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Alivira Animal Health walk-in interview for ADL/ R&D on 1st June 2024

Alivira Animal Health is a leading global company in the animal health sector, with a strong presence in various regions such as the EU, Latin America, Turkey, Africa, India, and CIS. With a total worth of USD 150 million, we specialize in animal health APIs and formulations, providing a wide range of products for food-producing and companion animal species in the feed, nutritional, and therapeutic segments. Our goal is to become the top integrated platform in the highly lucrative global Animal Health market, offering excellence from APIs to Formulations.

Greetings from Alivira Animal Health!

Alivira Animal Health is conducting a walk-in interview on 1st June 2024 at our Visakhapatnam plant. We have open positions for Officer/Executive – Research & Development (1-3 years experience) and Officer/Executive – Quality Control – ADL (2-4 years experience). Candidates with a pharma background are preferred. Enjoy perks such as free transportation, canteen facility, and bonus.

We are conducting walk-in interview for various roles in R&D/ ADL on 1st June 2024 for our plant located at Visakhapatnam.

Officer/Executive – Research & Development

Experience: 1-3 Yrs

No. of Open Positions: 05

Role & responsibilities :

  • To Conduct the lab experiments as per plan.
  • To Demonstration of plant batches in house & outsourcing.
  • To Disposal of effluents and old chemicals.
  • To Labelling of chemicals Equipment maintenance and Housekeeping.
  • To have knowledge in R&D Documentation in line with SOP
  • To Evaluation of Analytical results & chromatograms.
  • To interpret NMR, IR, MASS chromatogram

Preferred candidate profile: Pharma background

Perks and benefits: Free Transportation, Free canteen facility, Bonus

Officer/Executive – Quality Control – ADL

Experience: 2-4 Yrs

No. of open Positions: 05

Role & responsibilities:

  • To handle HPLC, GC, Wet Analysis.
  • Sound knowledge in documentation.

Preferred candidate profile: Pharma background

Perks and benefits: Free Transportation, Free canteen facility, Bonus

Walk-in interview details

Date & Time: 1st June , 9.30 AM – 4.30 PM
Venue: Ramky Pharma City India Limited, SEZ, Parwada, Visakhapatnam, India – 531019.
Contact – Haritha

Walk-in interview for Freshers at Chemveda Lifesciences on 29th May 2024

Chemveda Life Sciences is a rapidly expanding service provider catering to the pharmaceutical, biotechnology, agrochemical industries, and academia. As a contract research organization (CRO),  Chemveda is enhancing its value proposition by offering a wide range of drug discovery and drug development services, focusing on improving cost and timeline efficiencies for its global clients. Leveraging its scientific and technological capabilities,  Chemveda provides comprehensive support for drug discovery chemistry services, including lab-scale chemical synthesis, Process R&D, and large-scale custom chemical development of drug substances, key intermediates, and starting materials across various chemistry classes. Recently, we have been investing in building internal expertise in cutting-edge scientific platforms to address both current and emerging challenges in basic and applied research.

Greetings from Chemveda life Sciences

Join Chemveda Life Sciences as a DQA and contribute to the effective implementation of quality systems in R&D and AR&D projects. Freshers with M.Pharma qualification (2023,2024 Passed outs) are encouraged to apply. Walk-in interview on 29th May 2024.

We have vacancy in DQA

Department: DQA
Qualification – M.Pharma (2023,2024 Passed outs)
Experience: Freshers (Preferred for Male)

Roles and Responsibilities:

  1. To monitor the Quality Systems for their effective implementation and compliance during the development of Projects at R&D and AR&D.
  2. To follow a controlled document system for projects in Research & Development, Analytical Research & Development, Development Quality Assurance and other relevant departments.
  3. Responsible to receive reviewing and archive all records relevant to Technology transfer
  4. To review Technical report along with R&D and finalise the Technical report for Technology transfer discussion.
  5. To review of Spec & MOA.
  6. To review and verify completeness of Technology transfer documents through checklist.
  7. Coordinating with Contract Manufacturing Organisations for document closures.
  8. To share Technology transfer documents to Manufacturing QA.
  9. To review of R&D and AR&D LNBs for completeness and as per GDP.
  10. Good knowledge on Guidelines.

Desired Candidate Profile:

  • 0 – 6 Months of experience in the Pharmaceutical Industry.
  • Must be Proficient in written, verbal, and Computer skills.
  • Should be self-motivated and result-oriented.
  • Should be a keen learner, proactive, and have good analytical skills.
  • Ability to multitask and prioritize responsibilities.

