Biopharm Manufacturing Associate

Randstad USA; King of Prussia (Montgomery County); On-site; USD 60,000 - 80,000; Full time

Job summary

A leading company in biopharmaceuticals is seeking a Biopharm Manufacturing Associate II to perform key production operations. This role offers the chance to ensure safety, quality, and manufacturing excellence while engaging with an experienced team. Ideal candidates will possess relevant educational qualifications and cGMP experience, along with essential teamwork and communication skills.

Benefits

Comprehensive benefits package

401K plan

Medical, dental, and vision insurance

Short-term disability

Life insurance offerings

Qualifications

• Experience in cGMP manufacturing environments is important.
• Ability to accurately document processing tasks.
• Strong teamwork and communication skills are necessary.

Responsibilities

• Complete and document daily manufacturing tasks safely.
• Monitor equipment and critical process parameters.
• Engage in investigations related to safety or compliance.

Skills

GMP

Verbal skills

Written skills

Teamwork

Education

BS/BA degree with cGMP manufacturing experience

Associate's degree in Biotechnology

High School diploma with 1+ years of cGMP experience

Tools

MS-WORD

MS-EXCEL

MS-PowerPoint

Job description

job summary:
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.


location: King Of Prussia, Pennsylvania
job type: Contract
salary: $22.00 - 24.50 per hour
work hours: 9 to 5
education: Bachelors

responsibilities:

• 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:
Required:

• 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

Preferred:

• Demonstrated level of high performance
• Strong verbal and written skills
• The ability to work well in a team environment
• Must be able to follow detailed processing instructions as well as accurately document all necessary documentation

#LI-AL1


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 [e-mail].

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.

Required:

• 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

Preferred:

• Demonstrated level of high performance
• Strong verbal and written skills
• The ability to work well in a team environment
• Must be able to follow detailed processing instructions as well as accurately document all necessary documentation

#LI-AL1