Qa manual testing jobs in Ankleshwar

 ...Summarize the main purpose of the role Analyze quality standards for components, materials or services. Apply measures, sampling methods, testing methodology and other procedures that ensure that quality standards are met. Main Responsibilities List the main... 

Preferred candidate profile Education : M.Sc- Chemistry Experience : 10 to 15+ years of exp in API Pharma Industry experience. Job Profile : Quality professional with 10+ years of progressive experience with strong knowledge of Specialty Ingredient, Bulk Chemicals...

 ...in a regulatory-approved OSD manufacturing large unit. Job Responsibilities & Accountabilities We are looking for an experienced QA professional to join our team and lead Deviation & Complaint Investigations, along with core QMS activities. Key Responsibilities... 

 ...Job description for the Assistant Manager, Quality Assurance (QA)  We at Alchemie Finechem Pvt. Ltd. (Aarti Group) are looking for an experienced and dedicated  Assistant Manager, Quality Assurance to join our team in the  Quality Assurance department! If you have a strong... 

 ...Position title: ESO QA Specialist University degree in Pharmacy, Chemistry, Biology, or relevant Life Science Minimum of 5 years in a similar role or equivalent experience in a GMP-related environment Job location - Ankleshwar, Gujarat, India MISSION STATEMENT... 

 ...procurement process with the Client. Responsible for installation, testing and commissioning of equipment related to all service (...  ...as per vendor contracts, receipt of all relevant documents like manuals and test certificates, as built drawings. Need to follow all the... 

 ...POSITION PURPOSE The QA Portfolio Development Manager ESO manages all quality aspects of projects aimed to develop the portfolio of ESO products. Participates to launch management meetings and provides quality evaluation for projects lead by BD (In Licensing department and... 

Job Description Position: Quality Alert Expert Mandatory Requirements ~ Graduated / Post-graduate in Pharmacy/Medicine or Chemistry ~10 to 12 years minimum experience in Quality or Regulatory Affairs ~ Experience obtained in pharmaceutical manufacturing sites...

Ensure compliance with quality standards and regulatory requirements Perform quality checks and audits on raw materials, in-process, and finished products Monitor production processes to maintain product quality Prepare and maintain quality documentation and reports...

Key Responsibilities (Performance Indicators) Regularize the QC activities as per cGMP requirements. Regulatory and Pharmacopeia requirement for lab compliance. Review of hybrid and electronic data for IPQC and FG analysis.; Analytical method validation, OOS and ...

 ...with core QMS activities pertaining to QC. Key Responsibilities Trigger out of specification investigations upon detection of test results outside predefined specifications. Design and execute tests to confirm or rule out suspected root causes. Handling QMS... 

Job Title: Sr. Executive - Quality Compliance (Supplier Quality Assurance) Department: Quality Compliance Reports to: Quality Compliance Manager Location: Ankleshwar Position Type: Full-time Qualifications And Experience Education: B.Pharm / M.Pharm...

Job Description For Executive - Quality Assurance, Pharma Educational Qualification ~ B. Pharm / M. Pharm from a reputed university Experience ~1 to 4 years of similar experience in a regulatory-approved OSD manufacturing large unit. Quality Management...

Key Responsibilities Quality professional with 15.0+ years of progressive experience with strong knowledge of Speciality Ingredient, Bulk Chemicals, Food additive/ Food supplement and API Manufacturing, QMS, Qualification, Validation and other Manufacturing functions.; ...

 ...goals - Your path Responsible for performing and supervising the testing of Epoxy/Concrete/Mortar/Admixture/Flooring/RM and PM as per the...  ...and Measurement of product procedure' mentioned in our Quality Manual is followed in his location. Responsible for the calibration of... 

 ...one-stop solution for all your research and development needs. Role Description This is a full-time, on-site role for an OECD GLP QA Auditor located in Kim, Surat. The OECD GLP QA Auditor will be responsible for conducting study based/process based/facility based... 

 ...Practices, Safety and Good Housekeeping requirements. For review testing of Raw Materials like Tubes, Chemical for treatment, etc. &...  ...procedure within the plant. Revises and updates the Quality Systems Manual to ensure the program continues to be suitable and effective so... 

 ...is not mandatory, but strong programming logic and a willingness to learn are essential. Key Responsibilities: Design, develop, test, and maintain windows desktop applications using VB.Net and SQL Server. Work with databases to design schemas, write queries, and...