Walk-in interview details
Walk-In Date: 29th May 2024 (Wednesday)
Timings: 10.00 AM to 12.00 PM
Venue Details: Chemveda life Sciences, Admin Building,1st Floor, Plot No. B-11/1, IDA Uppal, Hyderabad – 500072, India.

Note – Females Not Eligible

If anyone is unable to attend an interview kindly share your profiles to ramasatish.uppuluri@chemvedals.com

Anjan Drug Private Limited (A Sekhmet Pharma Company) walk-in interview for Freshers and Experience candidates on 28th May – 1st June 2024

Anjan Drugs stands as a prominent Indian manufacturer of exceptional Active Pharmaceutical Ingredients (API). Holding the esteemed USFDA approval, it provides Valproic Acid, Sodium Valproate, Divalproex Sodium, Magnesium Valporate, and Gabapentin to renowned drug manufacturers in Brazil, India, the U.S.A., Canada, and other countries.

Greetings from Anjan Drug Private Limited (A Sekhmet Pharmaventures Company)!

Anjan Drug Private Limited is hosting walk-in interviews for Production Executive role. Ideal candidates have B.Sc (Chemistry) or Diploma background, 0-2 years experience in Pharma Production. Freshers with relevant qualifications are encouraged to apply!

Production Executive

Preferred candidate profile:

We are looking for candidates with B.Sc (Chemistry) or Diploma background with 0-2 years of experience in Pharma Production preferably API Manufacturing Industry. Freshers with B.Sc (Chemistry) or Diploma are also welcome.

Role & responsibilities

  • Compliance with GMP norms and to be following cGMP in manufacturing area.
  • Responsible to maintain the production blocks tidy and maintain clean room as per the classification and compliance for all types of regulatory audits, Inspection and / or internal quality audit.
  • Follow the procedure and production activities are preventing contamination or cross contamination.
  • Responsible for executing the production planning and achieving the maximum production without compromising the quality and safety.
  • Responsible for requesting the BMR & ECR to QA as per the production planning.
  • Raising request of the raw material and packing material, Verification of Raw material/ packaging material during dispensing as per master data and receipt of raw materials and packaging materials as per Batch manufacturing record and PMRO from Warehouse.
  • Responsible for recording of temperature, relative humidity and different pressure in manufacturing, packing area and raw material and finished goods storage areas.
  • Performing and online updating of equipment cleaning, area cleaning, manufacturing operations as per BMR/ECR and relevant SOP.
  • Filters, accessories usage & cleaning and storage as per SOP
  • Packing of finished product and labelling of intermediate, finished products, and its storage as per SOP.

Perks and benefits: As per Industry Standard

Walk-in interview details

Date & Time: 28 May – 1st June , 10.00 AM – 4.30 PM
Venue: Anjan Drug Private Limited (A Sekhmet Pharmaventures Company) Plot No. 109, 110,115 & 116, SIDCO Pharmaceutical, Industrial Estate, Alathur, Tamil Nadu 602003.
Contact – Subha Krishnan ( 09445025402 )

Sunrise international Labs walk-in interview for Production, QC on 28th & 29th May 2024

Sunrise International Labs Ltd., founded in 1986 in Cherlapally,  Hyderabad India, is currently a subsidiary of Perdaman Pharmaceuticals Pvt. Ltd. For more than 25 years, it has been supplying both the domestic Indian market and the international market with branded and generic pharmaceutical formulations. Additionally, Sunrise has actively engaged in contract manufacturing for numerous national and multinational companies.

Don’t miss the opportunity to work at Sunrise International Labs Ltd. We are conducting walk-in interviews for experienced candidates in Production/Quality Control on 28th & 29th May 2024. Apply for the Executive – OSD or HPLC Instrumentation roles. Male candidates with B.Sc/M.Sc/B.Pharm qualifications and 02-05 yrs experience are invited. Visit us at Plot No. 100, Lane-5, Sector II, Phase II, IDA Cherlapally, Hyderabad-500 051, INDIA.

Department: Production

  • Section: Granulation, Compression & Coating
  • Designation: Executive – OSd
  • Qualification: B.Sc/ B.Pharm
  • Experience: 02-05 yrs Experience
  • Male candidates only

Department: Quality Control 

  • Section: HPLC Instrumentation
  • Qualification: B.Sc / M.Sc
  • Experience: 02-05 yrs Experience
  • Male candidates only

Job Location: Hyderabad
Cell: 9121011003

Walk-In Interview Details:
Interview Date: 28th & 29th May 2024
Time: 10:00 AM to 4:00 PM
Venue: SUNRISE INTERNATIONAL LABS LTD. Plot No. 100, Lane-5, Sector II, Phase II, IDA Cherlapally, Hyderabad – 500051, INDIA.

