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Resumes 51 - 60 of 299 |
Lowell, MA
... GMP standards. Read work orders, routings and bills of materials, and have a basic computer skill, computer programs (Oracle/Agile) Assemble high quality assemblies using manufacturing procedures, assembly prints, schematics, and bills of materials. ...
- 2022 Nov 04
Canton, MA
... Developed GMP policies and procedures related to production control and reporting, inventory control and materials usage. Responsible for all Supply Chain Logistics and Transportation functions, negotiated LTL & small package delivery services. ...
- 2022 Sep 15
Foxborough, MA
... Two years of biotech experience as a process chemist in a GMP environment. Lifetime of experience collaborating with co-workers, as well as working independently without supervision. Education B.A. in Biology B.A. in Spanish Rhode Island College, ...
- 2022 Aug 16
Northborough, MA
... R A J U N I V A R T H I, P H D 3 Performed SME review and data verification of GMP, GLP, GCP records of QC release: Physical description, Color, Clarity, Visual Assessment, pH, Particulate testing, Osmolality, Extractable volume, Virus Particle ...
- 2022 Apr 20
Bedford, MA, 01730
... com LinkedIn.com/in/ChristianRandhahn Bedford, MA 01730 Global Sourcing & Supply Chain KPI & Financial Performance GMP & Compliance Cost Reduction / Cost Modeling RFQ / RFP, Vendors, Contracts Operations & Trend Analysis Product Development ...
- 2022 Mar 14
Lawrence, MA, 01843
... Lexington MA Feb 2003-Dec2005 Responsible for daily operations of the QC/ Microbiology lab to ensure the following assays are performing according to GMP’s and GLP’s regulations for Sterility, Endotoxin and Bioburden testing for water and in-process ...
- 2022 Jan 29
Waltham, MA
... anything mechanical was mine to take care of Process Mechanic Acorda Therapeutics July 2018 to July 2018 • Responsible for performing and documenting the required maintenance and monitoring of the facility, systems and equipment in a GMP Facility. ...
- 2021 Aug 17
Boston, MA
... Affairs § 510K, PMA, IVD, HDE, AL/ML based SaMD § ISO 13485, ISO 14971, IEC 60601, ICH § EU MDD, MDR 2017/745, STEDs, UDI § GLP, GMP, 21 CFR 820, CAPA, Labeling § MDSAP, Device Registration & Licensing Clinical Operations § IDE, IRBs, Clinical Study ...
- 2021 Apr 06
Boston, MA
... (May 2014- March 2016) • Drafting, revising and reviewing GMP quality documents like Batch Production records, SOPs, Master Formula Records, CMC sections of regulatory filing, logbooks, annual product Quality reports, validation/qualification ...
- 2021 Jan 03
Boston, MA
... Siemens NX, Tableau, EduPack, PDM Functional: GD&T, Tolerance Stack, DFMA, Lean Six Sigma, Injection Mold Analysis, FEA, GMP, ISO 9001, ISO 13485, Statistical Analysis, FMEA, Verification and Validation, Gage R&R, Stress Analysis, DOE, Shop floor ...
- 2020 Dec 15