- Merck & Co. (Rahway, NJ)
- …development activities, compliance investigation, change management and the authoring of GMP documentation in any of our enabling facilities.Additional Supported ... molecule processes, enabling gain of critical internal experience with scale-up of manufacturing GMP steps, demonstration of new manufacturing … more
- Merck & Co. (Durham, NC)
- …Description: Senior Specialist , Manufacturing Automation The Senior Specialist Manufacturing Automation person is primarily responsible for supporting ... a production regulated industryMinimum of five (5) years of experience in a GMP manufacturing automation-related role and direct experience with SDLC and change… more
- Merck & Co. (Rahway, NJ)
- …pilot plant enables gain of critical internal experience with scale-up of manufacturing GMP steps, demonstration of new manufacturing technology/processes, ... Job Description SSO Operations Specialist Job Description The Small Scale Organics (SSO)...The Small Scale Organics (SSO) Pilot Plant is a GMP (Good Manufacturing Practices) manufacturing … more
- Merck & Co. (Rahway, NJ)
- …is a new multi-modality (small molecule, biologics, vaccine) Drug Product development and GMP clinical manufacturing plant in Rahway, New Jersey.- The role at ... the Specialist level will be responsible for analyzing monthly forecasts...experienceRequired Experience and Skills: Knowledge of sterile drug product manufacturing or development.Evidence of good oral and written communication… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …productsThe Position This position is responsible for performing reviews of manufacturing and support documentation and records to certify compliance ... Novo Nordisk's life-saving treatments are brought to life. Our manufacturing facility produces a global supply of our hemophilia...with in-house specifications/standards and GMP for all NNUSBPI products. This position has QA… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …you ready to realize your potential? The Position This position will reviews manufacturing and support documentation and records to certify compliance with ... Novo Nordisk's life-saving treatments are brought to life. Our manufacturing facility produces a global supply of our hemophilia...in-house specifications/standards and GMP for all NNUSBPI products. This position has QA… more
- Catalent (Manassas, VA)
- …nutraceuticals, as well as small batch lozenges. With extensive development and manufacturing expertise and a wide range of flavors, ingredients, and colors ... to help create engaging new products consumers will love.The Document Control Specialist - 2nd Shift is responsible for creating and maintaining the Quality… more
- Catalent (Manassas, VA)
- …nutraceuticals, as well as small batch lozenges. With extensive development and manufacturing expertise and a wide range of flavors, ingredients, and colors ... to help create engaging new products consumers will love.The Quality Assurance Specialist I - Quarantine is responsible for auditing the products and processes… more
- Integrated Resources, Inc (Bothell, WA)
- …Deviations, Management Monitoring and Self Inspection auditing, QA reporting, and approval of GMP documentation . * Strong computer skills with Word and Excel and ... Job Title: QA Shop Floor Specialist Job Location: Bothell, WA Job Duration: 6...$43/hr. on W2 Top Skills: . 3-5 years of GMP work experience . Familiarity with Batch Records .… more
- Sunrise System inc (Bothell, WA)
- …Deviations, Management Monitoring and Self Inspection auditing, QA reporting, and approval of GMP documentation . Strong computer skills with Word and Excel and ... **Schedule- 9:00pm - 7:30am, Sun - Wed** **Top Skills: 3-5 years of GMP work experience Familiarity with Batch Records Deviations Experience Preferred Associates or… more
- Aequor (Seattle, WA)
- …Lead REQUIRED COMPETENCIES: Knowledge, Skills, and Abilities: Must have basic GMP and Quality knowledge. Intermediate skills to navigate a document management ... per procedure. Review training form submissions for adherence to good documentation principals, accuracy and completion. Oversee the creation, edit and/or retirement… more
- Novo Nordisk Inc. (Durham, NC)
- …of people around the world. In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling different steps in our injectable ... party instrument services Accurately & legibly records all activities in appropriate documentation . Writes work orders Reviews documentation for accuracy &… more
- Dexian - DISYS (Seattle, WA)
- …(LMS). REQUIRED COMPETENCIES: Knowledge, Skills, and Abilities: * Must have basic GMP and Quality knowledge. * Intermediate skills to navigate a document management ... per procedure. * Review training form submissions for adherence to good documentation principals, accuracy and completion. * Oversee the creation, edit and/or… more
- Spectraforce Technologies Inc (Bothell, WA)
- …Deviations, Management Monitoring and Self Inspection auditing, QA reporting, and approval of GMP documentation . * Strong computer skills with Word and Excel and ... Title: Quality Assurance Specialist (Pharma ONLY - NON IT JOB) Duration:...Sun - Wed** **Top Skills: - 3-5 years of GMP work experience - Familiarity with Batch Records -… more
- United Therapeutics (Eden Prairie, MN)
- …help patients with liver and kidney disease. How you'll contribute The Senior QA Specialist - GMP Manufacturing , is responsible for supporting quality ... operations during GMP clinical manufacturing of bioengineered organs at Miromatrix. The...Metrics: Compile and analyze data with respect to QA manufacturing metrics + Manufacturing Documentation :… more
- United Therapeutics (Eden Prairie, MN)
- …/ CofA: Create Certificates of Analysis and/or Certificates of Conformance + Manufacturing Documentation : Perform peer-review and contribute to the content of ... the Miromatrix are manufactured in accordance with current Good Manufacturing Practices ( GMP ) and meet all internal... manufacturing related documentation including SOPs, Work Instructions… more
- Randstad US (Burlington, MA)
- quality assurance specialist - gmp . + burlington , massachusetts + posted april 4, 2024 **job details** summary + $45 - $50 per hour + temp to perm + bachelor ... 6 PM education: Bachelors Responsibilities + Provide quality on-the-floor support of manufacturing , reviewing documentation , and providing real-time support of … more
- Reyes Holdings (Grand Rapids, MI)
- …of the manufacturing plant's on-the-job training program. The Training Documentation Specialist facilitates the training and qualification process for ... subject to the rule governing the program. **Position Summary:** The Training Documentation Specialist develops, designs and ensures delivery of the Standard… more
- Grifols Shared Services North America, Inc (Clayton, NC)
- … manufacturing , maintenance, and engineering documents including BPRs, SOPs, CCRs, Manufacturing Methods, etc. The senior technical document specialist will ... than 110 countries and regions. **Summary:** The senior technical document specialist is responsible for using technical knowledge/concepts while partnering with … more
- Amgen (Thousand Oaks, CA)
- …Become the professional you are meant to be in this meaningful role. ** Specialist Manufacturing , New Product Introductions** **Live** **What you will do** Let's ... In this vital role you will work as a Manufacturing Specialist supporting New Product Introductions (NPI)...or Life Science Field & 2 years of directly-related GMP manufacturing experience OR + Bachelor's degree… more
