Quality Control Jobs

As a Quality Assurance Engineer, you will be responsible for ensuring the quality and performance of our products through rigorous testing and evaluation.**Key Responsibilities:**- **Test Planning:** Create and implement detailed test plans that outline the scope, approach, resources, and schedule for testing activities, ensuring all aspects of the product are covered.- **Test Case Development:** Design and write clear and comprehensive test cases based on product specifications, to effectively evaluate functionality and identify any issues.- **Manual Testing:** Execute manual tests on software and applications to confirm performance, usability, and reliability meet our quality standards.- **Bug Reporting:** Identify, document, and track defects in a clear and concise manner, collaborating with the development team to ensure timely issue resolution.- **Regression Testing:** Conduct regression testing after fixes or enhancements to confirm that no new issues have been introduced and that existing functionality works as intended.- **Collaboration:** Work closely with developers and other team members to understand product requirements and provide feedback on areas for improvement.**Required Skills and Expectations:**Candidates should possess strong attention to detail and analytical thinking skills to identify problems and propose solutions. You should have basic knowledge of software development processes and testing methodologies. Effective communication skills are essential for collaborating with team members and reporting findings. A willingness to learn and adapt in a fast-paced environment is important, especially for those with less experience.

Designation :- OfficerDepartment:- Quality Assurance Qualification:- B.Pharma/M.PharmaExperience :- 2 Years To 3 Years Salary:- As Per Interview Gender:- Male Key Responsibilities:- i) To review all documents pertaining to vendor qualification and maintain the same in proper order and ensure proper filing for easy traceability.ii) To prepare and update approved vendor list as per schedule and distribute the same to concern departments.iii) To handle all pre shipment samples from new vendors for its documents and submission to QC.iv) Review and Handling of Documents for Qualification of API, RM and PM Vendors.v) Preparation and review of Vendor SOP and associated formats related to Vendor SOP.vi) To communicate with vendor with respect to any non-conformance and to obtain required Corrective Action and Preventive Action from vendor based on Audit report or CAPA received from vendor/ prepared Audit Closer documents.vii) To prepare Audit Closer documents.viii) To evaluate excipients vendor documents for the preparation of Quality Risk Management and evaluate the requirement of audits.ix) Archival of documents in respective file (received from vendor).x) Maintaining tracker and coordination with purchase and DQA team at R & D for any documents that is expired or not received.xi) Distribution of vendor qualification documents to the concerned department as an when required.Job Location:- Vapi, Gujarat Industry:- Reputed Manufacturing Industry

Company: Aevia HRWorkplace: RemoteJob location: New York, United States of America (USA)Work type: Full-time.Position: Data Entry Clerk We are seeking a meticulous and dedicated Data Entry Clerk to join our dynamic team. In this role, you will be responsible for accurately inputting and managing critical data that supports our operations and ensures the highest standards of quality and compliance. The ideal candidate will have a keen eye for detail, exceptional organizational skills, and the ability to handle sensitive information with confidentiality. Responsibilities

key Responsibilities:Oversee daily business operations and process efficiencyManage teams, budgets, and performance metricsEnsure smooth workflow and operational excellenceBrief Summary:Drives operational efficiency and ensures business processes run effectively.

Responsible for ensuring quality standards in the manufacturing of HDPE Pipe and components. The role includes monitoring raw materials, in-process production, and finished goods to ensure they meet technical specifications and industry standards.

As a Senior Biomedical Engineer, you will play a crucial role in developing and maintaining medical devices and systems. Your expertise will ensure that healthcare technologies are safe, effective, and innovative. **Key Responsibilities:**- **Design and Development:** Create and improve biomedical devices, ensuring they meet regulatory standards and patient needs. This includes working on prototypes and testing equipment for functionality.- **Testing and Validation:** Conduct rigorous testing to validate that devices perform as intended. This involves analyzing data and troubleshooting any issues that arise during testing.- **Collaboration with Healthcare Professionals:** Work closely with doctors, nurses, and other health professionals to understand their needs and incorporate their feedback into product designs, leading to enhanced patient care.- **Technical Support:** Provide ongoing technical support and training for users of biomedical equipment. This includes troubleshooting any operational issues and guiding users on proper usage.- **Regulatory Compliance:** Ensure that all products comply with relevant health and safety regulations. Keep up to date with industry standards to maintain compliance.**Required Skills and Expectations:**Candidates should have a solid background in biomedical engineering with 3 to 9 years of experience. A strong understanding of engineering principles, design software, and medical device regulations is essential. You should possess excellent problem-solving skills and be able to work independently as well as part of a team. Good communication skills are necessary to effectively liaise with various stakeholders. A passion for improving healthcare technology and a commitment to patient safety will set you apart in this role.

