- 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)
- …a crucial role in supporting the process automation systems within clinical manufacturing .-The Automation Specialist - Engineering Auto Eng position will report ... as sterile fill finish processes, to ensure optimal automation in pharmaceutical manufacturing .Understand and adhere to CFR, GMP , and data integrity regulations… more
- Merck & Co. (Rahway, NJ)
- …database querying and data programming.Ensure compliance with data integrity, CFR, GMP /regulations, and system life cycle documentation methodology specific to ... development and/or sterile fill finish principles.Knowledge of data integrity, CFR, GMP /regulations, and system life cycle documentation methodology.Ability to… more
- Aequor (Devers, TX)
- …warehousing, Quality, and compliance environments. Prefer to also have knowledge of GMP Manufacturing operations and processes. Directs quality initiatives that ... procedures and batch records, providing real time review of manufacturing batch record documentation and logbooks, and... and logbooks, and working with operations to resolve manufacturing issues. The Contractor Field QA Specialist … 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
- Legend Biotech USA, Inc. (Raritan, NJ)
- … facility, preferably cell therapy, testing facility, quality assurance, or manufacturing compliance. Expertise in GMP compliance knowledge including knowledge ... the treatment of multiple myeloma. Legend Biotech is seeking a Systems Engineer Specialist as part of the Commissioning and Qualification team based in Raritan, NJ.… 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
- 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
- ConsultNet (American Fork, UT)
- Document Control Specialist - manufacturing environmentDirect HireSalary Target $70,000 - $85,000Provo metro area work site.Job Description:This role works very ... standards, and quality manufacturing systems within the manufacturing environmentIt is a critical role for documentation...regulatory and quality management systems such as ISO 9001, GMP , FDA, etc ) Experience with Solidworks Electrical 2D… 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
- System One (Devens, MA)
- …warehousing, Quality, and compliance environments. Prefer to also have knowledge of GMP Manufacturing operations and processes. + Directs quality initiatives ... Job Title: Biologics GMP QA Specialist Location: Devens, MA...review of manufacturing batch records. + Review manufacturing shop floor documentation . Requirements EDUCATION REQUIREMENTS… 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
- Bausch Health (Santa Rosa, CA)
- …of improving peoples lives with our health care products. The Quality Assurance Specialist , GMP provides Quality support for Petaluma site and ensures adherence ... and fast-paced organization as a member of cross-functional teams. . Working in a GMP laboratory environment or manufacturing environment a plus. As required by… 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
