GeneSys Biologics is Hiring Manufacturing Professionals (Biologics Experience) Details are provided below 1. Position: Manufacturing Professionals (Biologics Experience) 2. Qualification: M.Sc./ BTech (Biotechnology) 3. Experience: 5-8 Years of experience in Upstream Manufacturing 4. Job Description: -To oversee daily shop-floor manufacturing, compliance & scheduling to ensure efficient batch execution. -Responsible for preparation & execution of process validation & cleaning validation protocol & report. -Assist with equipment validations (IQ, OQ,DQ & PQ) & coordinate for preventive maintenance periodically. -To oversee cleaning in place (CIP) & sterilization in place (SIP) of fermenters with associated process vessels & Cell bank preparation with smooth handling. -To prepare & review batch manufacturing records (BMR), handle quality deviations, OOS (out of specification), CAPA & change controls....
Emcure Pharmaceuticals is hiring Officer/Executive/AM for QC Microbiology Department
Emcure Pharmaceuticals is looking for dedicated and detail-oriented professionals for QC Microbiology team.
Details are provided below
1. Position:Officer/Executive / AM
2. Job Location: Sanand, Ahmedabad
3. Experience: 2 to 8 Years
5. Department: QC Micro
6. Qualification: B.Sc./M.Sc. Microbiology (or) B.Pharm / M.Pharm
7. Key areas of Work :
-Water Testing: Perform analysis of purified-water, WFI, potable water and water for injection as per IP/USP/EP guidelines.
-Sterility Testing: Perform sterility testing of pharmaceutical products, raw materials and components as per IP/USP.
-Microbial Limit Testing (MLT): Conduct microbial limit tests of raw materials, in-process and finished products.
-Environmental Monitoring (EM): Perform monitoring of viable and non-viable particles in clean areas as per SOP
-Media & Reagent Preparation: Prepare, sterilize and perform quality checks of culture media and reagents.
-Instrument Handling: Operate, calibrate and maintain microbiology laboratory instruments and equipment.
-Data Review & Reporting: Review raw data, analyze results and prepare accurate reports.
-Documentation: Ensure documentation as per GLP, GDP and cGMP guidelines.
-Compliance: Ensure adherence to quality standards, SOPs and regulatory requirements.
8. Key Responsibilities:
-Perform routine analysis and release testing of samples as per specifications.
-Ensure timely and accurate execution of tests.
-Maintain laboratory cleanliness and follow safety procedures.
-Participate in investigations, method validations and qualification activities.
-Support in audits and regulatory inspections.
-Continually drive quality improvement initiatives.
8. How to Apply:
Interested candidates can share their updated CV by sharing following information:
On mail id
dhruvi.rana@emcure.com
Current Organization:
Department:
Current Designation:
Current CTC:
Expected CTC:
Total Experience:
Suitable date and time for Interview within next 5 working days:
WHATSAPP 7383556373
MALE CANDIDTAES ARE PREFERED
NOTE: CANDIDATES WITH ONLY INJECTABLE MANUFACTURING ARE PREFERRED
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