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Call to HR between 10AM to 5PM At Ozone Pharmaceuticals Recruitment for QA/QC

Ozone Pharmaceuticals ltd Walk-in Interview 2022   B.Pharma for Quality Assurance / Quality Control At Gurgaon/Gurugram. Ozone Pharmaceuticals ltd Notification full details below.Interested and eligible candidates send Your Resume.

  • Vacancy details:
  • Post Name: Quality Assurance / Quality Control
  • Qualification: B.Pharma
  • Experienced :2 to 5 years
  • Salary:₹ 3,00,000 – 4,50,000 P.A.
  • Openings:NA

Job Description: Ozone Pharmaceuticals ltd Hiring For Technician-Production (Injectable) ! 

  • Important Details :
  • Location: Gurgaon/Gurugram
  • Post of date:24/05/2022
  • Contact Person-Sakshee Saini-+91 9910488937 (call between 10 AM to 5 PM)
  • Note:Interested candidates send their updated resume at [email protected]
  • Selection Process: The selection will be on the basis of Interview.

Roles and Responsibilities

  • To prepare SOPs, procedures, formats and amend, revised them time to time as and when required, ensure all
  • SOPs are up to date, make/ amend list of SOPs and share with all employees along with new version number.
  • Actively participate to complete OOS and OOT as per SOP and train others on SOP.
  • Liaise with GLP and QC team to perform hypothesis and closure of OOS, OOT in time.
  • Ensure all Deviations completed in time and document.
  • Ensure all Incidents completed in time with documents, risk assessment along with impact analysis to be done.
  • Responsible for quality review on change control complete as per predefined time line and documented.
  • Prepare documents, SOPs, Procedures, formats in such a way to make compliance for regulatory requirement like FDA, USFDA.
  • Responsible to support in customer audits and NABL, FDA, Ayush, FSSAI and USFDA and ensure zero non-compliance. Read latest guideline and implement.
  • Ensure correct formats are being used in the laboratory and all are controlled no uncontrolled documents available in the lab.
  • All required formats are bind and no loose sheet available in the lab.
  • Ensure latest guidelines are implemented ASAP.
  • Handle customer complaints and make them satisfied by providing technical support and clarifications.
  • Perform deviation, incident, change control and complete CAPA for each customer complaint and documents.
  • Ensure the data, document retrieval and traceability. No data integrity issue left.
  • Prepare TNI and ensure to communicate in time and execute.
  • Responsible to collect the feedback from costumer and its evaluation along with CAPA
  • Issuance, archival and retrieval of documents.
  • Prepare documents, SOPs, Procedures, formats in such a way to make compliance for regulatory requirement like FDA, USFDA.
  • Ensure correct formats are being used in the laboratory and all are controlled no uncontrolled documents available in the lab.
  • Responsible to support in ensuring the validity of test results.

Roles and Responsibilities

  • Responsible for chemical analysis of Pharmaceutical, Herbals, Food, Raw and Finish Products.
  • Responsible for Preparation of SOPs and Maintenance of records & log books related to food section.
  • Responsible for Internal calibration Check of all equipment related to food section.
  • Responsible for Operation & Calibration of other routine equipments.
  • To prepare SOPs / procedures/ formats and amendment/ revised them time to time as and when required, ensure all SOPs are up to date, make/ amendment list of SOPs and share with all employees along with new version number.
  • Developing and validating methods for testing of raw materials, intermediates and finished products, existing products on the stability programme and cleaning validation exercises.
  • To support for preparing Quality reports, including analytical reports (for raw materials and finished products), Certificates of Analysis (COA) (for finished products) and stability reports.
  • To support GLP team for calibrating analytical equipment, as and when required. Supporting all QC activities.
  • To support GLP Team for validation analytical equipment as and when required.
  • To support for validation of master excel sheet used for analytical calculation.
  • To ensure the full compliance of 21 CFR in the analytical equipments used in analytical laboratory.
  • To support and raise the lab requirement and coordinate to purchase team if required.
  • Ensuring that procedures are carried out carefully and accurately to eliminate errors.
  • Ensuring good relations and communications with all members of the team and responding politely and in a timely fashion to internal and external customers.
  • Working with all members of staff to maintain and develop the positive progressive culture within the Laboratory.
  • Observing and complying with Good Documentation Practices, Good laboratory practices and Good review practices.
  • Observing and complying with Data Integrity in laboratory.
  • Observing and complying with company Health and Safety Policies.
  • Observing and complying with company Standard Operating Procedures (SOPs

About Company

 Ozone Pharmaceuticals ltd is a major player in the Gurgaon/Gurugramn pharmaceuticals sector with the vision of becoming a global entity. Torrent Pharma enjoys dominance in the niche therapeutic areas like, cardiovascular and central nervous system, gastro-intestinal, pain management and oral anti-diabetic segments. Torrent Pharma owes its success in the domestic market to its thrust on frontline research, strategic marketing and world-class manufacturing.

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