Intas Pharma – Interview For QA/ QC/ QC Micro/ Packing/ Parenteral/ Instrumentation/ Engineering on 18 Feb 2024

Intas Pharma – Interview For QA/ QC/ QC Micro/ Packing/ Parenteral/ Instrumentation/ Engineering on 18 Feb 2024

Intas Pharma - Interview

Positions:OFFICER/SR. OFFICER

Department:Solid Oral Packing-Primary/Secondary Packing Area
Qualification:B.Sc/B.Pharma/M.Pharma
Experience: 2 to 6 Years
For Staff above level good knowledge in primary & secondary
tablet packing area
Positions:.TECHNICIAN/SR.OFFICER/EXECUTIVE
Department:Engineering – Instrumentation (Parenteral/Injectable)

Qualification:ITI/Diploma Eng/BE
Experience: 4 to 7 Years
Walk in Drive at Vadodara
Positions:TECHNICIAN/SR. OFFICER/EXECUTIVE

DepartmentParenteral (Injectable) Mfg – Aseptic/Autoclave/ Mfg Clean Area/Lyopholizer/Skidd/NDDS

Qualification:ITI/Diploma Eng/D.Pharm/B.Sc/B.Pharm/M.Pharm

Experience: 2 to 7 Years
For Technician & Staff Leval requrie good knowledge in Autoclave, Mfg Clean Area. Lyopholler, Skid, NODS & Aseptic Area
Candidate who should have good knowledge in Instrumentation & Plant Maintenance related work (Parenteral & Solid Oral Dosage) have good knowledge in trouble shooting related to equipment and machineries.
Positions:EXECUTIVE TO SR. EXECUTIVE
DepartmentQuality Control-Supervisor (QC-Supervisor)

Qualification:M.sc/B.Pharma/M.Pharma

Experience: 5 to 9 Years
Supervisor: To Verify sequence before start of analysis. Controlling the human error. Trouble shoot the instrument & method of technique. Reduction of unconfirmed OOS /OOT. Review of calibration & qualification activities of QC.

Positions:OFFICER/SR. OFFICER

Department:QA-Qualificaiton Parenteral & Solid Oral/ IPQA Parenteral & Solid Oral

Qualification:B.Pharma/M.Pharma
Experience: 2 to 6 Years
Candidate who should have good knowledge in QA Qualificaton & Validation Parenteral & Solid Oral/ POA Parenteral & Solid Oral Area
TECHNICIAN/SR.OFFICER/EXECUTIVE
Department:Engineering – Plant Maintenance (Parenteral/Injectable) Qualification:ITI / Diploma Eng/BE
Experience: 4 to 7 Years
Candidate who should have good knowledge in Instrumentation & Plant Maintenance related work Parenteral & Solid Oral Dosage) have good knowledge in trouble shooting related to equipment and machineries

PositionsOFFICER TO SR. EXECUTIVE

 Department Quality Control (QC-FG/Stability/AMV)

Qualification:M.sc/B.Pharma/M. Pharma
Experience: 2 to 12 Years
Analyst: Finished, AMV & Stability Section, knowledge of Instrument HPLC/GC Preferably know-how of Chromeleon Software.

PositionsOFFICER TO SR. EXECUTIVE
Department:Quality Control MICRO (Microbiology)

Qualification:M.sc Micro
Experience: 2 to 7 Years
-Analyst: Having exposure related Environment Monitoring in formulation, water analysis, various Microbiological test like sterility. BET, MLT etc. Having exposure related to regulatory plant and basic know of GLP GMP. Ready to work in rotational shift.

Date: 18th February, 2024 (Sunday) Time: 09:00 am to 02:00 pm Venue: Lemon Tree Hotel, Vadodara Opposite Parsi Agyari, Sayajigunj, Vadodara, Gujarat 390020

JOB LOCATION: INTAS PHARMEZ, AHMEDABAD

Please Note: Intas Pharmaceuticals Ltd. does
not directly or indirectly charge any fee for job application, processing, training or testing. Do not participate in any such invitations

Please carry your updated resume all educational, experience & salary documents
Candidates who have appeared for an interview at intas in
the last six months are requested not to apply Candidates must be open to work in shift duties and having pharma experience in regulated plant like USFDA, MHRA should apply.
INTAS PHARMACEUTICALS LTD.

Job Category: pharma
Job Type: Full Time
Job Location: Ahmedabad

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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