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- ...setup time and changeover losses 3. Quality & Compliance (Pharma Focus) * Ensure compliance with GMP, GDP, ISO, and customer quality... ...* Control mix-ups, traceability, line clearance, and batch documentation * Coordinate with QA for in-process and final inspections *...SuggestedShift work
Rs 6 - 10 lakhs p.a.
...laboratory associates Write, review and/or approve analytical documentation in timely and high-quality manner, such as releases, analytical... ...chemistry or equivalent and a minimum 6 years experience or M. Pharma/M. Sc with a minimum of 12 years experience in the...SuggestedWork at office- ...on queries raised Liaison with Front Office and Customer. Required Skill Set: Experience in Import & Export Operations, documentation Any graduate Minimum 3+ years from Shipping Background * Job Location: Hyderabad, Kondapur * Payroll: MOL IT (MOL...SuggestedPermanent employmentFull timeContract workWork at office
Rs 2.5 - 3.5 lakhs p.a.
...opportunities, we strive to be a leader in the tech education sector. Roles and Responsibilities : • Collect, review, and verify student documents such as ID proofs, academic records, admission letters, fee details, and financial documents. • Coordinate with banks and financial...SuggestedRs 1 - 3 lakhs p.a.
...Contribute to metadata and data modeling activities. Track and manage data issues using tools such as JIRA and document processes in Confluence. Apply Life Sciences/Pharma industry context to ensure data standards and compliance. Basic Qualifications and Experience Master'...Suggested- ...requiring awareness of the S/4HANA landscape and delta changes. A pharma industry background is mandatory. The position is based in... ...of pharma domain processes and regulatory compliance. Strong documentation and communication skills. Ability to collaborate with cross-...Suggested
- ...have an urgent requirement for a Pharmacist in a new start up Pharma company in Hyderabad Gachibowli. - Qualification: B Pharma and... ...on medication adherence and side effects. - Ensure pharmacy documentation is audit-ready and compliant. Key Result Areas (KRAs): - 1...SuggestedImmediate start
- ...Were Hiring! CSV Validation Engineer Pharma Project | Multiple Locations Position: CSV Validation Engineer Company: INSTRUMENTATION... ...of manufacturing systems (SCADA, HMI, PLC). Conduct and document Computer System Validation (CSV) activities for pharmaceutical/life...SuggestedImmediate start
- Client : Altimetrik Project : Novartis ( PHARMA - gaint) Work Module : Hybrid ( Altimetrik office ) Look for Immediate Joiners... ...overall improvement of our existing DWH&BI product. Improve documentation, quality, testing and operational standards Skills Preferred...SuggestedHybrid workWork at officeImmediate start
- ...UV, and Wet Chemistry techniques Conduct in-process, raw material, and finished product quality checks Maintain accurate QC documentation and reports Ensure compliance with internal quality standards and regulatory guidelines Support investigation of deviations...Suggested
- ...Satellites. We are renowned manufacturers of healthy food products, Pharma, innovative and cost-efficient composites, Satellites... ...returns such as GST, TDS, Excise, and Service Tax. Assist in documentation and represent the company along with auditors/lawyers before authorities...Suggested
- ...immediately Key Skills: * Liquid Filling Operations * GMP / SOP Compliance * BMR / BPR Documentation * Packaging Line Handling * Basic Machine Troubleshooting * Pharma Production Eligibility Criteria: Qualification: Diploma / B.Sc (Pharmacy / Chemistry /...SuggestedImmediate start
- ...Opportunity to head the Quality function for a renown Pharma in Hyderabad. Opportunity to be one of the key contributors to the company... ...stability governance. .Ensure batch release discipline and documentation integrity across sites. 4) CAPA, Investigations & Change...SuggestedRelocation
- ...andu00A0 maintain u00A0 design specifications, configuration documentation, and validation test scripts u00A0for IQ/OQ/PQu00A0 activities... ...LabVantage . u00A0 ~ Working knowledge ofu00A0 QC lab processes in pharma /life sciences. u00A0 ~ Familiarity withu00A0 instrument...SuggestedLong term contract
Rs 3.5 - 18 lakhs p.a.
