Job Description

Biopharma Manufacturing Associate - Need Associates in Sciences or Certification in Biopharma Manufacturing; 

• They are looking for people that are planning to stay in this role for a bit of time and grow, so Candidates without degrees coming from VoTech and trade schools will be considered for candidacy.
• Masters and Ph.D. will be over qualified; Please apply for Scientist Roles with us.

Shift Timings: 10 Hours Shifts; Shift Timings may vary;
Candidate should be OK with  24x7 Rotational Shift

Description:

• Under the direction of senior personnel, performs production operations including fermentation or cell culture operations, preparation of solutions, chromatographic separation, filtration and concentration operations, autoclave and parts washing of process assemblies, and area cleaning/upkeep.
• Will be responsible for completing daily manufacturing tasks and increasing competency in different production areas over time.
• Will participate in safety and compliance initiatives, as well as investigations.
• Will engage in the organization in Production System to continuously improve safety, quality, and schedule/cost performance.

Requirements:

• • Applies organization Values and Expectations into daily tasks by engaging positively with the team, using a patient and team-first mentality to achieve personal goals.
• • With good documentation and data integrity practices, safely and compliantly completes and documents daily manufacturing tasks per standard operating procedures, batch document instructions, and logbooks
• • Proactively works with senior staff to achieve competency in production operations
• • Monitors equipment and critical process parameters, and escalates any issues or abnormalities and participating the resulting troubleshooting activities
• • Strives to maintain a high level of competency with current and emerging digital platforms (SAP, EBR, AR/VR, etc)
• • During production transition times, support commissioning, decommissioning, validation, document revisions, engineering activities and execution of technical protocols.
• • Maintain a clean and orderly production area in accordance with good housekeeping practices.
• • Proactively ensures all processing equipment and necessary materials are adequate and available to set the team up for success
• • Transparently participates in investigations that are the result of safety or compliance issues.
• • Applies organization Values and Expectations into daily tasks by engaging positively with the team, using a patient and team-first mentality to achieve personal goals.
• • With good documentation and data integrity practices, safely and compliantly completes and documents daily manufacturing tasks per standard operating procedures, batch document instructions, and logbooks
• • Proactively works with senior staff to achieve competency in production operations
• • Monitors equipment and critical process parameters, and escalates any issues or abnormalities and participating the resulting troubleshooting activities
• • Strives to maintain a high level of competency with current and emerging digital platforms (SAP, EBR, AR/VR, etc)

Education:

• BS/BA in life sciences/engineering, or Associates Degree with 1 or more years of directly related experience. Degree in other discipline (or lack of degree) may be considered if sufficient technical depth has been achieved from professional experience