Monday, September 16, 2024

Walk in Drive - R&D Medicinal Chemistry & Peptide Chemistry | Bengaluru & Hyderabad | Sunday, 22nd Sept' 24

 Walk in Drive - R&D Medicinal Chemistry & Peptide Chemistry | Bengaluru & Hyderabad | Sunday, 22nd Sept' 24




We are thrilled to announce a walk-in drive for the role of Scientist in Medicinal Chemistry & Peptide chemistry at our cutting-edge R & D facility. If you have 2 to 5 years of experience with synthetic skills in performing various kinds of reactions, execute the synthesis of peptide molecules, purifications skills and has passion for drug discovery, we want to meet you!


Working in our Medicinal chemistry & Peptide Chemistry team offers unique opportunities to contribute to groundbreaking research and make a meaningful impact on patients' lives. Join us in our mission to develop innovative therapies and shape the future of healthcare.


If you meet the qualifications and are passionate about advancing drug discovery, we invite you to attend our walk-in drive. Come prepared to showcase your expertise and learn more about the exciting opportunities at Aurigene.


Job Location will be Bengaluru, however, walk in drives are being conducted at Hyderabad & Bengaluru at our office locations.


For any help regarding walk in drive on 22nd Sept 2024, You can reach out to us on apslta@aurigeneservices.com

Sunday, September 15, 2024

Openings at Dr. Reddy’s – Injectable Packing & Engineering, QC department

 

Openings at Dr. Reddy’s – Injectable Packing & Engineering, QC department






Dr. Reddy’s Laboratories, a global pharmaceutical leader, is currently offering exciting job opportunities in its Injectable Formulations division. As the company continues to expand, it seeks talented professionals to join its team, particularly in the fields of Packing, Engineering, and Quality Control (QC).

Dr. Reddy’s Laboratories is known for its commitment to innovation and quality in the pharmaceutical industry.



By joining the team, you will be part of a global organization that focuses on making life-saving medications available worldwide. The company offers competitive benefits and a dynamic working environment that fosters professional growth.

1.Department: Packing

Experience: 2 – 5 Years

Qualification:Diploma / B-Tech -Engg (Minimum 60% Marks)


Job profile :
• Expertise in handling packing line end to end operations & experience in any of the mentioned equipment:
Automatic Labelling, CVC – Auto
Cartonator, Vial Labelling, Jeckson Track and Trace, Secondary packing



2.Department: Engineering

Experience:2 – 6 Years

Qualification: Diploma / B.Tech /(Mechanical,
Instrumentation) –
(Minimum 60% Marks)


Job profile :
HVAC, Utility, Water systems, SME-Instrumentation Process control.
SME – Instrumentation must have exposure in filling machine, Autoclave, Isolators Electrical maintenance should have 33kv Licence with experience in black utilities.





3.Department :Equipment 

Experience:4-8 Years

Qualification:B.Pharm/ MPharm/Engineering (Minimum 60% Marks)

Job profile :
Experience in sterile manufacturing equipment qualification
Preparation and Execution of qualification protocols for Equipment’s, Autoclave, Tunnel, Filling and capping machine, Lyophilizer, Washing machine, bung processor etc.


Preparation, review and execution of SAT, IQ, OQ, PQ

4.Department :Quality Control

Experience :2- 6 Years

Qualification:M.Sc (Minimum 60% Marks)


Job profile:

Hands on experience in Handling of HPLC, GC.
Expertise in Handling of KF instrument, IR UV & Chemical Analysis.
Working experience in a GMP with a special emphasis on GDP(Good
Documentation Practices
Knowledge on Stability
Must have experience with USDA regulatory environment and process.

Work location: Vishakapatnam (pydibhimavaram)

Date : 21 September 2024 , Saturday
Time: 9.00am-3.00pm onwards

Venue – Ginger – Gajuwaka,
27-8-308/1/1, Near vadlapudi,

Sri Ramnagar, Sri Nagar,
Railway Gate, Visakhapatnam,
https://forms.office.com/r/w8cdJm8XnD
Andhra Pradesh – 530044




FDC Limited Hiring for Production/QA Positions: Walk-In Interviews on 18th & 21st September 2024

 

FDC Limited Hiring for Production/QA Positions: Walk-In Interviews on 18th & 21st September 2024




FDC Limited is conducting walk-in interviews for Production and Quality Assurance (QA) positions on 18th & 21st September 2024. This is a great opportunity for candidates with relevant experience in pharmaceutical production and quality assurance to join one of India’s leading pharmaceutical companies.

click here

Department: Production

Designation: Officer/ Senior Officer

Area: Packing

Qualifications: B. Pharma / M. Pharma

Experience required: 1-4 Years

Department: Production

Designation: Supervisor

Area: Granulation/ Capsule Filling

Qualifications: 12th with ITI

Experience required: 1-4 Years

Department: Quality Assurance

Designation: Executive

Area: QMS

(Market Complaint/ APQR/ Stability/ Change Control/ Investigation)

Qualifications: B. Pharma / M. Pharma

Experience required: 5-8 Years

Interview Schedule 18-09-2024 & 21-09-2024

FDC Limited, Village Khol-Bhud, Near Dr. Reddy, Tehsil Baddi, Distt. Solan, (HP) 173205


Contact Person: Mr. Sushil Kumar

Contact Number: 9736880100






Aarti Pharmalab Hiring For BΕ/BTech/ΜΕ/MTech Chemical Engineering - Technology Transfer

 

