Amneal -Hiring For Sterile/ Injectable Manufacturing

 Amneal -Hiring For Sterile/ Injectable Manufacturing

EVALUATION ACTIVITIES – THE QUALITY SYSTEMS MODEL

amneal We are Hiring
We are looking for competent, dynamic and motivated candidates for suitable position in Amneal Injectables Pvt.Ltd. Unit based at – Palli (Kadi)
Sterile/Injectable Manufacturing:
1) Designation: Executive/ Sr. Executive/Sr. Officer/Officer
Experience: 2-7 years (Only Sterile/Injectable Experience Required)
Qualification: M. Pharm/B. Pharm/M.Sc/B.sc

1.Candidate should have experience of Production Planning, change control, Line clearance, deviation handling, Autoclave operation (TS and component).Vial washing dehydrogenation and filling, Compounding Aseptic & control area operation, documentation, both SVP and LVP manufacturing etc.
2. Should have sound experience Injectable /parenteral /sterile manufacturing only.
2) Designation: Associate/Sr Assistant/Assistant/Operators
Experience: 2-7 years (Only Sterile/Injectable Experience Required) Qualification: ITI/B.Sc/Diploma Engineering/D.Pharma
Job Profile:
1. Candidate should have experience of bulk Manufacturing/Aseptic filling Control/Aseptic area operation. Vial Filling Capping, Large volume Bag filling., Vessel operation including CIP/SIP process handling, machine operation (Steam Sterilizer, Vial Washing) and GMP Documentation. Please do not apply if you are from API and other than pharma background
Note: Candidate should have 02 to 07 years of relevant experience in USFDA regulatory approved pharmaceuticals (Preferred 21 CFR compliance) organisation. All interested candidates can share CV on: digant.joshi@amneal.com

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Job Category: pharma
Job Type: Full Time
Job Location: Palli (Kadi)

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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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