Vertex Pharmaceuticals
2nd shift Medical Device Assembly (Contract)
Vertex Pharmaceuticals, Providence, Rhode Island, us, 02912
Job Description:
2nd Shift Manufacturing Operations TechnicianHours 1:30 to 10:00 pmThe Manufacturing Operations Technician is responsible for supporting daily cGMP manufacturing operations, including disassembly, and cleaning of the facility and process equipment.Job Description:This role will focus on the fabrication of cell encapsulation devices for delivering proprietary cells, including manufacturing of all components and final assembly of the finished device. The Successful Candidate will join the Device Manufacturing Team and work closely with the Device Process Development, Device Quality Control, and Device Quality Assurance Functions, as required. The position will be located in Providence, R.I..
Key Responsibilities:
Execute daily maintenance and startup activities of all manufacturing Unit Operations.
Manufacture and assemble Medical Devices in an ISO 7/8 Environment, ensuring compliance with c.G.M.P.
Procedures and all Cleanroom Practices in each Unit Operation.
Complete and compile Batch Records in a manner that complies with c.G.M.Ps. / c.G.D.Ps., and all relevant Procedures.
Comply with all Company Policies including Health, Safety, and Environmental Regulations, Personal Protective Equipment Requirements, and Standard Operating Procedures.
Ensure upkeep of Manufacturing Areas to allow for a clean, safe, and organized Work Environment.
Review and train to Work Instructions and other relevant documents on an as-needed basis.
Prioritize and plan work activities, and adapt to changing Production Schedules and other conditions, as required.
Participate in Process Capability Assessments, Process Validation Activities, Root Cause Investigations, Corrective and Preventative Actions, Physical Inventory, Cycle Counts, Variance Investigation and Reconciliation, and other Cross-Functional Activities, as required.
Review all Manufacturing Documentation, including Assembly, Inspection, Test, and Packaging Procedures, and provide feedback.
Key Duties and Responsibilities:Support facility operation, taking direction from Facilities/Operations, Quality, EH&S, Materials Management and the Release and Stability LaboratoryFollows SOPs, policies and all other relevant work instructions to ensure the successful and compliant operation of the drug product facilityCleans the facility and process equipmentEnters data into log booksMaintains understanding of, and strict adherence, to cGMP requirementsComplies with all on-going training requirementsKnowledge and Skills:Ability to follow verbal and written instructions in EnglishVisual AcuityAbility to distinguish between the colors red, yellow, blue and greenAbility to lift up to 50lbs.Communication skills, as well as documentation skillsBasic computer skills and demonstrated ability to learn new systems and understand new technologies.Flexibility to support shift work as required. This position may require overtime, as needed, supporting operations on late or early production shifts.Education and Experience:High School Diploma or GEDTypically requires less than 1 year experience or the equivalent combination of education and experience
Pay Range:$30/HRShift/Hours:2nd Shift Manufacturing Operations TechnicianHours 1:30 to 10:00 pmRequisition Disclaimer:This job posting is for a is for a temporary role with a third-party agency partner on assignment at Vertex Pharmaceuticals. The individual selected for this role will be offered the role as an employee of a third-party agency partner; compensation, medical benefits, fringe benefits and other terms and conditions of employment shall be presented by the third-party agency partner upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on a number of factors, including skills, competencies, experience, location and/or being pursued and other job-related factors permitted by law. In addition, this role will be eligible for overtime pay, in accordance with federal and state requirementsBy applying for this position, you agree to the Terms and Conditions. Agreeing to these terms, includes permission to use the email address and mobile phone number you provide during the application process or throughout the duration of your prospective or actual employees to notify you of job openings, profiles, articles, news, and other employment-related information, as well as to notify you of special promotions or additional products and services offered by us or our affiliates and partners (collectively, Atrium Alerts). Atrium Alerts may be sent by email, phone, or text message. Your personal information will be safely stored in our database. Atrium does not sell your personal information to third parties. Text message and data rates may apply. To OPT OUT of text messaging or to modify your communication preferences for Atrium Alerts at any time, please contact us at privacyadministrator@atriumstaff.com.If you do not agree with the Atrium Terms and Conditions, you can still complete your application for this position by emailing your resume to our team at tempstaffing@vrtx.com. Please include the job title in the subject of your email.
