.,/M.Sc.,/ B. Pharmacy
2 to 5 Years
Required Skills (Injectables)

⚫ Labeling Operators
• Line Chemists:
Inspecting and verifying packaging materials, preparing and labeling products for distribution, and maintaining accurate records of the packaging process.
Venue: Gland Pharma Ltd. Near Gandimaisamma ‘X’ Road, Dundigal, Qutbullapur Mandal, Hyderabad
Job Locations:Dundigal & Pashamylaram

PS: Preference will be given for immediate joiners and willing to work in 3 rotational shifts
Disclaimer: Gland Pharma does not seek any kind of payment 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: Dundigal & Pashamylaram

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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