Aarti Pharmalab Hiring For BΕ/BTech/ΜΕ/MTech Chemical Engineering - Technology Transfer





Aarti Pharmalab Hiring For BΕ/BTech/ΜΕ/MTech Chemical Engineering - Technology Transfer



Job Title: Executive / Sr. Executive / Dy Manager

Department: Technology Transfer



Location: Dombivli, Maharashtra,

Positions: 07

Qualification: B.Ε./B.Tech/Μ.Ε./M.Tech Chemical Engineering

Experience: 3 to 7 years

Responsibilities

• scale up technology from R&D to Kilo scale/ pilot scale/ commercial scale

• Coordination with R&D team for generating negative study data, concluding to optimize process parameters

• Observe R&D demo batches & preparation of demo batches report

Aarti Pharmalab Hiring For BΕ/BTech/ΜΕ/MTech Chemical Engineering - Technology Transfer

 Preparation of BFD, PFD, P&ID, mass balance, energy balance sheets

• Monitor process optimization & validation batches at pilot/commercial scale at different manufacturing sites of APL (Tarapur, Vapi, Atali)



Send your resume

Baxter Hiring For Quality Control Dept

 Baxter Hiring For Quality Control Dept





Position: Assoc, Quality Control - QMS

Location: Ahmedabad, Gujarat, India

Job Category: Quality


Job Description:

To review, update, report and inform Supervisor as & when deviation is initiated.

To ensure that the recording of NCR is done in line with standard operating procedure

To ensure the implementation of GMP, GDP practices and review of issues and impact of the same, if any, & take corrective actions.

To carry out GLP rounds in the Quality Control lab.

To work as a Good Manufacturing Practice (GMP) inspector in the plant

To train/update the team members on various regulatory guidelines

To identify, monitor the deviation/abnormalities in process/documents/systems are captured and resolve them according to Quality management System.

To ensure that all the deviations and OOS are reported to QA within required time frame.

To prepare, review, Implement and update SOP’s according to current regulations systems.

To conduct Technical committee meeting on CCN impact assessment.

To conduct monthly corrective and Preventive Action Meeting.

To review the CAPA summary report and ensure that all CAPA are closed within time frame.

To review Change Control Note and NCR report before sending to Quality Committee for final closure and ensure the timely closure of Change Control Note and NCR

To train/update the personnel for the various aspect of current Good Manufacturing Practices.

To investigate and close the QMS elements in timely manner.


Click on below link for apply

https://www.jobavailables.com/2024/09/baxter-hiring-for-quality-control-dept.html



Piramal Pharma Hiring For QC Department

 Piramal Pharma Hiring For QC Deptartment




Position: Executive - Quality Control

Qualification: MSc.


Required Skills: HPLC Analysis

Job Description : 


To execute analysis of finished goods / Stability samples / Raw materials / Packing materials In-process and cleaning samples along with relevant laboratory documentation.

Intimation & result reporting after completion of analysis & relevant documentation.

Checking and ensuring proper status labels after confirming availability of all the requirements (as applicable) for analysis such as approved control procedure, analytical protocol, reference standards, chemicals, reagents, GC/HPLC Columns, glassware, water preparation equipment, water bath, sonication baths, mobile phase bottle etc.

Ensure the online documents pertaining to day-to-day analysis are efficiently completed in timely manner. Reporting the activities daily to immediate supervisor.

Calibration of equipment’s / instruments.

Destruction of respective records & QC samples like retention samples of raw materials, analyzed samples.

To take out the quality reports, data / results entry in SAP system.

To prepare and maintain the working standards & documentation.

Ensure timely raising and closure of deviations, quality events, change controls, OOS/OOT.

Execution of analytical method validation, cleaning validation of products.

Preparation and maintenance of Analytical data sheets and Excel spread sheets.

Adequate knowledge of all equipment/instruments & their functioning in the laboratory & assist in equipment/instrument qualification activities.

Ensuring the quality and integrity of all GxP data and documentation generated.

Ensuring effective execution requirements of food regulations (US)-21 CFR Part 111.

Ensure fully Engagement and Involvement regarding awareness, clarity maintained related to data integrity.

Ensuring good house-keeping and accident free working in the laboratory.

To perform safe Laboratory operations (as per MSDS) ensuring proper usage of PPEs, safe, secure storage of hazardous, toxic, explosive, corrosive, irritant materials.

Ensure proper maintenance of HPLC and GC column and related logbooks in QC lab.

To fulfill the analytical requirements of FSSAI regulation.

To undergo assigned trainings on cGMP, HSE & departmental procedures / policies.

To determine internal and external QEHS issues as well as needs and expectations of relevant interested parties and monitor the same.

To implement QEHS policy & objectives.

To ensure participation and consultation of worker.

To identify & communicate incidents, QEHS non conformities, investigate and take corrective actions on the same.

To ensure work permit system during maintenance activities.

To implement QEHS continual improvement projects at site and monitor.

To ensure disposal of waste.








Click on below link for apply









O2h Walk-In Interview on 22nd September (Sunday)

O2h Walk-In Interview on 22nd September (Sunday)




We are actively #hiring for multiple positions and are seeking passionate candidates to be a part of our vision of #seedingideas in life science, tech, and green innovation.


Open Positions are as below

✔ Junior Architect

✔ Research Associate/Sr. Research Associate Analytical

✔Research Assistant - Analytical


We are conducting walk-in interview in #Ahmedabad. Please refer to the creative for specific venue details, date, and timings.


If you know someone who can be a good fit for any of the open positions, mention them in the comment section and help them build their #career.

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