No C2C or Third-Party Vendors
2nd Shift Manufacturing Operations TechnicianHours 1:30 to 10:00 pmThe Manufacturing Operations Technician is responsible for supporting daily cGMP manufacturing operations, including disassembly, and cleaning of the facility and process equipment.Job Description:This role will focus on the fabrication of cell encapsulation devices for delivering proprietary cells, including manufacturing of all components and final assembly of the finished device. The Successful Candidate will join the Device Manufacturing Team and work closely with the Device Process Development, Device Quality Control, and Device Quality Assurance Functions, as required. The position will be located in Providence, R.I..
Key Responsibilities:
Execute daily maintenance and startup activities of all manufacturing Unit Operations.
Manufacture and assemble Medical Devices in an ISO 7/8 Environment, ensuring compliance with c.G.M.P.
Procedures and all Cleanroom Practices in each Unit Operation.
Complete and compile Batch Records in a manner that complies with c.G.M.Ps. / c.G.D.Ps., and all relevant Procedures.
Comply with all Company Policies including Health, Safety, and Environmental Regulations, Personal Protective Equipment Requirements, and Standard Operating Procedures.
Ensure upkeep of Manufacturing Areas to allow for a clean, safe, and organized Work Environment.
Review and train to Work Instructions and other relevant documents on an as-needed basis.
Prioritize and plan work activities, and adapt to changing Production Schedules and other conditions, as required.
Participate in Process Capability Assessments, Process Validation Activities, Root Cause Investigations, Corrective and Preventative Actions, Physical Inventory, Cycle Counts, Variance Investigation and Reconciliation, and other Cross-Functional Activities, as required.
Review all Manufacturing Documentation, including Assembly, Inspection, Test, and Packaging Procedures, and provide feedback.
Key Duties and Responsibilities:Support facility operation, taking direction from Facilities/Operations, Quality, EH&S, Materials Management and the Release and Stability LaboratoryFollows SOPs, policies and all other relevant work instructions to ensure the successful and compliant operation of the drug product facilityCleans the facility and process equipmentEnters data into log booksMaintains understanding of, and strict adherence, to cGMP requirementsComplies with all on-going training requirementsKnowledge and Skills:Ability to follow verbal and written instructions in EnglishVisual AcuityAbility to distinguish between the colors red, yellow, blue and greenAbility to lift up to 50lbs.Communication skills, as well as documentation skillsBasic computer skills and demonstrated ability to learn new systems and understand new technologies.Flexibility to support shift work as required. This position may require overtime, as needed, supporting operations on late or early production shifts.Education and Experience:High School Diploma or GEDTypically requires less than 1 year experience or the equivalent combination of education and experience
Pay Range:$30/HRShift/Hours:2nd Shift Manufacturing Operations TechnicianHours 1:30 to 10:00 pmRequisition Disclaimer:This job posting is for a is for a temporary role with a third-party agency partner on assignment at Vertex Pharmaceuticals. The individual selected for this role will be offered the role as an employee of a third-party agency partner; compensation, medical benefits, fringe benefits and other terms and conditions of employment shall be presented by the third-party agency partner upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on a number of factors, including skills, competencies, experience, location and/or being pursued and other job-related factors permitted by law. In addition, this role will be eligible for overtime pay, in accordance with federal and state requirementsBy applying for this position, you agree to the Terms and Conditions. Agreeing to these terms, includes permission to use the email address and mobile phone number you provide during the application process or throughout the duration of your prospective or actual employees to notify you of job openings, profiles, articles, news, and other employment-related information, as well as to notify you of special promotions or additional products and services offered by us or our affiliates and partners (collectively, Atrium Alerts). Atrium Alerts may be sent by email, phone, or text message. Your personal information will be safely stored in our database. Atrium does not sell your personal information to third parties. Text message and data rates may apply. To OPT OUT of text messaging or to modify your communication preferences for Atrium Alerts at any time, please contact us at privacyadministrator@atriumstaff.com.If you do not agree with the Atrium Terms and Conditions, you can still complete your application for this position by emailing your resume to our team at tempstaffing@vrtx.com. Please include the job title in the subject of your email.
No C2C or Third-Party Vendors