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Showing posts with the label ISO 13485 Jobs

Vickro Biopharma Production Jobs in Hyderabad for Freshers | B.Sc & M.Sc Candidates Apply

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Vickro Biopharma Production Jobs in Hyderabad for Freshers | B.Sc & M.Sc Candidates Apply (Vickro Biopharma Production Jobs) Introduction Vickro Biopharma has announced new Production job openings at its Hyderabad facility for candidates looking to build a career in probiotics and nutraceutical manufacturing. This opportunity is suitable for both freshers and professionals with up to 3 years of experience. Candidates with B.Sc or M.Sc qualifications from a science background can apply for these Production positions. The role offers practical exposure to fermentation processes, production equipment operation, manufacturing documentation, cGMP practices, media preparation, culture maintenance, and nutraceutical manufacturing operations. For candidates searching for freshers pharma jobs in Hyderabad, production jobs for B.Sc graduates, microbiology jobs, biotechnology jobs, fermentation jobs, and nutraceutical manufacturing careers, this recruitment opportunity may provide valuabl...

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Caldor Health Technologies Hiring Quality & Regulatory Associate | 0–3 Years | Coimbatore

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Caldor Health Technologies Hiring Quality & Regulatory Associate | Freshers & Experienced Candidates Can Apply (Caldor Health Technologies Hiring Quality & Regulatory Associate) Introduction Caldor Health Technologies has announced an excellent career opportunity for candidates interested in Medical Device Quality Assurance and Regulatory Affairs. The company is currently hiring for the position of Quality & Regulatory Associate at its Coimbatore location. This opportunity is suitable for fresh graduates as well as professionals with up to 3 years of experience who want to build a career in medical device compliance, quality systems, regulatory documentation, risk management, and product lifecycle management. Professionals interested in ISO 13485 Quality Management Systems, CDSCO regulations, Design History Files (DHF), Device Master Files (DMF), and medical device regulatory submissions may find this role highly valuable for long-term career growth. About C...

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