Repligen
Manufacturing Specialist
Repligen, Lebanon, New Hampshire, us, 03766
Overview
Check you match the skill requirements for this role, as well as associated experience, then apply with your CV below.Avitide is a platform technology company dedicated to the discovery and development of high-performance affinity chromatography resins for the biopharmaceutical manufacturing industry. Avitide's technology platform offers an industry-leading affinity chromatography resin discovery, development, and supply timeline to reduce the overall costs of biopharmaceutical manufacturing and facilitate the delivery of new medicines to patients.
Avitide seeks qualified candidates to join the resin manufacturing team who exhibit an understanding of basic scientific principles regarding production of consumables or reagent manufacturing. The candidate will be responsible for meeting production schedules in a collaborative, fast-paced setting. This position offers an exciting opportunity to contribute to the advancement of novel therapies and medicines that impact global health.
ResponsibilitiesResponsibilities and Duties
Maintain a manufacturing clean room to ISO 14644 Class 8 specifications
Develop and maintain clean room standards to enable sterile manufacturing
Work under the guidance of Avitide's Head of Manufacturing to meet delivery schedules
Execute batch records in the manufacturing of products
Work with the Manufacturing team to develop and implement improved manufacturing processes
Documentation of verification records for the clean room and all processing equipment
Completion of all necessary quality documentation for manufacturing operations
QualificationsRecommended Qualifications and Experience
Degree (AS/BS) in biological sciences, biochemistry, or biochemical/chemical engineering preferred
1-3 years manufacturing operations experience
Experience working in a clean room environment, under a quality management system or other regulated environment is desirable
Ability to work with a minimum of supervision and a strict attention to detail
Ability to manage multiple deadlines
Adept with standard software packages (e.g. Excel, PowerPoint, Word)
Timely and strong communication skills
PDN-9d5bb812-491a-447d-9c1d-3e1b1542ced6
Check you match the skill requirements for this role, as well as associated experience, then apply with your CV below.Avitide is a platform technology company dedicated to the discovery and development of high-performance affinity chromatography resins for the biopharmaceutical manufacturing industry. Avitide's technology platform offers an industry-leading affinity chromatography resin discovery, development, and supply timeline to reduce the overall costs of biopharmaceutical manufacturing and facilitate the delivery of new medicines to patients.
Avitide seeks qualified candidates to join the resin manufacturing team who exhibit an understanding of basic scientific principles regarding production of consumables or reagent manufacturing. The candidate will be responsible for meeting production schedules in a collaborative, fast-paced setting. This position offers an exciting opportunity to contribute to the advancement of novel therapies and medicines that impact global health.
ResponsibilitiesResponsibilities and Duties
Maintain a manufacturing clean room to ISO 14644 Class 8 specifications
Develop and maintain clean room standards to enable sterile manufacturing
Work under the guidance of Avitide's Head of Manufacturing to meet delivery schedules
Execute batch records in the manufacturing of products
Work with the Manufacturing team to develop and implement improved manufacturing processes
Documentation of verification records for the clean room and all processing equipment
Completion of all necessary quality documentation for manufacturing operations
QualificationsRecommended Qualifications and Experience
Degree (AS/BS) in biological sciences, biochemistry, or biochemical/chemical engineering preferred
1-3 years manufacturing operations experience
Experience working in a clean room environment, under a quality management system or other regulated environment is desirable
Ability to work with a minimum of supervision and a strict attention to detail
Ability to manage multiple deadlines
Adept with standard software packages (e.g. Excel, PowerPoint, Word)
Timely and strong communication skills
PDN-9d5bb812-491a-447d-9c1d-3e1b1542ced6