Process Coordinator Salary at Collabera BETA

Specialist, QA Engineering 100% Onsite Work Schedule: Monday - Friday, Business Hours Position Summary: This role is responsible for providing quality oversight on technology transfer into and out of the site, process understanding and enhancement, and other site qualification activities in a fast-paced, highly collaborative manufacturing facility. This team supports the Cell Therapy Development early clinical drug product manufacturing facility, which supplies autologous and allogeneic cell therapies for first-in-human and pivotal clinical trials. Duties/Responsibilities : QA lead on technology transfer activities (process): Ensure technology transfers on new product introduction and/or new trials and cohorts are compliant with internal standards and/or regulatory requirements, as applicable. Maintain knowledge of scientific literature, regulatory guidelines, internal standards/procedures and apply key concepts during project activities/plans. Interact and coordinate with other QA fun

Quality - Specialist, QA Engineering Location: 100% Onsite role, Warren NJ Duration: 8 Months Contract with high possibilities of extension Work Schedule: Monday - Friday, Business Hours Must Haves: Providing quality oversight on technology transfer Must have strong authorship and be able to critically review investigations and reports, interpret results, and generate technical conclusions consistent with quality risk management principles. Must have strong understanding of global cGMP, quality systems (especially change management), and guidance documents. Bachelor's degree required Position Summary: This role is responsible for providing quality oversight on technology transfer into and out of the site, process understanding and enhancement, and other site qualification activities in a fast-paced, highly collaborative manufacturing facility. This team supports the Cell Therapy Development early clinical drug product manufacturing facility, which supplies autologous and allogeneic cel

Quality Assurance Specialist- Technology Transfer Rate type: W2 only 100% Onsite role, Warren NJ Work Schedule: Monday - Friday, Business Hours Bachelor's degree required Must Haves: Providing quality oversight on technology transfer Must have strong authorship and be able to critically review investigations and reports, interpret results, and generate technical conclusions consistent with quality risk management principles. Must have strong understanding of global cGMP, quality systems (especially change management), and guidance documents. Position Summary: This role is responsible for providing quality oversight on technology transfer into and out of the site, process understanding and enhancement, and other site qualification activities in a fast-paced, highly collaborative manufacturing facility. This team supports the Cell Therapy Development early clinical drug product manufacturing facility, which supplies autologous and allogeneic cell therapies for first-in-human and pivotal

Hope you are doing well. I am Srinivas from Futran Solutions. My client is looking for the below requirement. If you are interested. Please reach me out msrinivas@futransolutions.com / (609)-945-2335, Ext: 9068 Job Title: Quality - Specialist, QA Engineering - 61017-1 Location: Warren NJ – 100% Onite Work Schedule: Monday - Friday, Business Hours Bachelor's degree required. Must Haves: Providing quality oversight on technology transfer Must have strong authorship and be able to critically review investigations and reports, interpret results, and generate technical conclusions consistent with quality risk management principles. Must have strong understanding of global cGMP, quality systems (especially change management), and guidance documents. Position Summary: This role is responsible for providing quality oversight on technology transfer into and out of the site, process understanding and enhancement, and other site qualification activities in a fast-paced, highly collaborative manuf

Job Description Job Description Position: Payroll Analyst Location: REMOTE POSITION Contract Position on W2 (USC OR GC) SHIFT - MON-FRI 8:30AM - 4:30PM EST. DURATION - 3-6 MONTHS This position is directly responsible for supporting the U.S. Payroll Team in the efficient and timely completion of payroll processing, maintenance of employee tax withholding elections, delivery of net payments and garnishments. Responsibilities: · Interfaces with various functions to address daily issues. · Addresses identified issues in a timely and compliant manner. · Ensuring compliance with identified payroll deadlines as it relates to internal controls and payroll processing. · Coordinate with HR Sites to ensure timely and accurate pay to employees. · Responsible for the preparation of adhoc payments and pay adjustment calculations for both ON-cycle and OFF-cycle payments. · Responsible for the preparation of import files for inclusion in ON-cycle and OFF-cycle payment processing. · Research and resolv

Job Summary Talent Acquisition (TA) Coordinator is responsible for the timely and efficient support of the day-to-day Talent Acquisition operations, from recruitment through the initial onboarding process. In addition, will participate in special projects and liaise with other functional groups. At all times, the TA Coordinator strives to provide the best customer experience, both internally and externally, that creates a positive impression of Terumo. Job Details/Responsibilities Partner with the Recruiting team to best organize and effectively manage the day-to-day administrative operations of the Talent Acquisition department, from the initial job opening through the onboarding process. Coordinate interview schedules with candidates and internal interview teams, taken into account the dynamics of the organization/team/individuals as well as priorities. Make and maintain any necessary travel arrangements and ensure all parties are informed and related expenses are submitted promptly.

Job Description Job Description Summary: We are seeking a dedicated Shift Supervisor to oversee production and quality on the third shift, working Tuesday through Saturday from 12:45 AM to 8:15 AM. In this role, you will ensure that production activities align with customer requirements and delivery deadlines by effectively supervising the shift's operations. Essential Functions: Oversee and coordinate manufacturing functions to ensure timely product delivery. Supervise and support staff, ensuring proper training and adherence to performance standards. Manage all aspects of the injection molding process, including machine setup, process adjustments, inspections, troubleshooting, maintenance, and material loading to maintain efficient production. Ensure the production of high-quality parts in line with production schedules and quality standards. Collaborate with departments such as Quality, Maintenance, Planning (OpEx), and Warehouse to address process issues and ensure both internal an

Job Description Job Description We offer an exciting and rewarding opportunity for an enterprising manufacturing professional to be part of multiple and related start-up success stories in the biotech and biopharma industries. You will work closely with the founders, who are themselves accomplished entrepreneurs who have successfully launched and scaled-up similar businesses in the past, and who are also actively involved in launching this new enterprise. The Production Supervisor will be responsible for leading, planning, organizing, and directing all daily activities for three related manufacturing operations in start-up mode. These operations produce various proprietary components and parts for rapidly growing segments of biotech and biopharma processing equipment markets. The products are made from various synthetic polymer and elastomer materials using injection molding processes and equipment, typically manufactured in batch mode. Essential Duties and Responsibilities Plans and d