As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Focusing on immune diseases like HIV that affect a large percentage of the population, the work our longtime partner conducts is imperative to a better, healthier future. To be recognized as a crucial part to furthering this goal, join this growing team now!
location: King Of Prussia, Pennsylvania
job type: Contract
salary: $34.00 - 35.76 per hour
work hours: 9 to 5
education: Bachelors
responsibilities:
As a Biopharm Manufacturing Associate II, you will perform 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 Production System to continuously improve safety, quality, and schedule/cost performance. The purpose of this role is to be a part of a dynamic, multi-tiered operations team that brings life changing and lifesaving medicine to patients around the world. They will demonstrate Values (Patient Focus, Transparency, Respect, & Integrity) and Expectations (Courage, Accountability, Development, & Teamwork) daily by engaging positively with team members and production support groups. Under the direction of senior personnel, the biopharmaceutical manufacturing associate II performs a
variety of largescale production operations, interacting with automated equipment and
monitoring/processing data. Will be responsible for completing daily manufacturing tasks and increasing competency in different production areas over time. They will participate in safety and compliance initiatives, investigations, and help solve technical and organizational problems while working with different teams of experts. Will work within these teams to continuously improve safety, quality, and schedule/cost performance.
This role will provide YOU the opportunity to lead key activities to progress YOUR career.
- Demonstrate company Values - Patient Focus, Transparency, Respect, and Integrity - in every interaction, in every work task, and with every responsibility of the job role.
- Live company's Expectations of Courage, Accountability, Development, and Teamwork to achieve high performing behaviors in the workplace.
- 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 work with senior staff to achieve competency in production operations.
- Supports in cross-functional activities, such as engineering actions, validation actions and Tech Transfer actions, including proactive safety and compliance input prior to execution.
- Primarily these activities are within the production suite but sometimes require out-of-suite or off-site work (i.e. FAT support).
- Monitors equipment and critical process parameters and escalate any issues or abnormalities and participating in the resulting troubleshooting activities.
- Strives to maintain a high level of competency with current and emerging digital platforms (SAP, EBR, AR/VR, etc).
- By learning the production schedule and assessing it daily, 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.
qualifications:
- BS/BA degree, with cGMP manufacturing experience.
- OR an Associate's degree from Montgomery county community college in Biotechnology or related technical field with cGMP manufacturing experience.
- OR High School degree, 1+ years of cGMP manufacturing experience.
- Open to any other scientific background education or experience.
skills: MS-WORD, MS-EXCEL, MS-Powerpoint, GMP (Good Manufacturing Practice)
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.
Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).
This posting is open for thirty (30) days.
