Materials Control Associate

Materials Control Associate III

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.

Materials Control Associate

• Title: Materials Control Associate III
• Location: Harmans, MD (onsite)
• Industry: Pharmaceutical
• Hours: 7AM-7PM 2-2-3 rotating schedule: 2 on, 2 off, 3 on one week / 2 off, 2 on, and 3 off next week
• Salary: $35/ hour paid weekly with benefits options
• Employment Type: Contract: 6-months (potential for extension)

Environment: This role is responsible for supporting the overall GMP materials control/warehousing operations for BWI / Cavalier facility. The position requires practical experience and knowledge of a variety of activities such as materials receipt/quarantine/release, logistical support in a manufacturing facility, electronic inventory control.
The Manufacturing Associate III is accountable for the execution procedures for upstream manufacturing of clinical and commercial products. Supporting areas of upstream manufacturing by using SOP s and batch records to execute pre and post processing activities.

Job Scope:

• Collaborate with MST and development groups to assist with tech-transfer, scale-up, and translation activities.
• Will lead for one or more areas in upstream manufacturing as directed by the supervisor.
• Interface with engineering group to source new production equipment.
• Interface with Quality Assurance department to execute corrective actions / preventative actions.
• Represent the department to clients and on cross-functional project teams.
• Work with manufacturing manager and supervisors to develop and maintain training materials and curricula.
• Ability to work with bioreactor operation and cell culture including aseptic technique
• Execute and monitor critical processes supporting mammalian, microbial, and fill finish production facilities
• Solid experience with the following: large-scale centrifuges, washers, autoclaves
• Performs the weighing, dispensing of raw materials for media and buffers
• Performs the preparation of small and large volume media and buffer solutions, filtration and transfer of product.
• Operates bench top equipment including pH, conductivity, osmo meters, pumps, tubing welders, filter integrity testers etc.
• Dispensing, labeling, transfer/staging of raw materials and parts
• Assembly/disassembly, cleaning and sterilization of components, parts and equipment
• Ability to contribute to the development of new concepts, techniques, and standards
• Assist Facilities and Engineering personnel as necessary on equipment maintenance and calibration
• Interface with Quality Control department to submit in-process samples and coordinate environmental monitoring during key process steps.
• Provide support to cross-functional teams to meet production or timeline demands.
• Demonstrate understanding in scientific concepts, technical operations, safety, and Good Manufacturing Practice.
• Adhere to Quality standards and learn and comply with regulatory requirements.
• Provide suggestions for process optimization and efficiency, where applicable.
• Operate manufacturing equipment in assigned area
• Write standard operating procedures (SOP s) and other documents as necessary
• Complete manufacturing documents such as batch records, logbooks
• Assist in the execution of validation protocols

Skills Needed:

• Bachelor s degree in a Scientific, Engineering or Biotech field with 4 years experience with upstream (fermentation/bioreactor) biologic production processes under GMP compliance.
• OR HS Diploma or Associate s Degree with 5 6 years experience with upstream (fermentation/bioreactor) biologic production processes under GMP compliance.

EOE/ADA

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