Showing posts with label Biotechnology. Show all posts
Showing posts with label Biotechnology. Show all posts

Thursday, 26 January 2023

Shilpa Biologicals Private Limited #Hiring #wearehiring #Hiringalert #HPLC #LCMS #UHPLC #Proteins #Peptides #Biotechnology #

 Shilpa Biologicals Private Limited



Looking for Analytical R&D scientists

Exp required: 5-10 yrs
Qualification: MSc ,MTech,PhD in Biotechnology

Job Responsibilities

1. Planning and review of daily activities in ARD
2. Sound knowledge on Analytical techniques LC MS, GC MS, GC, HPLC, CE, IC, Zeatsizer, CD, Fluorescence and MALS
3. Technical knowledge on Characterization and Lot release activities
4. Knowledge on method development, qualifications, validations, stability and method transfer
5. Experience on Bio molecules like mAbs, proteins and peptides
6. Good presentation skills and technical writing capability using the analytical data
7. Good communication skills
8. Knowledge on regulatory guidelines
9. Good managerial skills to lead the team efficiently
10. To implement GLP and GDP in ARD

Intrested candidates can share your cv to
harikrishnau@shilpabio.com
asasidharan@shilpabio.com

Saturday, 17 April 2021

Research Associate | Noida

We are hiring!!

Urgent opportunity

Position: Research Associate

Location: Sector 63 Noida

Vacancies: 6

Freshers 2 Vacancies, 4-Expereinced

Qualification: Biotechnology

Must have experience in COVID testing

Kindly share your profile at hr@redcliffels.com

Wednesday, 10 January 2018

Walk-in interview’s freshers for #Production, #QA, #QC, #Microbiology, BD




Experience: Fresher’s

Qualification: B.Sc., B. Pharmacy, M. Pharmacy, B.Tech & M.Tech(Biotechnology),M.Sc.(life science),MBA

Designation: Trainee
 
Dates: 17/01/2018 to 19/01/2018.

Timings: 09:00 to 14:00 Hrs.

Preferably Male Candidates for QC & Production.

Request you to refer if any candidate is suitable.

Venue: Virchow biotech Pvt. ltd, Survey No. 172, Gagillapur, Next to Nehru Outer Ring Road,Dundigal Mandal, Medchal Dist.,

Landmark: Beside Granules India Pvt Ltd


Monday, 8 January 2018

Walk-in on 10th & 11th Jan 2018 for B.Sc Lifesciences freshers!

Experience: 0 - 6 months (Fresher can apply)
Job Location: Chennai

Qualification: B.Sc / M.Sc - Microbiology / Applied Microbiology / Biotechnology / Genetics / Genomics / Virology / Biochemistry / Molecular Biology / Bioinformatics

Job Description:
  • Apply coding and indexing to patent documents in line with editorial policies and conventions. 
  • Achieve production volume and quality targets.
  • Recording of performance against target.
  • Taking an active role within the team to ensure targets are met.
  • Maintain awareness of current developments in own technology areas.
  • Achieve and maintain consistent quality standards.
  • Effective personal planning and time management.
  • Maintain a flexible and adaptable approach towards process change.
  • To deputize for team members as and when required.
  • To take responsibility for identifying technology training and developmental needs for yourself on an on-going basis.
  • To make positive efforts to promote personal safety and that of others by taking reasonable care at work, by carrying out the requirements of the law or following recognized codes of practice provided or advised by management to ensure safe working practices.
  • To undertake any other reasonable duties as requested by your line manager / director on a permanent or temporary basis.
Interview Process:
1st round: Process Test [Written]
2nd round: Technical interview [In person with Hiring Manager]

Date: 10th Jan 2018
Time: 9 AM to 12 Noon

Address: Acropolis, 11th Floor, 148 Radhakrishna Salai, CIT Colony, Mylapore, Chennai, Tamil Nadu 600004. (Landmark: Sear Savera Hotel)
Contact Person: Elodie [Talent Acquisition - HR]

Contact Number: 044 3018 73

Saturday, 23 April 2016

Regulatory Affairs Biologics

Company Name: Biocon

Experience : 4-8 years

Qualification:  M.Sc. / M.tech Biotechnology / Ph.D. Life Science / Biotechnology

Job Description
  • Write & review regulatory submissions like IND, IMPD, MAA, NDA, DMF and documents for regulatory advices.
  • Guidance to cross functional teams on regulatory expectations for US, EU, Japan and major markets.
  • Ensuring regulatory compliance in cross functional teams and managing cross functional team deliverables.
  • Review of CMC, clinical, bioanalytical development related documents & ensure compliance to CTD requirements.
Apply 
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