Ind Swift – Interview For QC/ Packing/ Production on 11th May 2024

Ind Swift – Interview For QC/ Packing/ Production on 11th May 2024

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Ind-Swift Limited – Jawaharpur, Derabassi
is the Ace unit of Ind-Swift Limited, was created in the year 2006 with an aim to globalize the Ind-Swift brand for finished dosage forms. We are a 100% Export Oriented Formulation Unit dealing in regulated markets having approval like MHRA-UK, MOH-CANADA, TGA & ROW etc.
Department
Analyst HPLC (QUALITY CONTROL)
Candidate should have knowledge of HPLC & related instruments for RM/Stability/FG section.
B.Pharma/ M Sc. Chemistry
3-5 yrs
Officer (PACKING FORMULATION)
Candidate should have knowledge of packing operations. Knowledge of BQS, Autocarnator and Bottle packing. Responsible to adherence cGMP guidelines.

B.Pharma
3-6 yrs

Operator
(PACKING FORMULATION)
Candidate should have knowledge of packing operations. Knowledge of BQS, Autocarnator and Bottle packing. Responsible to adherence cGMP guidelines.

+2, ITI Diploma
2-8 yrs

Officer/Sr.Officer (PRODUCTION)
Candidate should have knowledge of manufacturing operations of granulation, compression, coating & capsule filling, responsible to adherence cGMP guidelines.
B.Pharma
3-6 yrs
Operator (PRODUCTION)
Candidate should have knowledge of manufacturing operations of granulation, compression, coating & capsule filling.
+2, ITI Diploma
3-6 yrs
Note: Only MHRA & USFDA exposure candidates will be entertained.
WALK-IN
Saturday, 11th May 2024 (10:00 am to 5:00 pm)
Please forward you Cv’s on the following contacts:
708 797 8441
[email protected]
708 797 8441
Ind-Swift Ltd., Off. NH-21, Vill. Jawaharpur, Derabassi, Distt. Mohali, Punjab -140507

Job Category: pharma
Job Type: Full Time
Job Location: Derabassi (Punjab)

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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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