Dasami Lab – Interview For QC/ Production/ Production (Documentation) on 7th Jan’ 2024

Dasami Lab – Interview For QC/ Production/ Production (Documentation) on 7th Jan’ 2024

Interview

We are Leading API Bulk Drug Manufacturing Company Approved by USFDA Requires The Following Personnel for Our Facility Located Near Choutuppal.

1) Department: Quality Control

Designation: Executive/Asst. Manager

Qualification: B.Sc/ M.Sc(Chemistry

Experience: 03-12 Years

Job Profile: Should Have Experience in HPLC Analysis Activities, LIMS Activities, Masters Creation/CSV Activities

2) Department: Production

Designation: Sr.Chemist/ Sr. Executive

Qualification: B.Sc/ M.Sc(Chemistry

Experience: 03-12 Years

Job Profile: Should Have Experience in Handling all Types of Equipments Knowledge in CGMP Activities

3) Department: Production (Documentation)

Designation: Sr. Chemist/ Sr. Executive

Qualification: B.Sc/ M.Sc(Chemistry

Experience: 03-12 Years

Job Profile: Should Have Experience in Online Documentation, Handling of Incidents in QMS and CGMP Activities.

4) Department: Engineering

Designation: Asst. Manager/Dy. Manager

Qualification: Diploma/ B.Tech/ M.Tech

Experience: 08-15Years

Job Profile: Providing Engineering Expertise and Providing Input on Safety, Design and Equipment Selection of API Processes Handling Engineering BOQ. Material Procurement and Budget and Equipment Selection of API Processes

Maintenance Works of Production Blocks by Meeting the Needs and Requirements. Maintaining Required Spare Parts Stock for Breakdowns and Preventive Maintenance Carrying out Preventive Maintenance and Investigate Calibration Failures

Date: 7th January 2024(Sunday)

Time: 9.00AM-1.00PM

Venue: “Hetero Corporate, 7-2-A2, Industrial Estates, Sanath Nagar, Hyderabad, Telengana-500018”.

Please Bring the following

Latest copy of Resume.

All educational certificates Xerox Copies.

Increment Letter & 3 Months pay slips.

Previous Employer relieving letters.

Aadhar & Pan Card

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

Apply for this position

Allowed Type(s): .pdf, .doc, .docx

ABHA

Abha is the Author  of pharmaceutical guidance, she is a pharmaceutical professional having more than 22 years of rich experience in pharmaceutical field. During her career, she works in the quality assurance department with multinational companies i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd. During his experience, she faces many regulatorily audits 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. She is currently leading a regulatory pharmaceutical company as a Head Quality. You can join him by Email, Facebook, Google+, Twitter, and YouTube