We are seeking a skilled Moulding Engineer with 3 to 7 years of experience to join our team in Mahalunge, Pune. This role involves designing and managing the production of moulds for various applications, ensuring high-quality output.Key Responsibilities:1. **Mould Design and Development**: Create detailed designs and specifications for new moulds, using standard engineering software and tools to ensure precision and efficiency.2. **Production Oversight**: Supervise the moulding process to maintain quality standards, ensuring that the production schedule meets deadlines while adhering to safety and compliance regulations.3. **Troubleshooting and Maintenance**: Identify any issues during the moulding process and implement effective solutions to minimize downtime and enhance production efficiency.4. **Collaboration**: Work closely with the production team and other engineers to refine processes and improve overall operational performance.5. **Quality Control**: Conduct inspections and tests on moulds to ensure they meet industry standards and customer specifications.Required Skills and Expectations:Candidates should possess a degree in engineering and have strong analytical and problem-solving skills. Proficiency in moulding techniques, materials, and manufacturing processes is essential. The ideal candidate must have excellent communication skills and be able to work well in a team environment, demonstrating leadership qualities when needed. Attention to detail and the ability to multitask in a fast-paced setting are crucial for this position.

Company DescriptionTrueZenix is a trusted transformation partner for Pharma and Life Sciences industries, specializing in innovation, compliance, and efficiency. With expertise in Consulting, Lean Labs, AI services, and Smart Labs grounded in Industry 4.0 principles, TrueZenix empowers clients to achieve faster, safer, and smarter operations. Their technology solutions include AI-enabled platforms for Validation, Risk Assessment, and Audit Management, offering enhanced compliance and predictive insights while reducing manual efforts. TrueZenixs offerings span multiple platforms such as ServiceNow, Salesforce, LIMS, and MES, ensuring a blend of digital innovation and domain knowledge. As a strategic partner, TrueZenix is committed to delivering measurable benefits, enabling businesses to thrive in a competitive and regulated landscape.Role DescriptionThis is a full-time on-site position located in Hyderabad for the Caliber LIMS (Internship QC transitioning to Fulltime over a span of two years) role. The intern will gain hands-on experience with Quality Control (QC) workflows, assist in implementing and utilizing Lab Information Management Systems (LIMS), and support quality management efforts within the pharmaceutical and life sciences domain. Responsibilities include executing quality assurance activities, ensuring Good Manufacturing Practices (GMP), and participating in quality audits to maintain compliance. Successful candidates will have opportunities to transition to a permanent role based on performance and organizational needs.QualificationsProficiency in Quality Control processes and Good Manufacturing Practices (GMP)Experience or knowledge in Quality Assurance, Quality Auditing, and Quality Management principlesStrong analytical and problem-solving skills related to quality and compliance activitiesAbility to work with Lab Information Management Systems (LIMS) and other digital quality management toolsDetail-oriented mindset and excellent organizational skillsBasic understanding of pharmaceutical and life sciences operations is a plusBachelors degree in Life Sciences, Pharmacy, Chemistry, Engineering, or a related field 5 months to 2 years of relevant QC experience Ready to work from Hyderabad (No WFH) Immediate availability preferred Must have excellent english communication skills and QC Skills.send your updated CV (PDF)Subject Line: Application for Caliber MDM - QCPlease include the following details in your email: Total & Relevant Experience Reason for Job Change Notice Period Current Location Educational Qualification Last/Current Organization Current & Expected CTCShortlisted candidates will be contacted for the next steps.Follow TrueZeniX Services Private Limited in LinkedIn for more updates Dont miss this opportunity apply now or share with someone who fits!

Designation :- Lab Assistant ( Documentation) Qualification:- BSC chemistry, Physics, Organic chemistry Experience :- Fresher to 1 YearsSalary:- As per interview Gender:- Male or Female Job Time:- 09:00 AM 06:00 PMJob Location :- Boiser Interview Location - VirarIndustry:- Service Company

Designation :- QA HeadQualification:- Bsc, MSc Chemistry,D Pharm,B PharmExperience :- 10 to 15 Year Exp in Pharma And Camical Background Salary:- 13 LPA to 14 LPA Gender:- Male Job Time :- General ShiftJob Location :- Palghar, Maharashtra

Designation :- Lab AssistantQualification:- BSc Or MSc Or D.Pharma/B. Pharma Experience:- Fresher To 1 YearsSalary:- As Per InterviewGender:- MaleJob Time:- 09:00 Am To 05:30/06:00 PmJob Location:- Umbergaon, Gujarat Area Of Work:- Pan IndiaIndustry:- Manufacturing Company