walk in interview on March 08, 2025 @ Indoco Remedies Limited Unit-3, Baddi:

Position: Officer

Qualification: B.Pharm / M.Sc

Experience: 2 to 8 years

Key Skills: FG, AMV, RM, HPLC & GLP Users.

For Engineering Department:

Position: Officer

Qualification: B.Tech & Diploma

Experience: 3 to 8 years

Key Skills: HVAC

For Quality Assurance Department:

Position Officer: IPQA

Qualification- B. Pharma

Experience: 3 to 8 years

For Production Department:

Position: Officer/Executive and Operators (Granulation, Compression and Packing)

Qualification: B. Pharma and iti

Experience: 2 to 10 years

Interested candidates can share their updated CVs at Avinash.kumar@indoco.com

In the pharmaceutical industry, the Quality Assurance (QA), Quality Control (QC), Research & Development (R&D), and Production departments play crucial roles in ensuring the development, manufacturing, and delivery of safe and effective medicines. Here’s an overview of each department:

1. Quality Assurance (QA)

QA focuses on preventing defects and ensuring compliance with Good Manufacturing Practices (GMP), regulations, and company policies.

• Develops and maintains Standard Operating Procedures (SOPs)
• Ensures GMP, FDA, WHO, and other regulatory compliance
• Conducts internal audits and inspections
• Manages deviation investigations and corrective actions (CAPA)
• Oversees documentation and batch release

2. Quality Control (QC)

QC is responsible for detecting defects in raw materials, intermediates, and finished products through testing and analysis.

• Performs chemical, physical, and microbiological testing
• Conducts stability studies to determine shelf life
• Ensures raw material and packaging material quality
• Uses analytical instruments (HPLC, GC, UV, FTIR, etc.)
• Verifies product compliance with specifications

3. Research & Development (R&D)

R&D is responsible for innovation, formulation, and process development of new pharmaceutical products.

• Develops new drug formulations and dosage forms
• Conducts preclinical and clinical trials
• Works on process development and optimization
• Studies drug stability and bioavailability
• Supports technology transfer from lab to production

4. Production (Manufacturing) Department

The Production department is responsible for manufacturing pharmaceutical products while ensuring compliance with GMP guidelines.

• Manufactures tablets, capsules, injections, syrups, ointments, etc.
• Operates granulation, mixing, compression, coating, filling, and packaging machines
• Ensures batch records and GMP compliance
• Works with QA & QC to maintain product quality
• Handles equipment validation and cleaning procedures

Each of these departments works together to ensure that pharmaceutical products are developed, manufactured, and delivered with the highest standards of safety, efficacy, and quality.

WALK IN INTERVIEW!!!

HOTEL HAMPTON BY HILTON, BARODA

DATE: 20TH FEBRUARY 2025 (THURSDAY)

TIME: 11:00 AM TO 08:00 PM

VENUE: HOTEL HAMPTON BY HILTON 14, FRIENDS CO. OP. SOCIETY, ALKAPURI, VADODARA, GUJARAT.

DURATION: 11:00 AM TO 08:00 PM

CONTACT INFO: 02717610000 EXT-6133/6122/6830

WALK IN WITH YOUR UPDATED RESUME & CTC PROOF/BREAKUP, ADHAR CARD PROOF WITH PHOTOCOPY EMAIL YOUR CV: DITEE.THAKAR@EMCURE.COM/AJABHAL MAKWANA@EMCURE.COM

WALK-IN INTERVIEW FOR ZYDUS LIFESCIENCES LIMITED AT SIKKIM

We are recruiting for our Ahmedabad Units

• Production - OSD

Tablet / Capsule-Granulation, Compression, Coating, Inspection, Capsule Filling and Wurster coater.

Blister Line (BQS)

RM, PM, FG, Dispensing. Dispatch, Documentation

RM. PM. Dispensing and dispatch

Process Equipment (Electrical / Instrumentation), BMS Engineer (Instrumentation), Utility Engineer

Instrument Technician - Process equipment's - Fitter / Electrical / Instrumentation / HVAC Operation //Water system

HPLC/GC/IR/UV/Dissolution and other OC Equipment/ QC Method Validation and Transfer

Job location 

Ahmedabad

3-8 years

M. Pharm/B. Pharm/M.Sc./B.sc/Diploma/ITI

Date:16th February 2025

Time:9 am to 5 pm

Venue: Sundar Hotel & Resort Majhitar, East Sikkim 737136

Location BDR Pharmaceuticals International Private Limited

Survey No. 51/1/2, 52/1/2, Vanseti Village, PO-Tajpura, TA-Halol, District: Baska, Gujarat.

