hplc qc in pharma

Wings Biotech LLP is steadfast in creating drugs in the Prescriptions and Branded Formulations segments with solutions to counter the problems We are on a constant hunt for talented professionals If you are an experienced healthcare professional who is skilled qualified and innovative If you are one of those who redeem challenges to meet success with...

qc review ,glp,hplc,qc gc,qc chemical Job Types: Full-time, Permanent, FresherPay: ₹15, ₹50,000.00 per monthBenefits:Health insuranceLeave encashmentProvident FundEducation:Bachelor's (Preferred)Experience:total work: 1 year (Preferred)Work Location: In person

Required QC Analyst exp 4-5 year, Finish Good HPLCsalary -Hike on current salary Male onlyLocation - Baddi Call

Hi we are hiringExperience;- 1 to 3 years Post;- QC CTC;- 20 to 35 k Location;-Baddi Knowledge ;- HPLC Interested candidate Apply;-Mail ID ;-Contact number ;

Role & responsibilitiesYou will be working as Head QC for USFDA approved Formulation Plant at Baddi and will be responsible for:You will be responsible for Establish the project goals and priorities.You will be responsible for team management and leadership.You will be handle 50 Plus Products and handle business turnover.You will be reporting to Head Quality...

Role & responsibilitiesComprehensive Oversight: Manage day-to-day activities in Quality Control .Instrument Expertise: Demonstrate hands-on experience with a variety of QC instruments, including HPLC, Dissolution, and other chemical and analytical tools.Lab Development: Utilize your expertise to develop the lab, ensuring compliance with the latest Revised...

Wings Biotech LLP provides a platform for candidates to prove themselves Profile Requirements Company Name Wings Biotech LLP Profile QC Chemist- RM Testing Vacancy 1 Position Location Baddi Salary Payable Hike on current package Required Experience 1 to 3 years in RM Testing Qualification B Pharma B sc or M Sc Email ID ...

Key Responsibilities 1 Stability Study Management Execute stability studies as per ICH guidelines Q1A-Q1E and company protocols Place withdraw and test samples from stability chambers accelerated intermediate and long-term Perform analysis of stability samples for physical chemical and microbiological parameters Monitor and document...

Responsibilities:Collaborate with cross-functional teams on product developmentEnsure compliance with regulatory standardsConduct method validations and HPLC analysisMonitor QMS procedures and document changes

Role & responsibilitiesTo be responsible for review of samples on HPLC, UV etc. as per specified in method of analysis.1 To be responsible for all the investigations related to any incident, OOS, OOT and deviation relatedto raw material and packing material.2 To ensure and implementation of pharmaceutical quality system, cGMP, GLP and gooddocumentation...