Similar posts
Biopharmaceutical Manufacturing Associate
- Contract
- Good Manufacturing Practice (GMP)
- United States
This vacancy has now expired. Please see similar roles below...
Biopharmaceutical Manufacturing Associate - Contract - Cambridge, MA
Proclinical is seeking a Biopharmaceutical Manufacturing Associate for our client. This is a contract position located in Cambridge, MA.
Primary Responsibilities:
The successful candidate will be responsible for various manufacturing tasks, including setting up processes, ensuring room readiness, and completing necessary paperwork. This role offers the opportunity to lead key activities and progress your career in a dynamic and inclusive environment.
Skills & Requirements:
- Bachelor's degree in a biological, chemical science, engineering or equivalent professional experience.
- High School Diploma with manufacturing production, cGMP experience.
- Previous manufacturing or laboratory experience requiring aseptic or sterile technique.
- Mechanical aptitude to operate pumps, scales, and PH meters.
- Ability to maintain attention to detail and quality, and a high level of integrity and confidentiality.
- Ability to read, understand, follow and comply with technical and written documents (SOPs.)
- Ability to work around acids, bases, oxidizers and cleaning solvents while wearing appropriate PPE.
- Ability to perform calculations using simple mathematical formulas.
- Basic computer skills.
The Biopharmaceutical Manufacturing Associate will:
- Operate processing equipment in accordance with SOPs in all classified areas.
- Use proper aseptic technique while performing tasks in the ISO 7 and ISO 8 areas.
- Troubleshoot process equipment and interact with maintenance personnel.
- Load and unload materials, label according to SOPs, assemble valves, connectors.
- Report deviations or potential issues immediately to the management team.
- Comply with applicable EHS/GMP regulations, guidelines, policies, and standard operating & safety procedures.
- Complete and document daily manufacturing tasks per standard operating procedures, batch document instructions, and logbooks.
- Maintain a high level of competency with current and emerging digital platforms (SAP, EBR, AR/VR, etc).
If you are having difficulty in applying or if you have any questions, please contact Jackie Cerchio at (+1) 267-846-2026 or j.cerchio@proclinical.com.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
INDCQA
Related jobs
US$25 - US$30 per hour
Norton, USA
Proclinical is on the hunt for bold, innovative thinkers who are ready to help push the boundaries of science and make a tangible difference in the world.
Highly Competitive
Visp, Schweiz
Proclinical is seeking a QC Analyst to join our client's team in Switzerland.
Highly Competitive
Solothurn, Switzerland
Proclinical is seeking an Associate Quality Control professional to join our client's team in Switzerland.
Highly Competitive
Basel-Stadt, Schweiz
Are you passionate about quality and precision? Join our client as a dedicated Quality Manager and help ensure top-tier standards every day.
Highly Competitive
Visp, Switzerland
Proclinical is seeking a QC Associate to join the Bioanalytics Microbial Team at our client's facility.
US$0.00 - US$25 per hour + Highly Competitive Salary
Fremont, USA
Proclinical is seeking a Maintenance Technician to ensure the smooth operation of facility systems and equipment.
Highly Competitive
King of Prussia, USA
Are you passionate about quality and precision? Join our client as a GMP Cleaning Associate and help ensure top-tier standards every day.
Highly Competitive
Paris, France
Proclinical is seeking a dedicated professional to join our client's team as a Device Regulatory Documentation & Compliance Senior Manager.