Daniel Thomas Email & Phone Number

Haverhill, Ma, Us

Haverhill, Ma, Us

Basel, Ch

The Senior Manufacturing Project Specialist is responsible to lead manufacturing projects in partnership with the Manufacturing Leadership Team and capable to drive cross-functionally projects to completion. This person will work closely with Manufacturing Management to support the achievement of department goals, technology transfers, interdepartmental readiness and batch release requirements. The Senior Manufacturing Project Specialist is SME for their area and general business processes. This person is key contributor to technology transfer and all activities directly support campaign readiness. The Senior Project Specialist can effectively represent his functional area on site initiatives and capable interfacing with Lonza customers.The individual will manage and execute a collection of projects in addition to ensuring Manufacturing CAPA closures, Change Controls, LIRs, OTN and site deviations. The Senior Manufacturing Project Specialist has responsibility for the planning, preparation, implementation and delivery of projects assigned. The individual works cross-functionally and in collaboration with internal support departments, customers and Manufacturing suites to develop or update internal policies, procedures or steps, identifies and escalate risks, communicates changes and plan for execution.The Project Specialist is responsible for owning and driving manufacturing improvement projects from concept to completion, with a particular focus on creating efficiencies that contribute to quality, cost, on-time delivery and right first time performance.This role may include the mentoring, management and oversight of other manufacturing Project Associates, specialists and temp labor.

Basel, Ch

The Senior Asset Training Specialist acts as a liaison with the Technical & Good Manufacturing Practices (GMP) Training Department regarding training content, delivery and metrics and ensures that activities are appropriately tracked in the LMS. The Senior Asset Training Specialist role provides advanced technical proficiency and consultative guidance as a business subject matter expert (SME) in the creation of On-The Job training materials. This position is a vital business partner who is passionate about training & committed to excellence while ensuring Asset’s personnel is properly trained prior to performance. Collaborates with supported Asset to ensure training plan objectives are met through effective learning and training solutions. The role is the Asset’s POC (Point of Contact) for consulting on curriculum development for new or modified roles, and cross-assets training projects. The Senior Asset Training Specialist is a role model in the organization, understanding and promoting GMP mindset and behaviors that drive a Quality Culture.

Basel, Ch

The Asset Training Specialist II acts as a liaison with the Technical & Good Manufacturing Practices (GMP) Training Department regarding training content, delivery and metrics and ensures that activities are appropriately tracked in the LMS. The Asset Training Specialist II role provides advanced technical proficiency and consultative guidance as a business subject matter expert (SME) in the creation of On-The Job training materials. This position is a vital business partner who is passionate about training & committed to excellence while ensuring Asset’s personnel is properly trained prior to performance. Collaborates with supported Asset to ensure training plan objectives are met through effective learning and training solutions. The role is the Asset’s POC (Point of Contact) for consulting on curriculum development for new or modified roles, and cross-assets training projects. The Asset Training Specialist II is a role model in the organization, understanding and promoting GMP mindset and behaviors that drive a Quality Culture.

Basel, Ch

The Asset Training Specialist acts as a liaison with the Technical & Good Manufacturing Practices (GMP) Training Department regarding training content, delivery and metrics and ensures that activities are appropriately tracked in the LMS. The Asset Training Specialist role provides technical proficiency and consultative guidance as a business subject matter expert (SME) in the creation of On-The Job training materials. This position is a vital business partner who is passionate about training & committed to excellence while ensuring Asset’s personnel is properly trained prior to performance. Collaborates with supported Asset to ensure training plan objectives are met through effective learning and training solutions. The role is the Asset’s POC (Point of Contact) for consulting on curriculum development for new or modified roles, and cross-assets training projects. The Asset Training Specialist is a role model in the organization, understanding and promoting GMP mindset and behaviors that drive a Quality Culture.

Basel, Ch

The Senior Manufacturing Associate is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions. Senior Associates are expected to demonstrate expertise and breadth of knowledge in executing process recipes across a variety of production activities, following written procedures (SOPs), monitoring equipment and processes, independently performing laboratory tasks, including pH, conductivity testing, product sampling, and conducting routine sanitization tasks to maintain facility and equipment and train other operators on these tasks. They are expected to demonstrate expertise and technical leadership in cGMP compliance and an in-depth understanding of process flow and be able to make decisions based on that experience. Senior Manufacturing Associates are able to troubleshoot complex and non-routine equipment events, initiate and assess deviations, review batch records and logbooks. May be asked to assume responsibilities for covering shift supervisor absences/vacations.

Basel, Ch

The Manufacturing Associate Level III is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions. Level III associates are expected to be fully proficient in executing process recipes, following written procedures (SOPs), monitoring equipment and processes, independently performing laboratory tasks, including pH, conductivity testing, product sampling, and conducting routine sanitization tasks to maintain facility and equipment and train other operators on these tasks. They are expected to demonstrate a significant knowledge of cGMP compliance and an in-depth understanding of process flow and be able to make decisions based on that experience. Level III Operators are able to troubleshoot routine and non-routine equipment events, initiate deviations, review batch records and logbooks.

Dover, Nh, Us

Basel, Ch

The Technology Transfer Lead is primarily responsible for activities related to process development and technology transfer from R&D into production but also includes ongoing technical support for manufacturing. Specific responsibilities include the following:• Utilize quality principles to ensure products under development (R&D) meet their critical quality attributes.• Interface with Operations, Regulatory and Quality Assurance and Quality Control departments to complete experimental/optimization trials and technology transfer of new products to production.• Development and coordination of related manufacturing transfer documentation.• Standard Operating Procedure (SOP) creation and revisions.• Investigation of Manufacturing Events.• Performing Process Development/Improvement & Engineering studies.• Creating and updating documentation needed for Regulatory Submissions.• Assists in the preparation and presentation of department Key Performance Indicators through routine progress report updates to the management team.• Collaborate and communicate with other specialists and leaders to coordinate cross-project initiatives and activities.• Work with both internal and external resources to achieve technical business solutions within project guidelines.• Respond to operational issues and information requests within defined areas of responsibility while progressing on work assignments.

Basel, Ch

The Manufacturing Associate Level III is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions. Level III associates are expected to be fully proficient in executing process recipes, following written procedures (SOPs), monitoring equipment and processes, independently performing laboratory tasks, including pH, conductivity testing, product sampling, and conducting routine sanitization tasks to maintain facility and equipment and train other operators on these tasks. They are expected to demonstrate a significant knowledge of cGMP compliance and an in-depth understanding of process flow and be able to make decisions based on that experience. Level III Operators are able to troubleshoot routine and non-routine equipment events, initiate deviations, review batch records and logbooks.

Responsible for creating a unique computer record of each immigrant visa petition that comes to the NVC. Responsible for the verification of original documents, and IRS tax forms. Department of State security clearance, Qualified to work with Sensitive but Unclassified information. Able to pass a typing test at 30 words per minute and 6,200 keystrokes per hour with no more than 10 errors.

Laval, Québec, Ca

The assistant manager is a lead part of a fully functioning team. Ensuring all employees are working together simultaneously to keep a store at an above-average company standard, while entertaining and satisfying customers. Routine daily duties include: paperwork processing, time management, scheduling, problem solving, cleaning, organizing, monthly audit accountability.

Bachelor'S Degree, Social Studies Teacher Education

Associate'S Degree, Liberal Arts And Sciences/Liberal Studies