Unichem Laboratories- Interview For Production/ EHS/ QA on 16th Jul to 19th Jul 24

Unichem Laboratories- Interview For Production/ EHS/ QA on 16th Jul to 19th Jul 24

Unichem Laboratories- Interview

Unichem Laboratories Walk-In Interview For Production/ EHS/ QA

We are hiring For Pithampur Site (API)

Venue: Unichem Laboratories Limited
Plot No. 197, Sector-1, Industrial; Area, Pithampur- Dist. Dhar- 454775 (Μ.Ρ.)

Interview Date- 16th Jul 24 to 19th Jul 24

Time- 11:00 to 16:00

1) Department: Production

A) Designation: Associate

Section: Intermediate+ Finished area (Adhere to Safety & CGMP Norms) (Distillation/Layer Separation, Solvent Handling, SRP/ Hydrogenation/ Micronization/DCS Automation)

Experience: 1.5 Yrs. – 3.5 Yrs.

Qualification: B. Sc./ Diploma Chemical

B) Designation: Sr. Officer/ Officer

Section: Qualification (URS/IQ/OQ/PQ) QMS (CCP/Deviation/OOS/OOT) (Adhere to Safety & CGMP Norms) (Distillation/Layer Separation, Solvent Handling, SRP/ Hydrogenation/ Micronization/DCS Automation)

Experience: 3.5 Yrs.- 4.5 Yrs.

Qualification: M. Sc./B. Sc./ Diploma

2) Department: EHS

Designation: Officer

Section: Fire & Safety

Experience: 2.0 Yrs-3.0 Yrs

Qualification: B. Tech (Fire & Safety)/ Diploma (Fire & Safety, AIDS, PGAIDS)

3) Department: Quality Assurance

A) Designation: Sr. Officer/Officer

Section: IPQA

Experience: 2.5 Yrs. – 4.5 Yrs.

Qualification: B. Pharma/ M. sc.

B) Designation: Sr. Executive/ Asst. Manager

Section: Investigation, Deviation, QMS

Experience: 5 Yrs. – 8 Yrs.

Qualification: B. Pharma/ M. sc.

Job Category: pharma
Job Type: Full Time
Job Location: Pithampur (MP)

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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