Amneal Pharma | Walk-in for Production-QC on 15 Dec 2019 | Pharma Jobs in Ahmedabad

We are looking for competent, dynamic and motivated candidates for suitable positions for Injectable & OSD (oral solid dosage) unit for our Ahmedabad SEZ Matoda Plant.

Date: 1st December,2019 (Sunday)
Timing: 9:00 AM to 12:00 PM

Venue:
Amneal Pharmaceuticals Pvt. Ltd.
Plot No 15,16,17 Pharmez
Village: Matoda
Sarkhej Bavla Road, Abad

Please find the Job details below:

1. Sterile Manufacturing ( Injectable unit /Parenteral Unit)

Designation: Officer /Sr. Officer/Operators
Qualification: B.Pharm/M.sc/ITI/Diploma
Total Experience: 0 to 05 years
Position: 50

Desired Profile :

1. To observe & follow all rules and regulations of the production department.
2. Must be from Parenteral background
3. To be aware and responsible for achieving quality objective and fulfilling the requirements of the quality of the company's service by means of applicable quality procedures.
4. Sound technical knowledge of Aseptic area and controlled are related activities.
5. Technical exposure and expertise on vial filling, sealing, Autoclave, Lyophilizer, PFS filling, cartridge filling machine.
6. Knowledge of Regulatory guidelines and exposure of USFDA audits.
7. Knowledge of Eye drop filling machine and related batch mfg. process.
8. Knowledge of Quality Management System (QMS) i.e. change control, Deviation, CAPA, and documentation in manufacturing area of injectable.
9. Expertise in batch manufacturing and preparation related activities.
10. Knowledge of equipment validation and qualifications in injectable.

2. Quality Control (QC - OSD)Designation: Officer/ Sr. Officer/ Executive
Qualification: B.sc/ M.sc /B.pharm /M.pharm
Total experience: 02 to 07 years

Position: 10
Area : Technology Transfer, RM, FP, Stability, LIMS

Desired Profile :

1. Able to perform sampling of raw-materials and packing materials within the specified time frame to support manufacturing activities.

2. Should have experience to perform analysis & documentation of Raw-materials, In-process, Finished products, stability & validation samples by using Caliber LIMS software

3. Exposure to for management of working/reference standards on Caliber LIMS

4. Should have exposure to perform analytical method transfer, method verification and method validation activities as per ICH guideline and as per SOP's

5. Exposure to prepare and standardization of volumetric solutions/reagents

6. Responsible to perform all activities in laboratory in GLP compliance manner

7. Caliber LIMS knowledge is preferable

Required Candidate profile

The candidate with good communication and inter personal skills computer knowledge and exposure to cGMP/ GLP Knowledge and understanding of regulatory requirement is essential.

Note : Candidate should have 02 to 07 years of relevant experience in USFDA regulatory approved pharmaceuticals (Preferred 21 CFR compliance) organisation. You may walk in for interview with current CV along with CTC proof Appointment letter Increment letter & last 3 months salary slip & Bank statement Aadhar & PAN card and 2 passport size photograph.

If you are unable to attend interview you can share cv on neha.modi@amnealindia.com kishan.soni@amnealindia.com chandanid@amnealindia.com

Reach us on : WhatsApp

Mail us to Advertise/ Share your job information: thepharmavacancy@gmail.com

Reach us on social media: