Senior Quality Control Associate

Innova Solutions has a client that is immediately hiring for Quality Control Senior Associate. Position type: Fulltime – Contract Duration: 12 Months Location: West Greenwich, RI As Quality Control Senior Associate, you will: Job Description: Fully onsite at Rhode Island Standard business hours Under general supervision, this position will...

Innova Solutions has a client that is immediately hiring for Quality Control Senior Associate.  Position type: Fulltime – Contract  Duration: 12 Months Location: West Greenwich, RIAs Quality Control Senior Associate, you will:  Job Description: Fully onsite at Rhode IslandStandard business hoursUnder general supervision, this position will perform...

Job DescriptionJob DescriptionDescription:Note:Fully onsite at Rhode IslandStandard business hours Under general supervision, this position will perform routine procedures and testing in support of the Bioanalytics Team. Main responsibility will be routine release and stability testing. Preferred qualifications will be experience with ELISA, general...

Job Description:Primary focus is enhancing systems by which client assures the safety of our biologic products. Under general supervision, this position will perform routine procedures and testing in support of the Bioanalytics Team. Main responsibility will be routine release and stability testing. Preferred qualifications will be experience with ELISA,...

Job Description:Primary focus is enhancing systems by which client assures the safety of our biologic products. Under general supervision, this position will perform routine procedures and testing in support of the Bioanalytics Team. Main responsibility will be routine release and stability testing. Preferred qualifications will be experience with ELISA,...

Description:Fully onsite at Rhode IslandStandard business hoursPrimary focus is enhancing systems by which Client assures the safety of our biologic products. Under general supervision, this position will perform routine procedures and testing in support of the Bioanalytics Team. Main responsibility will be routine release and stability testing. Preferred...

Description:Fully onsite at Rhode IslandStandard business hoursPrimary focus is enhancing systems by which Client assures the safety of our biologic products. Under general supervision, this position will perform routine procedures and testing in support of the Bioanalytics Team. Main responsibility will be routine release and stability testing. Preferred...

Job Details: Title: Quality Assurance Senior AssociateDuration: 1 YearLocation: West Greenwich, RIPay Rate: $35.17/hrShift : 7 PM – 7 AM ET (12 hour day)Five (5) working days in one week and two (2) working days the following weekJob Description:Job Details:In this vital role, will be responsible for PQA (Plant Quality Assurance) On the Floor in support of...

Description: Note: Responsibilities: Primary focus is the support and oversight of Amgen’s Quality Management Systems ensuring key requirements and initiatives are implemented, maintained and reviewed in accordance with cGMP regulations. Additional detail responsibilities, accountabilities or decision authorities are defined in procedures to execute...

Job Title: Senior Quality Assurance SpecialistAbout the Job:The Senior Quality Assurance Specialist will be responsible for supporting and overseeing Amgen's Quality Management Systems to ensure key requirements and initiatives are implemented, maintained, and reviewed in accordance with cGMP regulations. This role will also involve leading and directing the...

Summary: The primary focus is the support and oversight of the company's Quality Management Systems ensuring key requirements and initiatives are implemented, maintained and reviewed in accordance with cGMP regulations. Additional detail responsibilities, accountabilities or decision authorities are defined in procedures to execute assigned task for the role...

Job Details:In this vital role, will be responsible for PQA (Plant Quality Assurance) On the Floor in support of Manufacturing activities. This position requires working directly with Manufacturing staff during bulk drug substance operations to facilitate real-time decision-making regarding quality requirements and deviations.Responsibilities Include the...

Job Details:In this vital role, will be responsible for PQA (Plant Quality Assurance) On the Floor in support of Manufacturing activities. This position requires working directly with Manufacturing staff during bulk drug substance operations to facilitate real-time decision-making regarding quality requirements and deviations.Responsibilities Include the...

Job Summary:The primary focus of this role is to support and oversee Aditi Consulting's Quality Management Systems, ensuring key requirements and initiatives are implemented, maintained, and reviewed in accordance with cGMP regulations.Responsibilities:Leading and directing the Quality functions for assigned plant(s) or functional area(s)Providing Quality...

About Client: The client is one of the world's largest independent biotechnology companies, focusing on the discovery, development, and manufacturing of innovative human therapeutics. The company's areas of expertise include oncology, hematology, cardiovascular disease, inflammation, bone health, and neuroscience. It has developed a wide range of biologic...

Summary: In this vital role, will be responsible for PQA (Plant Quality Assurance) On the Floor in support of Manufacturing activities. This position requires working directly with Manufacturing staff during bulk drug substance operations to facilitate real-time decision-making regarding quality requirements and deviations. Responsibilities Include the...

Job Details: In this vital role, will be responsible for PQA (Plant Quality Assurance) On the Floor in support of Manufacturing activities. This position requires working directly with Manufacturing staff during bulk drug substance operations to facilitate real-time decision-making regarding quality requirements and deviations. Responsibilities Include the...

Description: Note: This position works a rotating shift schedule, Week 1: Monday, Tuesday, Friday, Saturday Week 2: Sunday, Wednesday, Thursday, ~12 hours per day 6:50 AM – 7:00 PM Ideal Candidate: GMP experience is a must, drive, Independent but able to work within a team structure, Proficient in Microsoft Office (e.g., Outlook, Word, Excel,...

Job SummaryWe are seeking a skilled Quality Assurance Assistant to join our team at Access Anvil Corp. As a key member of our Scott System QA team, you will play a critical role in ensuring the quality of our products and services.About UsThe Fort Miller Group, Inc. is a leading manufacturer of plastic and urethane formliners, concrete foam formwork, and...

About Client: The client is one of the world's largest independent biotechnology companies, focusing on the discovery, development, and manufacturing of innovative human therapeutics. The company's areas of expertise include oncology, hematology, cardiovascular disease, inflammation, bone health, and neuroscience. It has developed a wide range of biologic...