Interested candidates may walk-in with an updated CV, last three month payslip*, Original Degree*, 10th Certificate*. Candidates who are unable to walk-in may send in their CV’s to hr@sunriseintlabs.com
Note: * MANDATORY DOCUMENTS.
Contact: 9121011003

Sunrise international Labs walk-in interview for Production, QC on 28th & 29th May 2024

Neuland Laboratories walk-in interview for QC/ Microbiology on 28th – 31st May 2024

Neuland Laboratories Limited, founded in 1984, is now a publicly listed company headquartered in Hyderabad, India. It is a prominent manufacturer of active pharmaceutical ingredients (APIs) and offers comprehensive solutions for the chemistry requirements of the pharmaceutical industry.  Neuland caters to a wide range of needs, including the synthesis of library compounds, supplying NCEs and advanced intermediates at different stages of the clinical life-cycle, and supporting commercial launches. Our strength lies in our expertise in manufacturing APIs and advanced intermediates, which are produced in our facilities approved by the US FDA. We excel in applying robust process chemistry in a regulatory compliant environment, thanks to our highly qualified team of over 1600 employees.

Greetings from Neuland Laboratories!

Neuland Laboratories invites you to attend walk-in interviews for exciting opportunities in Quality Control & Microbiology departments. We are hiring for Chemist/Officer – Quality Control and Microbiology roles. Candidates with experience in HPLC (Empower 3 Software) for Quality Control and Microbiology background are preferred. Immediate joiners are highly appreciated. Male candidates preferred.

We are conducting walk-in interview for various roles in Quality Control & Microbiology departments on 28th May to 31st May 2024.

Chemist/Officer – Quality Control

Job Description for Quality Control

  • Experience: 03 to 06 years of Exp in HPLC (Empower 3 Software)
  • Candidate from API Background are highly preferrable.
  • Immediate joiner’s are Highly Appreciated.
  • Male Candidate are preferrable for this Role.

Roles & Responsibilities: (HPLC)

  • Ensuring the cleanliness of the instruments and work place.
  • Carry out the IR, UV and SOR analysis of in process, intermediates, stability and finished product samples as per controlled method of analysis.
  • Sampling and testing of finished products as per the controlled method of analysis.
  • Carryout the HPLC analysis of In-Process, Raw material, Intermediates, finished products and stability samples as per the controlled method of analysis.
  • Recording the analysis details in respective work book and other relevant log books for each analysis.
  • Responsible for the maintenance of HPLC Columns and instruments.
  • Review of analytical test data and reports related to chemical and HPLC analysis.
  • Calibration of FTIR, UV, SOR and balances in Quality control laboratory as per schedule.
  • Responsible for the investigation of OOS, OOT, Deviations and Laboratory Occurrences and incidents as per the controlled procedures.
  • Trouble shooting of HPLC instruments.
  • Supporting to R&D for analysis and related activities.
  • Any other relevant entrusted to the person by the immediate supervisor.

Job Description for Microbiology

  • Qualification: B.sc / M.sc ( Micro Biology Background)
  • Experience: 02 to 03 years of Exp in Microbiology.
  • Candidate from API Background are highly preferrable.
  • Immediate joiner’s are Highly Appreciated.
  • Male Candidate are preferrable for this Role.

Roles & Responsibilities: (Microbiology)

  • Responsible for day to day activities of Microbiology laboratory.
  • Reports to Section In-charge-Microbiology.
  • Responsible for Environmental monitoring in microbiological lab.
  • Preparation of Media for Microbial analysis of water, Environmental and API analysis.
  • Performing TOC analysis of water samples with online documentation.
  • Performing the “Bacterial Endotoxin Test”” test for API & water and completion of relevant documents.
  • Responsible for water & API sample collection & analysis and completion of relevant documents.
  • Microbiological Environment monitoring by Passive & Active air samples collection and documentation of relevant calculations pertaining to the analysis.
  • Responsible for making sure that materials are appropriately tested and the results are
    reported in microbiology lab as per the SOP / Protocols.
  • Performing the product method validations as per the Harmonized procedures and online documentation of relevant calculations pertaining to the analysis
  • Responsible for preparation of water and environmental monitoring trend analysis.
  • Responsible for microbial culture maintenance preparation and documentation.
  • Responsible for review of reports and documents related to Microbiology section.
  • Any other relevant entrusted to the person by the immediate supervisor.

Walk-in interview details

Date & Time: 28 May – 31st May , 11.00 AM – 3.00 PM
Venue: Neuland U1, Survey No: 474, 347, 490/2, Veerabhadraswamy Temple Road, Jinnaram, Bonthapally Village, Telangana 502313
Contact – Priyanka

Share your Resume : priyankapandey@neulandlabs.com

Please carry your 03 months Pay slip & Updated CV along with you.

