Team Leader - QC
at Julphar
Ras al-Khaimah, رأس الخيمة, United Arab Emirates -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 18 Jan, 2025 | Not Specified | 19 Oct, 2024 | N/A | Good communication skills | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
Job Description:
- Responsible for the planning and supervision of all QC labs finished products and maintain online compliance in all activities.
- To assign the work for analysts and supervise the analysis of finished products and ensure on time completion of analysis.
- To coordinate with Production plants for planning of analysis.
- Handling and supervision of Technology transfer projects.
- To check and ensure proper usage of all the QC equipment.
- To train the QC personnel on all the applicable procedures, specifications, testing methods and qualify analysts to perform various QC analysis.
- Processing and approve for all HPLC &GC analytical data for all analysts, review and check all the Audit trial for all the instruments.
- To train the QC personnel on all the applicable procedures, specifications, testing methods and qualify analysts to perform various QC analysis.
- To prepare and revise the SOPs and work instructions.
- To ensure the analysis are performed correctly as per applicable procedures and the raw data is checked for correctness, accuracy and compliance.
- To perform investigation for the lab incidents, OOS, OOL results, deviations and take appropriate corrective and preventive actions.
- Follow up &Close all the EQMS actions ( CAPA , OOS , Deviations , CCF )
- To lock the results in SAP, to create notifications & reservations for maintaining enough stock of chemicals & consumables.
- To involve and support in external and internal audits and to close the audit observations on time.
- Review and approve protocols and reports such as method validation, method transfer, process validation and stability.
- To handle and close the Quality management system actions like Deviations, OOS, CAPAs, AMS and Change controls using Amplelogic system.
- To follow and ensure data integrity and good documentation practices are implemented in the QC labs.
- To ensure and follow GLP, GMP, safety procedures and maintain hygienic conditions in lab.
- Shall be authorized designee for responsibilities of QC Sr Manager.
- Apart from above, the works assigned by the Head of the department/designee.
Core Competencies:
- Bachelor’s degree in Pharmacy / Science.
- Proficient with computer software application
- In terms of competency you are highly result oriented with strong sense of accountability & ownership.
- High on communication and collaboration, having an ability to manage multiple stakeholders at a time.
- Strong eye for details, having expertise to understand, review and implement the compliance inputs from Quality point of view.
- In-depth knowledge of the industry’s standards and regulations guidelines excellent knowledge of reporting procedures and record keeping.
- Must be able to manage tasks and priorities and easily adapt to changing situations.
- Ability to create cross functional relations and manage conflicts.
- Problem Solving and high agility on taking right scientific decisions.
Responsibilities:
Please refer the Job description for details
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Pharmacy science
Proficient
1
Ras al-Khaimah, United Arab Emirates