Executive - Quality Control Desirous Global Consulting

2.0 - 6.0 years

0 Lacs

chennai, tamil nadu

On-site

You will be responsible for analyzing raw materials, in-process, and finished product stability samples of various formulation products such as oral solids and injectable ophthalmic products. This includes utilizing QC Instruments like HPLC, GC, UV, FTIR, pH Meter, etc. You should have exposure to software like Empowers and Labware LIMS and possess knowledge of GLP GDP practices. Your role will involve executing validation, qualification, and calibration activities in the QC laboratory, as well as preparing SOPs, GTPs, STPs, specifications, protocols, IOCPs, records of analysis, and analysis reports. You will also be responsible for handling, issuing, and maintaining consumables, glassware, chemicals, reference standards, working standards, and cinematographic columns. Candidates with exposure to regulatory audits like USFDA will be preferred. Additionally, you will be required to review various types of samples and documents, including raw materials, finished products, stability samples, qualification documents, and calibration AMT documents. Your responsibilities will also include investigating OOS test results and laboratory incidents, as well as ensuring compliance with safety standards and maintaining Good Laboratory Practices at all times.,

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Mechanical Draughtsman cum QC Engineer Virani Dynamics LLP

2.0 - 6.0 years

0 Lacs

surat, gujarat

On-site

You will be joining a team of innovative and creative individuals who are dedicated to providing core Research and Development for new products and technical support to our affiliated companies such as Jyoti CNC Automation in Rajkot and KARP Group in Surat. Our office is based in Surat city and we are currently seeking a Mechanical Draughtsman cum QC Engineer to fulfill the following responsibilities. As a Mechanical Draughtsman, your main tasks will involve creating detailed and precise technical drawings utilizing computer-aided design (CAD) software or traditional drafting tools. These drawings will encompass plans, elevations, sections, and detailed views of mechanical components. In addition, you should be proficient in operating QC instruments like Vernier Caliper, Height gauge, Micrometer, Dial gauges, and possess knowledge in interpreting technical drawings with GD&T. Familiarity with workshop machines and manufacturing processes is also essential. Key Responsibilities: - Develop detailed 2D and 3D technical drawings using CAD software. - Transform rough sketches, specifications, and verbal instructions into accurate drawings. - Ensure drawings meet industry standards, regulations, and project specifications. - Incorporate feedback and revisions into drawings based on input from senior team members. Quality Control Responsibilities: - Measure and prepare QC reports for manufactured parts. - Maintain thorough documentation related to quality control processes, test outcomes, and corrective actions. Candidate Profile: Education: Bachelor's degree or Diploma in Mechanical Engineering from a reputable institution. Experience: Minimum of 2 years of relevant experience. Software Skills: Proficiency in PTC Creo, AutoCAD, Microsoft Office, etc. Location: Virani Dynamics LLP, Surat, Gujarat. Working Hours: 9:00 am to 6:00 pm. Salary: Commensurate with experience. This is a full-time, permanent position with benefits such as provided meals. The work schedule is during day shift and on-site.,

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Manager_Analytical Data Reviewer Spectrum Talent Management

8.0 - 13.0 years

10 - 15 Lacs

Mumbai

Work from Office

Role & responsibilities :- Job overview :- The role requires strong analytical data review skills and experience with various QC instruments . The position involves supporting their North American sites , Potentially requiring the candidate to work according to US time zone. Key Responsibilities & Required Experience: Strong exposure to Analytical Data Review and electronic data review from QC instruments such as HPLC, GC, Dissolution Apparatus, and Malvern 3000 Thorough understanding of Quality Control investigations, including Lab Incidents, OOS, and OOT Preparation and Review of Method validation, Method Transfer, Method Verification and Equivalency documents, etc Review of Analytical raw data, Chromatography, and LIMS for Raw Materials/In-process/Finished Products. Preparation and Review of new SOPs. Candidates must have relevant experience in Oral Solid Dosage (OSD) formulations and/or Active Pharmaceutical Ingredient (API) processes. Kindly note the following: The selected candidate will support one of their sites in North America and will be required to work as per the US time zone . Strong communication skills are essential for this role.

Posted 3 months ago

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Quality Control Supervisor ( Pharma / FMCG) Holistic Solutions India

2.0 - 3.0 years

3 - 4 Lacs

Hyderabad

Work from Office

B.Sc, 2+ yrs Exp in QC in Pharma / FMCG Industry Sampling & Analysis of Raw Material, In Process Material & Finish Product Maintaining & Calibrating QC Instruments Conditioning& Casing Cylender Moisture & Temparatures Maintaining Chemical Flow Meters Required Candidate profile B.Sc with 2+ yrs Exp in QC in Pharma / FMCG Industry Sampling & Analysis of Raw Material, In Process Material & Finish Product Maintaining & Calibrating QC Instruments Chemical Flow Meters Temparature

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