Team Leader - QC

at  Julphar

Ras al-Khaimah, رأس الخيمة, United Arab Emirates -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate18 Jan, 2025Not Specified19 Oct, 2024N/AGood communication skillsNoNo
Add to Wishlist Apply All Jobs
Required Visa Status:
CitizenGC
US CitizenStudent Visa
H1BCPT
OPTH4 Spouse of H1B
GC Green Card
Employment Type:
Full TimePart Time
PermanentIndependent - 1099
Contract – W2C2H Independent
C2H W2Contract – 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