O2h hiring Research and Senior Research Associate – Synthesis R&D

The o2h group fosters fresh concepts in science, technology, and eco-friendly advancements. Our team transcends barriers by embracing a cooperative and collective strategy towards innovation. This involves joint investments, collaborative creation, and shared execution to realize these concepts. The o2h group consists of 6 interconnected divisions: o2h ventures, o2h discovery, o2h therapeutics, o2h technology, o2h co-work, and o2h community.

We’re seeking a dynamic individual to conduct synthesis and purification of oligonucleotides on a milligram scale.

The ideal candidate will have proficiency in interpreting HPLC/LCMS analysis of oligonucleotides and peptides, along with experience in oligonucleotide purification techniques using AKTA. From project initiation to completion, they’ll be focused on delivering high-quality results and collaborating effectively with our leadership and management team.

Research and Senior Research Associate – Synthesis R&D

Qualification & Experience

  • M.Sc/M.Pharma/Ph.D. (Organic Chemistry)
  • 3-5 years of experience

Work Location: Ahmedabad, Gujarāt, India

Job description

  • Responsible to perform routine organic synthesis. (mg to gram scale) & work independently under the guidance of the leader.
  • Independently support the scientific team with instrumentation and equipment operation and maintenance.
  • Able to understand & interpret various instruments like NMR, Mass, HPLC.
  • Instrument purification like Combiflash, big columns, column packing. Deciding the mobile phase for purification.
  • Independently handling all types of glassware assembly arrangement, reaction reagent charging, maintaining temperature, nitrogen, etc.
  • Should be able to understand the written instruction from the scientist including patents and reprints where procedure highlighted by scientists.
  • To train and support the team members.
  • Meticulous Documentation & proper data management.
  • To maintain the record book of the work done like purification or reaction.

Job requirements

  • Minimum of 2 year to 4 years of experience working in CRO Industry.
  • Strong organizational, project management and problem-solving skills with impeccable multi-tasking abilities.
  • Exceptional interpersonal skills.
  • Friendly and professional demeanor.
  • Ability to write reports and prepare spreadsheets and presentations.
  • Excellent organizational skills with an ability to think proactively and prioritize work.
  • Proactive, highly motivated with a “can-do” attitude.
  • Strong and accurate attention to detail.

For more information related to the job role, responsibilities, and to apply, please scan the QR code or visit – https://lnkd.in/dpdhP9M5

Take the next step in your career journey by applying now!

O2h hiring Research and Senior Research Associate - Synthesis R&D

Job opportunity for B Tech/ M Tech at Virchow Biotech

Virchow Biotech Pvt. Ltd, located in  Hyderabad, is a prominent global player in the Bio-Pharma sector with over 15 years of operational expertise. Our company is ISO 13485:2015 and WHO-GMP certified, showcasing our commitment to quality. Additionally, we have offices in the USA. Our strength lies in our innovative research team and dedicated manufacturing team, both of which are driven by motivation and a commitment to providing top-notch products.

We have an immediate requirement for Sr Executive to Manager (Engineering-Projects) for VIRCHOW BIOTECH PVT LTD, Hyderabad,

Department: Engineering-Projects
Designation: Sr Executive or Manager
No of Vacancies: 2
Qualification: B. Tech or M. Tech (Mech, Ele or CIVIL)
Experience: 8 to 15 years
Budget: 9 lpa to 16 lpa

JOB DESCRIPTION:

Responsibilities:

  1. Planning and Designing of Injectable project activities of India and Oversees for strategic utilization of available resources as per schedules; executing cost saving techniques to achieve reduction in terms of man-days, raw materials & energy consumption.
  2. Should have experience in managing both green field and Brown Field from conceptualization to commissioning stage.
  3. Should have Feasibility, Conceptual, Basic detail engineering studies commissioning and qualification and qualification.
  4. Should have exposure on technical specification progress monitoring site management manpower planning.
  5. Review of Design and Execution phase to commissioning of HVAC, Utilities (Raw Utilities and Clen Utilities) and process equipment with documents, Checklists and review reports.
  6. Should be familiar with budget forecast of Capex & Apex
  7. Should have an idea on EHS requirements in line with project requirement.
  8. Should have an idea on Installation and commissioning of process equipment’s and Utility equipment’s.
  9. Should be keen on Commissioning of LVPs (PFS, Vial, Cartridge, Ampule, Autoclave and Lyophilized as well
  10. Monthly data presentation to the top management (Actual Vs WIP)

Interested candidates can share with the below mentioned mail-Id.
raghu@virchowbiotech.com

Preference will be given to immediate joiners.

