Register Here to Apply for Jobs or Post Jobs. X

QA Validation Specialist - Sterile Dosage Forms

Job in UAE/Dubai
Note that applications are not being accepted from your jurisdiction for this job currently via this jobsite. Candidate preferences are the decision of the Employer or Recruiting Agent, and are controlled by them alone.
For jobs on this site that accept applications from your location / country,
Company: Julphar
Full Time position
Listed on 2020-09-25
Job specializations:
  • Pharmaceutical
    Validation Engineer
  • Manufacturing
    Validation Engineer
Job Description & How to Apply Below
Location: Ras Al-Khaimah

Job Description:

Purpose: The QA Validation Specialist will adhere with the cGMP principles and perform Qualification and Validations as per approved master plan. Key responsibilities & Accountability: Responsible for the preparation and review of validation documentation (Protocols and Reports) and SOPs to support site validation activities. Conducts validation activities for Process and cleaning. Supports and monitors Media fill simulation activities. Conducts validation activities of equipment such as Autoclave, Tunnel Sterilizer, Lyophilizer, Terminal Sterilizer, Vial washing machine, vessels CIP/SIP, filling and capping machine, etc. Conducts validation activities of Utilities such as HVAC, Water System, Compressed Air and Nitrogen gas. Involve in product hold time activities. Temperature mapping studies of storage facilities. Perform all activities in compliance with safety standards and SOPs.  Qualifications: - Education Bachelor / Master degree in Science/Pharmacy/Engineering - Experience: 3-5 years in pharmaceutical industry in qualification/validation sections sterile manufacturing. Real Time Experience in the companies having GMP approval from USFDA/MHRA/TGA/ANVISA/EU authorities. - Training: Key Competencies: Flexible to work in all shifts and not sensitive to B-Lactams. Strong written and verbal communication skills for English language. Honesty & Integrity Self-confident. Technical Competencies: Basic IT skills and knowledge in Microsoft office (word, excel, etc.)Technical Documents (Protocols & Reports) writing in English. Knowledgeable with Pharmaceutical cGMP guidelines, qualifications and validations.
Position Requirements
Less than 1 Year work experience
Note that applications are not being accepted from your jurisdiction for this job currently via this jobsite. Candidate preferences are the decision of the Employer or Recruiting Agent, and are controlled by them alone.
For jobs on this site that accept applications from your location / country,
Search for further Jobs Here:
(Enter less keywords for more results. Suggestions may be selected)
Location
Employment Category
Education (minimum level)
Filters
Education Level
Experience Level (years)
Posted in last:
LOGIN Area - Jobsite