Name: Jobpe
Address: T-Hub, Plot No 1/C, Sy No 83/1, Raidurgam panmaktha, Knowledge City Rd, Hyderabad, Telangana, 500081, IN
Telephone: +91-83339-09630
Price range: Free

Engineer - CMM Quality / Lab QA (Tier1 European Auto MNC) 5LPA Max Adonis Recruitment Consultants

4.0 - 6.0 years

4 - 5 Lacs

Chengalpattu, Chennai

Work from Office

Focus on IN-PROCESS QUALITY INSPECTION, CMM INSPECTION, CALIBRATION, QMS, MEASURING INSTRUMENTS, DRAWING SPECIFICATIONS, GD&T, DAILY REJECTION MONITORING, 8D, 7QC, CFT ACTIVITIES, LAYERED PROCESS AUDIT, PROCESS AUDIT, PRODUCT AUDIT, SPC, GARAGE R&R.. Required Candidate profile DIP/BE 4+yrs exp into CMM QA / Lab QA handling CMM INSPECTION, CALIBRATION, QMS, MEASURING INSTRUMENTS, DRAWING SPECIFICATIONS, GD&T, 8D, 7QC, CFT ACTIVITIES, LAYERED PROCESS AUDIT, IPB, IQF, FTT etc Perks and benefits Excellent Perks. Send CV to adonis@adonisstaff.in

Posted 2 days ago

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Scientist - F&D - Technology Transfer - EU Market Unison Pharmaceuticals

3.0 - 8.0 years

3 - 7 Lacs

Ahmedabad

Work from Office

Great Opportunity to work with one of the fastest growing Pharmaceuticals in India!! About us: Unison Pharmaceuticals Private Limited (Formerly known as Unison Pharmaceuticals) was established in 1981 with a vision of providing quality and affordable medicines across the nation. With more than 4 decades of medical service to society, Unison is today one of the fastest-growing companies in Gujarat State. In addition to this, the company is ranked 82 among the top companies of India (Rupee wise sales) MAT March 2020. This makes Unison a distinguished company across the pharma industry. We are expanding our team!! Looking for passionate Formulation Scientist - Technology Transfer - EU market at our dedicated R&D center. Department : Formulation Development - Technology Transfer Formulation : Solid Orals Market : Europe Experience Required : 4-7 years Designation : Sr. Officer / Executive / Sr. Executive Location : R&D Center, Moraiya, Ahmedabad (Transportation from specific route if Ahmedabad is provided) Roles & responsibilities (Not Limited to): Execution of Scale-up, exhibit batches, validation batches for Regulated market products Feasibility trial, evaluation, execution of commercial validation batches for site variation contract manufacturing projects Document preparation, review related to SU/EB and validation batches Perks & Benefits: Dynamic work environment Career development opportunities Work-life balance Free transportation Canteen facility Free insurance coverage for self, spouse, and kids Range of learning opportunities to help employees grow and thrive If you are passionate about continuing to work in the pharmaceutical R&D and possess the required skills & experience, we encourage you to apply for this position. Interested one can revert with their resume on career@unisonpharmaceuticals.com Regards, Team HR

Posted 1 week ago

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Assistant Manager/ Deputy Manager - Production SV Management Consultants

10.0 - 14.0 years

6 - 16 Lacs

Bengaluru

Work from Office

Delivering Gate performances (SQDCEP) KPI in line with Departmental objectives Secure / improve the Safe Work Environment (with PPE adherence) Securing FTT (First Time Through) & control the Product Audit Remarks Securing the Delivery as per Customer delivery committment Encourage team towards Improvements with Cost savings implementation Maintaining 5S (Good House Keeping Practices) & Maintaining team's balanced leave plan Resource and Facility Management Evaluate theoretical volume capacities and recommend appropriate manning requirements Responsible for securing the Multi model mix with same takt time adherence Responsible for planning and securing the Tools, Fixtures etc. Lead & participate productivity improvements to reduce the manufacturing lead time Competence development with Contingency plan Securing Competence plan (Skill Matrix - 3:3:3) Identify/bridge the knowledge gap by securing respective Training Review and display the update Process documents maintenance Responsible for Work activity conclusion & Secure/Maintain the PCC/PIS/PCN document Responsible for Work/Method study to release/Maintain the SWS/OBC document Responsible for Man hour norms for all regular and project vehicles Responsible for Process audits & review on actions Responsible for Special process audit & review on actions Team development Handling Team grievance Responsible to appraise, giving constructive feedback on performance Support, guide and motivate team members towards our culture, way of working Support in continuous improvement on Function level Implementing IMS requirements Responsible for securing the Quality systems requirements Responsible for HIRA study Securing Environmental (Aspect/Impact study) requirements

Posted 3 weeks ago

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