Regards,
P. Raghurami Reddy,
Asst General Manager-HR,
Virchow Biotech Pvt Ltd,
Hyderabad.

Baxter International Inc. is Hiring Freshers | Apply Now

Baxter International Inc. (Baxter) is a medtech company that has been making medical innovations for almost a century. The company was founded in 1931 by Dr. Ralph Falk and Dr. Don Baxter, and was the first commercial manufacturer of prepared IV solutions. Baxter’s products and therapies are used in hospitals, clinics, and homes, and include diagnostic, critical care, kidney care, nutrition, hospital, and surgical products.

Baxter International Inc. is Hiring Freshers 
Regulatory Affairs 

Designation ⏩ Regulatory Affairs Specialist 

Location ⏩ Bengaluru, Karnataka, India

Req ⏩ JR – 137117

Mode Of Work ⏩ WFO

JOB Type ⏩ Full Time 

Educational Qualification ⏩ B. Pharm/ M. Pharm / B.Sc. / M.Sc. / life sciences graduate

Experience needed ⏩ Freshers

Job Description:

  • Create and Review regulatory documentation for Drug, Device and Combination product renewals.
  • Interact with non-regulatory support groups (i.e., manufacturing, product stability, quality, clinical, etc.) to request documentation necessary to support product renewals
  • Track status and progress of regulatory documentation that will be used for renewals
  • Coordinate and compile responses to regulatory authority renewal questions (under supervision)
  • Use an electronic document management system to compile documents to support product renewals for submission to Health Authorities
  • Answer internal queries for assigned products
  • Maintain Database of Regulatory Requirements for renewals
  • Knowledge of regulations
  • Scientific knowledge
  • Administrative and project management skills
  • Ability to contribute to multiple projects from a regulatory affairs perspective
  • Ability to multitask and prioritize
  • Interpersonal and communication skills
  • Technical system skills (e.g. word processing, spreadsheets, databases, online research)
  • Proofreading and editing skills
  • Ability to independently identify compliance risks and resolve or escalate as necessary

Interested and Eligible candidates can apply online by link given below.

Apply Now

Baxter International Inc. is Hiring Freshers | Apply Now

Job openings for BSc, MSc – Quality Control at BDR Pharmaceuticals

BDR Pharmaceuticals, founded in 2002, specializes in API manufacturing and has established a strong presence in both the domestic and global markets. In the ever-changing global pharmaceutical industry,  BDR Pharmaceuticals has successfully positioned itself by offering a diverse range of specialty medications. Our innovative approach of multi-branding guarantees accessibility to essential and life-saving drugs at reasonable prices. With API and formulation facilities located in Gujarat and Uttarakhand, as well as a pellet facility in  Hyderabad, we are committed to meeting the healthcare needs of individuals worldwide.

Job openings at BDR Pharmaceuticals!!

Join BDR Pharmaceuticals in Baska, Gujarat for a rewarding career in Quality Control Chemical. Officer to executive positions available with multiple vacancies. Minimum 2-5 years of experience and B.Sc./M.Sc. in chemistry required. Apply today!

Location: Baska, Gujarat
Position: Officer to executive (multiple vacancies)
Department: Quality Control Chemical
Function: AMT/IP/ FP/RM/PM/Water sampler & analyst/Documentation/GLP
Desired experience: minimum 2 to 5 years
Desired Qualification: B.Sc./M.Sc. in chemistry.

Interested & Relevant candidates can share their updated CV on: tanvi.gandhi@bdrpharma.com

Biozenta Lifesciences hiring for Freshers and Experience candidates

Biozenta Lifescience Pvt. Ltd. is a renowned pharmaceutical and life sciences corporation engaged in the production, distribution, exportation, trading, and provision of a wide range of anticancer injections, tablets, and various other products. Founded in 2018, this esteemed company has successfully established its presence on a global scale. Situated at DNA House B3, Opp. Godrej Interio Raipur, Biozenta Lifescience Pvt. Ltd. operates from a prime location.

Greetings from Biozenta Lifesciences!
We are for following positions

Department: Injection Manufacturing/ QC/ QMS/ RA/ RM/ Admin/ Fresher

Designation: Trainee/ Officer/ Chemist/ Executive/ Store In-charge

Experience: Freshers / 2 – 5 years of relevant experience

Qualification: ITI, B.Sc., M.Sc., B Pharm, Graduate

Interested candidates can Share Resume At: hr@biozenta.com

Biozenta Lifesciences hiring for Freshers and Experience candidates