162 Biologics Jobs - Page 7

Dear Candidate , we are hiring for Down Stream Process Executives & Operators Position . Experiance in handling the following Equipment Qualification: Bsc/Msc/ITI/B Pharmacy • M Pharmacy/Diploma/Btech/Any Degree 1 Chromatography column and system handling. 2 Column Packing (BPG And Chromoflow) 3 TFF System 4 Centrifuge system 5 Filtration, Filter Integrity,Buffer Preparation, CIP_SIP 6 Expertise in documentation QMS/GMP Compliance/Process Awareness Male Candidates & Biologics Company's only Preferable. "IMMEDIATE JOINERS ARE PREFERABLE"

Job Context: To support MIBG I-131 clinical programs and other JDI innovative products in the pipeline, The Regulatory Specialist will be reporting to the director of Regulatory Affairs and support the development of regulatory strategies related to JDI clinical programs, marketing applications in US and Canada and post-marketing activities. Challenges: 3. SCOPE and SIZE OF THE ROLE (Please indicate key metrics defining the size and scope of the role) Revenue / Operating Budget As per JDI RA budget plans Geographical Responsibilities (Global / International / Country / Area with in Country Will work with the team in Canada and based out of India Area of Impact (Dept. Location / Function or B...

ONLY FOR MALE CANDIDATES 2 TO 10 YRS EXPERIANCE IN BIOPHARMACEUTICAL SECTOR JOINING BONUS:25K-50K FOR EARLY JOINING Roles and Responsibilities Manage microbial fermentation processes, including upstream processing, downstream purification, and sterile filtration. Conduct microbial limit testing (MLT) and media fill simulations to ensure product quality. Operate bioreactors, centrifuges, incubators, autoclaves, and other equipment related to microbiological techniques. Perform routine maintenance tasks such as cleaning and sanitizing of equipment and work areas.

Role & responsibilities Quality Management system Review / approve Master documents like Batch documents, Specifications, Standard Test Procedures, artworks, Methods and other Good Manufacturing Practices (GMP) / quality related documents. Review/approve Site Master File (SMF), Validation Master Plan (VMP), Quality Manual and other organizational Quality Management System (QMS) related documents. Authorize to approve GMP/QMS documents, policies & protocols. Ensure that documents are prepared & implemented that meet GMP requirements. Approve/Reject Change Control, Deviation, CAPA and follow up for the closer of the same. Review / approve investigations, CAPA proposal & risk assessment. Attend...

Role & responsibilities Lead or support process design, continuous improvement, and optimization of upstream unit operations (e.g., seed train, production bioreactors, harvest systems) Develop, review, and approve process documentation including P&IDs, process descriptions, interface to Automation Work collaboratively with cross-functional teams in MSAT, Quality, Engineering and Operations to ensure seamless tech transfer and process implementation Troubleshoot process-related issues during manufacturing campaigns and provide real-time support Participate in capital projects involving design or retrofit of biopharmaceutical facilities, including equipment selection, specification, and commis...

Greetings from Kashiv Biosciences!!! We are looking for Upstream Process Specialist for our Biosimilar manufacturing facility based out of Ahmedabad. Following are the Roles and Responsibilities Roles & Responsibilities Responsible for Upstream Process for Mammalian Cell culture. Should have exposure on various Fermentation techniques and Single use Bio reactors. Qualification and validation of equipment. Exposure to Perfusion process and technique is must. Candidate Details The candidate should have worked in Biosimilars Upstream production (Mammalian Culture) for atleast 10 Years and exposure to Perfusion technology is must Exposure to Regulatory Audit is Must. Should be aware of QMS Docum...

WE ARE HIRING Department: QA-IPQA DS Activities Note: Only for Biological Companies Only Male candidates Experience: 3 to 6 years Qualification: MSC /M Pharmacy/B Pharmacy Job Responsibilities: Line clearance and Monitoring of batches manufactured at multiple stages / Activities in Production DS Experience in Downstream process with respect to Handling of AKTA Chromatography Systems, Column Packing and unpacking, TFF system Review and monitoring of In-Process quality checks in manufacturing area Additional Responsibilities: Involvement in review of Deviations, CAPAs, Risk Assessments, Market Complaints and Product Recalls Any job assigned by the head of the department and immediate superviso...

Novo Nordisk Global Business Services (GBS) India Department: GCM DP RoW Location Hyderabad, India Are you an experienced aseptic manufacturing project manager with a strong technical background and a passion for making a direct impact on patients'' livesDo you thrive in an international environment where cultural awareness is key to your successIf so, this could be your dream role! ApplyNow! The Position As a Project Manager in Aseptic Manufacturing, you will lead and mentor cross-functional teams, including both Novo Nordisk and our Contract Manufacturing Organisation (CMO) partners. It includes, Ensure the seamless Technology Transfer and manufacturing of our commercial products, always u...

YOUR TASKS AND RESPONSIBILITIES Development of marketing and promotional plans for products to support the end consumers need Monitor business performance and support the portfolio with the help of regular tracking Market intelligence through primary research and customer connect Writing and executing strategic business and marketing plans in collaboration with important prescribers, opinion leaders, round tables, and other advisory groups Joint financial responsibility for budgets (advertising and promotion, conferences and symposia, sales brochures and other product documentation, website content, literature), as well as analysis of budget income and costs; initiating and coordinating mark...

Dear Candidates, We are looking for a Zonal Sales Manager (Third Line Manager) candidates in our Derma Segment. HQ: Mumbai, Delhi & Bangalore. Role & responsibilities High Result orientation: To ensure achievement of Zonal Volume wise, Brand wise, Market Share wise Business Objectives. To ensure leadership position of Brands in Derma segment. Strategic thinking ability to work out strategies to realize the sales and service targets. Interpreting events and building scenario by taking overview. Innovative thinking & Application - Ability to suggest multiple ideas, variety of options to improve business, surpass competition and resolve problems. Leadership - Competitiveness, High initiative an...

Hi, We are hiring for the Executive / Sr Executive R&D - Downstream role Experience - Location - Hinjewadi phase 2 Key Responsibilities: Planning & Scheduling: Prepare monthly experimentation plans, ensuring the availability of resources such as manpower, raw materials, consumables, and equipment. Team Leadership: Lead a small team, ensuring optimal utilization of processes, equipment, and consumables. Provide training and guidance to team members Key Responsibilities: Problem-Solving & Troubleshooting: Proactively identify and resolve issues in experimentation, batch processing, and equipment operation in the PDL and Pilot Plant section. Safety & Compliance: Ensure strict adherence to cGMP,...

Role & responsibilities Ensure All Biopharmaceutical Development Lab Equipment are in state of GLP and Safety Compliance by rectifying equipment breakdowns, maintaining critical spares & consumables and carrying out equipment installations as per approved protocols. Attend breakdown of S1, S2 & S20 Equipment/ Instrument in lab and get it operational with support from instrument vendor and E&M team. Responsible for IQ, OQ, PQ for new instrument installation, calibration and maintain the supporting documents in coordination with DQA and E&M team. Responsible for the equipment requalification and completion of documents coordination with DQA and E&M team. Ensure that the S1, S2 & S20 Equipment/...