job summary: We are seeking a highly skilled and experienced Senior QA Specialist to join our dynamic team. In this role, you will be responsible for overseeing the quality assurance process, supporting batch disposition of drug substance, ensuring that our products meet both Local and Global quality standards. location: Cambridge, Massachusetts job type: Contract salary: $59.00 - 61.63 per hour work hours: 9 to 5 education: Bachelors resp
job summary: We are seeking a highly skilled and experienced Senior QA Specialist to join our dynamic team. In this role, you will be responsible for overseeing the quality assurance process, supporting batch disposition of drug substance, ensuring that our products meet both Local and Global quality standards. location: Cambridge, Massachusetts job type: Contract salary: $59.00 - 61.63 per hour work hours: 9 to 5 education: Bachelors resp
Are you an experienced Maintenance Technician with a solid understand of manufacturing equipment and electrical components in a GMP environment? Our client, a local company in North Billerica, is seeking experienced professionals for a direct hire position. If you are looking for a great company culture and a new opportunity with great benefits and pay, then look no further. Apply today! You will provide high level maintenance and repair services to autom
Are you an experienced Maintenance Technician with a solid understand of manufacturing equipment and electrical components in a GMP environment? Our client, a local company in North Billerica, is seeking experienced professionals for a direct hire position. If you are looking for a great company culture and a new opportunity with great benefits and pay, then look no further. Apply today! You will provide high level maintenance and repair services to autom
job summary: Description of the position: Facilitate and coordinate the sending out of testing samples and ensuring timely receipt of results and disposition of materials. Leading the document control process for Pure programs. location: Sudbury, Massachusetts job type: Contract salary: $24.00 - 24.50 per hour work hours: 9 to 5 education: Bachelors responsibilities: Description of principal responsibilities: Daily Responsibilities: Pr
job summary: Description of the position: Facilitate and coordinate the sending out of testing samples and ensuring timely receipt of results and disposition of materials. Leading the document control process for Pure programs. location: Sudbury, Massachusetts job type: Contract salary: $24.00 - 24.50 per hour work hours: 9 to 5 education: Bachelors responsibilities: Description of principal responsibilities: Daily Responsibilities: Pr
job summary: Description of the position: Facilitate and coordinate the sending out of testing samples and ensuring timely receipt of results and disposition of materials. Leading the document control process for Pure programs. location: Sudbury, Massachusetts job type: Contract salary: $24.00 - 24.50 per hour work hours: 9 to 5 education: Bachelors responsibilities: Description of principal responsibilities: Daily Responsibilities: Pr
job summary: Description of the position: Facilitate and coordinate the sending out of testing samples and ensuring timely receipt of results and disposition of materials. Leading the document control process for Pure programs. location: Sudbury, Massachusetts job type: Contract salary: $24.00 - 24.50 per hour work hours: 9 to 5 education: Bachelors responsibilities: Description of principal responsibilities: Daily Responsibilities: Pr
Reporting to the Associate Director of Quality Control, Moderna is seeking a QA Quality Systems and Distribution specialist based at their Norwood, MA site. The individual in this role will perform QC Raw Material activities in support of GMP Manufacturing and further support special projects as assigned. This position will be 1 st shift working Monday through Friday or (W-Sat shift, 10 hour days)salary: $45 - $60 per hourshift: Firstwork hours:
Reporting to the Associate Director of Quality Control, Moderna is seeking a QA Quality Systems and Distribution specialist based at their Norwood, MA site. The individual in this role will perform QC Raw Material activities in support of GMP Manufacturing and further support special projects as assigned. This position will be 1 st shift working Monday through Friday or (W-Sat shift, 10 hour days)salary: $45 - $60 per hourshift: Firstwork hours:
job summary: - Collaborate with immunogenicity team members to develop and establish a new version of an in vitro immunopeptidomics assay by advancing the sensitivity, robustness and throughput of an existing methodology - Contribute to the new assay qualification design, execution, and establishment of quality control parameters - Apply the qualified method to support ongoing biologic drug project immunogenicity analyses - Maintain analytical mass spectr
