Unichem laboratories-Walk in for Production, QC, & QA on 4th&11th June 2023

Unichem laboratories-Walk in for Production, QC, & QA on 4th&11th June 2023

Unichem laboratories Ltd. is looking for young dynamic candidates with ambition and drive for the following departments at our state-of-the-art Pharma Formulations Manufacturing facility at Pilerne Goa.

PRODUCTION
Experience in Oral Solid Dosage Manufacturing / CVC Packaging. Exposure to the latest manufacturing and packing techniques

QUALITY ASSURANCE
Familiar with cGMP guidelines and Quality Systems as per the international regulatory requirements.

FORMULATION DEVELOPMENT ANALYTICS (ADL)
Perform and prepare reports for analytical method development. method validation and query response for the finished product.

MATERIALS
Experience in Materials / Stores functions and should be fully conversant with pharmaceutical stores procedures.

QUALITY CONTROL
Experience in handling HPLC / GC / UV / IR Spectrometer

Exposure to regulatory environment is a must. Exposure to International Audits would be an added advantage.
Qualification : M.Pharm, B.Pharm, M.Sc, B.Sc
Experience : 1 – 7 year experience in respective segment with pharma background

Sunday, 04th June 2023
Treebo Trend Green Park Hotel, Guirim Bypass Junction, Mapusa, Goa
09:00 a.m. – 14:30 p.m.
Sunday, 11th June 2023
Hotel Grace Majestic. Next to Collectorate, Fatorda, Margao, Goa.
Time : 09:30 a.m. – 16:00 p.m

Send your resumes directly on hrgoa@unichemlabs.com for openings In Information Technology (B.E./BCA), Engineering(B.E./l)Diploma) and Formulation Development (M.Pharm).

Note : The candidate should bring along updated resume, passport size photo, all educational certificates, previous work experience certificates and current CTC statement.

Job Category: Phrama
Job Type: Full Time
Job Location: Goa

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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