- 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!
- 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.
location: King Of Prussia, Pennsylvania
job type: Contract
work hours: 9 to 5
education: Bachelors
responsibilities:
- Preparation, cleaning, sterilization, batching, pasteurization or filtration and delivery of media and solutions for cell culture and purification operations.
- Perform the set-up, operation, cleaning and break-down of process equipment.
- Perform sampling procedures on various analytical instruments to analyse cell culture, solution and/or product concentration characteristics. Operate Filter integrity devices to confirm the integrity of filters pre and post use.
- Perform process operations, equipment and instrument monitoring and trending to enable proactive identification of issues to escalate and correct with applicable departments.
- Set-up of fixed and mobile process equipment and parts with CIP skids to carry out validated cleaning and sterilization processes.
- Follow appropriate standard operating procedures (SOPs), protocols and batch records/logbooks to safely perform process operations and document compliantly with good documentation and data integrity practices.
- Follow all related safety policies and procedures and Put safety first by playing an active role in identifying and correcting unsafe behaviours and conditions.
- Ability to choose a type of communication that is most effective in each situation.
qualifications:
Must have:
- Bachelor of Science degree in Chemical Engineering, Biology, Chemistry, or other engineering or scientific field
- Familiarity with Good Manufacturing Practices (GMP) regulations
- Experience and knowledge of cGMP guidelines and standards. (1+ years)
- Knowledgeable of upstream equipment (aka unit operations) and process overview (media prep, small scale, large scale), Analytical equipment (VI-Cell, NOVA, Centrifuge, tubing welder), PLC / DCS / HMI
skills: SOP, MS-WORD, MS-EXCEL, MS-Powerpoint, Biology, Chemistry, 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: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).
This posting is open for thirty (30) days.
