Home / Job / Cipla Limited – Walk-In Interviews on 03rd’ October 2021

Cipla Limited – Walk-In Interviews on 03rd’ October 2021

Cipla Limited – Walk-In Interviews on 03rd’ October 2021

Cipla Walk-In Interview for Quality Assurance (Oral Solid Dosage)

Date & Time : 03rd October 2021,  09AM to 04PM

 Cipla Academy, Cipla Limited , Verna Industrial Estates, Verna, Goa
Job Location : Goa, India

Post/Eligibility Criteria

Officers – IPQA: Candidate with B.Pham / M.Pharm with 2-5yrs experience in In-Process Quality check, giving line clearance, Reviewing BMR BPR

Officer – QMS: Candidate with B.Pharm / M.Pharm with 2-5yrs experience in handling QMS Activities, Investigations, CAPA, Market complaint, Internal Audit.

Officers – Validation : Candidate with B.Pharma / M.Pharm with 2-5yrs experience in handling validation & Qualification Activities of OSD line.

Officers – Lab QA: Candidate with B.Pharma / M.Pharm with 2-5yrs experience in handling Lab QA Activities.

Candidates can walk-in with a recent copy of their resume, all relevant qualification certificates / Marksheets, Pan Card, Aadhar Card, Latest Increment Letter, experience letter of previous organization if any and salary slips of last 3 months.

Those who are unable to attend the walk-in may send their resume on below mail id: [email protected] & [email protected]

Candidates with Goan domicile will be preferred

All the candidates interested attend the walk-in are requested to take adequate COVID protection measures such as compulsory wearing of mask, maintaining a social distance and hand sanitization. No candidates will be permitted without a mask at venue.


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About Pharmaceutical Guidanace

Mr. Shiv Kumar is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 14 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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