...Innovative mindset Expertise in authoring and executing technical documentation following industry standards and methodologies (SDLC, AGILE)... ...and/or A&E firm using discrete event simulation in the pharma industry is strongly preferred; prior experience as an automation...SuggestedFull timeNight shift- Purpose of Job As a Business Analyst in our Commercial Pharma Tech Consulting team, you will act as a strategic bridge between client... ...requirements Develop user stories, data workflows, and documentation to guide technical teams Capture 'as-is' vs. 'to-be' process...
- ...We are hiring – RTR Executive (Pharma Industry) - French Process Location: Dundigal, Hyderabad Work Mode: Work from Office only Venkat Tech Global Solutions Pvt. Ltd. is looking to HIRE FOR ITS CLIENT French- Record-to-Report (RTR) Accountant to support a French subsidiary...Work at officeLocal area
Rs 1.5 - 3 lakhs p.a.
...Title- Project Manager (Pharma manufacturing) Job Description- To plan, execute, control and ensure closure of projects, while managing people and delivery excellence in all parameters of time, cost and processes in projects. Drive execution of the project roadmap and...Immediate start- ...Analytical) Location : Hyderabad, India Qualification : M. Pharma/M.Sc. in Pharma Chemistry from reputed University. Experience... ...project requirements. Carry Out Author and review Analytical documents, not limited to method development reports, justification...
- ...be responsible for developing, reviewing, and approving protocol documents and supporting materials for various clinical projects.... ...subject, including protocol design, development, and training, Pharma co economics, Outcomes Research, Health Technology Assessment, New...Relocation packageLocal area
Rs 1 - 4 lakhs p.a.
...metadata and data modeling activities. Track and manage data issues using tools such as JIRA and document processes in Confluence. Apply Life Sciences/Pharma industry context to ensure data standards and compliance. Basic Qualifications and Experience...- ...CuraTeQ Biologics, a wholly owned subsidiary of Aurobindo Pharma Ltd., is an EU GMP certified biopharmaceutical company headquartered... ...goals. The role also involves preparing reports and maintaining documentation for quality assurance purposes. Qualifications...Full time
- ...Care Piramal Critical Care (PCC), a business unit of Piramal Pharma, is the fourth-largest producer of inhaled anesthetics and a... ...will work on new product development, preparation of technical documentation for regulatory files (i.e., FDA 510k and CE mark technical files...
- ...Preparing and maintaining cash flow reports (Daily, Fortnightly, Monthly). • Coordinating with accountants to manage financial documentation and payment-related communications. • Managing CRM entries for expenses and payment adjustments. • Handling payables and receivables...Work at officeLocal area
- ...queries and supporting clients throughout the sales process. Preparing and maintaining accurate sales reports and commercial documentation . Managing business correspondence and coordinating with internal stakeholders. Representing the company at industry events...Full time
- ...Job Title: Senior Executive – Purchase Department (Pharma Company) Company : Sain Medicaments Pvt Ltd. Department: Procurement /... .... * Maintain and update the Approved Vendor List (AVL). Documentation & Compliance * Ensure all procurement processes adhere to cGMP...
- ...Be the First to Apply Division Piramal Pharma Solutions Piramal Pharma Solutions is a contract development and manufacturing... ...regulatory inspections and inspection readiness Experience in documentation and compilation of data for regulatory submissions (IND), i.e.,...Contract workWorldwide
- ...Authority queries, scientific/medical input to other safety related documentation including Health Hazard Evaluations, clinical study protocols,... ...Global Lighthouse Network. We aspire to be the most efficient pharma operations in the world. Our productivity improvement and...Relocation packageLocal area
- ...collaboration with physicians to ensure therapeutic effectiveness and minimize risks. Adverse Drug Event (ADE) Reporting: ~ Identify, document, and report adverse drug reactions and medication errors per hospital and regulatory protocols. Medication Management: ~...
Rs 2 - 5 lakhs p.a.
...The Associate Specialist, Global Commercial Pharma Pipeline Analytics, HHDDA will be responsible for developing and delivering data and analytics, generating strategic insights, and addressing global brand lead s business questions to inform pharma pipeline investments and...
