Similar posts
Biopharmaceutical Manufacturing Associate
- Contract
- Manufacturing
- United States
This vacancy has now expired. Please see similar roles below...
BPMA - Contract - King of Prussia, PA
Proclinical is seeking a skilled BPMA to join a dynamic team in an exciting contract opportunity. This position offers an opportunity to work collaboratively across functions, contribute to process improvements, and develop expertise in cutting-edge digital platforms.
Primary Responsibilities:
The successful candidate will support manufacturing operations by ensuring compliance with standard operating procedures and maintaining high standards of safety and documentation.
Skills & Requirements:
- A degree in one of the following:
- BS/BA with cGMP manufacturing experience.
- Associate's degree in biotechnology or a related technical field with cGMP manufacturing experience.
- High school diploma with at least 1 year of cGMP manufacturing experience.
- Strong verbal and written communication skills.
- Ability to work effectively in a team environment.
- Demonstrated ability to follow detailed processing instructions and maintain accurate documentation.
- A high level of performance and attention to detail is preferred.
The BPMA's responsibilities will be:
- Perform daily manufacturing tasks safely and compliantly, adhering to standard operating procedures and batch documentation.
- Maintain accurate and thorough documentation with a focus on data integrity.
- Collaborate with senior staff to build competency in production operations.
- Support cross-functional activities, including engineering, validation, and tech transfer actions, while providing proactive safety and compliance input.
- Monitor equipment and critical process parameters, escalating issues and participating in troubleshooting as needed.
- Stay current with and utilize emerging digital platforms such as SAP, EBR, and AR-VR.
- Assess production schedules daily to ensure all necessary equipment and materials are prepared and available.
- Participate transparently in investigations related to safety or compliance concerns.
If you are having difficulty in applying or if you have any questions, please contact Jackie Cerchio at j.cerchio@proclinical.com
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.
By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - https://www.proclinical.com/privacy-policy
Related jobs
Highly Competitive
Zaventem, België
Join our client where engineering meets impact and take the next leap in your career with this Technical Support Representative position!
Highly Competitive
Moreton, England
Step into a UK CSO Technician role where innovation meets precision in clinical trial packaging excellence.
Highly Competitive
Visp, Switzerland
Where environmental monitoring expertise meets precision, compliance, and process excellence.
Highly Competitive
Zaventem, Belgium
Join a company where engineering meets impact! Your next position in Diagnostics starts here.
Highly Competitive
Visp, Switzerland
Step into a pivotal role at a global CMO and help shape the future of healthcare infrastructure.
Highly Competitive
Visp, Schweiz
Where smart scheduling meets GMP-compliant engineering excellence.
Highly Competitive
Visp, Schweiz
Be the driving force behind seamless logistics for a global CMO, where precision and efficiency are key to supporting world-class manufacturing.
Highly Competitive
Basel, Schweiz
Keeping lab operations running seamlessly through precise logistics, inventory control, and supplier coordination.