234 Gdp Jobs - Page 5

We are looking for a meticulous Junior Engineer to contribute to the efficient maintenance and operation of our API manufacturing facility at Synnat Pharma. As a Junior Engineer, you will be integral to ensuring the reliability of our mechanical and electrical systems, contributing to our commitment to quality and compliance. This role involves a blend of hands-on equipment maintenance, detailed record-keeping, and active participation in equipment validation and qualification processes. You will collaborate closely with senior technicians and engineers, assisting in breakdown maintenance, equipment installation, and process improvement projects. Your dedication to following safety procedure...

Quality Control Analysts needed with 4+ years of experience in HPLC/GC, troubleshooting, and software integration (mpower 3, LIMS). GMP, GLP, GDP, and DI knowledge required. Shift operations experience necessary. Pharma API experience Mandatory.

To supervise all IPQA/QMS function activity on daily basis and update to Section Manager. To conduct and participate in CAPA meetings and review summary report of the same within defined time period monthly. To ensure the implementation of GMP, GDP practices and review of issues and impact of the same, if any, and take corrective actions. To ensure the investigation for complaints and deviations and CAPA after reviewing instruments. To prepare, review, Implement and update SOPs according to current regulations systems. To review Master Batch Document (MBD) / Master Packing Document (MPD) and get approval in advance from Head of Department of Production & QA. To train/update about new procedu...

• Execute product/prototype testing as per SOP/WI and protocols. • Prepare specimens, samples, and test equipment setup. Record, interpret, and analyze data; prepare test reports. Required Candidate profile Operate and maintain lab equipment; perform calibration and maintenance activities. Ensure strict compliance with safety procedures, GLP, GDP, and 5S standards

MAIN PURPOSE: Responsible for the manufacturing of raw materials components (uncut sheet and reagent). May includes some peoples of managements and reporting requirements. Responsible for the production of Rapid Diagnostic kits. Responsible to monitor and supervise following processes such as environmental conditions monitoring, Strip cutting, reagent preparation, lamination, cassette assembly, cassette poaching and pouch sealing etc. To Assist operation of an assigned area in terms of production quality, cost, Delivery, technically Safety, &HR, whilst reporting in the define goals responsible for the day to day Managements of peoples within production. Authority & Responsibility: Ensuring a...

Gurugram Job ID: SS202500088 Function: Lab Testing Role: Lab Desired Skills: Lab Testing, Calibration, Product/Protype Testing,IQ,OQ,PQ,DLP,DGP,5S Job Description Mechanical testing & analysis of products/prototypes ? Test planning & scheduling for multiple projects ? Sample preparation & test equipment setup ? Equipment operation, preventive maintenance & troubleshooting ? Equipment qualification (IQ, OQ, PQ) ? Calibration execution & vendor results review ? Root Cause Analysis (RCA) ? Preparation & review of SOPs, WIs, and test protocols ? Compliance with GLP, GDP & 5S standards ? Safety procedures & hazard control ? Experiment planning & coordination with internal/external labs ? Support ...

QC officer -04 Qc Executive - 01 Perform chromatographic analyses and tests, including HPLC, Gas Chromatography (GC), and Thin-Layer Chromatography (TLC), on raw materials, in-process materials, and finished products. LIMS knowledge preferred. Required Candidate profile We are looking for Male candidate due to work in rotation shift ( First/Second/Night) preferred B.Sc./MSc chemist & required experience of pharma formulation Sterile/Non Sterile product.

Looking for Quality NPI Engineer for gurgaon location.

To Identify & resolve the problem in electrical equipment like Transformer, DG sets, UPS & Battery bank, APFC Panel, VFD, ACB & VCB breaker job related to WRF & take follow-up for completion job. Note: Please share your CV on kchoudhary@embio.co.in

As a member of the ACG Capsules team based in Shirwal, your primary responsibilities will include: - Checking the allocated post production (ATS/Printing/camera) line(s) during each shift according to the CTQ (Critical to Quality) / CTP (Critical to Productivity) checklist. - Following the plan outlined in the color change note to minimize change over time at each sub-section. - Adhering to instructions from the shift lead to ensure timely change over by making sure roller(s)/ink are available. - Performing In-Process Quality Checks (IPQC) after every roller cleaning and checking camera rejections hourly to achieve zero defects. - Operating cameras according to the Standard Operating Procedu...

