Stelis Biopharma-Walk in Interview for DP Manufacturing, DP Packing on 03rd December 2023,

Stelis Biopharma-Walk in Interview for DP Manufacturing, DP Packing on 03rd December 2023,

We are a fully integrated pure-play biologics Contract Development and Manufacturing Organization (CDMO), offering the complete spectrum of services, from cell line technology transfer to clinical and commercial manufacturing with capabilities to convert drug substance into stable formulations and fill and finish formats. We have proven technical expertise in microbial, mammalian, viral vectors, and various other technology platforms with world-class cGMP manufacturing facilities that offer high-quality services for your global programs.

DP (Drug Product) Manufacturing Department
Exp : 2 to 8 years
Work Location : Stelis – Unit 2, Doddaballapur, Bangalore

Key responsibilities
• Responsible for DP facility manufacturing activities like Compounding, Filtration, Filling and lyophilization of the Vial line products.
• Assist the installation and commissioning activities like FAT, SAT etc. of the Filling lines for vials, formulation vessels, Sterilisers, Lyophilizers, ALUS, Sealing Machine, Isolator etc.
• Preparation and review of the OQ protocols, CLIA, QRM of all associated equipment and area.
• Ensure QMS compliance in manufacturing related activities.
• Assist the validations of equipment and facility and the process (aseptic media fill).
• Identify and implement the manufacturing and warehouse procedures with compliance to current GMP requirements.
• Good communication and writing skills.

DP Packing Department
Work Location : Stelis – Unit 2, Doddaballapur, Bangalore
Exp : 2 to 8 years

Key responsibilities
• Should have the knowledge and hand experience on handling of Packaging line with diversity of products packaging.
• Should have the knowledge and hands on experience with Labelling machines, Blister packing machine, Automatic Cartoning Machine, Pen Assembling machines.
• Should have the knowledge and hands on experience with Track and trace system and aggregation system.
• Should have the knowledge and hands on experience with Preparation and review of the URS, QRM, IQ, OQ and PQ protocols.
• Should have the basic knowledge of handling the Cold chain products.

Walk in Interview
Date : 03rd December 2023, Sunday
Time : 9:00 am to 01:00 pm
Venue : Hotel Sitara Grand 15-24-20/21/22, 1st Road, MIG Phase 1&2, KPHB Colony, Kukatpally, Hyderabad, Telangana 500072

Job Category: pharma
Job Type: Full Time
Job Location: Doddaballapur Unit 2

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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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