SRG offers flexible staffing solutions with a national presence. We provide contract, contract-to-hire, direct hire and executive search services. SRG utilizes an innovative approach to identify and qualify talent that is unique to the Staffing industry, featuring a cutting-edge platform that allows us to rapidly and precisely match professionals to client requirements. We have a proprietary database of over one million candidates and maintain continuous contact with our qualified talent.
Environment: A global leader and trusted supplier in the pharma, biotech and specialty ingredients markets. Headquartered in Basel, Switzerland, the company is focused on advanced manufacturing, high-quality control systems, regulatory expertise, and research and development (R&D) capabilities. The company s products and services include active pharmaceutical ingredients (API), stem cell therapies, drinking water sanitizers, vitamin B compounds, organic personal care ingredients, industrial preservatives and microbial control solution to combat viruses, bacteria and other dangerous pathogens.
Title: Manufacturing Associate - Biotech
Location: Walkersville, MD
Hours: 3rd Shift - 11pm - 7am
Salary: Up to $27hr based on Experience paid weekly (Benefits Available)
Employment Type: Long Term Contract (Possible Extension)
The Manufacturing Associate is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions. Level I associates are expected to execute process recipes, follow written procedures (SOPs), monitor equipment and processes, perform basic laboratory tasks, including pH, conductivity, sampling, and conduct routine sanitization tasks to maintain facility and equipment. They are expected to attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique in handling of products and materials
Responsible for executing aseptic processing in a clean room environment adhering to Standard Operating Procedures (SOPs)
o Complete documentation concurrently with completion of manufacturing processes
o Responsible for performing personal and environmental monitoring
o Be able to gown aseptically and work in an aseptic environment
o Process production batches in a LFBSC (Laminar Flow Biological Safety Cabinet)
o Wrap and assemble filling materials in preparation for autoclaving
o Assist in drum filling operations when required
o Responsible for completing assigned tasks (for example, cleaning, lab setup etc.) related to departmental functions
o Perform preventative maintenance and general upkeep on equipment and facilities including environmental monitoring
o Responsible for reviewing SOPs, MBRs and other associated forms for revision; Revise SOPs, Batch Records or other documentation as needed.
o Review and sign manufacturing batch records
o Responsible for keeping current on all job relevant trainings
o Maintain accurate production bin inventory in responsible area.
o Assist in writing deviations and supporting investigations
o Assist in training entry level staff members
o Being available for business necessitated overtime is required
o High School Diploma or GED is required; Bachelor s degree in a life sciences, engineering or related field is preferred
o Working manufacturing or technical skills are required
o Questioning attitude to drive problem solving
o Ability to collaborate with cross-functional teams
o Ability to communicate effectively to share learning and provide training to manufacturing
o Must have the ability to work in a fast paced, high workload environment.
o Must be able to read and follow defined SOPs and policies, work independently and as part of a team on various manufacturing tasks, identify and communicate non-routine events.
o Must be proactive, action oriented, and have the ability to adapt to a change.
o Must have strong communication skills both verbally and written.
o Must be able to support other members of the team through mentoring and training.
Bioscience/biopharmaceutical experience preferred