job summary: - Collaborate with immunogenicity team members to develop and establish a new version of an in vitro immunopeptidomics assay by advancing the sensitivity, robustness and throughput of an existing methodology - Contribute to the new assay qualification design, execution, and establishment of quality control parameters - Apply the qualified method to support ongoing biologic drug project immunogenicity analyses - Maintain analytical mass spectr
job summary: As a Quality Systems Specialist, you will be responsible for providing effective and efficient support to the Quality Management Systems (QMS) team by maintaining compliance with company policies, QMS standards, and local regulations. You will report to the QMS Manager. This position provides the opportunity to work directly with Manufacturing, Facilities, QA, and QC staff to manage QA Compliance activities for the Binney St. site in Cambridg
job summary: As a Quality Systems Specialist, you will be responsible for providing effective and efficient support to the Quality Management Systems (QMS) team by maintaining compliance with company policies, QMS standards, and local regulations. You will report to the QMS Manager. This position provides the opportunity to work directly with Manufacturing, Facilities, QA, and QC staff to manage QA Compliance activities for the Binney St. site in Cambridg
The individual in this role will be part of a cohesive team responsible for supporting cGMP mRNA drug products produced at this facility. He/she will provide quality oversight and expertise to enable technical success with stringent adherence to a Quality System that respects global regulatory expectations. The successful candidate will have experience in quality oversight or manufacturing experience in early stage clinical products. They will be able to i
The individual in this role will be part of a cohesive team responsible for supporting cGMP mRNA drug products produced at this facility. He/she will provide quality oversight and expertise to enable technical success with stringent adherence to a Quality System that respects global regulatory expectations. The successful candidate will have experience in quality oversight or manufacturing experience in early stage clinical products. They will be able to i
The individual in this role will be part of a cohesive team responsible for supporting cGMP mRNA drug products produced at this facility. He/she will provide quality oversight and expertise to enable technical success with stringent adherence to a Quality System that respects global regulatory expectations. The successful candidate will have experience in quality oversight or manufacturing experience in early stage clinical products. They will be able to i
The individual in this role will be part of a cohesive team responsible for supporting cGMP mRNA drug products produced at this facility. He/she will provide quality oversight and expertise to enable technical success with stringent adherence to a Quality System that respects global regulatory expectations. The successful candidate will have experience in quality oversight or manufacturing experience in early stage clinical products. They will be able to i
Reporting to the Associate Director of Quality Control, Moderna is seeking a Quality Control Raw Materials Associate I based at their Norwood, MA site. The individual in this role will perform QC Raw Material activities in support of GMP Manufacturing and further support special projects as assigned. This position will be 1 st shift working Monday through Friday.salary: $32 - $38 per hourshift: Firstwork hours: 8 AM - 4 PMeducation: BachelorsRes
Reporting to the Associate Director of Quality Control, Moderna is seeking a Quality Control Raw Materials Associate I based at their Norwood, MA site. The individual in this role will perform QC Raw Material activities in support of GMP Manufacturing and further support special projects as assigned. This position will be 1 st shift working Monday through Friday.salary: $32 - $38 per hourshift: Firstwork hours: 8 AM - 4 PMeducation: BachelorsRes
job summary: BioMedicine Design (BMD) High-Throughput Protein Production (HTP) Group is seeking a highly motivated scientist to support the molecular biology & protein production workflows: DNA construct design/assembly, PCR, sample preparation for sequencing, DNA production & quantitation, mammalian cell culture & transfections, protein purification & quantitation, and automated liquid handling. The candidate will play a major role in a core group that c
job summary: BioMedicine Design (BMD) High-Throughput Protein Production (HTP) Group is seeking a highly motivated scientist to support the molecular biology & protein production workflows: DNA construct design/assembly, PCR, sample preparation for sequencing, DNA production & quantitation, mammalian cell culture & transfections, protein purification & quantitation, and automated liquid handling. The candidate will play a major role in a core group that c
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