As a part of this role in the pharmaceutical industry, you will be responsible for handling CAPA (Corrective and Preventive Actions), OOS (Out of Specification) incidents, and deviations effectively. Your duties will also include the generation of Standard Operating Procedures (SOPs) to ensure smooth operations within the organization. Additionally, you will be involved in validation processes and maintaining compliance with Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP). This is a full-time position with a day shift schedule. The ideal candidate should have a total work experience of 1 year in a similar role within the pharmaceutical sector. The work location for ...

Rubicon Research Limited is a rapidly growing pharmaceutical formulation company focused on developing, manufacturing, and marketing branded specialty and generic prescription pharmaceutical products in regulated markets. With a diverse product portfolio of over 250 SKUs spanning more than 70 product families, we have established marketing, sales, and distribution platforms in the US through our subsidiaries AdvaGen Pharma and Validus Pharmaceuticals. Our US FDA-inspected R&D facilities in India and Canada, along with manufacturing facilities in Maharashtra, India, equipped with various drug development and manufacturing capabilities, demonstrate our commitment to quality and innovation. As ...

You will be working as a Production Chemist with a focus on knowledge of BRM, BPR, and exposure to GDP, GMP. Your role will involve experience in Sterile and Sterilization processes. As a Production Chemist, your responsibilities will include Batch Planning and Batch Manufacturing. The qualifications required for this position include relevant education details. The required skills for this role are a strong knowledge of BRM, BPR, exposure to GDP, GMP, and experience in Sterile and Sterilization processes. Preferred skills include proficiency in Batch Planning and Batch Manufacturing. Our company is committed to diversity and inclusivity, promoting an equal opportunity environment for all em...

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Apply today! Job Details Summary As a pharmacist you will be responsible for Maintaining and compliance of all local legislation and World Courier Standard Operating Procedures. Responsibilities Maintain and assure compliance with applicable ICH, GMP, GCP, GDP and FDA Good Clinical Practices, local regulatory affairs, legal require...

The job is based in Hyderabad/Bangalore/Chennai and at Gramener, you will find a welcoming work environment with diverse colleagues, a clear career path, and ample opportunities for growth and innovation. The company aims to develop a range of easily configurable data applications focused on storytelling for both public and private use. As part of your role, you will be involved in various impactful customer technical data platform projects, taking the lead on strategic initiatives that cover the design, development, and deployment of cutting-edge solutions. Collaboration with platform engineering teams will be key in implementing Data Brick services effectively within the company's infrastr...

You will be responsible for managing day-to-day warehouse operations in compliance with company SOPs, cGMP, and safety guidelines. Your role will involve overseeing the accurate and compliant handling, storage, and distribution of raw materials, packaging materials, and finished goods. This includes supervising receipt, unloading, verification, and de-dusting of materials, monitoring temperature and humidity, maintaining proper housekeeping, and handling equipment properly. Your essential functions will include overseeing the receipt, unloading, de-dusting, and weight verification of raw materials and packaging materials. You will manage the storage and handling of these materials according ...

You will be joining our client ACLDigital, a US-based company, for the position of Senior C++ Developer. This is a permanent opportunity with ACLDigital based in Bangalore, following a hybrid work model. The ideal candidate for this role should have 6 to 10 years of experience. The employment type is permanent with ACLDigital, and the expected notice period is immediate to a maximum of 15 days. In terms of compensation, the budget for this position is up to 25 LPA, depending on the candidate's experience and additional qualifications. Your responsibilities will include demonstrating robust UNIX/Linux experience to ensure operational efficiency. You should showcase exceptional coding proficie...

As a member of ACG Capsules in Shirwal, your primary responsibilities include checking the allocated post production line(s) such as ATS/Printing/camera in each shift according to the CTQ (critical to Quality) / CTP (Critical to Productivity) checklist. You will need to adhere to the plan outlined in the color change note, minimizing change over time at each sub-section. Following instructions from the shift lead is crucial for timely changeover, ensuring the availability of necessary equipment like roller(s) and ink. Furthermore, it is essential to execute In-Process Quality Control (IPQC) after each roller cleaning, checking camera rejections hourly to achieve zero defects. Operating the c...

