Senior Manager, Biopharmaceuticals - Middleton

Are you a results-driven biopharmaceutical sales professional looking to be part of an organization that values being curious, adaptable and accountable? · Lundbeck is a global biopharmaceutical company focusing exclusively on brain health.Business Planning & Account Leadership - ...

The LMS Training Project Manager is responsible for supporting the Manufacturing operations and cross-functional teams initiating, developing and distributing training compliance metrics, reporting on training trends, and overseeing training curricula content, structure and assig ...

We are seeking a highly qualified Capital Projects Engineer to support a strategic, year-long initiative within the Capital Projects group at a major biopharmaceutical facility located in Andover, MA. · ...

We are seeking a highly qualified Capital Projects Engineer to support a strategic, year-long initiative within the Capital Projects group at a major biopharmaceutical facility located in Andover, MA. · This role offers significant exposure to site-level capital project planning ...

+This role will provide non-testing support for raw material testing for new and existing products in a cGMP Quality Control Analytical (QCA) department.+ · + Revise and author GMP documents · Create and submit change requests to laboratory information management system (LIMS) bu ...

Provide QA Validation support to validation activities associated with Quality Control (QC) Laboratory instruments. · Candidate requires strong interpersonal oral and written communication skills as there is a high degree of collaboration required between members of QA Validation ...

We are seeking a highly qualified Capital Projects Engineer to support a strategic, year-long initiative within the Capital Projects group at a major biopharmaceutical facility located in Andover, MA. · Serve as the engineering lead for assigned capital projects. · Oversee the de ...

+Job summary · Capital Projects Engineer (12-Month Assignment Onsite) · +ResponsibilitiesServe as the engineering lead for assigned capital projects, managing the design process in collaboration with architectural/engineering (AE) firms and equipment vendors. · Oversee the develo ...

+ 12 month contract in Andover, MA. · Top 3 critical skills:Strong working knowledge of the validation lifecycle including computer system validation. · Working knowledge of data integrity regulations. · ...

A Technical Writer position is available at an undisclosed company. The role involves authoring technical protocols, reports, and related correspondence. · ...

Our client, a leading biopharmaceutical manufacturing organization, is seeking a dedicated and detail-oriented Quality Assurance Inspector to join their team. · ...

The Data Integrity Analyst will provide Quality Assurance oversight in support of a site project to remediate Data Integrity (DI) commitments. · The individual will be responsible for the quality review and approval of validation and change control documentation such as protocols ...

The technology transfer project support position serves as a key support role to the technology transfer project manager in managing logistical, scheduling, and documentation aspects of certain technology transfer projects. · ...

This role will provide non-testing support for raw material testing for new and existing products in a cGMP Quality Control Analytical (QCA) department. · This support includes writing and revising technical documents (procedures, test methods, raw material specifications) for ne ...

A highly motivated entry-level associate process scientist or engineer to join our interdisciplinary bioprocessing team.Execute routine laboratory studies to support portfolio of marketed biological products. · Perform work in a controlled laboratory environment. · ...

The individual will be responsible for the quality review and approval of validation and change control documentation such as protocols test plans various computer validation testing documents deviations and change controls in relation to DI remediation activities.The documentati ...

At Pfizer, every day is an opportunity to make a difference in patients' lives. Your contributions will directly impact patient care, as you work within a flexible, innovative and customer-oriented culture rooted in science and risk-based compliance. · ...

This role will provide non-testing support to the QC Analytical department for product life cycle management and technology transfer activities. · The technical skills within scope will require understanding of the scientific principles of test methods, data analysis and cGMP req ...

The individual will be responsible for the quality review and approval of validation and change control documentation such as protocols, test plans, various computer validation testing documents, deviations, · and change controls in relation to DI remediation activities.The docum ...

The technical services support position provides technical logistical administrative and documentation support for activities pertaining to biologics drug substance production at the Andover location. · Authoring of technical protocols reports memorandum records regulatory submis ...

The technical writer provides technical writing, administrative, and logistical support for technology projects. · Authoring of technical protocols, reports, memorandum, records, and related correspondence · Retrieve and compile data from electronic sources / databases and paper ...