Quality Control Job Vacancies in Panchkula

Ensuring all QC activities adhere to GMP (Good Manufacturing Practices), GLP (Good Laboratory Practices), and other relevant regulations. Maintaining accurate and complete QC documentation, including test reports, logs, and records. Participating in internal and external audits to ensure regulatory compliance. Supporting method validation, calibration, and equipment qualification activities. Testing and Analysis:Performing sampling, testing, and analysis of raw materials, in-process, and finished injectable products. Operating and maintaining laboratory instruments, such as HPLC, GC, UV, etc. Conducting stability studies to assess the shelf life of injectable products. Problem Solving and Improvement:Identifying and reporting deviations from quality standards, ensuring corrective and preventive actions (CAPA) are taken. Collaborating with production, QA, and other teams to resolve quality-related issues. Participating in the investigation of batch failures and OOS (Out of Specification) situations. Supporting the development and implementation of quality control systems. Supervision and Training:Supervising QC inspectors and ensuring they adhere to SOPs (Standard Operating Procedures). Providing training to QC staff on relevant procedures and techniques. Documentation and Reporting:Preparing and maintaining test reports, logs, and other QC documentation. Ensuring the timely completion and traceability of all testing activities. Maintaining accurate records of all QC data and results.

We are looking for a Quality Control Executive to ensure our products meet high standards of quality. The ideal candidate will have 3 to 6 years of experience in quality control and will be a proactive individual dedicated to maintaining excellence in product standards. Key Responsibilities:1. **Inspection of Products:** Conduct thorough inspections on finished products to identify any defects or deviations from quality standards. This involves using specific measurement tools and techniques to ensure compliance.2. **Testing Procedures:** Execute detailed testing procedures to assess product functionality and safety. This includes both physical tests and analytical methods to confirm product integrity.3. **Quality Documentation:** Maintain accurate records of quality checks and inspections. Document any non-conformance and generate reports to help improve processes. 4. **Collaboration with Teams:** Work closely with production and supply chain teams to provide quality feedback and ensure adherence to quality standards throughout the manufacturing process.5. **Continuous Improvement:** Contribute to the development and implementation of quality improvement initiatives. Stay updated on industry trends to enhance quality control processes.Required Skills and Expectations:The candidate must have a strong attention to detail and the ability to identify subtle differences in products. Effective communication skills are essential for working with various teams and presenting findings clearly. Candidates must also demonstrate problem-solving abilities and a commitment to maintaining high standards in a fast-paced environment. A graduate degree is required, and preference is given to male candidates for this role.

We are seeking a dedicated Quality Control Analyst to join our team in Nalagarh. The ideal candidate will have 2 to 4 years of experience and possess a degree in B.Pharma or B.Sc. This role requires a strong focus on ensuring product quality and compliance with regulatory standards.**Key Responsibilities:**- **Conduct Testing**: Perform various tests on raw materials and finished products to ensure they meet quality specifications. This includes physical, chemical, and microbiological analysis.- **Documentation and Reporting**: Maintain accurate records of test results and document deviations or issues. Timely reporting helps in identifying trends and implementing improvements.- **Quality Assurance Compliance**: Assist in maintaining compliance with quality standards and regulations set by industry and government bodies. This includes understanding and following standard operating procedures (SOPs).- **Collaboration with Teams**: Work closely with production and R&D teams to address quality-related concerns. Effective communication is essential for improving processes and products.- **Problem-Solving**: Identify root causes of quality issues and propose corrective actions. This analytical approach aims to prevent reoccurrence of defects.**Required Skills and Expectations:**Candidates must have strong analytical and critical thinking skills to assess complex quality issues effectively. Attention to detail is essential to ensure accurate testing and documentation. Knowledge of quality control regulations and practices is required. Proficiency in software applications for data analysis and reporting is preferred. A collaborative mindset is crucial for working well within a team. Candidates should also demonstrate a commitment to continuous learning and improvement in quality processes.