You have an opportunity as a Warehouse and Logistics Manager where you will be responsible for overseeing warehouse operations, inventory control, team management, safety compliance, and logistics and supply chain management in the pharmaceutical/API sector. Your key responsibilities include managing warehouse operations such as receipt, storage, and dispatch of materials, optimizing warehouse layout for efficiency, implementing inventory tracking systems, maintaining accurate inventory records, ensuring compliance with regulatory standards, and supervising warehouse staff. You will also be involved in coordinating with QA/QC for proper material handling, conducting training programs on safe...

We're Hiring: Junior Pharmacovigilance Specialist Location: Pune | Full-Time | Entry-Level / 01 Year Experience Are you a Life Science or Pharmacy graduate looking to kickstart your career in Pharmacovigilance Join our growing team and play a key role in ensuring drug safety and patient well-being through adverse event reporting and regulatory compliance, ???? Role Highlights ?? Analyze & process adverse event reports ?? Prepare regulatory safety submissions ?? Follow GCP, GDP, ICH & MedDRA coding standards ?? Collaborate with project managers and team leads ?? Ensure data accuracy and audit readiness ???? What Were Looking For ??? B Pharm / M Pharm Graduates ???? Freshers ???? Familiarity w...

Ensure current versions of all GMP documents are in use. Prepare, revise, and control SOPs . Implement and enforce (GDP). Conduct internal audits, maintain summaries and CAPA tracking Support in process validation, equipment qualification etc Required Candidate profile Ensure all QA activities comply with cGMP, regulatory requirements & internal quality standards for API & Specialty manufacturing. Contact Mr Deep at 9867038868, Email Id: ops@empowerrecruitments.com

As a valuable member of our team in the pharmaceutical industry, you will be responsible for various key tasks including CAPA, OOS, Deviation management, SOP's generation, and ensuring Validation, GDP, GMP compliance. Your role will play a crucial part in maintaining high quality standards and regulatory requirements. This is a full-time position with a day shift schedule. The ideal candidate should have a total work experience of 1 year, preferably within the pharmaceutical sector. The work location for this role will be in person, providing you with the opportunity to actively engage with the team and processes.,

The Quality Assurance (QA) Executive API (Bulk Drugs) role based in Savli, Gujarat requires a candidate with 2-5 years of experience and a qualification of B.Sc / M.Sc. As a QA Executive, your responsibilities will involve ensuring compliance with cGMP, ICH, and regulatory guidelines in API (bulk drug) manufacturing. You will be responsible for preparing, reviewing, and controlling SOPs, BMRs, BPRs, change controls, deviations, and CAPAs. In addition, conducting in-process checks for manufacturing and packaging activities, handling investigations for deviations, OOS/OOT results, and supporting root cause analysis are key components of this role. You will also be involved in participating in ...

As a Store Manager at our pharmaceutical manufacturing unit in Nadiad, you will be responsible for overseeing and managing the inventory and warehousing operations. With 7-10 years of experience in pharmaceutical warehousing, you will utilize your expertise in GMP and GDP to maintain compliance with regulatory guidelines. Your role will involve managing day-to-day store operations, ensuring proper storage conditions, and monitoring inventory levels to prevent stock-outs or overstocking. You will lead a team of store assistants, operators, and forklift drivers, while collaborating with various departments to ensure seamless operations. Your responsibilities will include overseeing material ha...

Hiring - ADL (AMD) - Nagpur Location Location - Nagpur MH Company - Pharma (MNC) Core OSD Formulation + Method Validation Experience Msc or Mpharm /bpharma Responsibility - Sr. Role Description 1. Analytical Method Development New analytical method development and troubleshooting of existing method of different types of Oral solids dosage form (Granules, Tablets, Pellets, Capsules etc.) for Regulated market projects or as per business need. 1. Ensure robust & cost effective method development of product by considering the available facility & resources 2. Conduct Literature survey, different pharmacopoeia & pharmacopeia forum search and review & application of same in AMD. 3. Conduct Pre-for...