Process Validation - 68+ job offers

Responsible for achieving a state of high-quality performance at our Supplier partners through the application and practice of Advanced Product Quality Planning ‘APQP’ during the industrialization of products/parts within the New Product Introduction ‘NPI’ process through process Validation, review

Jabil

At Jabil (NYSE: JBL), we are proud to be a trusted partner for the world's top brands, offering comprehensive engineering, supply chain, and manufacturing solutions. With 60 years of experience across industries and a vast network of over 100 sites worldwide, Jabil combines global reach with local e

Responsible for line clearance activity before commencing the different operations like dispensing, manufacturing, filling, inspection, sealing, labelling, and packing. Responsible for Process validation, cleaning validation/verification, hold time study, media fill & routine batch sampling as per p

SMC Ltd.

Key Accountabilities/Essential Functions: 1. To ensure Raw Material / Packing Material and finished goods testing in line with the SOPs. 2. To maintain device history records (DHR) & product release checklist for each lot. 3. To conduct inspections at in-process, in-coming and completes the final in

Baxter International Inc.

This is where your work makes a difference. At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a gre

Vicarious Surgical is seeking an Advanced Manufacturing Engineer to join our team in Bangalore, India. You will work with R&D and Manufacturing engineers to drive design for manufacturing and assembly activities during all phases of development. Vicarious Surgical is a US based next generation robot

SUN PHARMA

Experience: 3+ years Qualification: MSc Approval authority: Extra page issuance form. Batch internal release certificate and transfer note. Breakdown memo perform impact analysis on product quality and sign for QA. Tool set checking record. Release of bulk product for further stage. Key execution su

Ubique Systems

Exp-3-6 yrs Pune Location Np- Immediate Major Deliverables / Job Profile: BIW Robot simulation – - Simulation cell building - Reachability & feasibility study - BIW tool validation - Weld distribution, gun selection, gun sectioning - Cycle time chart preparation - Create layout from simulation cell

Vicarious Surgical is seeking a Senior Quality Assurance Engineer to join our team in Bangalore, India. This role will be tasked with supporting document and quality assurance activities equipment associated with our surgical robot. Vicarious Surgical is a US based next generation robotics company d

To review of URS, DQ, QRM, FAT, SAT, and vendor/ supplier’s documents related to qualification. To conduct sampling activities as per the protocols (Hold time, Process validation and cleaning validation etc.). To execute Qualification / Re-Qualification and Validation activities of Equipment / Syste

Apotex Research

Job Description About Apotex Inc. Apotex Inc. is a Canadian-based global health company that produces high-quality, affordable medicines for patients around the world. Apotex employs almost 6000 people worldwide in manufacturing, R&D, and commercial operations. Apotex medicines are accessible to

Amneal

Responsible for Process validation, cleaning validation/verification, hold time study, media fill & routine batch sampling as per protocol/SOP. Responsible for review of URS, DQ and vendor/ supplier’s documents related to qualification. Responsible for preparation and review of Validation/ Qualifica

Amneal

1. Responsible to perform Quality Function responsibilities pertaining to Validation. 2. Responsible for preparation and review of URS, DQ and vendor/ supplier’s documents related to qualification. 3. Responsible to co-ordinate with manufacturing, Engineering and QC personnel for respective Qualific

Job Description Literature Survey. Handle end to end responsibility of New Product development from conceptual stage to commercialization as per target timelines, planning, scheduling, monitoring and controlling of projects. Handling of Pilot plant, scale up studies, process development, process val

Apotex Research

Job Description About Apotex Inc. Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals and consumer heal

Job Description To ensure timely response of deficiencies raised by Agency on ANDA's. Review for all specifications and proposal from sites of approved ANDAs for supplement filings. Regulatory Support and review for pre-filing and development documentation such as development reports, BMR, BPR, spec

Apotex Research

Job Description About Apotex Inc. Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals and consumer heal

b Title Manager – MSTG NOSD Business Unit R&D1 Regulatory Affairs Job Classification Code New Function R&D Grade G10 Location Central India (Greenfield Project) Key Responsibilities At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at ever

Job DetailsJob Location: Prashanti Nagar IE Kukatpally Hyderabad, Telangana 500072Salary Range: ₹600,000.00 - ₹900,000.00 Responsible review of exhibit batch manufacturing records and exhibit batch packing records before execution of the batch. Responsible for review of process validation protocol a

We are looking for a skilled Process Validation Engineer to join our team in Pune. The ideal candidate will have 3+ years of experience and be available to start immediately. *Roles and Responsibility** Perform gap assessments and conduct remediation of documents with stakeholder inputs. Develop and