Location: On-site Nalagarh, Himachal PradeshExperience: 12 years (Mandatory)Qualification: B.Sc. in Chemistry / Microbiology / Biotechnology / Life SciencesAbout the Role:We are looking for a dedicated Quality Control (QC) Officer to join our pharmaceutical manufacturing team at our Nalagarh facility. The ideal candidate will have hands-on experience with laboratory testing and strong documentation practices in a GMP-regulated environment.Key Responsibilities:Conduct testing of raw materials, in-process samples, and finished products.Operate and maintain analytical instruments like HPLC, UV, IR, pH meter, etc.Ensure accurate and timely documentation as per cGMP and GLP guidelines.Perform stability studies and environmental monitoring (if required).Participate in lab audits, calibration, and equipment qualification.Maintain safety and hygiene in the lab environment.Desired Profile:B.Sc. in Chemistry / Microbiology / Biotechnology or relevant field12 years of QC experience in a pharmaceutical formulation unit (mandatory)Sound knowledge of GMP practices and analytical techniquesAttention to detail, good documentation habits, and strong analytical skillsMandatory Proficiency in written and verbal EnglishJoin a team committed to delivering high-quality, affordable medicines.Apply now to become part of our quality-driven organization!#QualityControl #PharmaJobs #ChemistryJobs #QCOfficer #PharmaceuticalIndustry #HimachalJobs #BScJobs #NalagarhJobs #PharmaCareers #GMPCompliance

Organization Name Grow Up Services Industry Type PHARMA / ELECTRICAL 3 No Of Position /Vacancies 500(FIVE HUNDRED ONLY) 4 Location Of the Job SEC 2,PARWANOO,DISTT.SOLAN,H.P. 1732205 Nature Of the job QC6Jd and KRA for the candidates=Detailed Brief of the job role - roles & Responsibilities QC7 Skills that are expected Reading Skill Any proficiency-need to be stated. No 9 Behavioural Skills expected Yes10 Behavioural Skills expected Yes11 Working Hours (shift timings) 8hours + OT(AS PER COMPANY REQUIREMENT) 100RS PER HOUR)12 Contact Person Name Chanchal Gupta, Shiva13 Contact Number +91-9045034151, 930637337414 Salary for 8 Hrs 14000rs15 PF/ESI Deduction (yes/no) yes 16 Dress code ( Who will provide dress or any deduction for dress code ) No, Over Coat will be given 17 Meal facility (YES / NO) Yes18 Mandatory Requisites ( Bike, Driving License) NO19 Minimum Qualification DMLT,D.pharma,B.pharma,B.Sc & M.Sc20 What is the mode of Salary (A/c transfer or Cash) Transfer

Designation: Quality Control ExecutiveQualification: Diploma/Degree in printing and Packaging.Reporting To: QC Team lead.Experience: Minimum 3-4 years. (Preferably in quality and production department)CTC Cost : 4 to 5.5 LacsSkills Needed:Computer literateOn site job approvalsKnowledge of colour ManagementExperience in offset/ Flexo paper base printing.

Sample Preparation and Analysis:- Prepare samples for analysis using various techniques, such as extraction, digestion, filtration, and dilution.- Perform analytical testing and characterization of samples using a wide range of analytical techniques and instrumentation, including HPLC, GC and UV-Vis, to determine chemical composition, identify impurities, and assess product quality.Data Interpretation and Reporting:- Analyse the experimental data, interpret results, and draw conclusions based on statistical analysis, and quality control criteria to support analytical findings and troubleshoot analytical issues.Instrument Maintenance and Calibration:- Maintain analytical instruments and equipment in proper working condition by performing routine maintenance, troubleshooting instrument malfunctions, and calibrating instruments according to manufacturer specifications to ensure data accuracy and instrument reliability.- Evaluate instrument performance, monitor quality control parameters, and implement corrective actions as needed to address deviations, minimize variability, and maintain analytical accuracy and precision.Quality Assurance and Compliance:Male Candidate OnlyBackground must be from Pharmaceutical Company

We are looking for 5 Quality Control Pharma Posts in Baddi with deep knowledge in Should have BSc of Msc in Microbiology and Required Educational Qualification is : B.Sc, M.Sc

Quality Assurance and Iso Documentation, Quality Standards Tools Tec, the job location is Rajpura

Walkin Interview Going On Baddi Pharmaceuticals Company..required Qa ( Ipqa ,Document Ion )production Executive /production Chemistqc Executive /microbiology qualification- Msc Chemistry ,Microbiologybsc,M Pharma/ B Pharmahr -luxmi

We are Looking for Quality Control Chemist. Analytical Testing & Documentation Experience in Tablet, Capsule & Liquid Oral Sections in Some Pharmaceutical Manufacturing Unit.