 Call No:- 9016580529, 9316305857, 9898898453, 7778054628

Email career@bdrpharma.com

Felix Generics Pvt Ltd.

Special Economic Zone, Phase II, Pithampur, Distt. Dhar, Madhya Pradesh, India - 454775

Stability Section In charge: 

Experience: 10-11 years. 

Qualification: M.Sc./M. Pharma/B. Pharma. 

Team Leading (Team management, Work allocation, preparation & Review of Stability Study Protocols, schedules, Summary Sheet, Resource management, troubleshoot in technical glitches). Stability Data Management: -Awareness of regulatory requirement, ANDA filing & new Product filing application, Handle Field Alert Report, Market complaint, Review & presentation of Data, Tracking of data. Chamber Management: Planning for sample pullout, Batch charging, storage & reconciliation, destruction & smooth functioning of Stability chamber/ Walk-in Chamber. Subject Matter Expertise: Awareness of operation of Stability Study as per regulatory requirement & able to handle the regulatory audits.

QC Validation Officer to Executive: Experience: 3-8 years. 

Qualification: M.Sc./M. Pharma/B. Pharma.

Analytical methods validation, verification and methods transfer, cleaning method Validation. Handling HPLC, GC, DR & other instruments. Preparing method validation and verification protocol and report. Reviewing analytical hard copy and electronics data.

QC Sr. Officer to Executive:

Experience: 4-8 years. 

Qualification: M.Sc./M. Pharma/B. Pharma. 

Working in QC analysing, Stability, In process, FP, RM sample. Handling instruments like HPLC, GC, FTIR, UV, DR, SSA, etc, versatile in handling SAP, documentation like preparing STPs and review of analytical hard copies and electronic data.

Granulation/Compression/Packing Officer: Experience: 2-4 years. 

Qualification: M. Pharma / B. Pharma. Working in granulation & compression & Packing area.

Experience: 4-10 years. 

Qualification: M. Pharma / B. Pharma. Working in granulation & compression area.

Area of Exposure: Material Handling, Electronic Batch Record filling and review, Good Knowledge of SAP System & T Codes for PP_PI, Machine Alarms handling, QMS, Deviation, Change Control, SOP, Reports Preparation, Manpower Handling and exposure in USFDA approved company.

Technician: 

Experience: 2-5 years. 

Qualification: D. Pharma / Diploma / ITI. Working in Granulation/Compression/Compression/Primary Bottle Packing (CVC Line)/Secondary Bottle Packing (CVČ Line). Area of Exposure: Good Computer knowledge/Machine Operation/Cleaning/Changeover/Alarm Handling.

Executive to DM (Plant Maintenance): Experience: 8-12 years. 

Qualification: BE Electrical / Instrumentation. Handle Preventive and breakdown maintenance of process equipment, Instruments of OSD plant. Maintain maintenance schedule, training records, protocols, and quality documentation.

Officer to Sr. Officer (Plant Maintenance): Experience: 4-8 years. 

Qualification: Diploma/BE Electrical /Mechanical/ Instrumentation. Preventive and breakdown maintenance of process equipment and Instruments of Injectable plant. To prepare, update and review planner & report.

Technician to Sr. Technician (Plant Maintenance): 

Experience: 4-8 years. 

Qualification: Diploma/BE Electrical / Mechanical/Instrumentation. Preventive and breakdown maintenance of process equipment and Instruments of Injectable plant. To prepare, update and review planner & report.

INTERVIEW VENUE: Hotel NOVOTEL Ahmedabad, Iscon Cross Roads, Sarkhej - Gandhinagar Hwy, next to Wide Angle Cinema, Ahmedabad, Gujarat-380015

Eligibility: Candidate having experience to work in USFDA approved unit with good communication skills, Interested Candidate can come for Walk In interview.

Date: 02nd February 2025

Timing: 10:00 am to 03:30 pm

Contact No.: 9109996408, 9109968966, Email ID: jobs@felixvet.com